Pavanello RC - Search Results

1

Linkage analysis in a large Brazilian family with van der Woude syndrome suggests the existence of a susceptibility locus for cleft palate at 17p11.2-11.1.

Sertié AL, Sousa AV, Steman S, Pavanello RC, Passos-Bueno MR. Sertié AL, et al. Among authors: pavanello rc. Am J Hum Genet. 1999 Aug;65(2):433-40. doi: 10.1086/302491. Am J Hum Genet. 1999. PMID: 10417286 Free PMC article.

2

Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?

Passos-Bueno MR, Byth BC, Rosenberg S, Takata RI, Bakker E, Beggs AH, Pavanello RC, Vainzof M, Davies KE, Zatz M. Passos-Bueno MR, et al. Among authors: pavanello rc. Am J Med Genet. 1993 Apr 15;46(2):172-5. doi: 10.1002/ajmg.1320460214. Am J Med Genet. 1993. PMID: 8484404

3

Exclusion of the 15q locus as a candidate gene for severe childhood autosomal recessive Duchenne-like muscular dystrophy in Brazilian families.

Passos-Bueno MR, Bakker E, Marie SK, Pavanello RC, Vainzof M, Carvalho AA, Cohen D, Beckmann J, Zatz M. Passos-Bueno MR, et al. Among authors: pavanello rc. Hum Mol Genet. 1993 Feb;2(2):201-2. doi: 10.1093/hmg/2.2.201. Hum Mol Genet. 1993. PMID: 8499908 No abstract available.

4

No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy families (FSHD) with 4q markers.

Passos-Bueno MR, Wijmenga C, Takata RE, Marie SK, Vainzof M, Pavanello RC, Hewitt JE, Bakker E, Carvalho A, Akiyama J, et al. Passos-Bueno MR, et al. Among authors: pavanello rc. Hum Mol Genet. 1993 May;2(5):557-62. doi: 10.1093/hmg/2.5.557. Hum Mol Genet. 1993. PMID: 8518794

5

Evidence that BCL3 plays a role in the etiology of nonsyndromic oral clefts in Brazilian families.

Gaspar DA, Matioli SR, Pavanello RC, Araújo BC, André M, Steman S, Otto PA, Passos-Bueno MR. Gaspar DA, et al. Among authors: pavanello rc. Genet Epidemiol. 2002 Nov;23(4):364-74. doi: 10.1002/gepi.10189. Genet Epidemiol. 2002. PMID: 12432504

6

The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than females.

Zatz M, Marie SK, Cerqueira A, Vainzof M, Pavanello RC, Passos-Bueno MR. Zatz M, et al. Among authors: pavanello rc. Am J Med Genet. 1998 May 1;77(2):155-61. Am J Med Genet. 1998. PMID: 9605290

7

Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD).

Tonini MM, Passos-Bueno MR, Cerqueira A, Matioli SR, Pavanello R, Zatz M. Tonini MM, et al. Neuromuscul Disord. 2004 Jan;14(1):33-8. doi: 10.1016/j.nmd.2003.07.001. Neuromuscul Disord. 2004. PMID: 14659410

8

A model to estimate the expression of the dystrophin gene in muscle from female Becker muscular dystrophy carriers.

Vainzof M, Passos-Bueno MR, Pavanello RC, Schreiber R, Zatz M. Vainzof M, et al. Among authors: pavanello rc. J Med Genet. 1992 Jul;29(7):476-9. J Med Genet. 1992. PMID: 1640426 Free PMC article.

9

Screening of male patients with autosomal recessive Duchenne dystrophy through dystrophin and DNA studies.

Vainzof M, Pavanello RC, Pavanello-Filho I, Rapaport D, Passos-Bueno MR, Zubrzycka-Gaarn EE, Bulman DE, Zatz M. Vainzof M, et al. Among authors: pavanello rc, pavanello filho i. Am J Med Genet. 1991 Apr 1;39(1):38-41. doi: 10.1002/ajmg.1320390110. Am J Med Genet. 1991. PMID: 1867262

10

Hypothesis: the existence of embryonic and adult isoforms of mRNA dystrophin provides an explanation for unusual clinical findings.

Zatz M, Passos-Bueno MR, Vainzof M, Pavanello RC. Zatz M, et al. Among authors: pavanello rc. Am J Med Genet. 1989 Mar;32(3):438-41. doi: 10.1002/ajmg.1320320336. Am J Med Genet. 1989. PMID: 2658593 No abstract available.

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