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Jerry Mendell

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Flanigan Kevin M; Dunn Diane M; von Niederhausern Andrew; Howard Michael T; Mendell Jerry; Connolly Anne; Saunders Carol; Modrcin Ann; Dasouki Majed; Comi Giacomo P; Del Bo Roberto; Pickart Angela; Jacobson Richard; Finkel Richard; Medne Livija; Weiss Robert B
DMD Trp3X nonsense mutation associated with a founder effect in North American families with mild Becker muscular dystrophy.
Elsheikh Bakri; Prior Thomas; Zhang Xiaoli; Miller Robert; Kolb Stephen J; Moore Dan; Bradley Walter; Barohn Richard; Bryan Wilson; Gelinas Deborah; Iannaccone Susan; Leshner Robert; Mendell Jerry R; Mendoza Michelle; Russman Barry; Smith Stephen; King Wendy; Kissel John T
An analysis of disease severity based on SMN2 copy number in adults with spinal muscular atrophy.
Mendell Jerry R; Rodino-Klapac Louise R; Rosales-Quintero Xiomara; Kota Janaiah; Coley Brian D; Galloway Gloria; Craenen Josepha M; Lewis Sarah; Malik Vinod; Shilling Christopher; Byrne Barry J; Conlon Thomas; Campbell Katherine J; Bremer William G; Viollet Laurence; Walker Christopher M; Sahenk Zarife; Clark K Reed
Limb-girdle muscular dystrophy type 2D gene therapy restores alpha-sarcoglycan and associated proteins.

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All Publications

2009: Flanigan Kevin M; Dunn Diane M; von Niederhausern Andrew; Howard Michael T; Mendell Jerry; Connolly Anne; Saunders Carol; Modrcin Ann; Dasouki Majed; Comi Giacomo P; Del Bo Roberto; Pickart Angela; Jacobson Richard; Finkel Richard; Medne Livija; Weiss Robert B
DMD Trp3X nonsense mutation associated with a founder effect in North American families with mild Becker muscular dystrophy.
Neuromuscular disorders : NMD 2009;19(11):743-8.
2009: Elsheikh Bakri; Prior Thomas; Zhang Xiaoli; Miller Robert; Kolb Stephen J; Moore Dan; Bradley Walter; Barohn Richard; Bryan Wilson; Gelinas Deborah; Iannaccone Susan; Leshner Robert; Mendell Jerry R; Mendoza Michelle; Russman Barry; Smith Stephen; King Wendy; Kissel John T
An analysis of disease severity based on SMN2 copy number in adults with spinal muscular atrophy.
Muscle & nerve 2009;40(4):652-6.
2009: Mendell Jerry R; Rodino-Klapac Louise R; Rosales-Quintero Xiomara; Kota Janaiah; Coley Brian D; Galloway Gloria; Craenen Josepha M; Lewis Sarah; Malik Vinod; Shilling Christopher; Byrne Barry J; Conlon Thomas; Campbell Katherine J; Bremer William G; Viollet Laurence; Walker Christopher M; Sahenk Zarife; Clark K Reed
Limb-girdle muscular dystrophy type 2D gene therapy restores alpha-sarcoglycan and associated proteins.
Annals of neurology 2009;66(3):290-7.
2009: Viollet Laurence; Gailey Susan; Thornton David J; Friedman Neil R; Flanigan Kevin M; Mahan John D; Mendell Jerry R
Utility of cystatin C to monitor renal function in Duchenne muscular dystrophy.
Muscle & nerve 2009;40(3):438-42.
2009: Elsheikh Bakri; Kissel John T; Christoforidis Gregory; Wicklund Matthew; Kehagias Dimitri T; Chiocca E Antonio; Mendell Jerry R
Spinal angiography and epidural venography in juvenile muscular atrophy of the distal arm "Hirayama disease".
Muscle & nerve 2009;40(2):206-12.
2009: Tsao Chang-Yong; Mendell Jerry R
Partial epilepsy in an adolescent male with limb-girdle muscular dystrophy 1B.
Journal of child neurology 2009;24(3):346-8.
2009: Thrush Philip T; Allen Hugh D; Viollet Laurence; Mendell Jerry R
Re-examination of the electrocardiogram in boys with Duchenne muscular dystrophy and correlation with its dilated cardiomyopathy.
The American journal of cardiology 2009;103(2):262-5.
2008: Rodino-Klapac L R; Lee J-S; Mulligan R C; Clark K R; Mendell J R
Lack of toxicity of alpha-sarcoglycan overexpression supports clinical gene transfer trial in LGMD2D.
Neurology 2008;71(4):240-7.
2008: Rosales Xiomara Q; Chu Mary-Lynn; Shilling Christopher; Wall Cheryl; Pastores Gregory M; Mendell Jerry R
Fidelity of gamma-glutamyl transferase (GGT) in differentiating skeletal muscle from liver damage.
Journal of child neurology 2008;23(7):748-51.
2008: Wagner Kathryn R; Fleckenstein James L; Amato Anthony A; Barohn Richard J; Bushby Katharine; Escolar Diana M; Flanigan Kevin M; Pestronk Alan; Tawil Rabi; Wolfe Gil I; Eagle Michelle; Florence Julaine M; King Wendy M; Pandya Shree; Straub Volker; Juneau Paul; Meyers Kathleen; Csimma Cristina; Araujo Tracey; Allen Robert; Parsons Stephanie A; Wozney John M; Lavallie Edward R; Mendell Jerry R
A phase I/IItrial of MYO-029 in adult subjects with muscular dystrophy.
