Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996
Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996
Leptomeningeal Carcinomatosis:Presenting Features and Prognostic Factors
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Critical Illness Myopathy and Neuropathy
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Motor Neuropathy Due to Docetaxel and Paclitaxel
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Hereditary Spastic Paraplegia:Advances in Genetic Research
Neurol 46:1507-1514, Fink,J.K.,et al, 1996
MR Imaging of the Meninges, Part II, Neoplastic Disease
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Evidence for Cardioembolic Stroke in a Case of Kearns-Sayre Syndrome
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Acute Bacterial Myositis Due to Staphylococcus Aureus Septicemia
Neurol 45:390-391, Sato,K.,et al, 1995
Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
Muscle & Nerve 18:267-275995., Ionasecu,V.V., 1995
Renal Cell Carcinomatous Meningitis:Pathologic and Immunohistochemical Features
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Clinicopath Conf
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Critical Illness Neuromuscular Disease in Children Manifested as Ventilatory Dependence
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Apolipoprotein E Allele E4, Dementia, and Cognitive Decline in a Population Sample
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Statement of Use of Apolipoprotein E Testing for Alzheimer Disease
JAMA 274:1627-1629, Farrer,L.A.,et al, 1995
Apoliprprotein E E4 Allele & the Lifetime Risk of Alzheimer's Disease:What Physicians Know, & What They Should Know
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Apolipoprotein E Genotype in Patients with Alzheimer's Disease:Implications for Risk of Dementia Among Relatives
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Inclusion Body Myositis and Myopathies
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Myasthenic Symptoms in Patients with Mitochondrial Myopathies
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Apolipoprotein E E4 in Inclusion Body Myositis
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Neurologic Aspects of Inflammatory Bowel Disease
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Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
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Late-Onset Mitochondrial Myopathy
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Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
Arch Neurol 52:25-31, Ricker,K.,et al, 1995
Diffuse Leptomeningeal Gliomatosis with Osteoblastic Metastases and No Evidence of Intraaxial Lesions
AJNR 16:1018-1020, Pingi,A.,et al, 1995
Medical Complications During Stroke Rehabilitation
Stroke 26:990-994, Kalra,L.,et al, 1995
Prolonged Paralysis After Neuromuscular Blockage
Muscle & Nerve, 18:937-94295., Gooch,J., 1995
The Prevention of Neurogenetic Disease
Arch Neurol 52:356-362, 3451995., Rosenberg,R.N.&Iannaccone,S.T., 1995
Mild Traumatic Brain Injury:Pathophysiology, Natural History, and Clinical Management
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Lyme Neuroborreliosis
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Myositis:Immunologic Contributions to Understanding Cause, Pathogenesis, and Therapy
Ann Int Med 122:715-724, Plotz,P.H.,et al, 1995
Proximal Myotonic Myopathy Syndrome in the Absence of Trinucleotide Repeat Expansions
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Mitochondrial DNA and Disease
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Primary Adhalin Deficiency as a Cause of Muscular Dystrophy in Patients with Normal Dystrophin
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Inclusion Body Myositis Presenting with Isolated Erector Spinae Paresis
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Common Variable Immunodeficiency and Inclusion Body Myositis:A Distinct Myopathy Mediated by Natural Killer Cells
Ann Neurol 37:806-810, Dalakas,M.C.&Illa,I., 1995
Amyloidosis Causing A Progressive Myopathy
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Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency
Ann Neurol 38:450-454, Wokke,J.H.J.,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
Neuroimaging and Cerebrospinal Fluid Cytology in the Diagnosis of Leptomeningeal Metastasis
Ann Neurol 38:51-57, Frelich,R.J.,et al, 1995
Detection of Cerebrospinal Fluid Metastasis:CT Myelography or MRI?
AJNR 16:1147-1151, Heinz,R.,et al, 1995
Neurological Multisystem Manifestation in Multiple Symmetric Lipomatosis:A Clinical and Electrophysiological Study
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Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
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Leptomeningeal Dissemination of Malignant Glioma Simulating Cerebral vasculitis:Case Report with Angiographic & Path
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Postcontrast MRI of Cranial Meninges:Leptomeningitis vs Pachymeningitis
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Anticonvulsant Hypersensitivity Syndrome
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Myasthenic Symptoms in Patients with Mitochondrial Myopathies
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Myotonic Dystrophy
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The Nondystrophic Myotonias
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Becker Muscular Dystrophy with Onset after 60 Years
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