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Zbigniew Wszolek
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71
Uitti, Ryan
61
Farrer, Matthew
49
dickson, dennis
26
Calne, Donald
25
Hutton, Michael
20
Ross, Owen
19
Gasser, Thomas
17
Aasly, Jan
16
Tsuboi, Yoshio
15
Boeve, Bradley
15
Baba, Yasuhiko
14
Hulihan, Mary
14
Lynch, Timothy
14
Stoessl, Jon
12
Kachergus, Jennifer
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All Publications
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2009: Dickson Dennis W; Braak Heiko; Duda John E; Duyckaerts Charles; Gasser Thomas; Halliday Glenda M; Hardy John; Leverenz James B; Del Tredici Kelly; Wszolek Zbigniew K; Litvan Irene
Neuropathological assessment of Parkinson's disease: refining the diagnostic criteria.
Lancet neurology 2009;8(12):1150-7.
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2009: Puschmann Andreas; Ross Owen A; Vilariño-Güell Carles; Lincoln Sarah J; Kachergus Jennifer M; Cobb Stephanie A; Lindquist Suzanne G; Nielsen Jørgen E; Wszolek Zbigniew K; Farrer Matthew; Widner Håkan; van Westen Danielle; Hägerström Douglas; Markopoulou Katerina; Chase Bruce A; Nilsson Karin; Reimer Jan; Nilsson Christer
A Swedish family with de novo alpha-synuclein A53T mutation: evidence for early cortical dysfunction.
Parkinsonism & related disorders 2009;15(9):627-32.
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2009: Krygowska-Wajs Anna; Cheshire William P; Wszolek Zbigniew K; Hubalewska-Dydejczyk Alicja; Jasinska-Myga Barbara; Farrer Matthew J; Moskala Marek; Sowa-Staszczak Anna
Evaluation of gastric emptying in familial and sporadic Parkinson disease.
Parkinsonism & related disorders 2009;15(9):692-6.
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2009: Cobb Stephanie A; Wider Christian; Ross Owen A; Mata Ignacio F; Adler Charles H; Rajput Alex; Rajput Ali H; Wu Ruey-Meei; Hauser Robert; Josephs Keith A; Carr Jonathan; Gwinn Katrina; Heckman Michael G; Aasly Jan O; Lynch Timothy; Uitti Ryan J; Wszolek Zbigniew K; Kapatos Gregory; Farrer Matthew J
GCH1 in early-onset Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2009;24(14):2070-5.
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2009: Wider Christian; Lincoln Sarah; Dachsel Justus C; Kapatos Gregory; Heckman Michael G; Diehl Nancy N; Papapetropoulos Spiridon; Mash Deborah; Rajput Alex; Rajput Ali H; Dickson Dennis W; Wszolek Zbigniew K; Farrer Matthew J
GCH1 expression in human cerebellum from healthy individuals is not gender dependent.
Neuroscience letters 2009;462(1):73-5.
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2009: Whitwell J L; Jack C R; Boeve B F; Senjem M L; Baker M; Ivnik R J; Knopman D S; Wszolek Z K; Petersen R C; Rademakers R; Josephs K A
Atrophy patterns in IVS10+16, IVS10+3, N279K, S305N, P301L, and V337M MAPT mutations.
Neurology 2009;73(13):1058-65.
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2009: Keeling Brett H; Vilariño-Güell Carles; Ross Owen A; Wszolek Zbigniew K; Uitti Ryan J; Farrer Matthew J
DRD3 Ser9Gly and HS1BP3 Ala265Gly are not associated with Parkinson disease.
Neuroscience letters 2009;461(2):74-5.
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2009: Jasinska-Myga B; Wider C; Opala G; Krygowska-Wajs A; Barcikowska M; Czyzewski K; Baker M; Rademakers R; Uitti R J; Farrer M J; Ross O A; Wszolek Z K
GRN 3'UTR+78 C>T is not associated with risk for Parkinson's disease.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2009;16(8):909-11.
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2009: Golub Yulia; Berg Daniela; Calne Donald B; Pfeiffer Ronald F; Uitti Ryan J; Stoessl A Jon; Wszolek Zbigniew K; Farrer Matthew J; Mueller Jakob C; Gasser Thomas; Fuchs Julia
Genetic factors influencing age at onset in LRRK2-linked Parkinson disease.
Parkinsonism & related disorders 2009;15(7):539-41.
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2009: Vilariño-Güell C; Chai H; Keeling B H; Young J E; Rajput A; Lynch T; Aasly J O; Uitti R J; Wszolek Z K; Farrer M J; Lin S-C
MEIS1 p.R272H in familial restless legs syndrome.
Neurology 2009;73(3):243-5.
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2009: Vilariño-Güell C; Wider C; Soto-Ortolaza A I; Cobb S A; Kachergus J M; Keeling B H; Dachsel J C; Hulihan M M; Dickson D W; Wszolek Z K; Uitti R J; Graff-Radford N R; Boeve B F; Josephs K A; Miller B; Boylan K B; Gwinn K; Adler C H; Aasly J O; Hentati F; Destée A; Krygowska-Wajs A; Chartier-Harlin M-C; Ross O A; Rademakers R; Farrer M J
Characterization of DCTN1 genetic variability in neurodegeneration.
Neurology 2009;72(23):2024-8.
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2009: Wider C; Van Gerpen J A; DeArmond S; Shuster E A; Dickson D W; Wszolek Z K
Leukoencephalopathy with spheroids (HDLS) and pigmentary leukodystrophy (POLD): a single entity?
Neurology 2009;72(22):1953-9.
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2009: Puschmann Andreas; Wszolek Zbigniew K; Farrer Matthew; Gustafson Lars; Widner Håkan; Nilsson Christer
Alpha-synuclein multiplications with parkinsonism, dementia or progressive myoclonus?
Parkinsonism & related disorders 2009;15(5):390-2.
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2009: Slowinski Jerzy L; Schweitzer Katherine J; Imamura Akiko; Uitti Ryan J; Strongosky Audrey J; Dickson Dennis W; Broderick Daniel F; Wszolek Zbigniew K
Brainstem atrophy on routine MR study in pallidopontonigral degeneration.
Journal of neurology 2009;256(5):827-9.
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2009: Wider Christian; Dickson Dennis W; Schweitzer Katherine J; Broderick Daniel F; Wszolek Zbigniew K
Familial idiopathic basal ganglia calcification: a challenging clinical-pathological correlation.
Journal of neurology 2009;256(5):839-42.
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2009: Hasegawa Kazuko; Stoessl A Jon; Yokoyama Teruo; Kowa Hisayuki; Wszolek Zbigniew K; Yagishita Saburo
Familial parkinsonism: study of original Sagamihara PARK8 (I2020T) kindred with variable clinicopathologic outcomes.
Parkinsonism & related disorders 2009;15(4):300-6.
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2009: Wider Christian; Dickson Dennis W; Stoessl A Jon; Tsuboi Yoshio; Chapon Françoise; Gutmann Ludwig; Lechevalier Bernard; Calne Donald B; Personett David A; Hulihan Mary; Kachergus Jennifer; Rademakers Rosa; Baker Matthew C; Grantier Linda L; Sujith O K; Brown Laura; Calne Susan; Farrer Matthew J; Wszolek Zbigniew K
Pallidonigral TDP-43 pathology in Perry syndrome.
Parkinsonism & related disorders 2009;15(4):281-6.
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2009: Wider Christian; Lincoln Sarah J; Heckman Michael G; Diehl Nancy N; Stone Jeremy T; Haugarvoll Kristoffer; Aasly Jan O; Gibson J Mark; Lynch Timothy; Rajput Alex; Rajput Michele L; Uitti Ryan J; Wszolek Zbigniew K; Farrer Matthew J; Ross Owen A
Phactr2 and Parkinson's disease.
Neuroscience letters 2009;453(1):9-11.
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2009: Ludolph A C; Kassubek J; Landwehrmeyer B G; Mandelkow E; Mandelkow E-M; Burn D J; Caparros-Lefebvre D; Frey K A; de Yebenes J G; Gasser T; Heutink P; Höglinger G; Jamrozik Z; Jellinger K A; Kazantsev A; Kretzschmar H; Lang A E; Litvan I; Lucas J J; McGeer P L; Melquist S; Oertel W; Otto M; Paviour D; Reum T; Saint-Raymond A; Steele J C; Tolnay M; Tumani H; van Swieten J C; Vanier M T; Vonsattel J-P; Wagner S; Wszolek Z K;
Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2009;16(3):297-309.
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2009: Whitwell J L; Jack C R; Boeve B F; Senjem M L; Baker M; Rademakers R; Ivnik R J; Knopman D S; Wszolek Z K; Petersen R C; Josephs K A
Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN.
Neurology 2009;72(9):813-20.
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2009: Vilariño-Güell Carles; Ross Owen A; Soto Alexandra I; Farrer Matthew J; Haugarvoll Kristoffer; Aasly Jan O; Uitti Ryan J; Wszolek Zbigniew K
Reported mutations in GIGYF2 are not a common cause of Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2009;24(4):619-20.
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2009: Haugarvoll Kristoffer; Toft Mathias; Skipper Lisa; Heckman Michael G; Crook Julia E; Soto Alexandra; Ross Owen A; Hulihan Mary M; Kachergus Jennifer M; Sando Sigrid B; White Linda R; Lynch Timothy; Gibson J Mark; Uitti Ryan J; Wszolek Zbigniew K; Aasly Jan O; Farrer Matthew J
Fine-mapping and candidate gene investigation within the PARK10 locus.
European journal of human genetics : EJHG 2009;17(3):336-43.
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2009: Young Jessica E; Vilariño-Güell Carles; Lin Siong-Chi; Wszolek Zbigniew K; Farrer Matthew J
Clinical and genetic description of a family with a high prevalence of autosomal dominant restless legs syndrome.
Mayo Clinic proceedings. Mayo Clinic 2009;84(2):134-8.
