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DEGENERATIVE DISEASES OF THE NERVOUS SYSTEM
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MCSHANE MA, BOYD S, HARDING B, et al: Progressive bulbar paralysis of childhood: A reappraisal of Fazio-Londe disease Brain 115:1889, 1992 MENDEZ MF, ADAMS NL, LEWANDOWSKI KS: Neurobehavioral changes associated with caudate lesions Neurology 39:349, 1989 MENDEZ MF, MENDEZ MA, MARTIN R, et al: Complex visual disturbances in Alzheimer s disease Neurology 40:439, 1990 MESULAM M-M: Slowly progressive aphasia without generalized dementia Ann Neurol 11:592, 1982 MESULAM MM, GROSSMAN M, HILLIS A, et al: The core and halo of primary progressive aphasia and semantic dementia Ann Neurol 54 (Suppl 5):S11, 2003 MITSUYAMA Y: Presenile dementia with motor neuron disease in Japan: Clinico-pathological review of 26 cases J Neurol Neurosurg Psychiatry 47:953, 1984 MOLLARET P: La Maladie de Friedreich Paris, Legrand, 1929 MORENO MARTINEZ JM, GARCIA DE LA ROCHA ML, MARTIN ARAQUEZ A: Monomelic segmental amyotrophy: A Spanish case involving the leg Rev Neurol (Paris) 146:443, 1990 MORRIS JC, COLE M, BANKER BQ, WRIGHT D: Hereditary dysphasic dementia and the Pick-Alzheimer spectrum Ann Neurol 16:458, 1984 MULDER DW, KURLAND LT, OFFORD KP, BEARD CM: Familial adult motor neuron disease: Amyotrophic lateral sclerosis Neurology 36:511, 1986 MUNSAT TL, SKERRY L, KORF B, et al: Phenotypic heterogeneity of spinal muscular atrophy mapping to chromosome 5q112-133 (SMA 5q) Neurology 40:1831, 1990 MURATA Y, YAMAGUCHI S, KAWAKAMI H: Characteristic magnetic resonance imaging ndings in Machado-Joseph disease Arch Neurol 55: 33, 1998 NACHMANOFF DB, SEGAL RA, DAWSON DM, et al: Hereditary ataxia with sensory neuronopathy: Biemond s ataxia Neurology 48:273, 1997 NAKANO KK, DAWSON DM, SPENCE A: Machado disease: A hereditary ataxia in Portuguese emigrants to Massachusetts Neurology 22:49, 1972 NEARY D: Non-Alzheimer s disease forms of cerebral atrophy J Neurol Neurosurg Psychiatry 53:929, 1990 NEARY D, SNOWDEN JS, BOWDEN DM: Neuropsychological syndromes in presenile dementia due to cerebral atrophy J Neurol Neurosurg Psychiatry 49:163, 1986 NEE LE, ELDRIDGE R, SUNDERLAND T, et al: Dementia of the Alzheimer type: Clinical and family study of 22 twin pairs Neurology 37:359, 1987 NIELSEN JE, KRABBE K, JENNUM P, et al: Autosomal dominant pure spastic paraplegia: A clinical, paraclinical and genetic study J Neurol Neurosurg Psychiatry 64:61, 1998 NIELSEN SL: Striatonigral degeneration disputed in familial disorder Neurology 27:306, 1977 NIKOSKELAINEN E, SAVONTAUS ML, WANNE OP, et al: Leber s hereditary optic neuroretinopathy A maternally inherited disease: A genealogic study in four pedigrees Arch Ophthalmol 105:665, 1987 NYGAARD TG, DUVOISIN RC: Hereditary dystonia-parkinsonism syndrome of juvenile onset Neurology 36:1424, 1986 NYGAARD TG, WILHELMSEN KC, RISCH NJ, et al: Linkage mapping of dopa-responsive dystonia (DRD) to chromosome 14q Nature Genet 5: 386, 1993 OKAZAKI H, LIPKIN LE, ARONSON SM: Diffuse intracytoplasmic ganglionic inclusions (Lewy type) associated with progressive dementia and quadriparesis in exion J Neuropathol Exp Neurol 20:237, 1961 OPPENHEIM H: Textbook of Nervous Diseases (A Bruce, transl) Edinburgh, Schulze, 1911, p 512 PAKKENBERG B, MOLLER A, GUNDERSEN HJG, et al: The absolute number of nerve cells in substantia nigra in normal subjects and in patients with Parkinson s disease estimated with an unbiased stereological method J Neurol Neurosurg Psychiatry 54:30, 1991 PAPP MI, KAHN JE, LANTOS PL: Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy (striatonigral degeneration, olivopontocerebellar atrophy and Shy-Drager syndrome) J Neurol Sci 94: 79, 1989
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