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Results 1 to 25 of 3492

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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

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

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

A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome lp21-q23CHUNG, Ming-Yi; LU, Yi-Chun; CHENG, Nai-Chia et al.Brain. 2003, Vol 126, pp 1293-1299, issn 0006-8950, 7 p., 6Article

CHROMOSOMAL INSTABILITY IN ATAXIA TELANGIECTASIAKOHN PH; WHANG PENG J; LEVIS WR et al.1982; CANCER GENETICS AND CYTOGENETICS; ISSN 0165-4608; NLD; DA. 1982; VOL. 6; NO 4; PP. 289-302; BIBL. 47 REF.Article

ERYTHROCYTE MEMBRANE LIPIDS IN FRIEDREICH'S ATAXIADRAPER P; HUANG YS; SHAPCOTT D et al.1979; CANAD. J. NEUROL. SCI.; CAN; DA. 1979; VOL. 6; NO 2; PP. 291-294; ABS. FRE; BIBL. 16 REF.Article

BEITRAG ZUM LOUIS-BAR-SYNDROM (ATAXIA TELANGIECTASIA) = ATAXIE TELANGIECTASIETENNSTEDT A.1978; ZBL. ALLG. PATHOL. PATHOL. ANAT.; DDR; DA. 1978; VOL. 122; NO 5; PP. 485-495; ABS. ENG; BIBL. 46 REF.Article

OSSERVAZIONI CLINICHE E IMMUNOLOGICHE NELL'ATASSIA-TELANGECTASIA. STUDIO DI 13 PAZIENTI. = OBSERVATIONS CLINIQUES ET IMMUNOLOGIQUES DANS L'ATAXIE-TELANGIECTASIE. ETUDE DE 13 MALADESMARCHETTI F; BUSINGO L; FINOCCHI M et al.1977; FOLIA ALLERGOL. IMMUNOL. CLIN.; ITAL.; DA. 1977; VOL. 24; NO 6; PP. 598-601; ABS. ANGL.; BIBL. 9 REF.Article

FRIEDREICH'S ATAXIA IN THE SOUTH OF ITALY: A CLINICAL AND BIOCHEMICAL SURVEY OF 23 PATIENTSCAMPANELLA G; FILLA A; DE FALCO F et al.1980; CAN. J. NEUROL. SCI.; ISSN 0317-1671; CAN; DA. 1980; VOL. 7; NO 4; PP. 351-357; ABS. FRE; BIBL. 27 REF.Article

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