Neurologic Disorders in Renal Failure (1st of Two Parts)
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Acute Quadriparesis with Muscle Spasms Related to Electrolyte Disturbances in Steatorrhea
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A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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Brugada Syndrome in Spinal and Bulbar Muscular Atrophy
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The Acquired Metabolic Disorders of the Nervous System, Dialysis Disequilibrium Syndrome
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Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis
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Degenerative Diseases of the Nervous System, Kennedy Syndrome (X-Linked Bulbospinal Muscular Atrophy)
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Heterogeneity of Coenzyme Q10 Deficiency
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Tired Legs - A Gut Diagnosis
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Amyotrophic Lateral Sclerosis
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Epidemiology, Pathophysiology, & Management of Hyponatremic Encephalopathy
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Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
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Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
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McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
JNNP 55:407-408, Felice,K.J.,et al, 1992
Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
Neurol 41:823-828, Olney,R.K.,et al, 1991
Autosomal Dominant Cramping Disease
Arch Neurol 47:810-812, Ricker,K.&Moxley,R.T., 1990
Familial X-linked Myalgia and Cramps:A Nonprogressive Myopathy Associated with a Deletion in the Dystrophin Gene
Neurol 39:1277-1280, Gospe,S.M.,et al, 1989
Autoantibodies to Glutamic Acid Decarboxylase in Pt with Stiff-Man Syndr, Epilepsy & Type I Diabetes Mellitus
NEJM 318:1012-1020, Solimena,M.,et al, 1988
Phosphorylase Deficiency
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McArdle's Disease in the 1980s
NEJM 312:370-371, Layzer,R.B., 1985
Cylindrical Spirals in a Familial Neuromuscular Disorder
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Celiac Sprue & Refractory Sprue
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