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FIELD TESTING OF AN ATAXIA SCORING AND STAGING SYSTEMPOURCHER E; BARBEAU A.1980; CAN. J. NEUROL. SCI.; ISSN 0317-1671; CAN; DA. 1980; VOL. 7; NO 4; PP. 339-344; ABS. FRE; BIBL. 8 REF.Article

HORBUS FRIEDREICH ALS NEUROKARDIOLOGISCHE KRANKHEIT. II: PATHOMORPHOLOGIE, PATHOGENESE, THERAPIE = LA MALADIE DE FRIEDREICH, UNE MALADIE NEUROCARDIOLOGIQUE. II. PATHOMORPHOLOGIE, PATHOGENESE, TRAITEMENTRUSER HR.1983; HERZ. KREISLAUF; ISSN 0046-7324; DEU; DA. 1983; VOL. 15; NO 1; PP. 14-17; ABS. ENG; BIBL. 37 REF.Article

EVOKED POTENTIAL ABNORMALITIES IN THE VARIOUS INHERITED ATAXIASNUWER MR; PERLMAN SL; PACKWOOD JW et al.1983; ANNALS OF NEUROLOGY; ISSN 0364-5134; USA; DA. 1983; VOL. 13; NO 1; PP. 20-27; BIBL. 41 REF.Article

Altered frequency-dependent inactivation and steady-state inactivation of polyglutamine -expanded α1A in SCA6HAIYAN CHEN; PIEDRAS-RENTERIA, Erika S.American journal of physiology. Cell physiology. 2007, Vol 61, Num 3, issn 0363-6143, C1078-C1086Article

Usefulness of the Scale for Assessment and Rating of Ataxia (SARA)YABE, Ichiro; MATSUSHIMA, Masaaki; SOMA, Hiroyuki et al.Journal of the neurological sciences. 2008, Vol 266, Num 1-2, pp 164-166, issn 0022-510X, 3 p.Article

DOSAGE DE LA PYRUVATE DESHYDROGENASE MUSCULAIRE DANS DEUX MODELES EXPERIMENTAUX D'ATAXIE.BUTTERWORTH RF; IZUMI K; LANDREVILLE F et al.1977; UN. MED. CANADA; CANADA; DA. 1977; VOL. 106; NO 4; PP. 468-471; ABS. ANGL.; BIBL. 10 REF.Article

Spinocerebellar ataxia type 6 and episodic ataxia type 2: differences and similarities between two allelic disordersMANTUANO, E; VENEZIANO, L; JODICE, C et al.Cytogenetic and genome research. 2003, Vol 100, Num 1-4, pp 147-153, issn 1424-8581, 7 p.Article

Spinocerebellar ataxia type 17 in the Yugoslav populationALENDAR, A; CULJKOVIC, B; SAVIC, D et al.Acta neurologica scandinavica. 2004, Vol 109, Num 3, pp 185-187, issn 0001-6314, 3 p.Article

Spinocerebellar ataxia 7 (SCA7)LEBRE, A.-S; BRICE, A.Cytogenetic and genome research. 2003, Vol 100, Num 1-4, pp 154-163, issn 1424-8581, 10 p.Article

Spontaneous and induced chromosome breakage in chorionic villus samples: a cytogenetic approach to first trimester prenatal diagnosis of ataxia telangiectasia syndromeLLERENA, J. JR; MURER-ORLANDO, M; MCGUIRE, M et al.Journal of medical genetics. 1989, Vol 26, Num 3, pp 174-178, issn 0022-2593, 5 p.Article

The hereditary spinocerebellar ataxias in JapanSASAKI, H; YABE, I; TASHIRO, K et al.Cytogenetic and genome research. 2003, Vol 100, Num 1-4, pp 198-205, issn 1424-8581, 8 p.Article

Falls in degenerative cerebellar ataxiasVAN DE WARRENBURG, Bart P. C; STEIJNS, Janneke A. G; MUNNEKE, Marten et al.Movement disorders. 2005, Vol 20, Num 4, pp 497-500, issn 0885-3185, 4 p.Article

