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TG Nygaard

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Johann Hagenah; Rachel Saunders-Pullman; Katja Hedrich; Kemal Kabakci; K Habermann; Karin Wiegers; Kathrin Mohrmann; Thora Lohnau; Deborah Raymond; Peter Vieregge; TG Nygaard; Laurie J Ozelius; Susan Bressman; Christine Klein
High mutation rate in dopa-responsive dystonia: detection with comprehensive GCHI screening.
Rachel Saunders-Pullman; N Blau; Keith Hyland; J Zschocke; TG Nygaard; Deborah Raymond; Vicki Shanker; Kathrin Mohrmann; L Arnold; SD Tabbal; D DeLeon; Blair Ford; Mitchell F Brin; S Chouinard; Laurie J Ozelius; Christine Klein; Susan Bressman
Phenylalanine loading as a diagnostic test for DRD: interpreting the utility of the test.
T Lynch; Mary Sano; Karen Marder; Karen L Bell; Norman L Foster; R F Defendini; Anders A F Sima; C Keohane; TG Nygaard; Stanley Fahn; Richard Mayeux; Lewis P Rowland; Kirk Wilhelmsen
Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex. 1994.

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All Publications

2005: Johann Hagenah; Rachel Saunders-Pullman; Katja Hedrich; Kemal Kabakci; K Habermann; Karin Wiegers; Kathrin Mohrmann; Thora Lohnau; Deborah Raymond; Peter Vieregge; TG Nygaard; Laurie J Ozelius; Susan Bressman; Christine Klein
High mutation rate in dopa-responsive dystonia: detection with comprehensive GCHI screening.
Neurology 2005;64(5):908-11.
2004: Rachel Saunders-Pullman; N Blau; Keith Hyland; J Zschocke; TG Nygaard; Deborah Raymond; Vicki Shanker; Kathrin Mohrmann; L Arnold; SD Tabbal; D DeLeon; Blair Ford; Mitchell F Brin; S Chouinard; Laurie J Ozelius; Christine Klein; Susan Bressman
Phenylalanine loading as a diagnostic test for DRD: interpreting the utility of the test.
Molecular genetics and metabolism 2004;83(3):207-12.
2001: T Lynch; Mary Sano; Karen Marder; Karen L Bell; Norman L Foster; R F Defendini; Anders A F Sima; C Keohane; TG Nygaard; Stanley Fahn; Richard Mayeux; Lewis P Rowland; Kirk Wilhelmsen
Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex. 1994.
Neurology 2001;57(10 Suppl 3):S39-45.
2000: Ichizo Nishino; antonella spinazzola; A Papadimitriou; S Hammans; I Steiner; C D Hahn; A M Connolly; Alain Verloes; J Guimarães; Ivan P Maillard; H Hamano; Maria Alice Donati; Carol E Semrad; J A Russell; Antoni L Andreu; Georgios M Hadjigeorgiou; Tuan H Vu; Saba Tadesse; TG Nygaard; I Nonaka; I Hirano; Eduardo Bonilla; Lewis P Rowland; Salvatore DiMauro; Michio Hirano
Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations.
Annals of neurology 2000;47(6):792-800.
1999: TG Nygaard; Deborah Raymond; C Chen; Ichizo Nishino; Paul Greene; D Jennings; Gary A Heiman; Christine Klein; Rachel Saunders-Pullman; Patricia L Kramer; Laurie J Ozelius; Susan Bressman
Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31.
Annals of neurology 1999;46(5):794-8.
1999: Paul R Jarman; N Del Grosso; Enza Maria Valente; Barbara Leube; E Cassetta; Anna Rita Bentivoglio; H M Waddy; Ryan Uitti; Demetrius M Maraganore; Alberto Albanese; Marina Frontali; Georg Auburger; Susan Bressman; Nicholas W Wood; TG Nygaard
Primary torsion dystonia: the search for genes is not over.
Journal of neurology, neurosurgery, and psychiatry 1999;67(3):395-7.
1999: Keith Hyland; TG Nygaard; JM Trugman; Kathryn J Swoboda; Lauren A Arnold; S P Sparagana
Oral phenylalanine loading profiles in symptomatic and asymptomatic gene carriers with dopa-responsive dystonia due to dominantly inherited GTP cyclohydrolase deficiency.
Journal of inherited metabolic disease 1999;22(3):213-5.
