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Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
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Inclusion Body Myositis, Observations in 40 Patients
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Cytochrome c Oxidase Deficiency in Leigh Syndrome
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Acid Maltase Deficiency
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Vascular Parkinsonism and Dementia in a CADASIL Case with Intact Nigrostriatal Dopaminergic System
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Generalized Arteriopathy in Patients with Cervical Artery Dissection
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Neurological Presentation of Fabry's Disease in a 52 Year Old Man
JNNP 73:340-342, Mohanraj,R.,et al, 2002
Neurologic Presentation of Whipple Disease
Medicine 81:443-457, Gerard,A.,et al, 2002
The Wide Spectrum of Myofibrillar Myopathy Suggests a Multifactorial Etiology and Pathogenesis
Neurol 51:1646-1655, Amato,A.A.,et al, 1998
Diagnostic Criteria for Sporadic Creutzfeldt-Jakob Disease
Arch Neurol 53:913-920, Kretzschmar,H.A.,et al, 1996
Cerebral Amyloid Angiopathy Manifesting as Recurrent Intracerebral Hemorrhage
Arch Neurol 41:330-333, Finelli,P.F.,et al, 1984
L'Angiopathie Amyloide Cerebrale
Rev Neurol (Paris) 137:181-194981., Regli,F.,et al, 1981
Alcoholic Myopathy in Heart & Skeletal Muscle
NEJM 301:28-33, Rubin,E., 1979
Neoplastic Angioendotheoliosis:Ultrastructural Study & Review of the Literature
Ann Neurol 3:393, Petito,C.K.,et al, 1978
Progressive Camptocormia with Head Drop and Dysphagia
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A 23-Year-Old Man With Seizures and Visual Deficit
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Weak at the Knees
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Adult-Onset Adrenoleukodystrophy Manifesting as Dementia
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Clinicopathological Conference Metachromatic Leukodystrophy (juvenile type)
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Lipomembranous Polycystic Osteodysplasia (Brain, Bone, & Fat Disease)
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Santavuori Disease:Diagnosis by Leukocyte Ultrastructure
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Diagnosis of Infatile Neuroaxonal Dystrophy by Skin Biopsy
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Juvenile Huntington Chorea:Clinical, Ultrastructural, & Biochemical Studies
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Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis
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Herpes Simplex & the Human Nervous System
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