Browsing by Author Zatz, M.

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Showing results 18 to 21 of 21 < previous 
Issue DateTitleAuthor(s)
15-Mar-1999Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian populationVainzof, M.; Passos-Bueno, M. R.; Pavanello, RCM; Marie, S. K.; Oliveira, ASB; Zatz, M.; Universidade de São Paulo (USP); Universidade Federal de São Paulo (UNIFESP)
1-Oct-2007Screening for mutations in the dynamin 2 gene in Brazilian patients with centronuclear myopathy and Charcot-Marie-Tooth neuropathySell, K.; Yamamoto, L.; Velloso, F.; Cerqueira, A.; Zanoteli, E. [UNIFESP]; Chimelli, L.; Kashiwagi, F.; Zatz, M.; Vainzof, M.; Universidade de São Paulo (USP); Universidade Federal de São Paulo (UNIFESP); Universidade Federal do Rio de Janeiro (UFRJ)
31-Jul-1992SCREENING of GLYCEROL KINASE-DEFICIENCY in PATIENTS AFFECTED BY DUCHENNE and BECKER MUSCULAR-DYSTROPHYSchreiber, R.; Passosbueno, M. R.; Rapaport, D.; Pavanello, R. D.; Vainzof, M.; Fernandes, MES; Zatz, M.; Universidade de São Paulo (USP); Universidade Federal de São Paulo (UNIFESP)
15-Apr-1993SEVERE NONSPECIFIC X-LINKED MENTAL-RETARDATION CAUSED BY A PROXIMALLY XP LOCATED GENE - INTRAGENIC HETEROGENEITY OR A NEW FORM of X-LINKED MENTAL-RETARDATIONPassosbueno, M. R.; Byth, B. C.; Rosenberg, S.; Takata, R. I.; Bakker, E.; Beggs, A. H.; Pavanello, R. C.; Vainzof, M.; Davies, K. E.; Zatz, M.; UNIV OXFORD; Universidade Federal de São Paulo (UNIFESP); LEIDEN UNIV; HARVARD UNIV