1998: Michio Hirano; J Garcia-de-Yebenes; AC Jones; Ichizo Nishino; Salvatore DiMauro; Jose R Carlo; A N Bender; A F Hahn; L M Salberg; D E Weeks; TG Nygaard
Mitochondrial neurogastrointestinal encephalomyopathy syndrome maps to chromosome 22q13.32-qter.
American journal of human genetics 1998;63(2):526-33.
1998: Jane H Morse; AC Jones; Robyn J Barst; Susan E Hodge; Kirk Wilhelmsen; TG Nygaard
Familial primary pulmonary hypertension locus mapped to chromosome 2q31-q32.
Chest 1998;114(1 Suppl):57S-58S.
1998: AC Jones; Y Yamamura; Laura A Almasy; S Bohlega; B Elibol; Jean P Hubble; S Kuzuhara; M Uchida; T Yanagi; D E Weeks; TG Nygaard
Autosomal recessive juvenile parkinsonism maps to 6q25.2-q27 in four ethnic groups: detailed genetic mapping of the linked region.
American journal of human genetics 1998;63(1):80-7.
1998: Kirk Wilhelmsen; C B Moskowitz; D E Weeks; M Neystat; TG Nygaard; L Clark; M Dancoup; E E Sobrevega; R Rosales; G L Gamez; O Pacioles; M Perez; Stanley Fahn
Molecular genetic analysis of Lubag.
Advances in neurology 1998;78():341-8.
1998: Susan Bressman; Deborah de Leon; Deborah Raymond; Laurie J Ozelius; Xandra O Breakefield; TG Nygaard; Laura A Almasy; Neil J Risch; Patricia L Kramer
Clinical-genetic spectrum of primary dystonia.
Advances in neurology 1998;78():79-91.
1997: Laura A Almasy; Susan Bressman; Deborah Raymond; Patricia L Kramer; Paul Greene; Gary A Heiman; Blair Ford; J Yount; Deborah de Leon; S Chouinard; Rachel Saunders-Pullman; Mitchell F Brin; R P Kapoor; A C Jones; H Shen; Stanley Fahn; Neil J Risch; TG Nygaard
Idiopathic torsion dystonia linked to chromosome 8 in two Mennonite families.
Annals of neurology 1997;42(4):670-3.
1997: Jane H Morse; AC Jones; Robyn J Barst; Susan E Hodge; Kirk Wilhelmsen; TG Nygaard
Mapping of familial primary pulmonary hypertension locus (PPH1) to chromosome 2q31-q32.
Circulation 1997;95(12):2603-6.
1996: Susan Bressman; T T Warner; Laura A Almasy; Ryan Uitti; Paul Greene; Gary A Heiman; Deborah Raymond; Blair Ford; Deborah de Leon; Stanley Fahn; Patricia L Kramer; N J Risch; Demetrius M Maraganore; TG Nygaard; A E Harding
Exclusion of the DYT1 locus in familial torticollis.
Annals of neurology 1996;40(4):681-4.
1996: O Bandmann; TG Nygaard; Robert Surtees; CD Marsden; Nicholas W Wood; AE Harding
Dopa-responsive dystonia in British patients: new mutations of the GTP-cyclohydrolase I gene and evidence for genetic heterogeneity.
Human molecular genetics 1996;5(3):403-6.
1995: TG Nygaard
Dopa-responsive dystonia.
Current opinion in neurology 1995;8(4):310-3.
1995: Daniel E Weeks; TG Nygaard; Michael Neystat; L D Harby; Kirk Wilhelmsen
A high-resolution genetic linkage map of the pericentromeric region of the human X chromosome.
Genomics 1995;26(1):39-46.
1994: Kirk Wilhelmsen; T Lynch; E Pavlou; M Higgins; TG Nygaard
Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22.
American journal of human genetics 1994;55(6):1159-65.
1994: T Lynch; Mary Sano; Karen Marder; K L Bell; Norman L Foster; R F Defendini; Anders A F Sima; C Keohane; TG Nygaard; Stanley Fahn
Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex.
Neurology 1994;44(10):1878-84.
1994: TG Nygaard; S P Waran; R A Levine; Ali Naini; A M Chutorian
Dopa-responsive dystonia simulating cerebral palsy.
Pediatric neurology 1994;11(3):236-40.
1994: H Takahashi; R A Levine; matthew galloway; BJ Snow; Donald B Calne; TG Nygaard
Biochemical and fluorodopa positron emission tomographic findings in an asymptomatic carrier of the gene for dopa-responsive dystonia.
Annals of neurology 1994;35(3):354-6.