Annals of neurology 2008;63(5):561-71.
2008: Haidet Amanda M; Rizo Liza; Handy Chalonda; Umapathi Priya; Eagle Amy; Shilling Chris; Boue Daniel; Martin Paul T; Sahenk Zarife; Mendell Jerry R; Kaspar Brian K
Long-term enhancement of skeletal muscle mass and strength by single gene administration of myostatin inhibitors.
Proceedings of the National Academy of Sciences of the United States of America 2008;105(11):4318-22.
2008: Kannanayakal Theresa J; Mendell Jerry R; Kuret Jeff
Casein kinase 1 alpha associates with the tau-bearing lesions of inclusion body myositis.
Neuroscience letters 2008;431(2):141-5.
2007: Tsao Chang-Yong; Mendell Jerry R
Autistic disorder in 2 children with mitochondrial disorders.
Journal of child neurology 2007;22(9):1121-3.
2007: Rodino-Klapac Louise R; Chicoine Louis G; Kaspar Brian K; Mendell Jerry R
Gene therapy for duchenne muscular dystrophy: expectations and challenges.
Archives of neurology 2007;64(9):1236-41.
2007: King W M; Ruttencutter R; Nagaraja H N; Matkovic V; Landoll J; Hoyle C; Mendell J R; Kissel J T
Orthopedic outcomes of long-term daily corticosteroid treatment in Duchenne muscular dystrophy.
Neurology 2007;68(19):1607-13.
2007: Mendell Jerry R; Csimma Cristina; McDonald Craig M; Escolar Diana M; Janis Scott; Porter John D; Hesterlee Sharon E; Howell R Rodney
Challenges in drug development for muscle disease: a stakeholders' meeting.
Muscle & nerve 2007;35(1):8-16.
2007: Rodino-Klapac Louise R; Janssen Paul M L; Montgomery Chrystal L; Coley Brian D; Chicoine Louis G; Clark K Reed; Mendell Jerry R
A translational approach for limb vascular delivery of the micro-dystrophin gene without high volume or high pressure for treatment of Duchenne muscular dystrophy.
Journal of translational medicine 2007;5():45.
2006: Miller Timothy M; Kim Soo H; Yamanaka Koji; Hester Mark; Umapathi Priya; Arnson Hannah; Rizo Liza; Mendell Jerry R; Gage Fred H; Cleveland Don W; Kaspar Brian K
Gene transfer demonstrates that muscle is not a primary target for non-cell-autonomous toxicity in familial amyotrophic lateral sclerosis.
Proceedings of the National Academy of Sciences of the United States of America 2006;103(51):19546-51.
2006: Mendell Jerry R; Boué Daniel R; Martin Paul T
The congenital muscular dystrophies: recent advances and molecular insights.
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 2006;9(6):427-43.
2006: Moore Steven A; Shilling Christopher J; Westra Steven; Wall Cheryl; Wicklund Matthew P; Stolle Catherine; Brown Charlotte A; Michele Daniel E; Piccolo Federica; Winder Thomas L; Stence Aaron; Barresi Rita; King Nick; King Wendy; Florence Julaine; Campbell Kevin P; Fenichel Gerald M; Stedman Hansell H; Kissel John T; Griggs Robert C; Pandya Shree; Mathews Katherine D; Pestronk Alan; Serrano Carmen; Darvish Daniel; Mendell Jerry R
Limb-girdle muscular dystrophy in the United States.
Journal of neuropathology and experimental neurology 2006;65(10):995-1003.
2006: Mendell Jerry R; Clark K Reed
Risks, benefits, and consent in the age of gene therapy.
Neurology 2006;66(7):964-5.
2006: Tsao Chang-Yong; Mendell J R
Coexisting muscular dystrophies and epilepsy in children.
Journal of child neurology 2006;21(2):148-50.
2006: Mendell Jerry R; Clark K Reed
Challenges for gene therapy for muscular dystrophy.
Current neurology and neuroscience reports 2006;6(1):47-56.
2006: Barohn R J; Herbelin L; Kissel J T; King W; McVey A L; Saperstein D S; Mendell J R
Pilot trial of etanercept in the treatment of inclusion-body myositis.
Neurology 2006;66(2 Suppl 1):S123-4.
2005: Sahenk Z; Nagaraja H N; McCracken B S; King W M; Freimer M L; Cedarbaum J M; Mendell J R
NT-3 promotes nerve regeneration and sensory improvement in CMT1A mouse models and in patients.
Neurology 2005;65(5):681-9.
2005: Buzin Carolyn H; Feng Jinong; Yan Jin; Scaringe William; Liu Qiang; den Dunnen Johan; Mendell Jerry R; Sommer Steve S
Mutation rates in the dystrophin gene: a hotspot of mutation at a CpG dinucleotide.
Human mutation 2005;25(2):177-88.
2004: Mendell Jerry R; Miller Andra
Gene transfer for neurologic disease: agencies, policies, and process.
Neurology 2004;63(12):2225-32.
2004: Miller T M; Dias da Silva M R; Miller H A; Kwiecinski H; Mendell J R; Tawil R; McManis P; Griggs R C; Angelini C; Servidei S; Petajan J; Dalakas M C; Ranum L P W; Fu Y H; Ptácek L J
Correlating phenotype and genotype in the periodic paralyses.
Neurology 2004;63(9):1647-55.