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2009: Farrer Matthew J; Hulihan Mary M; Kachergus Jennifer M; Dächsel Justus C; Stoessl A Jon; Grantier Linda L; Calne Susan; Calne Donald B; Lechevalier Bernard; Chapon Francoise; Tsuboi Yoshio; Yamada Tatsuo; Gutmann Ludwig; Elibol Bülent; Bhatia Kailash P; Wider Christian; Vilariño-Güell Carles; Ross Owen A; Brown Laura A; Castanedes-Casey Monica; Dickson Dennis W; Wszolek Zbigniew K
DCTN1 mutations in Perry syndrome.
Nature genetics 2009;41(2):163-5.
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2009: Wider Christian; Dachsel Justus C; Soto Alexandra I; Heckman Michael G; Diehl Nancy N; Yue Mei; Lincoln Sarah; Aasly Jan O; Haugarvoll Kristoffer; Trojanowski John Q; Papapetropoulos Spiridon; Mash Deborah; Rajput Alex; Rajput Ali H; Gibson J Mark; Lynch Timothy; Dickson Dennis W; Uitti Ryan J; Wszolek Zbigniew K; Farrer Matthew J; Ross Owen A
FGF20 and Parkinson's disease: no evidence of association or pathogenicity via alpha-synuclein expression.
Movement disorders : official journal of the Movement Disorder Society 2009;24(3):455-9.
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2009: Wider Christian; Wszolek Zbigniew K
Movement disorders: insights into mechanisms and hopes for treatment.
Lancet neurology 2009;8(1):8-10.
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2009: Imamura Akiko; Wszolek Zbigniew K; Lucas John A; Dickson Dennis W
Corticobasal syndrome with Alzheimer's disease pathology.
Movement disorders : official journal of the Movement Disorder Society 2009;24(1):152-3; author reply 153.
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2009: Xiao Jianfeng; Bastian Robert W; Perlmutter Joel S; Racette Brad A; Tabbal Samer D; Karimi Morvarid; Paniello Randal C; Blitzer Andrew; Batish Sat Dev; Wszolek Zbigniew K; Uitti Ryan J; Hedera Peter; Simon David K; Tarsy Daniel; Truong Daniel D; Frei Karen P; Pfeiffer Ronald F; Gong Suzhen; Zhao Yu; LeDoux Mark S
High-throughput mutational analysis of TOR1A in primary dystonia.
BMC medical genetics 2009;10():24.
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2008: Rademakers Rosa; Eriksen Jason L; Baker Matt; Robinson Todd; Ahmed Zeshan; Lincoln Sarah J; Finch Nicole; Rutherford Nicola J; Crook Richard J; Josephs Keith A; Boeve Bradley F; Knopman David S; Petersen Ronald C; Parisi Joseph E; Caselli Richard J; Wszolek Zbigniew K; Uitti Ryan J; Feldman Howard; Hutton Michael L; Mackenzie Ian R; Graff-Radford Neill R; Dickson Dennis W
Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia.
Human molecular genetics 2008;17(23):3631-42.
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2008: Nandhagopal R; Mak E; Schulzer M; McKenzie J; McCormick S; Sossi V; Ruth T J; Strongosky A; Farrer M J; Wszolek Z K; Stoessl A J
Progression of dopaminergic dysfunction in a LRRK2 kindred: a multitracer PET study.
Neurology 2008;71(22):1790-5.
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2008: Strongosky Audrey J; Farrer Matthew; Wszolek Zbigniew K
Are Parkinson disease patients protected from some but not all cancers?
Neurology 2008;71(20):1650; author reply 1650-1.
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2008: Ross Owen A; Soto Alexandra I; Vilariño-Güell Carles; Heckman Michael G; Diehl Nancy N; Hulihan Mary M; Aasly Jan O; Sando Sigrid; Gibson J Mark; Lynch Timothy; Krygowska-Wajs Anna; Opala Grzegorz; Barcikowska Maria; Czyzewski Krzysztof; Uitti Ryan J; Wszolek Zbigniew K; Farrer Matthew J
Genetic variation of Omi/HtrA2 and Parkinson's disease.
Parkinsonism & related disorders 2008;14(7):539-43.
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2008: Ross Owen A; Heckman Michael G; Soto Alexandra I; Diehl Nancy N; Haugarvoll Kristoffer; Vilariño-Güell Carles; Aasly Jan O; Sando Sigrid; Gibson J Mark; Lynch Timothy; Krygowska-Wajs Anna; Opala Grzegorz; Barcikowska Maria; Czyzewski Krzysztof; Uitti Ryan J; Wszolek Zbigniew K; Farrer Matthew J
Dopamine beta-hydroxylase -1021C>T association and Parkinson's disease.
Parkinsonism & related disorders 2008;14(7):544-7.
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2008: Van Gerpen J A; Wider C; Broderick D F; Dickson D W; Brown L A; Wszolek Z K
Insights into the dynamics of hereditary diffuse leukoencephalopathy with axonal spheroids.
Neurology 2008;71(12):925-9.
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2008: DelleDonne Anthony; Klos Kevin J; Fujishiro Hiroshige; Ahmed Zeshan; Parisi Joseph E; Josephs Keith A; Frigerio Roberta; Burnett Melinda; Wszolek Zbigniew K; Uitti Ryan J; Ahlskog J Eric; Dickson Dennis W
Incidental Lewy body disease and preclinical Parkinson disease.
Archives of neurology 2008;65(8):1074-80.
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2008: Wider C; Skipper L; Solida A; Brown L; Farrer M; Dickson D; Wszolek Z K; Vingerhoets F J G
Autosomal dominant dopa-responsive parkinsonism in a multigenerational Swiss family.
Parkinsonism & related disorders 2008;14(6):465-70.
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2008: Vilariño-Güell C; Soto A I; Young J E; Lin S-C; Uitti R J; Wszolek Z K; Farrer M J
Susceptibility genes for restless legs syndrome are not associated with Parkinson disease.
Neurology 2008;71(3):222-3.
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2008: Fujishiro Hiroshige; Ferman Tanis J; Boeve Bradley F; Smith Glenn E; Graff-Radford Neill R; Uitti Ryan J; Wszolek Zbigniew K; Knopman David S; Petersen Ronald C; Parisi Joseph E; Dickson Dennis W
Validation of the neuropathologic criteria of the third consortium for dementia with Lewy bodies for prospectively diagnosed cases.
Journal of neuropathology and experimental neurology 2008;67(7):649-56.
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2008: Healy Daniel G; Falchi Mario; O'Sullivan Sean S; Bonifati Vincenzo; Durr Alexandra; Bressman Susan; Brice Alexis; Aasly Jan; Zabetian Cyrus P; Goldwurm Stefano; Ferreira Joaquim J; Tolosa Eduardo; Kay Denise M; Klein Christine; Williams David R; Marras Connie; Lang Anthony E; Wszolek Zbigniew K; Berciano Jose; Schapira Anthony H V; Lynch Timothy; Bhatia Kailash P; Gasser Thomas; Lees Andrew J; Wood Nicholas W;
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study.
Lancet neurology 2008;7(7):583-90.
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2008: Markopoulou K; Dickson D W; McComb R D; Wszolek Z K; Katechalidou L; Avery L; Stansbury M S; Chase B A
Clinical, neuropathological and genotypic variability in SNCA A53T familial Parkinson's disease. Variability in familial Parkinson's disease.
Acta neuropathologica 2008;116(1):25-35.
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2008: Wider Christian; Uitti Ryan J; Wszolek Zbigniew K; Fang John Y; Josephs Keith A; Baker Matthew C; Rademakers Rosa; Hutton Michael L; Dickson Dennis W
Progranulin gene mutation with an unusual clinical and neuropathologic presentation.
Movement disorders : official journal of the Movement Disorder Society 2008;23(8):1168-73.
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2008: Haugarvoll K; Rademakers R; Kachergus J M; Nuytemans K; Ross O A; Gibson J M; Tan E-K; Gaig C; Tolosa E; Goldwurm S; Guidi M; Riboldazzi G; Brown L; Walter U; Benecke R; Berg D; Gasser T; Theuns J; Pals P; Cras P; De Deyn P Paul; Engelborghs S; Pickut B; Uitti R J; Foroud T; Nichols W C; Hagenah J; Klein C; Samii A; Zabetian C P; Bonifati V; Van Broeckhoven C; Farrer M J; Wszolek Z K
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease.
Neurology 2008;70(16 Pt 2):1456-60.
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2008: Imamura A; Geda Y E; Slowinski J; Wszolek Z K; Brown L A; Uitti R J
Medications used to treat Parkinson's disease and the risk of gambling.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2008;15(4):350-4.
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2008: Wider C; Melquist S; Hauf M; Solida A; Cobb S A; Kachergus J M; Gass J; Coon K D; Baker M; Cannon A; Stephan D A; Schorderet D F; Ghika J; Burkhard P R; Kapatos G; Hutton M; Farrer M J; Wszolek Z K; Vingerhoets F J G
Study of a Swiss dopa-responsive dystonia family with a deletion in GCH1: redefining DYT14 as DYT5.
Neurology 2008;70(16 Pt 2):1377-83.
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2008: Tsuboi Yoshio; Dickson Dennis W; Nabeshima Kazuki; Schmeichel Ann M; Wszolek Zbigniew K; Yamada Tatsuo; Benarroch Eduardo E
Neurodegeneration involving putative respiratory neurons in Perry syndrome.
Acta neuropathologica 2008;115(2):263-8.
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2008: Slowinski Jerzy; Imamura Akiko; Uitti Ryan J; Pooley Robert A; Strongosky Audrey J; Dickson Dennis W; Broderick Daniel F; Wszolek Zbigniew K
MR imaging of brainstem atrophy in progressive supranuclear palsy.
Journal of neurology 2008;255(1):37-44.
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2008: Rutherford Nicola J; Zhang Yong-Jie; Baker Matt; Gass Jennifer M; Finch Nicole A; Xu Ya-Fei; Stewart Heather; Kelley Brendan J; Kuntz Karen; Crook Richard J P; Sreedharan Jemeen; Vance Caroline; Sorenson Eric; Lippa Carol; Bigio Eileen H; Geschwind Daniel H; Knopman David S; Mitsumoto Hiroshi; Petersen Ronald C; Cashman Neil R; Hutton Mike; Shaw Christopher E; Boylan Kevin B; Boeve Bradley; Graff-Radford Neill R; Wszolek Zbigniew K; Caselli Richard J; Dickson Dennis W; Mackenzie Ian R; Petrucelli Leonard; Rademakers Rosa
Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis.
