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kw.\*:("Olivopontocerebellar")

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The olivopontocerebellar atrophiesDUVOISIN, R. C; PLAITAKIS, A.Advances in neurology. 1984, Vol 41, issn 0091-3952, 302 p.Serial Issue

Grading of neuropathology in multiple system atrophy : Proposal for a novel scaleJELLINGER, Kurt A; SEPPI, Klaus; WENNING, Gregor K et al.Movement disorders. 2005, Vol 20, pp S29-S36, issn 0885-3185, SUP12Conference Paper

The spectrum of pathological involvement of the striatonigral and olivopontocerebellar systems in multiple system atrophy: clinicopathological correlationsOZAWA, Tetsutaro; PAVIOUR, Dominic; REVESZ, Tamas et al.Brain. 2004, Vol 127, pp 2657-2671, issn 0006-8950, 15 p., 12Article

LA NOSOLOGIA DE LA ATROFIA OLIVOPONTOCEREBELOSA: REVISION CRITICA = LA NOSOLOGIE DE L'ATROPHIE OLIVO-PONTO-CEREBELLEUSE: REVISION CRITIQUEBERCIANO J.1981; ARCH. NEUROBIOL.; ISSN 0004-0576; ESP; DA. 1981; VOL. 44; NO 3; PP. 163-182; ABS. ENG; BIBL. 6 P.Article

The efficacy of combined estrogen and buspirone treatment in olivopontocerebellar atrophyHEO, Jae-Hyeok; LEE, Soon-Tae; CHU, Kon et al.Journal of the neurological sciences. 2008, Vol 271, Num 1-2, pp 87-90, issn 0022-510X, 4 p.Article

Rasagiline is neuroprotective in a transgenic model of multiple system atrophySTEFANOVA, Nadia; POEWE, Werner; WENNING, Gregor K et al.Experimental neurology (Print). 2008, Vol 210, Num 2, pp 421-427, issn 0014-4886, 7 p.Article

Immunohistochemical expression of microtubule-associated protein 5 (MAP5) in glial cells in multiple system atrophyARAI, N; NISHIMURA, M; ODA, M et al.Journal of the neurological sciences. 1992, Vol 109, Num 1, pp 102-106, issn 0022-510XArticle

Sensory and motor peripheral neuropathy in olivopontocerebellar atrophyROSSI, A; CIACCI, G; FEDERICO, A et al.Acta neurologica scandinavica. 1986, Vol 73, Num 4, pp 363-371, issn 0001-6314Article

Glutamate dehydrogenase deficiency in patients with olivopontocerebellar atrophyDUVOISIN, R. C; CHOKROVERTY, S; LEPORE, F et al.Neurology. 1983, Vol 33, Num 10, pp 1322-1326, issn 0028-3878Article

Menzel's hereditary ataxia with slow eye movements and myoclonus: a clinico-pathological studyRONDOT, P; DE RECONDO, J; DAVOUS, P et al.Journal of the neurological sciences. 1983, Vol 61, Num 1, pp 65-80, issn 0022-510XArticle

ATROPHIC MACULOPATHY ASSOCIATED WITH HEREDITARY ATAXIADUINKERKE EEROLA KU; CRUYSBERG JRM; DEUTMAN AF et al.1980; AM. J. OPHTHALMOL.; ISSN 0002-9394; USA; DA. 1980; VOL. 90; NO 5; PP. 597-603; BIBL. 25 REF.Article

ANTERIOR HORN CELL DISEASE ASSOCIATED WITH PONTOCEREBELLAR HYPOPLASIA IN INFANTS.GOUTIERES F; AICARDI J; FARKAS E et al.1977; J. NEUROL. NEUROSURG. PSYCHIATRY; G.B.; DA. 1977; VOL. 40; NO 4; PP. 370-378; BIBL. 19 REF.Article

