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

OLIVOPONTOCEREBELLAR ATROPHY. A REVIEW OF 117 CASESBERCIANO J.1982; J. NEUROL. SCI.; ISSN 0022-510X; NLD; DA. 1982; VOL. 53; NO 2; PP. 253-272; BIBL. 6 P.Article

SPINO-OLIVO-PONTO-CEREBELLO-NIGRAL ATROPHY WITH LEWY BODIES AND BINUCLEATED NERVE CELLS : A CASE REPORT = ATROPHIE SPINO-OLIVO-PONTO-CEREBELLO-NIGRALE AVEC CORPS DE LEWY ET CELLULES NERVEUSES BINUCLEES: RAPPORT D'UN CASKAIYA H.1974; ACTA NEUROPATHOL.; ALLEM.; DA. 1974; VOL. 30; NO 3; PP. 263-269; BIBL. 1P.Article

FORME HEREDITAIRE D'ATROPHIE CEREBELLEUSEKREJCOVA H; FILIPOVA M; SEEMANOVA E et al.1975; CESKOSL. NEUROL. NEUROCHIR.; CESKOSL.; DA. 1975; VOL. 38; NO 71; PP. 294-301; ABS. RUSSE ANGL.; BIBL. 11 REF.Article

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

DEGENERESCENCE STRIATO-NIGRIQUE. A PROPOS DE L'ETUDE CLINIQUE, THERAPEUTIQUE ET ANATOMIQUE DE 2 CASBOUDIN G; GUILLARD A; MIKOL J et al.1976; REV. NEUROL.; FR.; DA. 1976; VOL. 132; NO 2; PP. 137-156; ABS. ANGL.; BIBL. 2 P.Article

GENETIC AND CLINICAL PATTERNS OF HERITABLE CEREBELLAR ATAXIAS IN ADULTS. II: CLINICAL MANIFESTATIONSKONDO K; HIROTA K; KATAGIRI T et al.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 4; PP. 276-284; BIBL. 22 REF.Article

OLIVOPONTOCEREBELLAR ATROPHY IN CHILDREN: A REPORT OF SEVEN CASES IN TWO FAMILIESCOLAN RV; SNEAD OC; CEBALLOS R et al.1981; ANN. NEUROL.; ISSN 0364-5134; USA; DA. 1981; VOL. 10; NO 4; PP. 355-363; BIBL. 18 REF.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

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

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

THE HUMAN PURKINJE CELLS: A GOLGI STUDY IN PATHOLOGYFUJISAWA K; NAKAMURA A.1982; ACTA NEUROPATHOL.; ISSN 0001-6322; DEU; DA. 1982; VOL. 56; NO 4; PP. 255-264; BIBL. 25 REF.Article

ATROPHIE OLIVO-PONTO-CEREBELLEUSE FAMILIALE AVEC MYOCLONIES. LES LIMITES DE LA DYSSYNERGIE CEREBELLEUSE MYOCLONIQUE. (SYNDROME DE RAMSAY-HUNT.)BONDUELLE M; ESCOUROLLE R; BOUYGUES P et al.1976; REV. NEUROL.; FR.; DA. 1976; VOL. 132; NO 2; PP. 113-124; ABS. ANGL.; BIBL. 28 REF.Article

URINE VAPOR PATTERN FOR OLIVOPONTOCEREBELLAR DEGENERATION = PROFIL DES SUBSTANCES VOLATILES DE L'URINE DANS LA DEGENERESCENCE OLIVO-PONTO-CEREBELLEUSEROSENBERG RN; ROBINSON AB; PARTRIDGE D et al.1975; CLIN. BIOCHEM.; CANADA; DA. 1975; VOL. 8; NO 6; PP. 365-368; BIBL. 6 REF.Article

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

OLIVOPONTOCEREBELLAR DEGENERATION. CLINICOPATHOLOGIE CORRELATION OF THE ASSOCIATED RETINOPATHY = DEGENERESCENCE OLIVOPONTOCEREBELLEUSE. CORRELATION CLINICOPATHOLOGIQUE DE LA RETINOPATHIE ASSOCIEERYAN SJ JR; KNOX DL; GRENN WR et al.1975; ARCH. OPHTHALMOL.; U.S.A.; DA. 1975; VOL. 93; NO 3; PP. 169-172; BIBL. 5 REF.Article

Inositol 1,4,5-trisphosphate receptors and protein kinase C in olivopontocerebellar atrophyDESAIAH, D; VIG, P. J. S; SUBRAMONY, S. H et al.Brain research. 1991, Vol 552, Num 1, pp 36-40, issn 0006-8993, 5 p.Article

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

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

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