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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

HEREDODEGENERESCENCE REVELEE PAR UNE OPHTALMOPLEGIE.ARNOULD G; BARROCHE G; OUDOT P et al.1977; REV. OTO-NEURO-OPHTALMOL.; FR.; DA. 1977; VOL. 49; NO 1; PP. 33-38; BIBL. 14 REF.Article

Linkage between late onset, dominant spinocerebellar ataxia and HLAWERDELIN, L; PLATZ, P; LAMM, L. U et al.Human genetics. 1984, Vol 66, Num 1, pp 85-89, issn 0340-6717Article

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

AN INVESTIGATION OF PYRUVATE METABOLISM IN PATIENTS WITH CEREBELLAR AND SPINNOCEREBELLAR DEGENERATIONLIVINGSTONE IR; MASTAGLIA FL; PENNINGTON RJT et al.1980; J. NEUROL. SCI.; ISSN 0022-510X; NLD; DA. 1980; VOL. 48; NO 1; PP. 123-132; 123-132; BIBL. 19 REF.Article

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

EPIDEMIOLOGIE ET POLYMORPHISME CLINIQUE DES ATAXIES HEREDITAIRESSHUTOV AA; DEDIK GK.1978; ZH. NEVROPATOL. PSIKHIATR. S.S. KORSAKOVA; SUN; DA. 1978; VOL. 78; NO 6; PP. 825-830; ABS. ANGL.; BIBL. 29 REF.Article

Dysphagia in Huntington's diseaseLEOPOLD, N. A; KAGEL, M. C.Archives of neurology (Chicago). 1985, Vol 42, Num 1, pp 57-60, issn 0003-9942Article

DEGENERAZIONE SPINO-OLIVO-CEREBELLO-NIGRALE-STUDIO ANATOMO-CLINOCO DI UN CASO AD ESORDIO INFANTILE. = DEGENERESCENCE SPINO-OLIVO-CEREBELLO-NIGRALE. ETUDE ANATOMO-CLINIQUE D'UN CAS APPARU DANS L'ENFANCENARDELLI E; RIZZUTO N; PANIZON F et al.1976; ACTA NEUROL.; ITAL.; DA. 1976; VOL. 31; NO 3; PP. 392-403; ABS. ANGL.; BIBL. 1 P. 1/2Article

AUTOSOMAL DOMINANT MOTOR SYSTEM DISEASE OF THE PORTUGUESE: A REVIEWROSENBERG RN; FOWLER HL.1981; NEUROLOGY; ISSN 0028-3878; USA; DA. 1981; VOL. 31; NO 9; PP. 1124-1126; BIBL. 17 REF.Article

LIPIDS AND LIPOPROTEINS IN FRIEDREICH'S ATAXIAWALKER JL; CHAMBERLAIN S; ROBINSON N et al.1980; J. NEUROL. NEUROSURG. PSYCHIATRY; GBR; DA. 1980; VOL. 43; NO 2; PP. 111-117; BIBL. 45 REF.Article

PROGRESSIVE MYOCLONUS AND EPILEPSY WITH DENTATORUBRAL DEGENERATION. A CLINICOPATHOLOGICAL STUDY OF THE RAMSAY HUNT SYNDROME.BIRD TD; SHAW CM.1978; J. NEUROL. NEUROSURG. PSYCHIATRY; G.B.; DA. 1978; VOL. 41; NO 2; PP. 140-149; BIBL. 25 REF.Article

DOMINANT SPINOPONTINE ATROPHY. REPORT OF TWO ADDITIONAL MEMBERS OF FAMILY W.POGACAR S; AMBLER M; CONKLIN WJ et al.1978; ARCH. NEUROL.; U.S.A.; DA. 1978; VOL. 35; NO 3; PP. 156-162; BIBL. 7 REF.Article

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

MALOCCLUSION DENTAIRE DANS L'ATAXIE FAMILIALE DE FRIEDREICHGURSKAYA NZ; GORIN NN.1978; ZH. NEVROPATOL. PSIKHIATR. S.S. KORSAKOVA; S.S.S.R.; DA. 1978; VOL. 78; NO 3; PP. 355-357; ABS. ANGL.; BIBL. 10 REF.Article

Controlled trial of thyrotropin releasing hormone tartrate in ataxia of spinocerebellar degenerationsSOBUE, I; TAKAYANAGI, T; MARUYAMA, S et al.Journal of the neurological sciences. 1983, Vol 61, Num 2, pp 235-248, issn 0022-510XArticle

ELECTROENCEPHALOGRAPHIC FINDINGS IN FRIEDREICH'S ATAXIA AND AUTOSOMAL RECESSIVE SPASTIC ATAXIA OF CHARLEVOIX-SAGUENAY (ARSACS)BOUCHARD RW; BOUCHARD JP; BOUCHARD R et al.1979; CANAD. J. NEUROL. SCI.; CAN; DA. 1979; VOL. 6; NO 2; PP. 191-194; ABS. FRE; BIBL. 9 REF.Article

LIPID ABNORMALITIES IN HEREDITARY NEUROPATHY. I. SERUM NON-POLAR LIPIDS.YAO JK; ELLEFSON RD; DICK PJ et al.1976; J. NEUROL. SCI.; NETHERL.; DA. 1976; VOL. 29; NO 2-4; PP. 161-175; BIBL. 1 P. 1/2Article

Phenotypic heterogeneity in Huntington diseaseFOLSTEIN, S. E; ABBOTT, M. H; FRANZ, M. L et al.Journal of neurogenetics. 1984, Vol 1, Num 2, pp 175-184, issn 0167-7063Article

New type of spinocerebellar degeneration syndrome in a northern Swedish populationGUSTAVSON, K.-H; MODRZEWSKA, K; ERIKSON, A et al.Clinical genetics. 1987, Vol 32, Num 5, pp 306-312, issn 0009-9163Article

Potential impact of a predictive test on the gene frequency of Huntington diseaseSCHOENFELD, M; MYERS, R. H; BERKMAN, B et al.American journal of medical genetics. 1984, Vol 18, Num 3, pp 423-429, issn 0148-7299Article

JOSEPH DISEASE IN A NON-PORTUGUEUSE FAMILYSAKAI T; OHTA M; ISHINO H et al.1983; NEUROLOGY; ISSN 0028-3878; USA; DA. 1983; VOL. 33; NO 1; PP. 74-80; BIBL. 22 REF.Article

HEREDOATAXIA (SPINOCEREBELLAR DEGENERATION), ERG ALTERATIONS, TEMPORAL ASPECTSSTANESCU SEGAL B; MICHIELS J.1979; OPHTHALMOLOGICA; CHE; DA. 1979; VOL. 178; NO 5; PP. 267-272; ABS. GER/FRE; BIBL. 18 REF.Article

ADULT-ONSET HEREDITARY ATAXIA IN SCOTLAND.KOEPPEN AH; HANS MB; SHEPHERD DI et al.1977; ARCH. NEUROL.; U.S.A.; DA. 1977; VOL. 34; NO 10; PP. 611-618; BIBL. 17 REF.Article