PLoS genetics 2008;4(9):e1000193.
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2008: Wider Christian; Wszolek Zbigniew K
Etiology and pathophysiology of frontotemporal dementia, Parkinson disease and Alzheimer disease: lessons from genetic studies.
Neuro-degenerative diseases 2008;5(3-4):122-5.
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2008: Wider Christian; Wszolek Zbigniew K
Rapidly progressive familial parkinsonism with central hypoventilation, depression and weight loss (Perry syndrome)--a literature review.
Parkinsonism & related disorders 2008;14(1):1-7.
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2007: Boeve B F; Silber M H; Saper C B; Ferman T J; Dickson D W; Parisi J E; Benarroch E E; Ahlskog J E; Smith G E; Caselli R C; Tippman-Peikert M; Olson E J; Lin S-C; Young T; Wszolek Z; Schenck C H; Mahowald M W; Castillo P R; Del Tredici K; Braak H
Pathophysiology of REM sleep behaviour disorder and relevance to neurodegenerative disease.
Brain : a journal of neurology 2007;130(Pt 11):2770-88.
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2007: Rademakers Rosa; Baker Matt; Gass Jennifer; Adamson Jennifer; Huey Edward D; Momeni Parastoo; Spina Salvatore; Coppola Giovanni; Karydas Anna M; Stewart Heather; Johnson Nancy; Hsiung Ging-Yuek; Kelley Brendan; Kuntz Karen; Steinbart Ellen; Wood Elisabeth McCarty; Yu Chang-En; Josephs Keith; Sorenson Eric; Womack Kyle B; Weintraub Sandra; Pickering-Brown Stuart M; Schofield Peter R; Brooks William S; Van Deerlin Vivianna M; Snowden Julie; Clark Christopher M; Kertesz Andrew; Boylan Kevin; Ghetti Bernardino; Neary David; Schellenberg Gerard D; Beach Thomas G; Mesulam Marsel; Mann David; Grafman Jordan; Mackenzie Ian R; Feldman Howard; Bird Thomas; Petersen Ron; Knopman David; Boeve Bradley; Geschwind Dan H; Miller Bruce; Wszolek Zbigniew; Lippa Carol; Bigio Eileen H; Dickson Dennis; Graff-Radford Neill; Hutton Mike
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.
Lancet neurology 2007;6(10):857-68.
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2007: Ross Owen A; Haugarvoll Kristoffer; Stone Jeremy T; Heckman Michael G; White Linda R; Aasly Jan O; Mark Gibson J; Lynch Timothy; Wszolek Zbigniew K; Uitti Ryan J; Farrer Matthew J
Lack of evidence for association of Parkin promoter polymorphism (PRKN-258) with increased risk of Parkinson's disease.
Parkinsonism & related disorders 2007;13(7):386-8.
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2007: Bogaerts Veerle; Engelborghs Sebastiaan; Kumar-Singh Samir; Goossens Dirk; Pickut Barbara; van der Zee Julie; Sleegers Kristel; Peeters Karin; Martin Jean-Jacques; Del-Favero Jurgen; Gasser Thomas; Dickson Dennis W; Wszolek Zbigniew K; De Deyn Peter P; Theuns Jessie; Van Broeckhoven Christine
A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorder.
Brain : a journal of neurology 2007;130(Pt 9):2277-91.
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2007: Miklossy Judith; Qing Hong; Guo Jian-Ping; Yu Sheng; Wszolek Zbigniew K; Calne Donald; McGeer Edith G; McGeer Patrick L
Lrrk2 and chronic inflammation are linked to pallido-ponto-nigral degeneration caused by the N279K tau mutation.
Acta neuropathologica 2007;114(3):243-54.
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2007: Haugarvoll Kristoffer; Wszolek Zbigniew K; Hutton Michael
The genetics of frontotemporal dementia.
Neurologic clinics 2007;25(3):697-715, vi.
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2007: Whaley N R; Putzke John D; Baba Yasuhiko; Wszolek Zbigniew K; Uitti Ryan J
Essential tremor: phenotypic expression in a clinical cohort.
Parkinsonism & related disorders 2007;13(6):333-9.
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2007: Melrose H L; Kent C B; Taylor J P; Dachsel J C; Hinkle K M; Lincoln S J; Mok S S; Culvenor J G; Masters C L; Tyndall G M; Bass D I; Ahmed Z; Andorfer C A; Ross O A; Wszolek Z K; Delldonne A; Dickson D W; Farrer M J
A comparative analysis of leucine-rich repeat kinase 2 (Lrrk2) expression in mouse brain and Lewy body disease.
Neuroscience 2007;147(4):1047-58.
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2007: Baba Y; Baker M C; Le Ber I; Brice A; Maeck L; Kohlhase J; Yasuda M; Stoppe G; Bugiani O; Sperfeld A D; Tsuboi Y; Uitti R J; Farrer M J; Ghetti B; Hutton M L; Wszolek Z K
Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation.
Journal of neural transmission (Vienna, Austria : 1996) 2007;114(7):947-50.
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2007: Arvanitakis Zoe; Witte Robert J; Dickson Dennis W; Tsuboi Yoshio; Uitti Ryan J; Slowinski Jerzy; Hutton Michael L; Lin Siong-Chi; Boeve Bradley F; Cheshire William P; Pooley Robert A; Liss Julie M; Caviness John N; Strongosky Audrey J; Wszolek Zbigniew K
Clinical-pathologic study of biomarkers in FTDP-17 (PPND family with N279K tau mutation).
Parkinsonism & related disorders 2007;13(4):230-9.
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2007: Berger Zdenek; Roder Hanno; Hanna Amanda; Carlson Aaron; Rangachari Vijayaraghavan; Yue Mei; Wszolek Zbigniew; Ashe Karen; Knight Joshua; Dickson Dennis; Andorfer Cathy; Rosenberry Terrone L; Lewis Jada; Hutton Mike; Janus Christopher
Accumulation of pathological tau species and memory loss in a conditional model of tauopathy.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2007;27(14):3650-62.
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2007: Melquist Stacey; Craig David W; Huentelman Matthew J; Crook Richard; Pearson John V; Baker Matt; Zismann Victoria L; Gass Jennifer; Adamson Jennifer; Szelinger Szabolcs; Corneveaux Jason; Cannon Ashley; Coon Keith D; Lincoln Sarah; Adler Charles; Tuite Paul; Calne Donald B; Bigio Eileen H; Uitti Ryan J; Wszolek Zbigniew K; Golbe Lawrence I; Caselli Richard J; Graff-Radford Neill; Litvan Irene; Farrer Matthew J; Dickson Dennis W; Hutton Mike; Stephan Dietrich A
Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.
American journal of human genetics 2007;80(4):769-78.
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2007: Taylor Julie P; Hulihan Mary M; Kachergus Jennifer M; Melrose Heather L; Lincoln Sarah J; Hinkle Kelly M; Stone Jeremy T; Ross Owen A; Hauser Robert; Aasly Jan; Gasser Thomas; Payami Haydeh; Wszolek Zbigniew K; Farrer Matthew J
Leucine-rich repeat kinase 1: a paralog of LRRK2 and a candidate gene for Parkinson's disease.
Neurogenetics 2007;8(2):95-102.
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2007: Baba Yasuhiko; Uitti Ryan J; Boylan Kevin B; Uehara Yoshinari; Yamada Tatsuo; Farrer Matthew J; Couchon Elizabeth; Batish Sat Dev; Wszolek Zbigniew K
Aprataxin (APTX) gene mutations resembling multiple system atrophy.
Parkinsonism & related disorders 2007;13(3):139-42.
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2007: Lippa C F; Duda J E; Grossman M; Hurtig H I; Aarsland D; Boeve B F; Brooks D J; Dickson D W; Dubois B; Emre M; Fahn S; Farmer J M; Galasko D; Galvin J E; Goetz C G; Growdon J H; Gwinn-Hardy K A; Hardy J; Heutink P; Iwatsubo T; Kosaka K; Lee V M-Y; Leverenz J B; Masliah E; McKeith I G; Nussbaum R L; Olanow C W; Ravina B M; Singleton A B; Tanner C M; Trojanowski J Q; Wszolek Z K;
DLB and PDD boundary issues: diagnosis, treatment, molecular pathology, and biomarkers.
Neurology 2007;68(11):812-9.
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2007: Haugarvoll Kristoffer; Toft Mathias; Ross Owen A; Stone Jeremy T; Heckman Michael G; White Linda R; Lynch Timothy; Gibson John Mark; Wszolek Zbigniew K; Uitti Ryan J; Aasly Jan O; Farrer Matthew J
ELAVL4, PARK10, and the Celts.
Movement disorders : official journal of the Movement Disorder Society 2007;22(4):585-7.
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2007: Whittle A J; Ross O A; Naini A; Gordon P; Mistumoto H; Dächsel J C; Stone J T; Wszolek Z K; Farrer M J; Przedborski S
Pathogenic Lrrk2 substitutions and Amyotrophic lateral sclerosis.
Journal of neural transmission (Vienna, Austria : 1996) 2007;114(3):327-9.
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2007: Slowinski Jerzy; Dominik Jake; Uitti Ryan J; Ahmed Zeshan; Dickson Dennis D; Wszolek Zbigniew K
Frontotemporal dementia and Parkinsonism linked to chromosome 17 with the N279K tau mutation.
Neuropathology : official journal of the Japanese Society of Neuropathology 2007;27(1):73-80.
-
2007: Frank Andrew R; Wszolek Zbigniew K; Jack Clifford R; Boeve Bradley F
Distinctive MRI findings in pallidopontonigral degeneration (PPND).
Neurology 2007;68(8):620-1.
-
2007: Wszolek Zbigniew K; Brown Laura A
Prevalence and clinical characteristics of restless legs syndrome in Japanese patients with Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2007;22(2):284.
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2007: Imamura Akiko; Wszolek Zbigniew; Uitti Ryan
Neurodegenerative overlap syndrome: Parkinsonism and motor neuron disorder.
