A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Neurotoxicity of Commonly Used Antineoplastic Agents
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Clinicopathologic Conference, Hypocalcemic Myopathy Due to Hypoparathyroidism
NEJM 388:1513-1520, Case 12-2023, 2023
Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
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Spinal Muscular Atrophy
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Acute Flaccid Myelitis: Cause, Diagnosis, and Management
Lancet 394:334-397, Murphy, O.C.,et al, 2021
A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
Neurol 97:958-963, Davalos, L.,et al, 2021
Rapidly Progressive Gait Disorder and Cranial Nerves Involvement in a 9-year-old boy
Neurol 94:e330-e334, Lipp, A.,et al, 2020
Progressive Proximal Weakness in a 61-Year-Old Man
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A 54-year-old man with Dyspnea and Muscle Weakness
Neurol 92:e1136-e1140, Chertcoff, A.,et al, 2019
Muscular Dystrophies
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Young Adult with Dysphagia and Severe Weight Loss
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A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
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Myasthenia Gravis
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The Limbic-Girdle Muscular Dystrophies
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Family Paralysis
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New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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Clinicopath Conf,Hepatitis C,Type II Cryoglobulinemia,Vasculitis,B-cell Lymphoma,Mononeuritis Multiplex,Case 3-1999
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Adult Botulism
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CIDP:Clinical Features & Responses to Trtm in 67 Consecutive Pts with/without a Monoclonal Gammopathy
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Various Types of Hereditary Inclusion Body Myopathies Map to Chromosome 9p1-q1
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Bent Spine Syndrome
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Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996
Neurologic Aspects of Inflammatory Bowel Disease
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Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
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Lambert-Eaton Myasthenic Syndrome (LEMS) in Association with Lymphoproliferative Disorders
Muscle & Nerve 18:715-719995., Argov,Z.,et al, 1995
Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995
Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
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Myotonic Dystrophy
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Thyrotoxic Periodic Paralysis in the US, Report of 7 Cases & Review of the Literature
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Familial Inclusion Body Myositis:Evidence for Autosomal Dominant Inheritance
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Familial Adult-Onset Muscular Dystrophy with Leukoencephalopathy
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Neurologic Aspects of Cobalamin Deficiency
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Late Effects of Paralytic Poliomyelitis in Olmsted County, Minnesota
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Chronic Cardiomyopathy and WEakness or Acute Coma in Children with a Defect in Carnitine Uptake
Ann Neurol 30:709-716, Stanley,C.A.,et al, 1991
Neurologic Crises in Hereditary Tyrosinemia
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Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
Neuropediatrics 19:62-71, Voit,T.,et al, 1988
Neurotoxic Effects of Organophosphorus Insecticides:An Intermediate Syndrome
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Central Core Disease, Clinical Features in 13 Patients
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A Long-Term Follow-Up Study of Patients with Post-Poliomyelitis Neuromuscular Symptoms
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Severe Neurological Disease Associated with Hyperparathyroidism
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