2004: Yan Jin; Feng Jinong; Buzin Carolyn H; Scaringe William; Liu Qiang; Mendell Jerry R; den Dunnen Johan; Sommer Steve S
Three-tiered noninvasive diagnosis in 96% of patients with Duchenne muscular dystrophy (DMD).
Human mutation 2004;23(2):203-4.
2003: Collins M P; Periquet M I; Mendell J R; Sahenk Z; Nagaraja H N; Kissel J T
Nonsystemic vasculitic neuropathy: insights from a clinical cohort.
Neurology 2003;61(5):623-30.
2003: Flanigan Kevin M; von Niederhausern Andrew; Dunn Diane M; Alder Jonathan; Mendell Jerry R; Weiss Robert B
Rapid direct sequence analysis of the dystrophin gene.
American journal of human genetics 2003;72(4):931-9.
2003: Mendell Jerry R; Sahenk Zarife
Clinical practice. Painful sensory neuropathy.
The New England journal of medicine 2003;348(13):1243-55.
2002: Cohn Ronald D; Henry Michael D; Michele Daniel E; Barresi Rita; Saito Fumiaki; Moore Steven A; Flanagan Jason D; Skwarchuk Mark W; Robbins Michael E; Mendell Jerry R; Williamson Roger A; Campbell Kevin P
Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration.
Cell 2002;110(5):639-48.
2002: Tsao Chang-Yong; Mendell Jerry R; Kissel John T
Dermatomyositis in two siblings and a brief review of familial dermatomyositis.
Journal of child neurology 2002;17(7):540-2.
2002: Tsao Chang-Yong; Mendell Jerry R
Combined partial deficiencies of carnitine palmitoyltransferase II and mitochondrial complex I presenting as increased serum creatine kinase level.
Journal of child neurology 2002;17(4):304-6.
2002: Tsao Chang-Yong; Mendell Jerry R; Friemer Miriam L; Kissel John T
Lambert-Eaton myasthenic syndrome in children.
Journal of child neurology 2002;17(1):74-6.
2001: Novak V; Kanard R; Kissel J T; Mendell J R
Treatment of painful sensory neuropathy with tiagabine: a pilot study.
Clinical autonomic research : official journal of the Clinical Autonomic Research Society 2001;11(6):357-61.
2001: Kissel J T; McDermott M P; Mendell J R; King W M; Pandya S; Griggs R C; Tawil R;
Randomized, double-blind, placebo-controlled trial of albuterol in facioscapulohumeral dystrophy.
Neurology 2001;57(8):1434-40.
2001: Mendell J R; Buzin C H; Feng J; Yan J; Serrano C; Sangani D S; Wall C; Prior T W; Sommer S S
Diagnosis of Duchenne dystrophy by enhanced detection of small mutations.
Neurology 2001;57(4):645-50.
2001: Tsao C Y; Mendell J R; Bartholomew D
High mitochondrial DNA T8993G mutation (<90%) without typical features of Leigh's and NARP syndromes.
Journal of child neurology 2001;16(7):533-5.
2001: Fenichel G M; Griggs R C; Kissel J; Kramer T I; Mendell J R; Moxley R T; Pestronk A; Sheng K; Florence J; King W M; Pandya S; Robison V D; Wang H
A randomized efficacy and safety trial of oxandrolone in the treatment of Duchenne dystrophy.
Neurology 2001;56(8):1075-9.
2001: Novak V; Freimer M L; Kissel J T; Sahenk Z; Periquet I M; Nash S M; Collins M P; Mendell J R
Autonomic impairment in painful neuropathy.
Neurology 2001;56(7):861-8.
2001: Musumeci O; Naini A; Slonim A E; Skavin N; Hadjigeorgiou G L; Krawiecki N; Weissman B M; Tsao C Y; Mendell J R; Shanske S; De Vivo D C; Hirano M; DiMauro S
Familial cerebellar ataxia with muscle coenzyme Q10 deficiency.
Neurology 2001;56(7):849-55.
2001: Lindenbaum Y; Kissel J T; Mendell J R
Treatment approaches for Guillain-Barré syndrome and chronic inflammatory demyelinating polyradiculoneuropathy.
Neurologic clinics 2001;19(1):187-204.
2001: Mendell J R; Barohn R J; Freimer M L; Kissel J T; King W; Nagaraja H N; Rice R; Campbell W W; Donofrio P D; Jackson C E; Lewis R A; Shy M; Simpson D M; Parry G J; Rivner M H; Thornton C A; Bromberg M B; Tandan R; Harati Y; Giuliani M J;
Randomized controlled trial of IVIg in untreated chronic inflammatory demyelinating polyradiculoneuropathy.
Neurology 2001;56(4):445-9.
2000: Tsao C Y; Mendell J R; Luquette M; Dixon B; Morrow G
Mitochondrial DNA depletion in children.
Journal of child neurology 2000;15(12):822-4.
2000: Barresi R; Moore S A; Stolle C A; Mendell J R; Campbell K P
Expression of gamma -sarcoglycan in smooth muscle and its interaction with the smooth muscle sarcoglycan-sarcospan complex.
The Journal of biological chemistry 2000;275(49):38554-60.
2000: Tsao C Y; Mendell J R; Lo W D; Luquette M; Rennebohm R
Myasthenia gravis and associated autoimmune diseases in children.
Journal of child neurology 2000;15(11):767-9.