Movement disorders : official journal of the Movement Disorder Society 2007;22(1):151-2.
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2007: Wider Christian; Wszolek Zbigniew K
Clinical genetics of Parkinson's disease and related disorders.
Parkinsonism & related disorders 2007;13 Suppl 3():S229-32.
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2006: Chabolla David R; Wszolek Zbigniew K
Pharmacologic management of seizures in organ transplant.
Neurology 2006;67(12 Suppl 4):S34-8.
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2006: Ferman Tanis J; Smith Glenn E; Boeve Bradley F; Graff-Radford Neill R; Lucas John A; Knopman David S; Petersen Ronald C; Ivnik Robert J; Wszolek Zbigniew; Uitti Ryan; Dickson Dennis W
Neuropsychological differentiation of dementia with Lewy bodies from normal aging and Alzheimer's disease.
The Clinical neuropsychologist 2006;20(4):623-36.
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2006: Imamura Akiko; Uitti Ryan J; Wszolek Zbigniew K
Dopamine agonist therapy for Parkinson disease and pathological gambling.
Parkinsonism & related disorders 2006;12(8):506-8.
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2006: Putzke J D; Whaley N R; Baba Y; Wszolek Z K; Uitti R J
Essential tremor: predictors of disease progression in a clinical cohort.
Journal of neurology, neurosurgery, and psychiatry 2006;77(11):1235-7.
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2006: Gass Jennifer; Cannon Ashley; Mackenzie Ian R; Boeve Bradley; Baker Matt; Adamson Jennifer; Crook Richard; Melquist Stacey; Kuntz Karen; Petersen Ron; Josephs Keith; Pickering-Brown Stuart M; Graff-Radford Neill; Uitti Ryan; Dickson Dennis; Wszolek Zbigniew; Gonzalez John; Beach Thomas G; Bigio Eileen; Johnson Nancy; Weintraub Sandra; Mesulam Marsel; White Charles L; Woodruff Bryan; Caselli Richard; Hsiung Ging-Yuek; Feldman Howard; Knopman Dave; Hutton Mike; Rademakers Rosa
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration.
Human molecular genetics 2006;15(20):2988-3001.
-
2006: Brodkin Cynthia L; Wszolek Zbigniew K
Neurologic presentation of Erdheim-Chester disease.
Neurologia i neurochirurgia polska 2006;40(5):397-403.
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2006: Haugarvoll Kristoffer; Uitti Ryan J; Farrer Matthew J; Wszolek Zbigniew K
LRRK2 gene and tremor-dominant parkinsonism.
Archives of neurology 2006;63(9):1346-7.
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2006: Ishihara Lianna; Warren Liling; Gibson Rachel; Amouri Rim; Lesage Suzanne; Dürr Alexandra; Tazir Meriem; Wszolek Zbigniew K; Uitti Ryan J; Nichols William C; Griffith Alida; Hattori Nobutaka; Leppert David; Watts Ray; Zabetian Cyrus P; Foroud Tatiana M; Farrer Matthew J; Brice Alexis; Middleton Lefkos; Hentati Faycal
Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations.
Archives of neurology 2006;63(9):1250-4.
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2006: Baba Yasuhiko; Uitti Ryan J; Farrer Matthew J; Wszolek Zbigniew K
Atypical Parkinsonism and SCA8.
Parkinsonism & related disorders 2006;12(6):396.
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2006: Baba Yasuhiko; Putzke John D; Tsuboi Yoshio; Josephs Keith A; Thomas Natalie; Wszolek Zbigniew K; Dickson Dennis W
Effect of MAPT and APOE on prognosis of progressive supranuclear palsy.
Neuroscience letters 2006;405(1-2):116-9.
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2006: Wszolek Z K; Baba Y; Mackenzie I R; Uitti R J; Strongosky A J; Broderick D F; Baker M C; Melquist S; Hutton M L; Tsuboi Y; Allanson J E; Carr J; Kumar A; Calne S M; Miklossy J; McGeer P L; Calne D B; Stoessl A J
Autosomal dominant dystonia-plus with cerebral calcifications.
Neurology 2006;67(4):620-5.
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2006: Liss Julie M; Krein-Jones Kari; Wszolek Zbigniew K; Caviness John N
Speech characteristics of patients with pallido-ponto-nigral degeneration and their application to presymptomatic detection in at-risk relatives.
American journal of speech-language pathology / American Speech-Language-Hearing Association 2006;15(3):226-35.
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2006: Shiarli A-M; Jennings R; Shi J; Bailey K; Davidson Y; Tian J; Bigio E H; Ghetti B; Murrell J R; Delisle M B; Mirra S; Crain B; Zolo P; Arima K; Iseki E; Murayama S; Kretzschmar H; Neumann M; Lippa C; Halliday G; Mackenzie J; Khan N; Ravid R; Dickson D; Wszolek Z; Iwatsubo T; Pickering-Brown S M; Mann D M A
Comparison of extent of tau pathology in patients with frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration with Pick bodies and early onset Alzheimer's disease.
Neuropathology and applied neurobiology 2006;32(4):374-87.
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2006: Haugarvoll Kristoffer; Wszolek Zbigniew K
PARK8 LRRK2 parkinsonism.
Current neurology and neuroscience reports 2006;6(4):287-94.
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2006: Farrer Matthew J; Haugarvoll Kristoffer; Ross Owen A; Stone Jeremy T; Milkovic Nicole M; Cobb Stephanie A; Whittle Andrew J; Lincoln Sarah J; Hulihan Mary M; Heckman Michael G; White Linda R; Aasly Jan O; Gibson J Mark; Gosal David; Lynch Timothy; Wszolek Zbigniew K; Uitti Ryan J; Toft Mathias
Genomewide association, Parkinson disease, and PARK10.
American journal of human genetics 2006;78(6):1084-8; author reply 1092-4.
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2006: Baba Yasuhiko; Putzke John D; Whaley Nathaniel R; Wszolek Zbigniew K; Uitti Ryan J
Progressive supranuclear palsy: phenotypic sex differences in a clinical cohort.
Movement disorders : official journal of the Movement Disorder Society 2006;21(5):689-92.
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2006: Hirano S; Shinotoh H; Kobayashi T; Tsuboi Y; Wszolek Z K; Aotsuka A; Tanaka N; Ota T; Fukushi K; Tanada S; Irie T
Brain acetylcholinesterase activity in FTDP-17 studied by PET.
Neurology 2006;66(8):1276-7.
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2006: Baba Yasuhiko; Markopoulou Katerina; Putzke John D; Whaley Nathaniel R; Farrer Matthew J; Wszolek Zbigniew K; Uitti Ryan J
Phenotypic commonalities in familial and sporadic Parkinson disease.
Archives of neurology 2006;63(4):579-83.
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2006: de Silva Rohan; Lashley Tammaryn; Strand Catherine; Shiarli Anna-Maria; Shi Jing; Tian Jinzhou; Bailey Kathryn L; Davies Peter; Bigio Eileen H; Arima Kunimasa; Iseki Eizo; Murayama Shigeo; Kretzschmar Hans; Neumann Manuela; Lippa Carol; Halliday Glenda; MacKenzie James; Ravid Rivka; Dickson Dennis; Wszolek Zbigniew; Iwatsubo Takeshi; Pickering-Brown Stuart M; Holton Janice; Lees Andrew; Revesz Tamas; Mann David M A
An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R- and 4R-specific tau monoclonal antibodies.
Acta neuropathologica 2006;111(4):329-40.
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2006: Baba Yasuhiko; Ghetti Bernardino; Baker Matthew C; Uitti Ryan J; Hutton Michael L; Yamaguchi Keiji; Bird Thomas; Lin Wenlang; DeLucia Michael W; Dickson Dennis W; Wszolek Zbigniew K
Hereditary diffuse leukoencephalopathy with spheroids: clinical, pathologic and genetic studies of a new kindred.
Acta neuropathologica 2006;111(4):300-11.
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2006: Wszolek Z K; Slowinski J; Imamura A; Tsuboi Y; Broderick D F
New and reliable MRI diagnosis for progressive supranuclear palsy.
Neurology 2006;66(5):781; author reply 781.
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2006: Di Fonzo Alessio; Tassorelli Cristina; De Mari Michele; Chien Hsin F; Ferreira Joaquim; Rohé Christan F; Riboldazzi Giulio; Antonini Angelo; Albani Gianni; Mauro Alessandro; Marconi Roberto; Abbruzzese Giovanni; Lopiano Leonardo; Fincati Emiliana; Guidi Marco; Marini Paolo; Stocchi Fabrizio; Onofrj Marco; Toni Vincenzo; Tinazzi Michele; Fabbrini Giovanni; Lamberti Paolo; Vanacore Nicola; Meco Giuseppe; Leitner Petra; Uitti Ryan J; Wszolek Zbigniew K; Gasser Thomas; Simons Erik J; Breedveld Guido J; Goldwurm Stefano; Pezzoli Gianni; Sampaio Cristina; Barbosa Egberto; Martignoni Emilia; Oostra Ben A; Bonifati Vincenzo;
Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease.
European journal of human genetics : EJHG 2006;14(3):322-31.
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2006: Boeve Bradley F; Lin Siong-Chi; Strongosky Audrey; Dickson Dennis W; Wszolek Zbigniew K
Absence of rapid eye movement sleep behavior disorder in 11 members of the pallidopontonigral degeneration kindred.
Archives of neurology 2006;63(2):268-72.
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2006: Ross Owen A; Toft Mathias; Whittle Andrew J; Johnson Joseph L; Papapetropoulos Spiridon; Mash Deborah C; Litvan Irene; Gordon Mark F; Wszolek Zbigniew K; Farrer Matthew J; Dickson Dennis W
Lrrk2 and Lewy body disease.
Annals of neurology 2006;59(2):388-93.
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2006: Mata Ignacio F; Bodkin Cynthia L; Adler Charles H; Lin Siong-Chi; Uitti Ryan J; Farrer Matthew J; Wszolek Zbigniew K
Genetics of restless legs syndrome.
Parkinsonism & related disorders 2006;12(1):1-7.
