Campiotto S - Search Results

1

A deletion including the brain promoter of the Duchenne muscular dystrophy gene is not associated with mental retardation.

Rapaport D, Passos-Bueno MR, Takata RI, Campiotto S, Eggers S, Vainzof M, Makover A, Nudel U, Yaffe D, Zatz M. Rapaport D, et al. Among authors: campiotto s. Neuromuscul Disord. 1992;2(2):117-20. doi: 10.1016/0960-8966(92)90043-6. Neuromuscul Disord. 1992. PMID: 1422198

2

High proportion of new mutations and possible anticipation in Brazilian facioscapulohumeral muscular dystrophy families.

Zatz M, Marie SK, Passos-Bueno MR, Vainzof M, Campiotto S, Cerqueira A, Wijmenga C, Padberg G, Frants R. Zatz M, et al. Among authors: campiotto s. Am J Hum Genet. 1995 Jan;56(1):99-105. Am J Hum Genet. 1995. PMID: 7825608 Free PMC article.

3

Novel point mutations in the dystrophin gene.

Sitnik R, Campiotto S, Vainzof M, Pavanello RC, Takata RI, Zatz M, Passos-Bueno MR. Sitnik R, et al. Among authors: campiotto s. Hum Mutat. 1997;10(3):217-22. doi: 10.1002/(SICI)1098-1004(1997)10:3<217::AID-HUMU7>3.0.CO;2-F. Hum Mutat. 1997. PMID: 9298822

4

Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial cases.

Zatz M, Sumita D, Campiotto S, Canovas M, Cerqueira A, Vainzof M, Passos-Bueno MR. Zatz M, et al. Among authors: campiotto s. Am J Med Genet. 1998 Jul 24;78(4):361-5. doi: 10.1002/(sici)1096-8628(19980724)78:4<361::aid-ajmg11>3.0.co;2-g. Am J Med Genet. 1998. PMID: 9714440

5

Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers.

Sumita DR, Vainzof M, Campiotto S, Cerqueira AM, Cánovas M, Otto PA, Passos-Bueno MR, Zatz M. Sumita DR, et al. Among authors: campiotto s. Am J Med Genet. 1998 Dec 4;80(4):356-61. Am J Med Genet. 1998. PMID: 9856563

6

A Caucasian family with the 3271 mutation in mitochondrial DNA.

Marie SK, Goto Y, Passos-Bueno MR, Zatz M, Carvalho AA, Carvalho M, Levy JA, Palou VB, Campiotto S, Horai S, et al. Marie SK, et al. Among authors: campiotto s. Biochem Med Metab Biol. 1994 Aug;52(2):136-9. doi: 10.1006/bmmb.1994.1045. Biochem Med Metab Biol. 1994. PMID: 7993661

7

Geographic distribution of hepatitis C virus genotypes in Brazil.

Campiotto S, Pinho JR, Carrilho FJ, Da Silva LC, Souto FJ, Spinelli V, Pereira LM, Coelho HS, Silva AO, Fonseca JC, Rosa H, Lacet CM, Bernardini AP. Campiotto S, et al. Braz J Med Biol Res. 2005 Jan;38(1):41-9. doi: 10.1590/s0100-879x2005000100007. Epub 2005 Jan 18. Braz J Med Biol Res. 2005. PMID: 15665987 Free article.

8

Identification of three novel alleles of HLA-DRB1 and HLA-A in the Brazilian population.

Abdeen H, McErlean C, Moraes ME, Torres M, Campiotto S, Galvão S, Gouvea C, Middleton D. Abdeen H, et al. Among authors: campiotto s. Tissue Antigens. 2007 Jun;69(6):607-10. doi: 10.1111/j.1399-0039.2007.00835.x. Tissue Antigens. 2007. PMID: 17498272

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