2000: Collins M P; Mendell J R; Periquet M I; Sahenk Z; Amato A A; Gronseth G S; Barohn R J; Jackson C E; Kissel J T
Superficial peroneal nerve/peroneus brevis muscle biopsy in vasculitic neuropathy.
Neurology 2000;55(5):636-43.
2000: Feng B; Chen L; Drmanovic Z; Kakabadze I; Mendell J R; Marzluf G A; Sahenk Z
Intracellular processing and toxicity of the truncated androgen receptor: nuclear congophilia-associated cell death.
Journal of neuropathology and experimental neurology 2000;59(8):652-63.
2000: Tsao C Y; Mendell J R; Lo W D; Luquette M; Rusin J
Mitochondrial respiratory-chain defects presenting as nonspecific features in children.
Journal of child neurology 2000;15(7):445-8.
2000: Stedman H; Wilson J M; Finke R; Kleckner A L; Mendell J
Phase I clinical trial utilizing gene therapy for limb girdle muscular dystrophy: alpha-, beta-, gamma-, or delta-sarcoglycan gene delivered with intramuscular instillations of adeno-associated vectors.
Human gene therapy 2000;11(5):777-90.
2000: Tawil R; McDermott M P; Brown R; Shapiro B C; Ptacek L J; McManis P G; Dalakas M C; Spector S A; Mendell J R; Hahn A F; Griggs R C
Randomized trials of dichlorphenamide in the periodic paralyses. Working Group on Periodic Paralysis.
Annals of neurology 2000;47(1):46-53.
1999: Periquet M I; Novak V; Collins M P; Nagaraja H N; Erdem S; Nash S M; Freimer M L; Sahenk Z; Kissel J T; Mendell J R
Painful sensory neuropathy: prospective evaluation using skin biopsy.
Neurology 1999;53(8):1641-7.
1999: Sahenk Z; Mendell J R
Alterations in nodes of Ranvier and Schmidt-Lanterman incisures in Charcot-Marie-Tooth neuropathies.
Annals of the New York Academy of Sciences 1999;883():508-12.
1999: Orrell R W; Tawil R; Forrester J; Kissel J T; Mendell J R; Figlewicz D A
Definitive molecular diagnosis of facioscapulohumeral dystrophy.
Neurology 1999;52(9):1822-6.
1999: Sue C M; Bruno C; Andreu A L; Cargan A; Mendell J R; Tsao C Y; Luquette M; Paolicchi J; Shanske S; DiMauro S; De Vivo D C
Infantile encephalopathy associated with the MELAS A3243G mutation.
The Journal of pediatrics 1999;134(6):696-700.
1999: Sahenk Z; Chen L; Mendell J R
Effects of PMP22 duplication and deletions on the axonal cytoskeleton.
Annals of neurology 1999;45(1):16-24.
1999: Tsao C Y; Mendell J R
The childhood muscular dystrophies: making order out of chaos.
Seminars in neurology 1999;19(1):9-23.
1999: Kissel J T; Mendell J R
Muscular dystrophy: historical overview and classification in the genetic era.
Seminars in neurology 1999;19(1):5-7.
1998: Parsons D W; McAndrew P E; Iannaccone S T; Mendell J R; Burghes A H; Prior T W
Intragenic telSMN mutations: frequency, distribution, evidence of a founder effect, and modification of the spinal muscular atrophy phenotype by cenSMN copy number.
American journal of human genetics 1998;63(6):1712-23.
1998: Sciacco M; Gasparo-Rippa P; Vu T H; Tanji K; Shanske S; Mendell J R; Schon E A; DiMauro S; Bonilla E
Study of mitochondrial DNA depletion in muscle by single-fiber polymerase chain reaction.
Muscle & nerve 1998;21(11):1374-81.
1998: Bartolo C; Mendell J R; Prior T W
Identification of a missense mutation in a Friedreich's ataxia patient: implications for diagnosis and carrier studies.
American journal of medical genetics 1998;79(5):396-9.
1998: Tsao C Y; Mendell J R; Rusin J; Luquette M
Congenital muscular dystrophy with complete laminin-alpha2-deficiency, cortical dysplasia, and cerebral white-matter changes in children.
Journal of child neurology 1998;13(6):253-6.
1998: Vu T H; Sciacco M; Tanji K; Nichter C; Bonilla E; Chatkupt S; Maertens P; Shanske S; Mendell J; Koenigsberger M R; Sharer L; Schon E A; DiMauro S; DeVivo D C
Clinical manifestations of mitochondrial DNA depletion.
Neurology 1998;50(6):1783-90.
1998: Erdem S; Mendell J R; Sahenk Z
Fate of Schwann cells in CMT1A and HNPP: evidence for apoptosis.
Journal of neuropathology and experimental neurology 1998;57(6):635-42.
1998: Kissel J T; McDermott M P; Natarajan R; Mendell J R; Pandya S; King W M; Griggs R C; Tawil R
Pilot trial of albuterol in facioscapulohumeral muscular dystrophy. FSH-DY Group.
Neurology 1998;50(5):1402-6.
1998: Erdem S; Freimer M L; O'Dorisio T; Mendell J R
Procainamide-induced chronic inflammatory demyelinating polyradiculoneuropathy.
Neurology 1998;50(3):824-5.
1998: Mendell J T; Panicker S G; Tsao C Y; Feng B; Sahenk Z; Marzluf G A; Mendell J R
Novel compound heterozygous laminina2-chain gene (LAMA2) mutations in congenital muscular dystrophy. Mutations in brief no. 159. Online.