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2006: Baba Yasuhiko; Tsuboi Yoshio; Inoue Hirosato; Yamada Tatsuo; Wszolek Zbigniew K; Broderick Daniel F
Acute measles encephalitis in adults.
Journal of neurology 2006;253(1):121-4.
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2006: Klodowska-Duda Gabriela; Slowinski Jerzy; Opala Grzegorz; Gorzkowska Agnieszka; Jasinska-Myga Barbara; Wszolek Zbigniew K; Dickson Dennis W
Corticobasal degeneration -- clinico-pathological considerations.
Folia neuropathologica / Association of Polish Neuropathologists and Medical Research Centre, Polish Academy of Sciences 2006;44(4):257-64.
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2006: Uitti R J; Wszolek Z K
Concerning neuroprotective therapy for Parkinson's disease.
Journal of neural transmission. Supplementum 2006;(70):433-7.
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2006: Whaley N R; Uitti R J; Dickson D W; Farrer M J; Wszolek Z K
Clinical and pathologic features of families with LRRK2-associated Parkinson's disease.
Journal of neural transmission. Supplementum 2006;(70):221-9.
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2006: Wszolek Zbigniew K; Tsuboi Yoshio; Ghetti Bernardino; Pickering-Brown Stuart; Baba Yasuhiko; Cheshire William P
Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17).
Orphanet journal of rare diseases 2006;1():30.
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2005: Mata Ignacio F; Kachergus Jennifer M; Taylor Julie P; Lincoln Sarah; Aasly Jan; Lynch Timothy; Hulihan Mary M; Cobb Stephanie A; Wu Ruey-Meei; Lu Chin-Song; Lahoz Carlos; Wszolek Zbigniew K; Farrer Matthew J
Lrrk2 pathogenic substitutions in Parkinson's disease.
Neurogenetics 2005;6(4):171-7.
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2005: Baba Yasuhiko; Kuroiwa Ataru; Uitti Ryan J; Wszolek Zbigniew K; Yamada Tatsuo
Alterations of T-lymphocyte populations in Parkinson disease.
Parkinsonism & related disorders 2005;11(8):493-8.
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2005: Adams John R; van Netten Hinke; Schulzer Michael; Mak Edwin; Mckenzie Jessamyn; Strongosky Audrey; Sossi Vesna; Ruth Thomas J; Lee Chong S; Farrer Matthew; Gasser Thomas; Uitti Ryan J; Calne Donald B; Wszolek Zbigniew K; Stoessl A Jon
PET in LRRK2 mutations: comparison to sporadic Parkinson's disease and evidence for presymptomatic compensation.
Brain : a journal of neurology 2005;128(Pt 12):2777-85.
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2005: Krygowska-Wajs A; Kachergus J M; Hulihan M M; Farrer M J; Searcy J A; Booij J; Berendse H W; Wolters E Ch; Wszolek Z K
Clinical and genetic evaluation of 8 Polish families with levodopa-responsive parkinsonism.
Journal of neural transmission (Vienna, Austria : 1996) 2005;112(11):1487-502.
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2005: Baba Yasuhiko; Putzke John D; Whaley Nathaniel R; Wszolek Zbigniew K; Uitti Ryan J
Gender and the Parkinson's disease phenotype.
Journal of neurology 2005;252(10):1201-5.
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2005: Baba Yasuhiko; Hentschel Kenneth; Freeman William D; Broderick Daniel F; Wszolek Zbigniew K
Large paraspinal and iliopsoas muscle hematomas.
Archives of neurology 2005;62(8):1306.
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2005: Bodkin Cynthia L; Maurer Kenneth B; Wszolek Zbigniew K
Botulinum toxin type A therapy during pregnancy.
Movement disorders : official journal of the Movement Disorder Society 2005;20(8):1081-2; author reply 1082.
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2005: Strauss Karsten M; Martins L Miguel; Plun-Favreau Helene; Marx Frank P; Kautzmann Sabine; Berg Daniela; Gasser Thomas; Wszolek Zbginiew; Müller Thomas; Bornemann Antje; Wolburg Hartwig; Downward Julian; Riess Olaf; Schulz Jörg B; Krüger Rejko
Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease.
Human molecular genetics 2005;14(15):2099-111.
-
2005: Uitti R J; Baba Y; Whaley N R; Wszolek Z K; Putzke J D
Parkinson disease: handedness predicts asymmetry.
Neurology 2005;64(11):1925-30.
-
2005: Miklossy Judit; Mackenzie Ian R; Dorovini-Zis Katerina; Calne Donald B; Wszolek Zbigniew K; Klegeris Andis; McGeer Patrick L
Severe vascular disturbance in a case of familial brain calcinosis.
Acta neuropathologica 2005;109(6):643-53.
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2005: Baba Yasuhiko; Tsuboi Yoshio; Baker Matthew C; Uitti Ryan J; Hutton Michael L; Dickson Dennis W; Farrer Matthew; Putzke John D; Woodruff Bryan K; Ghetti Bernardino; Murrell Jill R; Boeve Bradley F; Petersen Ronald C; Verpillat Patrice; Brice Alexis; Delisle Marie-Bernadette; Rascol Oliver; Arima Kunimasa; Dysken Maurice W; Yasuda Minoru; Kobayashi Tomonori; Sunohara Nobuhiko; Komure Osamu; Kuno Sadako; Sperfeld Anne D; Stoppe Gabriela; Kohlhase Jürgen; Pickering-Brown Stuart; Neary David; Bugiani Orso; Wszolek Zbigniew K
The effect of tau genotype on clinical features in FTDP-17.
Parkinsonism & related disorders 2005;11(4):205-8.
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2005: Baba Yasuhiko; Broderick Daniel F; Uitti Ryan J; Hutton Michael L; Wszolek Zbigniew K
Heredofamilial brain calcinosis syndrome.
Mayo Clinic proceedings. Mayo Clinic 2005;80(5):641-51.
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2005: Putzke J D; Uitti R J; Obwegeser A A; Wszolek Z K; Wharen R E
Bilateral thalamic deep brain stimulation: midline tremor control.
Journal of neurology, neurosurgery, and psychiatry 2005;76(5):684-90.
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2005: Baba Yasuhiko; Uitti Ryan J; Farrer Matthew J; Wszolek Zbigniew K
Sporadic SCA8 mutation resembling corticobasal degeneration.
Parkinsonism & related disorders 2005;11(3):147-50.
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2005: Uitti Ryan J; Baba Yasuhiko; Wszolek Zbigniew K; Putzke D John
Defining the Parkinson's disease phenotype: initial symptoms and baseline characteristics in a clinical cohort.
Parkinsonism & related disorders 2005;11(3):139-45.
-
2005: Freeman William; Wszolek Zbigniew
Botulinum toxin type A for treatment of spasticity in spinocerebellar ataxia type 3 (Machado-Joseph disease).
Movement disorders : official journal of the Movement Disorder Society 2005;20(5):644.
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2005: Josephs Keith A; Uchikado Hirotake; McComb Rodney D; Bashir Rifaat; Wszolek Zbigniew; Swanson Jerry; Matsumoto Joseph; Shaw Gerry; Dickson Dennis W
Extending the clinicopathological spectrum of neurofilament inclusion disease.
Acta neuropathologica 2005;109(4):427-32.
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2005: Kachergus Jennifer; Mata Ignacio F; Hulihan Mary; Taylor Julie P; Lincoln Sarah; Aasly Jan; Gibson J Mark; Ross Owen A; Lynch Timothy; Wiley Joseph; Payami Haydeh; Nutt John; Maraganore Demetrius M; Czyzewski Krzysztof; Styczynska Maria; Wszolek Zbigniew K; Farrer Matthew J; Toft Mathias
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations.
American journal of human genetics 2005;76(4):672-80.
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2005: Eriksen Jason L; Wszolek Zbigniew; Petrucelli Leonard
Molecular pathogenesis of Parkinson disease.
Archives of neurology 2005;62(3):353-7.
-
2005: Toft Mathias; Aasly Jan; Bisceglio Gina; Adler Charles H; Uitti Ryan J; Krygowska-Wajs Anna; Lynch Timothy; Wszolek Zbigniew K; Farrer Matthew J
Parkinsonism, FXTAS, and FMR1 premutations.
Movement disorders : official journal of the Movement Disorder Society 2005;20(2):230-3.
-
2005: Cheshire William P; Wszolek Zbigniew K
Body mass index is reduced early in Parkinson's disease.
Parkinsonism & related disorders 2005;11(1):35-8.
-
2005: Wszolek Zbigniew K; Slowinski Jerzy; Golan Maciej; Dickson Dennis W
Frontotemporal dementia and parkinsonism linked to chromosome 17.
Folia neuropathologica / Association of Polish Neuropathologists and Medical Research Centre, Polish Academy of Sciences 2005;43(4):258-70.
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2004: Oliveira J R M; Spiteri E; Sobrido M J; Hopfer S; Klepper J; Voit T; Gilbert J; Wszolek Z K; Calne D B; Stoessl A J; Hutton M; Manyam B V; Boller F; Baquero M; Geschwind D H
Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease).
Neurology 2004;63(11):2165-7.
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2004: Uitti Ryan J; Calne Donald B; Dickson Dennis W; Wszolek Zbigniew K
Is the neuropathological 'gold standard' diagnosis dead? Implications of clinicopathological findings in an autosomal dominant neurodegenerative disorder.
Parkinsonism & related disorders 2004;10(8):461-3.
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2004: Zimprich Alexander; Biskup Saskia; Leitner Petra; Lichtner Peter; Farrer Matthew; Lincoln Sarah; Kachergus Jennifer; Hulihan Mary; Uitti Ryan J; Calne Donald B; Stoessl A Jon; Pfeiffer Ronald F; Patenge Nadja; Carbajal Iria Carballo; Vieregge Peter; Asmus Friedrich; Müller-Myhsok Bertram; Dickson Dennis W; Meitinger Thomas; Strom Tim M; Wszolek Zbigniew K; Gasser Thomas
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.
Neuron 2004;44(4):601-7.
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2004: Putzke J D; Wharen R E; Obwegeser A A; Wszolek Z K; Lucas J A; Turk M F; Uitti R J
Thalamic deep brain stimulation for essential tremor: recommendations for long-term outcome analysis.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2004;31(3):333-42.
