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Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy

Annals of neurology, 2012-03, Vol.71 (3), p.407-416

2012

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Myovascular innervation: Axon loss in small-fiber neuropathies

Muscle & nerve, 2015-04, Vol.51 (4), p.514-521

2015

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Defining SOD1 ALS natural history to guide therapeutic clinical trial design

Journal of neurology, neurosurgery and psychiatry, 2017-02, Vol.88 (2), p.99-105

2017

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Targeted sequencing and identification of genetic variants in sporadic inclusion body myositis

Neuromuscular disorders : NMD, 2015-04, Vol.25 (4), p.289-296

2015

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Clinical Delineation and Localization to Chromosome 9p13.3–p12 of a Unique Dominant Disorder in Four Families: Hereditary Inclusion Body Myopathy, Paget Disease of Bone, and Frontotemporal Dementia

Molecular genetics and metabolism, 2001-12, Vol.74 (4), p.458-475

2001

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Prevalence of Axonal sensory neuropathy with IgM binding to Trisulfated heparin disaccharide (TS-HDS) in patients with Fibromyalgia (P2.2-100)

Neurology, 2019-04, Vol.92 (15_supplement)

2019

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Prevalence of neuropathy in patients with minimally symptomatic hyperCKemia (2484)

Neurology, 2021-04, Vol.96 (15_supplement)

2021

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CANOMAD and other chronic ataxic neuropathies with disialosyl antibodies (CANDA)

Journal of neurology, 2018-06, Vol.265 (6), p.1402-1409

2018

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LTBP4 genotype predicts age of ambulatory loss in duchenne muscular dystrophy

Annals of neurology, 2013-04, Vol.73 (4), p.481-488

2013

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Cramps and small-fiber neuropathy

Muscle & nerve, 2013-08, Vol.48 (2), p.252-255

2013

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Myelinated and unmyelinated endoneurial axon quantitation and clinical correlation

Muscle & nerve, 2016-02, Vol.53 (2), p.198-204

2016

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The cooperative international neuromuscular research group Duchenne natural history study: Glucocorticoid treatment preserves clinically meaningful functional milestones and reduces rate of disease progression as measured by manual muscle testing and other commonly used clinical trial outcome measures

Muscle & nerve, 2013-07, Vol.48 (1), p.55-67

2013

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Myelinated and unmyelinated endoneurial axon quantitation and clinical correlation: Endoneurial Axon Quantitation

Muscle & nerve, 2016-02, Vol.53 (2), p.198-204

2016

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Motor neuron disease associated with copper deficiency

Muscle & nerve, 2006-12, Vol.34 (6), p.789-793

2006

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The cooperative international neuromuscular research group duchenne natural history study-a longitudinal investigation in the era of glucocorticoid therapy: Design of protocol and the methods used

Muscle & nerve, 2013-07, Vol.48 (1), p.32-54

2013

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Association Study of Exon Variants in the NF-κB and TGFβ Pathways Identifies CD40 as a Modifier of Duchenne Muscular Dystrophy

American journal of human genetics, 2016-11, Vol.99 (5), p.1163-1171

2016

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Safety and Efficacy of Topiramate in Individuals With Cryptogenic Sensory Peripheral Neuropathy With Metabolic Syndrome: The TopCSPN Randomized Clinical Trial

JAMA neurology, 2023-12, Vol.80 (12), p.1334

2023

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Characteristics of Patients Evaluated for Small Fiber Neuropathy with Skin Biopsy (P4.117)

Neurology, 2014-04, Vol.82 (10_supplement)

2014

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Prevalence of Axonal Sensory Neuropathy With IgM Binding to Trisulfated Heparin Disaccharide in Patients With Fibromyalgia

Journal of clinical neuromuscular disease, 2019-03, Vol.20 (3), p.103-110

2019

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Inflammatory Demyelinating Neuropathies

Current treatment options in neurology, 2011-04, Vol.13 (2), p.131-142

2011

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Selective staining of the cerebellar molecular layer by serum IgG in Miller-Fisher and related syndromes

Neurology, 1996-11, Vol.47 (5), p.1317-1320

1996

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Cooperative international neuromuscular research group duchenne natural history study demonstrates insufficient diagnosis and treatment of cardiomyopathy in duchenne muscular dystrophy

Muscle & nerve, 2014-08, Vol.50 (2), p.250-256

2014

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A controlled trial of intravenous immunoglobulin in multifocal motor neuropathy

Journal of the peripheral nervous system, 2013-12, Vol.18 (4), p.321-330

2013

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Editorial

Degenerative neurological and neuromuscular disease, 2011-03, p.1

Lopate, Glenn

2011

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Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy

Myovascular innervation: Axon loss in small-fiber neuropathies

Defining SOD1 ALS natural history to guide therapeutic clinical trial design

Targeted sequencing and identification of genetic variants in sporadic inclusion body myositis

Clinical Delineation and Localization to Chromosome 9p13.3–p12 of a Unique Dominant Disorder in Four Families: Hereditary Inclusion Body Myopathy, Paget Disease of Bone, and Frontotemporal Dementia

Prevalence of Axonal sensory neuropathy with IgM binding to Trisulfated heparin disaccharide (TS-HDS) in patients with Fibromyalgia (P2.2-100)

Prevalence of neuropathy in patients with minimally symptomatic hyperCKemia (2484)

CANOMAD and other chronic ataxic neuropathies with disialosyl antibodies (CANDA)

LTBP4 genotype predicts age of ambulatory loss in duchenne muscular dystrophy

Cramps and small-fiber neuropathy

Myelinated and unmyelinated endoneurial axon quantitation and clinical correlation

Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort

Myelinated and unmyelinated endoneurial axon quantitation and clinical correlation: Endoneurial Axon Quantitation

Motor neuron disease associated with copper deficiency

The cooperative international neuromuscular research group duchenne natural history study-a longitudinal investigation in the era of glucocorticoid therapy: Design of protocol and the methods used

Association Study of Exon Variants in the NF-κB and TGFβ Pathways Identifies CD40 as a Modifier of Duchenne Muscular Dystrophy

Safety and Efficacy of Topiramate in Individuals With Cryptogenic Sensory Peripheral Neuropathy With Metabolic Syndrome: The TopCSPN Randomized Clinical Trial

Characteristics of Patients Evaluated for Small Fiber Neuropathy with Skin Biopsy (P4.117)

Prevalence of Axonal Sensory Neuropathy With IgM Binding to Trisulfated Heparin Disaccharide in Patients With Fibromyalgia

Inflammatory Demyelinating Neuropathies

Selective staining of the cerebellar molecular layer by serum IgG in Miller-Fisher and related syndromes

Cooperative international neuromuscular research group duchenne natural history study demonstrates insufficient diagnosis and treatment of cardiomyopathy in duchenne muscular dystrophy

A controlled trial of intravenous immunoglobulin in multifocal motor neuropathy

Editorial

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