Human mutation 1998;12(2):135.
1998: Mendell J R
Charcot-Marie-Tooth neuropathies and related disorders.
Seminars in neurology 1998;18(1):41-7.
1997: Coovert D D; Le T T; McAndrew P E; Strasswimmer J; Crawford T O; Mendell J R; Coulson S E; Androphy E J; Prior T W; Burghes A H
The survival motor neuron protein in spinal muscular atrophy.
Human molecular genetics 1997;6(8):1205-14.
1997: McAndrew P E; Parsons D W; Simard L R; Rochette C; Ray P N; Mendell J R; Prior T W; Burghes A H
Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy number.
American journal of human genetics 1997;60(6):1411-22.
1997: Prior T W; Bartolo C; Papp A C; Snyder P J; Sedra M S; Burghes A H; Kissel J T; Luquette M H; Tsao C Y; Mendell J R
Dystrophin expression in a Duchenne muscular dystrophy patient with a frame shift deletion.
Neurology 1997;48(2):486-8.
1997: DiDonato C J; Ingraham S E; Mendell J R; Prior T W; Lenard S; Moxley R T; Florence J; Burghes A H
Deletion and conversion in spinal muscular atrophy patients: is there a relationship to severity?
Annals of neurology 1997;41(2):230-7.
1997: Fouad G; Dalakas M; Servidei S; Mendell J R; Van den Bergh P; Angelini C; Alderson K; Griggs R C; Tawil R; Gregg R; Hogan K; Powers P A; Weinberg N; Malonee W; Ptácek L J
Genotype-phenotype correlations of DHP receptor alpha 1-subunit gene mutations causing hypokalemic periodic paralysis.
Neuromuscular disorders : NMD 1997;7(1):33-8.
1997: Tawil R; McDermott M P; Pandya S; King W; Kissel J; Mendell J R; Griggs R C
A pilot trial of prednisone in facioscapulohumeral muscular dystrophy. FSH-DY Group.
Neurology 1997;48(1):46-9.
1996: Parsons D W; McAndrew P E; Monani U R; Mendell J R; Burghes A H; Prior T W
An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA-determining gene.
Human molecular genetics 1996;5(11):1727-32.
1996: Mendell J R; Garcha T S; Kissel J T
The immunopathogenic role of complement in human muscle disease.
Current opinion in neurology 1996;9(3):226-34.
1996: Tawil R; Forrester J; Griggs R C; Mendell J; Kissel J; McDermott M; King W; Weiffenbach B; Figlewicz D
Evidence for anticipation and association of deletion size with severity in facioscapulohumeral muscular dystrophy. The FSH-DY Group.
Annals of neurology 1996;39(6):744-8.
1996: Bartolo C; Papp A C; Snyder P J; Sedra M S; Burghes A H; Hall C D; Mendell J R; Prior T W
A novel splice site mutation in a Becker muscular dystrophy patient.
Journal of medical genetics 1996;33(4):324-7.
1996: Kissel J T; Mendell J R
Neuropathies associated with monoclonal gammopathies.
Neuromuscular disorders : NMD 1996;6(1):3-18.
1996: Prior T W; Bartolo C; Papp A C; Snyder P J; Sedra M S; Burghes A H; Mendell J R
Nonsense mutations in a Becker muscular dystrophy and an intermediate patient.
Human mutation 1996;7(1):72-5.
1995: Tsao C Y; Lo W D; Mendell J R; Batley R J
Critical illness polyneuropathy in a 2-year-old girl with hemorrhagic shock encephalopathy syndrome.
Journal of child neurology 1995;10(6):486-8.
1995: Griggs R C; Askanas V; DiMauro S; Engel A; Karpati G; Mendell J R; Rowland L P
Inclusion body myositis and myopathies.
Annals of neurology 1995;38(5):705-13.
1995: Mendell J R; Kissel J T; Amato A A; King W; Signore L; Prior T W; Sahenk Z; Benson S; McAndrew P E; Rice R
Myoblast transfer in the treatment of Duchenne's muscular dystrophy.
The New England journal of medicine 1995;333(13):832-8.
1995: Nadkarni N; Freimer M; Mendell J R
Amyloidosis causing a progressive myopathy.
Muscle & nerve 1995;18(9):1016-8.
1995: Prior T W; Bartolo C; Pearl D K; Papp A C; Snyder P J; Sedra M S; Burghes A H; Mendell J R
Spectrum of small mutations in the dystrophin coding region.
American journal of human genetics 1995;57(1):22-33.
1995: Mendell J R; Sahenk Z; Prior T W
The childhood muscular dystrophies: diseases sharing a common pathogenesis of membrane instability.
Journal of child neurology 1995;10(2):150-9.
1995: Winnard A V; Mendell J R; Prior T W; Florence J; Burghes A H
Frameshift deletions of exons 3-7 and revertant fibers in Duchenne muscular dystrophy: mechanisms of dystrophin production.
American journal of human genetics 1995;56(1):158-66.
1995: Guida M; Marger R S; Papp A C; Snyder P J; Sedra M S; Kissel J T; Mendell J R; Prior T W
A molecular protocol for diagnosing myotonic dystrophy.
Clinical chemistry 1995;41(1):69-72.
1995: Thompson T G; DiDonato C J; Simard L R; Ingraham S E; Burghes A H; Crawford T O; Rochette C; Mendell J R; Wasmuth J J
A novel cDNA detects homozygous microdeletions in greater than 50% of type I spinal muscular atrophy patients.