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2004: Woodruff Bryan K; Baba Yasuhiko; Hutton Michael L; Wszolek Zbigniew K; Tsuboi Yoshio; Kobayashi Tomonori; Ghetti Bernardino; Arima Kunimasa; Yasuda Minoru; Rascol Olivier
Haplotype-phenotype correlations in kindreds with the N279K mutation in the tau gene.
Archives of neurology 2004;61(8):1327; author reply 1327.
-
2004: Kumar Ajit; Calne Susan M; Schulzer Michael; Mak Edwin; Wszolek Zbigniew; Van Netten Chris; Tsui Joseph K C; Stoessl A Jon; Calne Donald B
Clustering of Parkinson disease: shared cause or coincidence?
Archives of neurology 2004;61(7):1057-60.
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2004: van Twillert G; van Eeden S; Nellen F J B; Cornelissen M; Wszolek Z; Westermann A M
Spinal cord compression due to Kaposi's sarcoma.
Annals of oncology : official journal of the European Society for Medical Oncology / ESMO 2004;15(7):1143-4.
-
2004: Furtado Sarah; Payami Haydeh; Lockhart Paul J; Hanson Melissa; Nutt John G; Singleton Andrew A; Singleton Amanda; Bower Jamel; Utti Ryan J; Bird Thomas D; de la Fuente-Fernandez Raul; Tsuboi Yoshio; Klimek Mary L; Suchowersky Oksana; Hardy John; Calne Donald B; Wszolek Zbigniew K; Farrer Matthew; Gwinn-Hardy Katrina; Stoessl A Jon
Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).
Movement disorders : official journal of the Movement Disorder Society 2004;19(6):622-9.
-
2004: Wszolek Z K; Pfeiffer R F; Tsuboi Y; Uitti R J; McComb R D; Stoessl A J; Strongosky A J; Zimprich A; Müller-Myhsok B; Farrer M J; Gasser T; Calne D B; Dickson D W
Autosomal dominant parkinsonism associated with variable synuclein and tau pathology.
Neurology 2004;62(9):1619-22.
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2004: Krygowska-Wajs Anna; Wszolek Zbigniew
[Advances in the genetic studies in Parkinson's disease]
Neurologia i neurochirurgia polska 2004;38(2):127-36.
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2004: Farrer Matt; Kachergus Jennifer; Forno Lysia; Lincoln Sarah; Wang Deng-Shun; Hulihan Mary; Maraganore Demetrius; Gwinn-Hardy Katrina; Wszolek Zbigniew; Dickson Dennis; Langston J William
Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplications.
Annals of neurology 2004;55(2):174-9.
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2004: Zimprich Alexander; Müller-Myhsok Bertram; Farrer Matthew; Leitner Petra; Sharma Manu; Hulihan Mary; Lockhart Paul; Strongosky Audrey; Kachergus Jennifer; Calne Donald B; Stoessl Jon; Uitti Ryan J; Pfeiffer Ronald F; Trenkwalder Claudia; Homann Nikolaus; Ott Erwin; Wenzel Karoline; Asmus Friedrich; Hardy John; Wszolek Zbigniew; Gasser Thomas
The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing interval.
American journal of human genetics 2004;74(1):11-9.
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2003: Baba Yasuhiko; Wszolek Zbigniew K; Normand Marlene M
Paroxysmal kinesigenic dyskinesia associated with central pontine myelinolysis.
Parkinsonism & related disorders 2003;10(2):113.
-
2003: Putzke J D; Wharen R E; Wszolek Z K; Turk M F; Strongosky A J; Uitti R J
Thalamic deep brain stimulation for tremor-predominant Parkinson's disease.
Parkinsonism & related disorders 2003;10(2):81-8.
-
2003: Tsuboi Y; Wszolek Z K; Graff-Radford N R; Cookson N; Dickson D W
Tau pathology in the olfactory bulb correlates with Braak stage, Lewy body pathology and apolipoprotein epsilon4.
Neuropathology and applied neurobiology 2003;29(5):503-10.
-
2003: Cordes Michael; Wszolek Zbigniew K
Deafness and cerebral plasticity.
Journal of nuclear medicine : official publication, Society of Nuclear Medicine 2003;44(9):1440-2.
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2003: Tsuboi Y; Slowinski J; Josephs K A; Honer W G; Wszolek Z K; Dickson D W
Atrophy of superior cerebellar peduncle in progressive supranuclear palsy.
Neurology 2003;60(11):1766-9.
-
2003: Ferman T J; McRae C A; Arvanitakis Z; Tsuboi Y; Vo A; Wszolek Z K
Early and pre-symptomatic neuropsychological dysfunction in the PPND family with the N279K tau mutation.
Parkinsonism & related disorders 2003;9(5):265-70.
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2003: Slowinski Jerzy; Wharen Robert E; Uitti Ryan J; Wszolek Zbigniew K; Krygowska-Wajs Anna; Mrówka Ryszard
[Current therapies for parkinson's disease. Part II: surgical treatment]
Neurologia i neurochirurgia polska 2003;37(3):677-86.
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2003: Krygowska-Wajs Anna; Wszolek Zbigniew K; Uitti Ryan J; Slowinski Jerzy; Szczudlik Andrzej
[The current therapies for parkinson's disease. Part I: pharmacological treatment]
Neurologia i neurochirurgia polska 2003;37(3):665-76.
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2003: Krygowska-Wajs Anna; Hussey Jennifer M; Hulihan Mary; Farrer Matthew J; Tsuboi Yoshio; Uitti Ryan J; Wszolek Zbigniew K
Two large Polish kindreds with levodopa-responsive Parkinsonism not linked to known Parkinsonian genes and loci.
Parkinsonism & related disorders 2003;9(4):193-200.
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2003: Tsuboi Yoshio; Wszolek Zbigniew K; Mizuno Yoshikuni; Kobayashi Tomonori; Yasuda Minoru; Yamada Tatsuo
[Japanese contribution to the understanding of frontotemporal dementia and parkinsonism linked to chromosome 17(FTDP-17)]
No to shinkei = Brain and nerve 2003;55(2):107-19.
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2003: Tsuboi Y; Uitti R J; Baker M; Hutton M L; Wszolek Z K
Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation.
Neurology 2003;60(3):525-6.
-
2003: Wszolek Zbigniew K; Krygowska-Wajs Anna; Barcikowska Maria
[Fronto-temporal dementia and parkinsonism linked to chromosome 17 (FTDP-17): clinical criteria]
Neurologia i neurochirurgia polska 2003;37(1):173-84.
-
2003: Caviness John N; Tsuboi Yoshio; Wszolek Zbigniew K
Clinical-electrophysiological correlation of tremor and myoclonus in a kindred with the N279K tau mutation.
Parkinsonism & related disorders 2003;9(3):151-7.
-
2003: Kobayashi Hirokazu; Krüger Rejko; Markopoulou Katerina; Wszolek Zbigniew; Chase Bruce; Taka Hikaru; Mineki Reiko; Murayama Kimie; Riess Olaf; Mizuno Yoshikuni; Hattori Nobutaka
Haploinsufficiency at the alpha-synuclein gene underlies phenotypic severity in familial Parkinson's disease.
Brain : a journal of neurology 2003;126(Pt 1):32-42.
-
2003: Uitti Ryan J; Wszolek Zbigniew K
Dopamine agonists, sleep disorders, and driving in Parkinson's disease.
Advances in neurology 2003;91():343-9.
-
2003: Wszolek Zbigniew K; Tsuboi Yoshio; Farrer Mathew; Uitti Ryan J; Hutton Mike L
Hereditary tauopathies and parkinsonism.
Advances in neurology 2003;91():153-63.
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2002: Tsuboi Y; Baker M; Hutton M L; Uitti R J; Rascol O; Delisle M-B; Soulages X; Murrell J R; Ghetti B; Yasuda M; Komure O; Kuno S; Arima K; Sunohara N; Kobayashi T; Mizuno Y; Wszolek Z K
Clinical and genetic studies of families with the tau N279K mutation (FTDP-17).
Neurology 2002;59(11):1791-3.
-
2002: Uitti Ryan J; Tsuboi Yoshio; Pooley Robert A; Putzke John D; Turk Margaret F; Wszolek Zbigniew K; Witte Robert J; Wharen Robert E
Magnetic resonance imaging and deep brain stimulation.
Neurosurgery 2002;51(6):1423-28; discussion 1428-31.
-
2002: Cheshire William P; Tsuboi Yoshio; Wszolek Zbigniew K
Physiologic assessment of autonomic dysfunction in pallidopontonigral degeneration with N279K mutation in the tau gene on chromosome 17.
Autonomic neuroscience : basic & clinical 2002;102(1-2):71-7.
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2002: Furtado S; Farrer M; Tsuboi Y; Klimek M L; de la Fuente-Fernández R; Hussey J; Lockhart P; Calne D B; Suchowersky O; Stoessl A J; Wszolek Z K
SCA-2 presenting as parkinsonism in an Alberta family: clinical, genetic, and PET findings.
Neurology 2002;59(10):1625-7.
-
2002: Kock Norman; Müller Birgitt; Vieregge Peter; Pramstaller Peter P; Marder Karen; Abbruzzese Giovanni; Martinelli Paolo; Lang Anthony E; Jacobs Helfried; Hagenah Johann; Harris Juliette; Meija-Santana Helen; Fahn Stanley; Hedrich Katja; Kann Martin; Gehlken Ulrike; Culjkovic Biljana; Schwinger Eberhard; Wszolek Zbigniew K; Zühlke Christine; Klein Christine
Role of SCA2 mutations in early- and late-onset dopa-responsive parkinsonism.
Annals of neurology 2002;52(2):257-8; author reply 258.
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2002: Tsuboi Yoshio; Uitti Ryan J; Delisle Marie-Bernadette; Ferreira Joaquim J; Brefel-Courbon Christine; Rascol Olivier; Ghetti Bernardino; Murrell Jill R; Hutton Michael; Baker Matthew; Wszolek Zbigniew K
Clinical features and disease haplotypes of individuals with the N279K tau gene mutation: a comparison of the pallidopontonigral degeneration kindred and a French family.
