Age and Cause of Death in Mitochondrial Diseases
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Sjogren-Larsson Syndrome, Clinical and MRI/MRS Findings in FALDH-Deficient Patients
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Is There a Familial Carpal Tunnel Syndrome? An Evaluation and Literature Review
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Hereditary Form of Parkinsonism-Dementia
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Limbic Encephalitis:Comparison of FDG PET and MR Imaging Findings
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Near-Fatal Heat Stroke During the 1995 Heat Wave in Chicago
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Follow-up of Nine Patients with Hurler Syndrome After Bone Marrow Transplantation
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Mucolipidosis Type IV; Characteristic MRI Findings
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Proton Spectroscopy in Myotonic Dystrophy, Correlations with CTG Repeats
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Congenital Muscular Dystrophy:Use of Brain MR Imaging to Predict Merosin Deficiency
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MR of Extraocular Muscles in Chronic Progressive External Ophthalmoplegia
AJNR 19:95-99, Carlow,T.J.,et al, 1998
Detection of a Varient Protein in Hair:New Diagnostic Method in Portuguese Type Familial Amyloid Polyneuropathy
BMJ 316:1500-1501, Ando,Y.,et al, 1998
Anesthetic and Surgical Complictions in 219 Cases of Myotonic Dystrophy
Neurol 49:1646-1650, Mathieu,J.,et al, 1997
Myotonic Dystrophy, The Role of Large Triplet Repeat Length in the Develop of Mental Retardation
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The Muscular Dystrophies-Clarity or Chaos
NEJM 336 650-651, Dubowitz,V., 1997
Prognosis in Familial ALS:Progr & Surv in Pts with glu100gly & ala4val Mutations in Cu, Zn Superoxide Dismutase
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Obstetric Aspects in Women with FSH Muscular Dystrophy, Limb-Girdle Musc Dyst, & Cogen Myopathies
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Primary Adhalinopathy (x-Sarcoglycanopathy) :Clin, Path & Genetic Correl in 20 Pts with Autosomal Recessive Muscular Dystrophy
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X-Linked Emery-Dreifuss Muscular Dystrophy Can Be Diagnosed from Skin Biopsy or Blood Sample
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Motor Neuron Syndromes in Cancer Patients
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Familial Nature and Continuing Morbidity of the Amyotrophic Lateral Sclerosis-Parkinsonism Dementia Complex of Guam
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Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
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An Acutely Confused 15-Year-Old Girl
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Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy
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Distal WEakness in Dystrophin-Deficient Muscular Dystrophy
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The Effect on Memory of Chronic Prednisone Treatment in Patients with Systemic Disease
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From Enigmatic to Problematic:The New Molecular Genetics of Childhood Spinal Muscular Atrophy
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Palliative Care in Neurology
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Neuroradiologic Findings in Polyarteritis Nodosa
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Memory, Attention, and Executive Function in Chronic Fatigue Syndrome
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Cognitive Dysfunction as the Major Presenting Feature of Becker's Muscular Dystrophy
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Clinical Heterogeneity of Adhalin Deficiency
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Prenatal Diagnosis of Duchenne Muscular Dystrophy Using a Single Fetal Nucleated Erythrocyte in Maternal Blood
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Is Chronic Respiratory Failure in Neuromuscular Diseases Worth Treating
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Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
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Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
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Investigation of Muscle Disease
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Cerebrovascular Complications of Fabry's Disease
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Mastocytosis-Induced Nyctalopia
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Paraneoplastic Limbic Encephalitis in Hodgkin's Disease
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Evaluation of the Cardiomyopathy in Becker Muscular Dystrophy
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Hypoglycaemia in Spinal Muscular Atrophy
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Natural History in Proximal Spinal Muscular Atrophy
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Proximal Myotonic Myopathy Syndrome in the Absence of Trinucleotide Repeat Expansions
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Deficiency of Brain Synaptic Dystrophin in Human Duchenne Muscular Dystrophy
Ann Neurol 38:446-449, Kim,T.W.,et al, 1995
Brain Abnormalities in Duchenne Muscular Dystrophy:Phosphorus-31 Magnetic Resonance Spectroscopy & Neuropsych Study
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Primary Adhalin Deficiency as a Cause of Muscular Dystrophy in Patients with Normal Dystrophin
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Myoblast Transfer in the Tratment of Duchenne's Muscular Dystrophy
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