Nature genetics 1995;9(1):56-62.
1994: Lynn D J; Woda R P; Mendell J R
Respiratory dysfunction in muscular dystrophy and other myopathies.
Clinics in chest medicine 1994;15(4):661-74.
1994: Ptácek L J; Tawil R; Griggs R C; Meola G; McManis P; Barohn R J; Mendell J R; Harris C; Spitzer R; Santiago F
Sodium channel mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis.
Neurology 1994;44(8):1500-3.
1994: Sahenk Z; Seharaseyon J; Mendell J R
CNTF potentiates peripheral nerve regeneration.
Brain research 1994;655(1-2):246-50.
1994: Prior T W; Bartolo C; Papp A C; Snyder P J; Sedra M S; Burghes A H; Mendell J R
Identification of a missense mutation, single base deletion and a polymorphism in the dystrophin exon 16.
Human molecular genetics 1994;3(7):1173-4.
1994: Sahenk Z; Barohn R; New P; Mendell J R
Taxol neuropathy. Electrodiagnostic and sural nerve biopsy findings.
Archives of neurology 1994;51(7):726-9.
1994: Prior T W; Papp A C; Snyder P J; Sedra M S; Western L M; Bartolo C; Moxley R T; Mendell J R
Heteroduplex analysis of the dystrophin gene: application to point mutation and carrier detection.
American journal of medical genetics 1994;50(1):68-73.
1994: Tawil R; McDermott M P; Mendell J R; Kissel J; Griggs R C
Facioscapulohumeral muscular dystrophy (FSHD): design of natural history study and results of baseline testing. FSH-DY Group.
Neurology 1994;44(3 Pt 1):442-6.
1994: Tan E; Lynn D J; Amato A A; Kissel J T; Rammohan K W; Sahenk Z; Warmolts J R; Jackson C E; Barohn R J; Mendell J R
Immunosuppressive treatment of motor neuron syndromes. Attempts to distinguish a treatable disorder.
Archives of neurology 1994;51(2):194-200.
1993: Griggs R C; Tawil R; Storvick D; Mendell J R; Altherr M R
Genetics of facioscapulohumeral muscular dystrophy: new mutations in sporadic cases.
Neurology 1993;43(11):2369-72.
1993: Prior T W; Papp A C; Snyder P J; Burghes A H; Bartolo C; Sedra M S; Western L M; Mendell J R
A missense mutation in the dystrophin gene in a Duchenne muscular dystrophy patient.
Nature genetics 1993;4(4):357-60.
1993: Amato A A; Barohn R J; Sahenk Z; Tutschka P J; Mendell J R
Polyneuropathy complicating bone marrow and solid organ transplantation.
Neurology 1993;43(8):1513-8.
1993: Weiffenbach B; Dubois J; Storvick D; Tawil R; Jacobsen S J; Gilbert J; Wijmenga C; Mendell J R; Winokur S; Altherr M R
Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromsome 4q35 recombination events.
Nature genetics 1993;4(2):165-9.
1993: Amato A A; Prior T W; Barohn R J; Snyder P; Papp A; Mendell J R
Kennedy's disease: a clinicopathologic correlation with mutations in the androgen receptor gene.
Neurology 1993;43(4):791-4.
1993: Prior T W; Papp A C; Snyder P J; Burghes A H; Sedra M S; Western L M; Bartello C; Mendell J R
Identification of two point mutations and a one base deletion in exon 19 of the dystrophin gene by heteroduplex formation.
Human molecular genetics 1993;2(3):311-3.
1993: Sahenk Z; Seharaseyon J; Mendell J R; Burghes A H
Gene delivery to spinal motor neurons.
Brain research 1993;606(1):126-9.
1993: Kissel J T; Lynn D J; Rammohan K W; Klein J P; Griggs R C; Moxley R T; Cwik V A; Brooke M H; Mendell J R
Mononuclear cell analysis of muscle biopsies in prednisone- and azathioprine-treated Duchenne muscular dystrophy.
Neurology 1993;43(3 Pt 1):532-6.
1993: Griggs R C; Moxley R T; Mendell J R; Fenichel G M; Brooke M H; Pestronk A; Miller J P; Cwik V A; Pandya S; Robison J
Duchenne dystrophy: randomized, controlled trial of prednisone (18 months) and azathioprine (12 months)
Neurology 1993;43(3 Pt 1):520-7.
1993: Ptacek L J; Gouw L; Kwiecinski H; McManis P; Mendell J R; Barohn R J; George A L; Barchi R L; Robertson M; Leppert M F
Sodium channel mutations in paramyotonia congenita and hyperkalemic periodic paralysis.
Annals of neurology 1993;33(3):300-7.
1993: Tan E; Hajinazarian M; Bay W; Neff J; Mendell J R
Acute renal failure resulting from intravenous immunoglobulin therapy.
Archives of neurology 1993;50(2):137-9.
1993: Mendell J R
Chronic inflammatory demyelinating polyradiculoneuropathy.
Annual review of medicine 1993;44():211-9.
1993: Prior T W; Papp A C; Snyder P J; Burghes A H; Sedra M S; Western L M; Bartolo C; Mendell J R
Exon 44 nonsense mutation in two-Duchenne muscular dystrophy brothers detected by heteroduplex analysis.
Human mutation 1993;2(3):192-5.
1992: Winnard A V; Jia-Hsu Y; Gibbs R A; Mendell J R; Burghes A H
Identification of a 2 base pair nonsense mutation causing a cryptic splice site in a DMD patient.
