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Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
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Various Types of Hereditary Inclusion Body Myopathies Map to Chromosome 9p1-q1
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Gene Locus for Autosomal Recessive Distal Myopathy with Rimmed Vacuoles Maps to Chromosome 9
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Inclusion Body Myositis and Myopathies
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Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
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A 42-year-old man with unilateral leg weakness
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Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
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Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
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A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
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Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
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A 23-Year-Old Man With Seizures and Visual Deficit
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Fragile X Premutation With Atypical Symptoms at Onset
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Inclusion Body Myositis
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Treatment of Inclusion-Body Myositis with High-Dose Intravenous Immunoglobulin
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Spectrum of Inclusion Body Myositis
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Inclusion Body Myositis
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Lafora Disease:Diagnosis by Liver Biopsy
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Human-To-Human Transmission of Rabies Virus by Corneal Transplant
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Abnormalties In Cultured Muscle & Periphral Nerve Of A Patient With Adrenomyeloneuropathy
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Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis
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Polyradiculoneuropathy in Addison's Disease:Case report & review of literature
Neurol 27:494, Abbas,D.H.,et al, 1977
Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger
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Epidemiology of Motor-Neuron Diseases
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