NEUROTRANSMITTER AMINO ACIDS IN DOMINANTLY INHERITED CEREBELLAR DISORDERSPERRY TL; KISH SJ; HANSEN S et al.1981; NEUROLOGY; ISSN 0028-3878; USA; DA. 1981; VOL. 31; NO 3; PP. 237-242; BIBL. 31 REF.Article

Dominant spinocerebellar ataxia: genetic counselingJACKSON, J. F; CURRIER, R. D; MORTON, N. E et al.Journal of neurogenetics. 1983, Vol 1, Num 1, pp 87-90, issn 0167-7063Article

CHOREE DE HUNTINGTON ET ATROPHIE CEREBELLEUSE. (A PROPOS D'UNE OBSERVATION ANATOMO-CLINIQUE).CASTAIGNE P; ESCOUROLLE R; GRAY F et al.1976; REV. NEUROL.; FR.; DA. 1976; VOL. 132; NO 4; PP. 233-240; ABS. ANGL.; BIBL. 27 REF.Article

Spinal muscular atrophy combined with sporadic olivopontocerebellar atrophyWEI LUO; ZHIYUAN OUYANG; YI GUO et al.Clinical neurology and neurosurgery. 2008, Vol 110, Num 8, pp 855-858, issn 0303-8467, 4 p.Article

MRI-based volumetric differentiation of sporadic cerebellar ataxiaBÜRK, K; GLOBAS, C; WAHL, T et al.Brain. 2004, Vol 127, pp 175-181, issn 0006-8950, 7 p., 1Article

Familial olivopontocerebellar atrophy with neonatal onset: a recessively inherited syndrome with systemic and biochemical abnormalitiesHARDING, B. N; DUNGER, D. B; GRANT, D. B et al.Journal of neurology, neurosurgery and psychiatry. 1988, Vol 51, Num 3, pp 385-390, issn 0022-3050Article

Olivopontocerebellar atrophy: immunocytochemical and golgi observationsKOEPPEN, A. H; MITZEN, E. J; HANS, M. B et al.Neurology. 1986, Vol 36, Num 11, pp 1478-1488, issn 0028-3878Article

Cytoskeletal protein abnormalities in patientw with olivopontocerebellar atrophy : an immunocytochemical and Gallyas silver impregnation studyKOBAYASHI, K; MIYAZU, K; KATSUKAWA, K et al.Neuropathology and applied neurobiology (Print). 1992, Vol 18, Num 3, pp 237-249, issn 0305-1846Conference Paper

Degeneration of the corticopontine tract in olivoponteocerebellar atrophyYAGISHITA, S; YOKOI, S; IWABUCHI, K et al.Virchows Archiv. A, Pathological anatomy and histopathology. 1991, Vol 418, Num 2, pp 99-103, issn 0174-7398Article

Glycerophosphoethanolamine concentration is elevated in brain of patients with dominantly inherited olivopontocerebellar atrophyKISH, S. J; ROBITAILLE, Y; BALL, M et al.Neuroscience letters. 1990, Vol 120, Num 2, pp 209-211, issn 0304-3940, 3 p.Article

Olivopontocerebellar atrophy in an infant (an autopsy case)JUCK JOON HWANG; YOON SEONG LEE; JUNG BIN LEE et al.Sehur huidai hagsur ji. (Seoul journal of medicine). 1987, Vol 28, Num 2, pp 149-153, issn 0253-2972Article

Familial ataxia with extreme difference in age of clinical onsetAMIT, R; GRANIT, G; SHAPIRA, Y et al.Neuropediatrics. 1986, Vol 17, Num 3, pp 165-167, issn 0174-304XArticle

Reduction of noradrenaline in cerebellum of patients with olivopontocerebellar atrophyKISH, S. J; SHANNAK, K. S; HORNYKIEWICZ, O et al.Journal of neurochemistry. 1984, Vol 42, Num 5, pp 1476-1478, issn 0022-3042Article

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