Human molecular genetics 1992;1(8):645-6.
1992: Weiffenbach B; Bagley R; Falls K; Hyser C; Storvick D; Jacobsen S J; Schultz P; Mendell J; Willems van Dijk K; Milner E C
Linkage analyses of five chromosome 4 markers localizes the facioscapulohumeral muscular dystrophy (FSHD) gene to distal 4q35.
American journal of human genetics 1992;51(2):416-23.
1992: Sahenk Z; Mendell J R
Alterations in slow transport kinetics induced by estramustine phosphate, an agent binding to microtubule-associated proteins.
Journal of neuroscience research 1992;32(4):481-93.
1992: Prior T W; Papp A C; Snyder P J; Mendell J R
Case of the month: germline mosaicism in carriers of Duchenne muscular dystrophy.
Muscle & nerve 1992;15(8):960-3.
1992: Kissel J T; Mendell J R
Vasculitic neuropathy.
Neurologic clinics 1992;10(3):761-81.
1992: Klein C J; Coovert D D; Bulman D E; Ray P N; Mendell J R; Burghes A H
Somatic reversion/suppression in Duchenne muscular dystrophy (DMD): evidence supporting a frame-restoring mechanism in rare dystrophin-positive fibers.
American journal of human genetics 1992;50(5):950-9.
1992: Williams L L; Kissel J T; Shannon B T; Wright F S; Mendell J R
Expression of Schwann cell and peripheral T-cell activation epitopes in hereditary motor and sensory neuropathy.
Journal of neuroimmunology 1992;36(2-3):147-55.
1992: Weiffenbach B; Bagley R G; Falls K; Dubois J; Hyser C; Storvick D; Schultz P; Mendell J R; Milner E C; Jacobsen S J
Framework multipoint map of the long arm of human chromosome 4 and telomeric localization of the gene for FSHD.
Mammalian genome : official journal of the International Mammalian Genome Society 1992;3(3):143-50.
1991: Fenichel G M; Florence J M; Pestronk A; Mendell J R; Moxley R T; Griggs R C; Brooke M H; Miller J P; Robison J; King W
Long-term benefit from prednisone therapy in Duchenne muscular dystrophy.
Neurology 1991;41(12):1874-7.
1991: Mendell J R; Sahenk Z; Gales T; Paul L
Amyloid filaments in inclusion body myositis. Novel findings provide insight into nature of filaments.
Archives of neurology 1991;48(12):1229-34.
1991: Barohn R J; Sahenk Z; Warmolts J R; Mendell J R
The Bruns-Garland syndrome (diabetic amyotrophy). Revisited 100 years later.
Archives of neurology 1991;48(11):1130-5.
1991: Fenichel G M; Mendell J R; Moxley R T; Griggs R C; Brooke M H; Miller J P; Pestronk A; Robison J; King W; Signore L
A comparison of daily and alternate-day prednisone therapy in the treatment of Duchenne muscular dystrophy.
Archives of neurology 1991;48(6):575-9.
1991: Kissel J T; Burrow K L; Rammohan K W; Mendell J R
Mononuclear cell analysis of muscle biopsies in prednisone-treated and untreated Duchenne muscular dystrophy. CIDD Study Group.
Neurology 1991;41(5):667-72.
1991: Burrow K L; Coovert D D; Klein C J; Bulman D E; Kissel J T; Rammohan K W; Burghes A H; Mendell J R
Dystrophin expression and somatic reversion in prednisone-treated and untreated Duchenne dystrophy. CIDD Study Group.
Neurology 1991;41(5):661-6.
1991: Griggs R C; Moxley R T; Mendell J R; Fenichel G M; Brooke M H; Pestronk A; Miller J P
Prednisone in Duchenne dystrophy. A randomized, controlled trial defining the time course and dose response. Clinical Investigation of Duchenne Dystrophy Group.
Archives of neurology 1991;48(4):383-8.
1991: Kissel J T; Halterman R K; Rammohan K W; Mendell J R
The relationship of complement-mediated microvasculopathy to the histologic features and clinical duration of disease in dermatomyositis.
Archives of neurology 1991;48(1):26-30.
1990: Griggs R C; Moxley R T; Mendell J R; Fenichel G M; Brooke M H; Miller P J; Mandel S; Florence J; Schierbecker J; Kaiser K K
Randomized, double-blind trial of mazindol in Duchenne dystrophy.
Muscle & nerve 1990;13(12):1169-73.
1990: Prior T W; Papp A C; Snyder P J; Highsmith W E; Friedman K J; Perry T R; Silverman L M; Mendell J R
Determination of carrier status in Duchenne and Becker muscular dystrophies by quantitative polymerase chain reaction and allele-specific oligonucleotides.
Clinical chemistry 1990;36(12):2113-7.
1990: Mendell J R; Jiang X S; Warmolts J R; Nichols W C; Benson M D
Diagnosis of Maryland/German familial amyloidotic polyneuropathy using allele-specific, enzymatically amplified, genomic DNA.
Annals of neurology 1990;27(5):553-7.
1990: Lo W D; Barohn R J; Bobulski R J; Kean J; Mendell J R
Centronuclear myopathy and type-1 hypotrophy without central nuclei. Distinct nosologic entities?
Archives of neurology 1990;47(3):273-6.
1990: Sahenk Z; Whitaker J N; Mendell J R
Immunocytochemical evidence for the retrograde transport of intraaxonal cathepsin D: possible relevance to the dying-back process.
