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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

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

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

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

Treatment of heredo-degenerative ataxias with amantadine hydrochlorideBOTEZ, M. I; YOUNG, S. N; BOTEZ, T et al.Canadian journal of neurological sciences. 1991, Vol 18, Num 3, pp 307-311, issn 0317-1671Article

Oligodendrogial microtubular tangles in olivopontocerebellar atrophyNAKAZATO, Y; YAMAZAKI, H; HIRATO, J et al.Journal of neuropathology and experimental neurology. 1990, Vol 49, Num 5, pp 521-530, issn 0022-3069Article

Reflex myoclonus in olivopontocerebellar atrophyRODRIGUEZ, M. E; ARTIEDA, J; ZUBIETA, J. L et al.Journal of neurology, neurosurgery and psychiatry. 1994, Vol 57, Num 3, pp 316-319, issn 0022-3050Conference Paper

An autopsy case of mitochondrial encephalomyopathy with prominent degeneration in olivo-ponto-cerebellar systemKAGEYAMA, Y; ICHIKAWA, K; FUJIOKA, A et al.Acta neuropathologica. 1991, Vol 83, Num 1, pp 99-103, issn 0001-6322Article

Olivopontocerebellar atrophy of neonatal onset and disialotransferrin developmental deficiency syndromeHORSLEN, S. P; CLAYTON, P. T; HARDING, B. N et al.Archives of disease in childhood. 1991, Vol 66, Num 9, pp 1027-1032, issn 0003-9888Article

Familial olivopontocerebellar atrophy with macular degeneration: a separate entity among the olivopontocerebellar atrophiesANTTINEN, A; NIKOSKELAINEN, E; MARTTILA, R. J et al.Acta neurologica scandinavica. 1986, Vol 73, Num 2, pp 180-190, issn 0001-6314Article

Selective loss of expression of glutamate glur2/r3 receptor subunits in cerebellar tissue from a patient with olivopontocerebellar atrophyDIRSON, Gregoire; DESJARDINS, Paul; TANNENBERG, Tony et al.Metabolic brain disease. 2002, Vol 17, Num 2, pp 77-82, issn 0885-7490Article

Patterns of neuropsychological performance in multiple system atrophy compared to sporadic and hereditary olivopontocerebellar atrophyBERENT, S; GIORDANI, B; GILMAN, S et al.Brain and cognition (Print). 2002, Vol 50, Num 2, pp 194-206, issn 0278-2626, 13 p.Article

XY sex reversal and a nonprogressive neurologic disorder : A new syndrome?MAHBUBUL HUQ, A. H. M; NIGRO, Michael A.Pediatric neurology. 2000, Vol 23, Num 4, pp 357-360, issn 0887-8994Article

Fatal outcome in a case of pontocerebellar hypoplasia type 2GRELLNER, W; ROHDE, K; WILSKE, J et al.Forensic science international. 2000, Vol 113, Num 1-3, pp 165-172, issn 0379-0738Conference Paper

Prolonged sympathetic reflex latency on Skin nerves in sporadic cerebellar degenerationSHINDO, K; TSUNODA, S.-I; SHIOZAWA, Z et al.Archives of neurology (Chicago). 1999, Vol 56, Num 4, pp 462-466, issn 0003-9942Article

Non-familial olivopontocerebellar atrophy combined with late onset Alzheimer's disease : a clinico-pathological case reportKOBAYASHI, K; FUKUTANI, Y; HAYASHI, M et al.Journal of the neurological sciences. 1998, Vol 154, Num 1, pp 106-112, issn 0022-510XArticle

Movement-related cortical potentials and contingent negative variation in olivopontocerebellar atrophyOISHI, M; MOCHIZUKI, Y; TAKASU, T et al.Clinical EEG electroencephalography. 1997, Vol 28, Num 4, pp 245-248, issn 0009-9155Article

Muscle morphology and mitochondrial investigations of a family with autosomal dominant cerebellar ataxia and retinal degeneration mapped to chromosome 3p12-p21.1FORSGREN, L; LIBELIUS, R; HOLMBERG, M et al.Journal of the neurological sciences. 1996, Vol 144, Num 1-2, pp 91-98, issn 0022-510XArticle

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