Archives of neurology 2002;59(6):943-50.
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2002: Tsuboi Y; Wszolek Z K; Kusuhara T; Doh-ura K; Yamada T
Japanese family with parkinsonism, depression, weight loss, and central hypoventilation.
Neurology 2002;58(7):1025-30.
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2002: Wszolek Z K; Gwinn-Hardy K; Wszolek E K; Muenter M D; Pfeiffer R F; Rodnitzky R L; Uitti R J; McComb R D; Gasser T; Dickson D W
Neuropathology of two members of a German-American kindred (Family C) with late onset parkinsonism.
Acta neuropathologica 2002;103(4):344-50.
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2002: Lockhart Paul J; Holtom Benjamin; Lincoln Sarah; Hussey Jennifer; Zimprich Alexander; Gasser Thomas; Wszolek Zbigniew K; Hardy John; Farrer Matthew J
The human sideroflexin 5 (SFXN5) gene: sequence, expression analysis and exclusion as a candidate for PARK3.
Gene 2002;285(1-2):229-37.
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2002: Farrer Matt; Hardy John; Hutton Mike; Maraganore Demetrius; Tsuboi Yoshio; Wszolek Zbigniew K
Identifying genetic factors in Parkinson disease.
JAMA : the journal of the American Medical Association 2002;287(6):715-6.
-
2002: Hussey Jennifer; Lockhart Paul J; Seltzer William; Wszolek Zbigniew K; Payami Haydeh; Hanson Melissa; Gwinn-Hardy Katrina; Farrer Matt
Accurate determination of ataxin-2 polyglutamine expansion in patients with intermediate-range repeats.
Genetic testing 2002;6(3):217-20.
-
2002: Caviness John N; Wszolek Zbigniew K
Myoclonus in pallido-ponto-nigral degeneration.
Advances in neurology 2002;89():35-9.
-
2001: West A B; Zimprich A; Lockhart P J; Farrer M; Singleton A; Holtom B; Lincoln S; Hofer A; Hill L; Müller-Myhsok B; Wszolek Z K; Hardy J; Gasser T
Refinement of the PARK3 locus on chromosome 2p13 and the analysis of 14 candidate genes.
European journal of human genetics : EJHG 2001;9(9):659-66.
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2001: Pal P K; Wszolek Z K; Uitti R; Markopoulou K; Calne S M; Stoessl A J; Calne D B
Positron emission tomography of dopamine pathways in familial Parkinsonian syndromes.
Parkinsonism & related disorders 2001;8(1):51-6.
-
2001: Arvanitakis Z; Wszolek Z K
Recent advances in the understanding of tau protein and movement disorders.
Current opinion in neurology 2001;14(4):491-7.
-
2001: Wszolek Z K; Tsuboi Y; Uitti R J; Reed L; Hutton M L; Dickson D W
Progressive supranuclear palsy as a disease phenotype caused by the S305S tau gene mutation.
Brain : a journal of neurology 2001;124(Pt 8):1666-70.
-
2001: Wszolek Z K; Kardon R H; Wolters E C; Pfeiffer R F
Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17): PPND family. A longitudinal videotape demonstration.
Movement disorders : official journal of the Movement Disorder Society 2001;16(4):756-60.
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2001: McRae C A; Diem G; Yamazaki T G; Mitek A; Wszolek Z K
Interest in genetic testing in pallido-ponto-nigral degeneration (PPND): a family with frontotemporal dementia with Parkinsonism linked to chromosome 17.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2001;8(2):179-83.
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2001: Reed L A; Wszolek Z K; Hutton M
Phenotypic correlations in FTDP-17.
Neurobiology of aging 2001;22(1):89-107.
-
2001: Zink M; Grim L; Wszolek Z K; Gasser T
Autosomal-dominant Parkinson's disease linked to 2p13 is not caused by mutations in transforming growth factor alpha (TGF alpha) (short communication).
Journal of neural transmission (Vienna, Austria : 1996) 2001;108(8-9):1029-34.
-
2001: Wszolek Z K; Uitti R J; Markopoulou K
Familial Parkinson's disease and related conditions. Clinical genetics.
Advances in neurology 2001;86():33-43.
-
2000: Wszolek Z K; Tsuboi Y; Uitti R J; Reed L
Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene.
Neurology 2000;55(12):1939.
-
2000: Wszolek Z K; Uitti R J; Hutton M
A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration.
Neurology 2000;54(10):2028-30.
-
2000: Lynch H T; McComb R D; Osborn N K; Wolpert P A; Lynch J F; Wszolek Z K; Sidransky D; Steg R E
Predominance of brain tumors in an extended Li-Fraumeni (SBLA) kindred, including a case of Sturge-Weber syndrome.
Cancer 2000;88(2):433-9.
-
1999: Wszolek Z K; Markopoulou K
Molecular genetics of familial parkinsonism.
Parkinsonism & related disorders 1999;5(4):145-55.
-
1999: Samii A; Markopoulou K; Wszolek Z K; Sossi V; Dobko T; Mak E; Calne D B; Stoessl A J
PET studies of parkinsonism associated with mutation in the alpha-synuclein gene.
Neurology 1999;53(9):2097-102.
-
1999: Markopoulou K; Wszolek Z K; Pfeiffer R F; Chase B A
Reduced expression of the G209A alpha-synuclein allele in familial Parkinsonism.
Annals of neurology 1999;46(3):374-81.
-
1999: Steg R E; Kessinger A; Wszolek Z K
Cortical blindness and seizures in a patient receiving FK506 after bone marrow transplantation.
Bone marrow transplantation 1999;23(9):959-62.
-
1999: Wszolek Z K; Koller W C
Rare and unusual parkinsonian syndromes.
Advances in neurology 1999;80():369-76.
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1998: Hong M; Zhukareva V; Vogelsberg-Ragaglia V; Wszolek Z; Reed L; Miller B I; Geschwind D H; Bird T D; McKeel D; Goate A; Morris J C; Wilhelmsen K C; Schellenberg G D; Trojanowski J Q; Lee V M
Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17.
Science (New York, N.Y.) 1998;282(5395):1914-7.
-
1998: Clark L N; Poorkaj P; Wszolek Z; Geschwind D H; Nasreddine Z S; Miller B; Li D; Payami H; Awert F; Markopoulou K; Andreadis A; D'Souza I; Lee V M; Reed L; Trojanowski J Q; Zhukareva V; Bird T; Schellenberg G; Wilhelmsen K C
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17.
Proceedings of the National Academy of Sciences of the United States of America 1998;95(22):13103-7.
-
1998: Wszolek Z K; Lagerlund T D; Steg R E; McManis P G
Clinical neurophysiologic findings in patients with rapidly progressive familial parkinsonism and dementia with pallido-ponto-nigral degeneration.
Electroencephalography and clinical neurophysiology 1998;107(3):213-22.
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1998: Reed L A; Schmidt M L; Wszolek Z K; Balin B J; Soontornniyomkij V; Lee V M; Trojanowski J Q; Schelper R L
The neuropathology of a chromosome 17-linked autosomal dominant parkinsonism and dementia ("pallido-ponto-nigral degeneration").
Journal of neuropathology and experimental neurology 1998;57(6):588-601.
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1998: Vaughan J R; Farrer M J; Wszolek Z K; Gasser T; Durr A; Agid Y; Bonifati V; DeMichele G; Volpe G; Lincoln S; Breteler M; Meco G; Brice A; Marsden C D; Hardy J; Wood N W
Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. The European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD).
Human molecular genetics 1998;7(4):751-3.
-
1998: Gasser T; Müller-Myhsok B; Wszolek Z K; Oehlmann R; Calne D B; Bonifati V; Bereznai B; Fabrizio E; Vieregge P; Horstmann R D
A susceptibility locus for Parkinson's disease maps to chromosome 2p13.
Nature genetics 1998;18(3):262-5.
-
1998: Wszolek Z K; Markopoulou K
Olfactory dysfunction in Parkinson's disease.
Clinical neuroscience (New York, N.Y.) 1998;5(2):94-101.
-
1997: Wszolek Z K; Vieregge P; Uitti R J; Gasser T; Yasuhara O; McGeer P; Berry K; Calne D B; Vingerhoets F J; Klein C; Pfeiffer R F
German-Canadian family (family A) with parkinsonism, amyotrophy, and dementia - Longitudinal observations.
Parkinsonism & related disorders 1997;3(3):125-39.
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1997: Markopoulou K; Larsen K W; Wszolek E K; Denson M A; Lang A E; Pfeiffer R F; Wszolek Z K
Olfactory dysfunction in familial parkinsonism.
Neurology 1997;49(5):1262-7.
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1997: Denson M A; Wszolek Z K; Pfeiffer R F; Wszolek E K; Paschall T M; McComb R D
Familial parkinsonism, dementia, and Lewy body disease: study of family G.
Annals of neurology 1997;42(4):638-43.
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1997: Gasser T; Müller-Myhsok B; Wszolek Z K; Dürr A; Vaughan J R; Bonifati V; Meco G; Bereznai B; Oehlmann R; Agid Y; Brice A; Wood N
Genetic complexity and Parkinson's disease.
Science (New York, N.Y.) 1997;277(5324):388-9; author reply 389.
-
1997: Wszolek Z K; Lynch T; Wilhelmsen K C
Rapidly progressive autosomal dominant Parkinsonism and dementia with Pallido-Ponto-Nigral Gegeneration (PPND) and Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex (DDPAC) are clinically distinct conditions that are both linked to 17q21-22.
Parkinsonism & related disorders 1997;3(2):67-76.
-
1997: Wszolek Z K; Steg R E; Armitage J O
Complex partial status epilepticus after bone marrow transplantation for non-Hodgkin's lymphoma.
Bone marrow transplantation 1997;19(6):637-8.
-
1997: Wszolek Z K; Steg R E
Seizures after orthotopic liver transplantation.
Seizure : the journal of the British Epilepsy Association 1997;6(1):31-9.