Cerebellar ataxia in the eastern and southern parts of NorwayKOHT, J; TALLAKSEN, C. M. E.Acta neurologica Scandinavica. Supplementum. 2007, Vol 115, Num 187, pp 76-79, issn 0065-1427, 4 p.Conference Paper

Uncommon features in Cuban families affected with Friedreich ataxiaCRUZ-MARINO, Tania; GONZALEZ-ZALDIVAR, Yanetza; LAFFITA-MESA, Jose Miguel et al.Neuroscience letters. 2010, Vol 472, Num 2, pp 85-89, issn 0304-3940, 5 p.Article

Uses of the postural stability test for differential diagnosis of hereditary ataxiasSCHWABOVA, J; ZAHALKA, F; KOMAREK, V et al.Journal of the neurological sciences. 2012, Vol 316, Num 1-2, pp 79-85, issn 0022-510X, 7 p.Article

The clinical, pathological and genetic aspects of sporadic late onset cerebellar ataxia: observations on a series of ten patientsKUMAR, D; TIMPERLEY, W. R.Acta neurologica scandinavica. 1988, Vol 37, Num 3, pp 181-186, issn 0001-6314Article

Phenotype Variability in Spinocerebellar Ataxia Type 2: A Longitudinal Family Survey and a Case Featuring an Unusual Benign Course of DiseaseHERING, Sascha; ACHMÜLLER, Clemens; KÖHLER, Andrea et al.Movement disorders. 2009, Vol 24, Num 5, pp 774-777, issn 0885-3185, 4 p.Article

SHORTENING REACTION IN PATIENTS WITH CEREBELLAR ATAXIAANGEL RW.1982; ANN. NEUROL.; ISSN 0364-5134; USA; DA. 1982; VOL. 11; NO 3; PP. 272-279; BIBL. 22 REF.Article

PATHOGENETIC AND PREVENTIVE ASPECTS OF NON-PROGRESSIVE ATAXIC SYNDROMES1979; DEVELOP. MED. CHILD NEUROL.; GBR; DA. 1979; VOL. 21; NO 5; PP. 663-671; ABS. FRE/GER/SPA; BIBL. 2 P.Article

Autosomal dominant cerebellar ataxias in Spain : molecular and clinical correlations, prevalence estimation and survival analysisINFANTE, J; COMBARROS, O; VOLPINI, V et al.Acta neurologica scandinavica. 2005, Vol 111, Num 6, pp 391-399, issn 0001-6314, 9 p.Article

Molecular genetics of spinocerebellar ataxia type 8 (SCA8)MOSEMILLER, A. K; DALTON, J. C; DAY, J. W et al.Cytogenetic and genome research. 2003, Vol 100, Num 1-4, pp 175-183, issn 1424-8581, 9 p.Article

PRENATAL DIAGNOSIS OF ATAXIA TELANGIECTASIAMEIRA SHAHAM; VOSS R; BECKER Y et al.1982; J. PEDIATR.; ISSN 0022-3476; USA; DA. 1982; VOL. 100; NO 1; PP. 134-137; BIBL. 10 REF.Article

DYSARTHRIC SYMPTOMATOLOGY OF FRIEDREICH'S ATAXIAJOANETTE Y; DUDLEY JG.1980; BRAIN AND LANGUAGE; USA; DA. 1980; VOL. 10; NO 1; PP. 39-50; BIBL. 16 REF.Article

GLYCOSYLATED HEMOGLOBINS IN FRIEDREICH'S ATAXIADRAPER P; SHAPCOTT D; LANGLOIS M et al.1980; CAN. J. NEUROL. SCI.; ISSN 0317-1671; CAN; DA. 1980; VOL. 7; NO 4; PP. 405-407; ABS. FRE; BIBL. 8 REF.Article

FAMILIAL SPASTIC ATAXIA: OCCURRENCE IN CHILDHOOD.HOGAN GR; BAUMAN ML.1977; NEUROLOGY; U.S.A.; DA. 1977; VOL. 27; NO 6; PP. 520-526; BIBL. 45 REF.Article

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