1994: Susan Bressman; Gary A Heiman; TG Nygaard; Laurie J Ozelius; A L Hunt; Mitchell F Brin; M F Gordon; C B Moskowitz; Deborah de Leon; Robert E Burke
A study of idiopathic torsion dystonia in a non-Jewish family: evidence for genetic heterogeneity.
Neurology 1994;44(2):283-7.
1993: TG Nygaard; Kirk Wilhelmsen; N J Risch; D L Brown; JM Trugman; T Conrad Gilliam; Stanley Fahn; Daniel E Weeks
Linkage mapping of dopa-responsive dystonia (DRD) to chromosome 14q.
Nature genetics 1993;5(4):386-91.
1993: BJ Snow; TG Nygaard; H Takahashi; Donald B Calne
Positron emission tomographic studies of dopa-responsive dystonia and early-onset idiopathic parkinsonism.
Annals of neurology 1993;34(5):733-8.
1993: CH Waters; H Takahashi; Kirk Wilhelmsen; R Shubin; BJ Snow; TG Nygaard; C B Moskowitz; Stanley Fahn; Donald B Calne
Phenotypic expression of X-linked dystonia-parkinsonism (lubag) in two women.
Neurology 1993;43(8):1555-8.
1993: CH Waters; P L Faust; J Powers; H Vinters; C Moskowitz; TG Nygaard; A L Hunt; Stanley Fahn
Neuropathology of lubag (x-linked dystonia parkinsonism).
Movement disorders : official journal of the Movement Disorder Society 1993;8(3):387-90.
1993: D M Lasser; Kirk Wilhelmsen; TG Nygaard; U Tantravahi
Characterization of microsatellite polymorphisms DXS691 and DXS692: genetic mapping to Xq26.2-Xq27 and Xq25-Xq26.2.
Genomics 1993;16(3):785-6.
1993: H Takahashi; BJ Snow; TG Nygaard; Donald B Calne
Clinical heterogeneity of dopa-responsive dystonia: PET observations.
Advances in neurology 1993;60():586-90.
1993: TG Nygaard
Dopa-responsive dystonia. Delineation of the clinical syndrome and clues to pathogenesis.
Advances in neurology 1993;60():577-85.
1992: TG Nygaard; H Takahashi; Gary A Heiman; BJ Snow; Stanley Fahn; Donald B Calne
Long-term treatment response and fluorodopa positron emission tomographic scanning of parkinsonism in a family with dopa-responsive dystonia.
Annals of neurology 1992;32(5):603-8.
1991: D Schuback; Patricia L Kramer; Laurie J Ozelius; Gösta Holmgren; L Forsgren; Mårten Kyllerman; Jan Wahlström; C M Craft; TG Nygaard; M Brin
Dopamine beta-hydroxylase gene excluded in four subtypes of hereditary dystonia.
Human genetics 1991;87(3):311-6.
1991: TG Nygaard; CD Marsden; Stanley Fahn
Dopa-responsive dystonia: long-term treatment response and prognosis.
Neurology 1991;41(2 ( Pt 1)):174-81.
1991: Kirk Wilhelmsen; Daniel E Weeks; TG Nygaard; C B Moskowitz; R L Rosales; D C dela Paz; E E Sobrevega; Stanley Fahn; T Conrad Gilliam
Genetic mapping of "Lubag" (X-linked dystonia-parkinsonism) in a Filipino kindred to the pericentromeric region of the X chromosome.
Annals of neurology 1991;29(2):124-31.
1991: David J Kwiatkowski; TG Nygaard; D E Schuback; S Perman; JM Trugman; Susan Bressman; Robert E Burke; Mitchell F Brin; Laurie J Ozelius; Xandra O Breakefield
Identification of a highly polymorphic microsatellite VNTR within the argininosuccinate synthetase locus: exclusion of the dystonia gene on 9q32-34 as the cause of dopa-responsive dystonia in a large kindred.
American journal of human genetics 1991;48(1):121-8.
1990: TG Nygaard; JM Trugman; J G de Yebenes; Stanley Fahn
Dopa-responsive dystonia: the spectrum of clinical manifestations in a large North American family.
Neurology 1990;40(1):66-9.
1989: TG Nygaard; RC Duvoisin; M Manocha; S Chokroverty
Seizures in progressive supranuclear palsy.
Neurology 1989;39(1):138-40.
1989: N A Fletcher; I J Holt; AE Harding; TG Nygaard; J Mallet; CD Marsden
Tyrosine hydroxylase and levodopa responsive dystonia.
Journal of neurology, neurosurgery, and psychiatry 1989;52(1):112-4.