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The sedentary arsacidsBOYCE, M.Iranica antiqua. 1994, Vol 29, pp 241-251, issn 0021-0870Article

CALCULS ASCENDANTS DU PROGRAMME D'ACKERMANN: ANALYSE DU PROGRAMME DE J. ARSAC.BERRY G.1977; R.A.I.R.O., INFORMAT. THEOR.; FR.; DA. 1977; VOL. 11; NO 2; PP. 113-126; BIBL. 19 REF.Article

Sacsin-related autosomal recessive ataxia without prominent retinal myelinated fibers in JapanHARA, Kenju; ONODERA, Osamu; ENDO, Minoru et al.Movement disorders. 2004, Vol 20, Num 3, pp 380-382, issn 0885-3185, 3 p.Article

HOMOZYGOUS CONTIGUOUS GENE DELETION OF 13q12 CAUSING LGMD2C AND ARSACS IN THE SAME PATIENTMCMILLAN, Hugh J; CARTER, Melissa T; JACOB, Pierre J et al.Muscle & nerve. 2009, Vol 39, Num 3, pp 396-399, issn 0148-639X, 4 p.Article

THE PROBLEMATIC MARRIAGES OF THE ARMENIAN KING ARSAK II: AN IRANIAN HYPOTHESIS = Les mariages problématiques du roi d'Arménie Arsace II: une hypothèse iranienneGARSOÏAN, Nina.Studia iranica (Paris). 2013, Vol 42, Num 1, pp 57-70, issn 0221-5004, 14 p.Article

New findings in the ataxia of Charlevoix―SaguenayGAZULLA, Jose; BENAVENTE, Isabel; TINTORE, María et al.Journal of neurology. 2012, Vol 259, Num 5, pp 869-878, issn 0340-5354, 10 p.Article

Novel SACS mutation in a Belgian family with sacsin-related ataxiaOUYANG, Y; SEGERS, K; BOUQUIAUX, O et al.Journal of the neurological sciences. 2008, Vol 264, Num 1-2, pp 73-76, issn 0022-510X, 4 p.Article

Novel compound heterozygous mutations of the SACS gene in autosomal recessive spastic ataxia of Charlevoix-SaguenayHAGS, Rie; MIKI, Yasuo; TAKIYAMA, Yoshihisa et al.Clinical neurology and neurosurgery (Dutch-Flemish ed.). 2012, Vol 114, Num 6, pp 746-747, issn 0303-8467, 2 p.Article

An inherited large-scale rearrangement in SACS associated with spastic ataxia and hearing lossTERRACCIANO, Alessandra; CASALI, Carlo; ZOLLINO, Marcella et al.Neurogenetics (Oxford. Print). 2009, Vol 10, Num 2, pp 151-155, issn 1364-6745, 5 p.Article

A novel genomic disorder : a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix-SaguenayBRECKPOT, Jeroen; TAKIYAMA, Yoshihisa; THIENPONT, Bernard et al.European journal of human genetics. 2008, Vol 16, Num 9, pp 1050-1054, issn 1018-4813, 5 p.Article

An unusual case of a spasticity-lacking phenotype with a novel SACS mutationSHIMAZAKI, Haruo; SAKOE, Kumi; NIIJIMA, Kenji et al.Journal of the neurological sciences. 2007, Vol 255, Num 1-2, pp 87-89, issn 0022-510X, 3 p.Article

ARSACS in the Dutch population : a frequent cause of early-onset cerebellar ataxiaVERMEER, Sascha; MEIJER, Rowdy P. P; KREMER, Berry et al.Neurogenetics (Oxford. Print). 2008, Vol 9, Num 3, pp 207-214, issn 1364-6745, 8 p.Article

NEUROPHYSIOLOGICAL STUDY IN A SPANISH FAMILY WITH RECESSIVE SPASTIC ATAXIA OF CHARLEVOIX-SAGUENAYGARCIA, Antonio; CRISCUOLO, Chiara; DE MICHELE, Giuseppe et al.Muscle & nerve. 2008, Vol 37, Num 1, pp 107-110, issn 0148-639X, 4 p.Article

Novel mutation of SACS gene in a Spanish family with autosomal recessive spastic ataxiaCRISCUOLO, Chiara; SACCA, Francesco; DE MICHELE, Giuseppe et al.Movement disorders. 2005, Vol 20, Num 10, pp 1358-1361, issn 0885-3185, 4 p.Article

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