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Autosomal dominant cerebellar ataxias = Les ataxies cérébelleuses autosomiques dominantesMARELLI, C; CAZENEUVE, C; BRICE, A et al.Revue neurologique (Paris). 2011, Vol 167, Num 5, pp 385-400, issn 0035-3787, 16 p.Article

Effect of ionizing radiation on synthesis of subreplicon size DNA in ataxia telangiectasia cellsHOULDSWORTH, J; LAVIN, M. F.Biochemistry international. 1983, Vol 6, Num 3, pp 349-356, issn 0158-5231Article

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

Dysarthria in Friedreich's ataxia: timing of speech segmentsACKERMANN, H; HERTRICK, I.Clinical linguistics & phonetics. 1993, Vol 7, Num 1, pp 75-91, issn 0269-9206Article

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

ADULT-ONSET HEREDITARY CEREBELLAR ATAXIA AND NEUROSENSORY DEAFNESS = ATAXIE CEREBELLEUSE ET SURDITE NEUROSENSORIELLE HEREDITAIRES A DEBUT ADULTESCHIMKE RN.1974; CLIN. GENET.; DENM.; DA. 1974; VOL. 6; NO 5; PP. 416-421; BIBL. 1 P. 1/2Article

Proposed mechanism of ataxia in Fisher's syndromeROPPER, A. H; SHAHANI, B.Archives of neurology (Chicago). 1983, Vol 40, Num 9, pp 537-538, issn 0003-9942Article

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

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

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

188 CASES OF NON-PROGRESSIVE ATAXIC SYNDROMES IN CHILDHOOD. ASPECTS OF AETIOLOGY AND CLASSIFICATION = 8 CAS DE SYNDROMES ATAXIQUES NON PROGRESSIFS CHEZ L'ENFANT. ASPECTS DE L'ETIOLOGIE ET DE LA CLASSIFICATIONSANNER G; HAGBERG B.1974; NEUROPAEDIATRIE; DTSCH.; DA. 1974; VOL. 5; NO 3; PP. 224-235; ABS. ALLEM.; BIBL. 25REF.Article

FLOOR ATAXIA TEST BATTERY. RESULTS FROM AN 8- TO 18- YEAR-OLD GROUP = BATTERIE DE TESTS D'ATAXIE SUR LE PLANCHER. RESULTATS D'UN GROUPE AGE DE 8 A 18 ANSCUNNINGHAM DR; GOETZINGER CP.1972; ARCH. OTOLARYNGOL.; U.S.A.; DA. 1972; VOL. 96; NO 6; PP. 559-564; BIBL. 10 REF.Serial Issue

ATAXIES DE L'ENFANTARTHUIS M.1972; REV. PRATICIEN; FR.; DA. 1972; VOL. 22; NO 30; PP. 4147-4158 (6P.); ABS. ANGL.; BIBL. 12REF.Serial Issue

Association d'un hypogonadisme hypogonadotrope et d'une ataxie cérébelleuse chez un homme : à propos d'un cas = Hypogonadotropic hypogonadism discovered in a patient with cerebellar ataxiaROBIN, G; JONARD, S; VUILLAUME, I et al.Annales d'endocrinologie. 2005, Vol 66, Num 6, pp 545-551, issn 0003-4266, 7 p.Article

Traitement des ataxies cérébelleuses à anticorps anti-GAD par cures séquentielles de corticoïdes = Steroid treatment in four cases of anti-GAD cerebellar ataxiaBONNAN, M; CABRE, P; OLINDO, S et al.Revue neurologique (Paris). 2008, Vol 164, Num 5, pp 427-433, issn 0035-3787, 7 p.Article

Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxiaGROS-LOUIS, Francois; DUPRE, Nicolas; DION, Patrick et al.Nature genetics. 2007, Vol 39, Num 1, pp 80-85, issn 1061-4036, 6 p.Article

Acetazolamide-responsive episodic ataxia syndromeZASORIN, N. L; BALOH, R. W; MYERS, L. B et al.Neurology. 1983, Vol 33, Num 9, pp 1212-1214, issn 0028-3878Article

Ataxic hindbrain thinking: the clumsy cerebellum syndromeLANDAU, W. M.Neurology. 1989, Vol 39, Num 3, pp 315-323, issn 0028-3878Article

On the nature of a defect in cells from individuals with ataxia-telangiectasiaCORNFORTH, M. N; BEDFORD, J. S.Science (Washington, D.C.). 1985, Vol 227, Num 4694, pp 1589-1591, issn 0036-8075Article

Ataxic Creutzfeldt-Jakob disease: diagnostic techniques and neuropathologic observations in early diseaseJONES, H. R. JR; HEDLEY-WHYTE, E. T; FREIDBERG, S. R et al.Neurology. 1985, Vol 35, Num 2, pp 254-257, issn 0028-3878Article

Deterioration of spinal reflex in quails orally ingesting clioquinolMORISHITA, S; GOTO, M; FUKUDA, H et al.Journal of pharmacobio-dynamics. 1985, Vol 8, Num 9, pp 751-756, issn 0386-846XArticle

A kindred with cerebellar ataxia and thermoanalgesiaGENIS, D; FERRER, I; MARQUEZ, F et al.Journal of neurology, neurosurgery and psychiatry. 2009, Vol 80, Num 5, pp 518-523, issn 0022-3050, 6 p.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

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