Authors:
VAINZOF M
MARIE SKN
REED UC
SCHWARTZMAN JS
PAVANELLO RCM
PASSOSBUENO MR
ZATZ M
Citation: M. Vainzof et al., DEFICIENCY OF MEROSIN (LAMININ-M OR ALPHA-2) IN CONGENITAL MUSCULAR-DYSTROPHY ASSOCIATED WITH CEREBRAL WHITE-MATTER ALTERATIONS, Neuropediatrics, 26(6), 1995, pp. 293-297
Citation: S. Rosemberg et al., CONGENITAL INSENSITIVITY TO PAIN WITH ANHIDROSIS (HEREDITARY SENSORY AND AUTONOMIC NEUROPATHY TYPE-IV), Pediatric neurology, 11(1), 1994, pp. 50-56
Authors:
MARIE SKN
GOTO Y
PASSOSBUENO MR
ZATZ M
CARVALHO AAS
CARVALHO M
LEVY JA
PALOU VB
CAMPIOTTO S
HORAI S
NONAKA I
Citation: Skn. Marie et al., A CAUCASIAN FAMILY WITH THE 3271-MUTATION IN MITOCHONDRIAL-DNA, Biochemical medicine and metabolic biology, 52(2), 1994, pp. 136-139
Authors:
PASSOSBUENO MR
WIJMENGA C
TAKATA RE
MARIE SKN
VAINZOF M
PAVANELLO RC
HEWITT JE
BAKKER E
CARVALHO A
AKIYAMA J
FRANTS RR
ZATZ M
Citation: Mr. Passosbueno et al., NO EVIDENCE OF GENETIC-HETEROGENEITY IN BRAZILIAN FACIOSCAPULOHUMERALMUSCULAR-DYSTROPHY FAMILIES (FSHD) WITH 4Q MARKERS, Human molecular genetics, 2(5), 1993, pp. 557-562
Authors:
PASSOSBUENO MR
RICHARD I
VAINZOF M
FOUGEROUSSE F
WEISSENBACH J
BROUX O
COHEN D
AKIYAMA J
MARIE SKN
CARVALHO AA
GUILHERME L
KALIL J
TSANACLIS AM
ZATZ M
BECKMANN JS
Citation: Mr. Passosbueno et al., EVIDENCE OF GENETIC-HETEROGENEITY IN THE AUTOSOMAL RECESSIVE ADULT FORMS OF LIMB-GIRDLE MUSCULAR-DYSTROPHY FOLLOWING LINKAGE ANALYSIS WITH 15Q PROBES IN BRAZILIAN FAMILIES, Journal of Medical Genetics, 30(5), 1993, pp. 385-387
Authors:
GOTO Y
NONAKA I
HORAL S
HAYASHI JI
MARIE SKN
Citation: Y. Goto et al., EVIDENCE FOR THE 3271 MUTATION IN THE MITOCHONDRIAL TRANSFER-RNA GENERELATING TO MITOCHONDRIAL ENCEPHALOMYOPATHIES, American journal of human genetics, 53(3), 1993, pp. 1166-1166