-
1996: Kishore A; Wszolek Z K; Snow B J; de la Fuente-Fernandez R; Arwert F; Wijker M; Schulzer M; Calne D B; Vingerhoets F J
Presynaptic nigrostriatal function in genetically tested asymptomatic relatives from the pallido-ponto-nigral degeneration family.
Neurology 1996;47(6):1588-90.
-
1996: Edwards L L; Wszolek Z K; Normand M M
Neurophysiologic evaluation of cyclosporine toxicity associated with bone marrow transplantation.
Acta neurologica Scandinavica 1996;94(5):358-64.
-
1996: Gasser T; Müller-Myhsok B; Supala A; Zimmer E; Wieditz G; Wszolek Z K; Vieregge P; Bonifati V; Oertel W H
The CYP2D6B allele is not overrepresented in a population of German patients with idiopathic Parkinson's disease.
Journal of neurology, neurosurgery, and psychiatry 1996;61(5):518-20.
-
1996: Wszolek Z K; McCashland T M; Witte R J; Brandenberg G A; Steg R E
Spinal epidural abscess in a liver transplant recipient.
Transplantation proceedings 1996;28(5):2978-9.
-
1996: Chelimsky G; Wszolek Z; Chelimsky T C
Gastrointestinal dysfunction in autonomic neuropathy.
Seminars in neurology 1996;16(3):259-68.
-
1996: Pavletic Z S; Bishop M R; Markopoulou K; Wszolek Z K
Drug-induced parkinsonism after allogeneic bone marrow transplantation.
Bone marrow transplantation 1996;17(6):1185-7.
-
1996: Wszolek Z K; Peeiffer R F; Denson M A; McComb R D
Danish-American family (family E) with 'Parkinson's Disease': Pitfalls of genetic studies.
Parkinsonism & related disorders 1996;2(1):47-9.
-
1996: Steg R E; Wszolek Z K
Electroencephalographic abnormalities in liver transplant recipients: practical considerations and review.
Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society 1996;13(1):60-8.
-
1996: Wijker M; Wszolek Z K; Wolters E C; Rooimans M A; Pals G; Pfeiffer R F; Lynch T; Rodnitzky R L; Wilhelmsen K C; Arwert F
Localization of the gene for rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration to chromosome 17q21.
Human molecular genetics 1996;5(1):151-4.
-
1996: Normand M M; Ashraf W; Quigley E M; Maurer K B; Edwards L; Pfeiffer R F; Wszolek Z K
Simultaneous electromyography and manometry of the anal sphincters in parkinsonian patients: technical considerations.
Muscle & nerve 1996;19(1):110-1.
-
1996: Gasser T; Wszolek Z; Supala A; Trofatter J; Ozelius L; Uitti R J; Pfeiffer R F; Gusella J; Calne D; Breakefield X O
Genetic linkage studies in autosomal dominantly inherited L-DOPA responsive parkinsonism. Evaluation of candidate genes.
Advances in neurology 1996;69():87-95.
-
1995: Edwards L L; Wszolek Z K; Normand M M
Neurophysiologic evaluation of cyclosporine toxicity associated with bone marrow transplantation.
Acta neurologica Scandinavica 1995;92(5):423-9.
-
1995: Wilhelmsen K C; Wszolek Z K
Is there a genetic susceptibility to idiopathic parkinsonism?
Parkinsonism & related disorders 1995;1(2):73-84.
-
1995: Wszolek Z K; Steg R E
Seizures after liver transplantation.
Liver transplantation and surgery : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society 1995;1(5):334-9.
-
1995: Ashraf W; Wszolek Z K; Pfeiffer R F; Normand M; Maurer K; Srb F; Edwards L L; Quigley E M
Anorectal function in fluctuating (on-off) Parkinson's disease: evaluation by combined anorectal manometry and electromyography.
Movement disorders : official journal of the Movement Disorder Society 1995;10(5):650-7.
-
1995: Markopoulou K; Wszolek Z K; Pfeiffer R F
A Greek-American kindred with autosomal dominant, levodopa-responsive parkinsonism and anticipation.
Annals of neurology 1995;38(3):373-8.
-
1995: Denson M A; Wszolek Z K
Familial parkinsonism: Our experience and review.
Parkinsonism & related disorders 1995;1(1):35-46.
-
1995: Ellingson R J; Wszolek Z K; Kendall J D; Donovan J P; Schafer D F
Brainstem auditory evoked potentials in liver transplant candidates.
The Nebraska medical journal 1995;80(7):167-70.
-
1995: Normand M M; Wszolek Z K; Klass D W
Temporal intermittent rhythmic delta activity in electroencephalograms.
Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society 1995;12(3):280-4.
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1995: Edwards L L; Normand M M; Wszolek Z K
Cervical dystonia: a review the role of botulinum toxin.
The Nebraska medical journal 1995;80(5):109-15.
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1995: Wszolek Z K; Pfeiffer B; Fulgham J R; Parisi J E; Thompson B M; Uitti R J; Calne D B; Pfeiffer R F
Western Nebraska family (family D) with autosomal dominant parkinsonism.
Neurology 1995;45(3 Pt 1):502-5.
-
1995: Wszolek Z K; Groover R V; Klass D W
Seizures presenting as episodic hypersomnolence.
Epilepsia 1995;36(1):108-10.
-
1994: Gasser T; Wszolek Z K; Trofatter J; Ozelius L; Uitti R J; Lee C S; Gusella J; Pfeiffer R F; Calne D B; Breakefield X O
Genetic linkage studies in autosomal dominant parkinsonism: evaluation of seven candidate genes.
Annals of neurology 1994;36(3):387-96.
-
1993: Wszolek Z K; Cordes M; Calne D B; Münter M D; Cordes I; Pfeifer R F
[Hereditary Parkinson disease: report of 3 families with dominant autosomal inheritance]
Der Nervenarzt 1993;64(5):331-5.
-
1992: Wszolek Z K; Pfeiffer R F; Bhatt M H; Schelper R L; Cordes M; Snow B J; Rodnitzky R L; Wolters E C; Arwert F; Calne D B
Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration.
Annals of neurology 1992;32(3):312-20.
-
1992: Wszolek Z K; Pfeiffer R F
Genetic considerations in movement disorders.
Current opinion in neurology and neurosurgery 1992;5(3):324-30.
-
1992: Herkes G K; Wszolek Z K; Westmoreland B F; Klass D W
Effects of midazolam on electroencephalograms of seriously ill patients.
Mayo Clinic proceedings. Mayo Clinic 1992;67(4):334-8.
-
1992: Wszolek Z K; Herkes G K; Lagerlund T D; Kokmen E
Comparison of EEG background frequency analysis, psychologic test scores, short test of mental status, and quantitative SPECT in dementia.
Journal of geriatric psychiatry and neurology 1992;5(1):22-30.
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1991: Wszolek Z K; Aksamit A J; Ellingson R J; Sharbrough F W; Westmoreland B F; Pfeiffer R F; Steg R E; de Groen P C
Epileptiform electroencephalographic abnormalities in liver transplant recipients.
Annals of neurology 1991;30(1):37-41.
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1990: Wszolek Z K; Williams D P; Kyle R A
Benedykt Dybowski--physician, explorer, scientist, political prisoner.
Mayo Clinic proceedings. Mayo Clinic 1990;65(10):1381.
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1990: Steg R E; Lefkowitz D M; Wszolek Z; Jordan A A
Optic nerve enlargement in acute optic neuritis.
The Nebraska medical journal 1990;75(10):284-7.
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1989: Wszolek Z K; McComb R D; Pfeiffer R F; Steg R E; Wood R P; Shaw B W; Markin R S
Pontine and extrapontine myelinolysis following liver transplantation. Relationship to serum sodium.
Transplantation 1989;48(6):1006-12.
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1989: Gasecki A P; Mawk J R; Hahn F J; Wszolek Z K; McComb R D; Bennett D R
Neurocysticercosis: a case report.
The Nebraska medical journal 1989;74(9):275-9.
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1989: Steg R E; Lefkowitz D M; Wszolek Z; Sison A S; Hahn F
Clinical diagnostic imaging. Cerebral venous thrombosis.
The Nebraska medical journal 1989;74(2):37-41.
-
1988: Sullivan J M; Wszolek Z K; Lund G; Pfeiffer R F
Thoracic outlet syndrome.
Neurosurgery 1988;23(2):271-2.
-
1988: Sullivan J M; Wszolek Z K; Lund G; Pfeiffer R F
Magnetic resonance imaging in thoracic outlet syndrome.
The Nebraska medical journal 1988;73(3):70-2.
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1988: Wszolek Z; Monsour H; Smith P; Pfeiffer R
Cryptococcal meningoencephalitis with parkinsonian features.
Movement disorders : official journal of the Movement Disorder Society 1988;3(3):271-3.
-
1987: Wszolek Z K; Schima E J; Phalen J J
Arteriovenous malformation of the brain.
The Nebraska medical journal 1987;72(12):404-5.
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1987: Wszolek Z; Monsour H; Smith P
"Erroneous elevation of creatinine caused by 5-fluorocytosine".
The Nebraska medical journal 1987;72(8):289.
-
1982: Wszolek Z
[Echoencephalographic studies in stroke]
Polski tygodnik lekarski (Warsaw, Poland : 1960) 1982;37(12):337-8.
-
1982: Wszolek Z; Hawranek M
[Traumatic spinal cord syndromes of the cervical spine]
Chirurgia narzadów ruchu i ortopedia polska 1982;47(3):153-7.
-
1981: Wszolek Z
[Unusual course of complicated migraine]
Neurologia i neurochirurgia polska 1981;15(4):515.
-
1980: Wszolek Z; Hawranek M
[Echoencephalography in the diagnosis of craniocerebral injuries]
Polski tygodnik lekarski (Warsaw, Poland : 1960) 1980;35(6):195-7.
-
1979: Gladych-Kielc I; Wszolek Z
[Case of narcolepsy with attacks of cataplexy, parahypnotic paralysis and hypnagogic hallucinations]
Wiadomosci lekarskie (Warsaw, Poland : 1960) 1979;32(24):1775-6.
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1978: Glowacki B; Wszolek Z
[Case of hemiphlegic migraine with atypical angiographic findings]
Neurologia i neurochirurgia polska 1978;12(4):795-6.
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