Brain research 1990;510(1):1-6.
1990: Barohn R J; Clanton T; Sahenk Z; Mendell J R
Recurrent respiratory insufficiency and depressed ventilatory drive complicating mitochondrial myopathies.
Neurology 1990;40(1):103-6.
1990: Mendell J R
Immunosuppressive therapy in Duchenne muscular dystrophy: considerations for myoblast transfer studies.
Advances in experimental medicine and biology 1990;280():287-95.
1989: Barohn R J; Kissel J T; Warmolts J R; Mendell J R
Chronic inflammatory demyelinating polyradiculoneuropathy. Clinical characteristics, course, and recommendations for diagnostic criteria.
Archives of neurology 1989;46(8):878-84.
1989: Mendell J R; Moxley R T; Griggs R C; Brooke M H; Fenichel G M; Miller J P; King W; Signore L; Pandya S; Florence J
Randomized, double-blind six-month trial of prednisone in Duchenne's muscular dystrophy.
The New England journal of medicine 1989;320(24):1592-7.
1989: Brooke M H; Fenichel G M; Griggs R C; Mendell J R; Moxley R; Florence J; King W M; Pandya S; Robison J; Schierbecker J
Duchenne muscular dystrophy: patterns of clinical progression and effects of supportive therapy.
Neurology 1989;39(4):475-81.
1989: Kissel J T; Riethman J L; Omerza J; Rammohan K W; Mendell J R
Peripheral nerve vasculitis: immune characterization of the vascular lesions.
Annals of neurology 1989;25(3):291-7.
1988: Fenichel G M; Brooke M H; Griggs R C; Mendell J R; Miller J P; Moxley R T; Park J H; Provine M A; Florence J; Kaiser K K
Clinical investigation in Duchenne muscular dystrophy: penicillamine and vitamin E.
Muscle & nerve 1988;11(11):1164-8.
1988: Hyser C L; Kissel J T; Warmolts J R; Mendell J R
Scapuloperoneal neuropathy: a distinct clinicopathologic entity.
Journal of the neurological sciences 1988;87(1):91-102.
1988: Pakalnis A; Drake M E; Barohn R J; Chakeres D W; Mendell J R
Evoked potentials in chronic inflammatory demyelinating polyneuropathy.
Archives of neurology 1988;45(9):1014-6.
1988: Hyser C L; Mendell J R
Recent advances in Duchenne and Becker muscular dystrophy.
Neurologic clinics 1988;6(3):429-53.
1988: Barohn R J; Levine E J; Olson J O; Mendell J R
Gastric hypomotility in Duchenne's muscular dystrophy.
The New England journal of medicine 1988;319(1):15-8.
1987: Warmolts J R; Mendell J R; O'Dorisio T M; Cataland S
Comparison of the effects of continuous subcutaneous infusion and split-mixed injection of insulin on nerve function in type I diabetes mellitus.
Journal of the neurological sciences 1987;82(1-3):161-9.
1987: Hyser C L; Province M; Griggs R C; Mendell J R; Fenichel G M; Brooke M H; Miller J P; Polakowska R; Doherty R A; Quirk S
Genetic heterogeneity in Duchenne dystrophy.
Annals of neurology 1987;22(4):553-5.
1987: Hyser C L; Doherty R A; Griggs R C; Mendell J R; Polakowska R; Quirk S; Brooke M H; Fenichel G M
Carrier assessment for mothers and sisters of isolated Duchenne dystrophy cases: the importance of serum enzyme determinations.
Neurology 1987;37(9):1476-80.
1987: Brooke M H; Fenichel G M; Griggs R C; Mendell J R; Moxley R T; Miller J P; Kaiser K K; Florence J M; Pandya S; Signore L
Clinical investigation of Duchenne muscular dystrophy. Interesting results in a trial of prednisone.
Archives of neurology 1987;44(8):812-7.
1987: Mendell J R; Kolkin S; Kissel J T; Weiss K L; Chakeres D W; Rammohan K W
Evidence for central nervous system demyelination in chronic inflammatory demyelinating polyradiculoneuropathy.
Neurology 1987;37(8):1291-4.
1987: Mendell J R; Province M A; Moxley R T; Griggs R C; Brooke M H; Fenichel G M; Miller J P; Kaiser K K; King W; Robison J
Clinical investigation of Duchenne muscular dystrophy. A methodology for therapeutic trials based on natural history controls.
Archives of neurology 1987;44(8):808-11.
1987: Hyser C L; Griggs R C; Mendell J R; Polakowska R; Quirk S; Brooke M H; Fenichel G M; Doherty R A
Use of serum creatine kinase, pyruvate kinase, and genetic linkage for carrier detection in Duchenne and Becker dystrophy.
Neurology 1987;37(1):4-10.
1986: Kissel J T; Mendell J R; Rammohan K W
Microvascular deposition of complement membrane attack complex in dermatomyositis.
The New England journal of medicine 1986;314(6):329-34.
1985: Kissel J T; Slivka A P; Warmolts J R; Mendell J R
The clinical spectrum of necrotizing angiopathy of the peripheral nervous system.
Annals of neurology 1985;18(2):251-7.
1981: Mendell J R; Sahenk Z; Warmolts J R; Marshall J K; Thibert P
The spontaneously diabetic BB Wistar rat. Morphologic and physiologic studies of peripheral nerve.
Journal of the neurological sciences 1981;52(1):103-15.

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