Brunoni D - Search Results

1

Limb deficiency with or without Möbius sequence in seven Brazilian children associated with misoprostol use in the first trimester of pregnancy.

Gonzalez CH, Vargas FR, Perez AB, Kim CA, Brunoni D, Marques-Dias MJ, Leone CR, Correa Neto J, Llerena Júnior JC, de Almeida JC. Gonzalez CH, et al. Among authors: brunoni d. Am J Med Genet. 1993 Aug 1;47(1):59-64. doi: 10.1002/ajmg.1320470113. Am J Med Genet. 1993. PMID: 8368254

2

Prenatal exposure to misoprostol and vascular disruption defects: a case-control study.

Vargas FR, Schuler-Faccini L, Brunoni D, Kim C, Meloni VF, Sugayama SM, Albano L, Llerena JC Jr, Almeida JC, Duarte A, Cavalcanti DP, Goloni-Bertollo E, Conte A, Koren G, Addis A. Vargas FR, et al. Among authors: brunoni d. Am J Med Genet. 2000 Dec 11;95(4):302-6. doi: 10.1002/1096-8628(20001211)95:4<302::aid-ajmg2>3.0.co;2-b. Am J Med Genet. 2000. PMID: 11186881

3

Complex toe syndactyly with characteristic facial phenotype: a new syndrome?

Sobreira NL, Cernach MC, Brunoni D, Perez AB. Sobreira NL, et al. Among authors: brunoni d. Am J Med Genet A. 2008 Jul 1;146A(13):1725-8. doi: 10.1002/ajmg.a.32377. Am J Med Genet A. 2008. PMID: 18512233

4

Use of misoprostol during pregnancy and Möbius' syndrome in infants.

Pastuszak AL, Schüler L, Speck-Martins CE, Coelho KE, Cordello SM, Vargas F, Brunoni D, Schwarz IV, Larrandaburu M, Safattle H, Meloni VF, Koren G. Pastuszak AL, et al. Among authors: brunoni d. N Engl J Med. 1998 Jun 25;338(26):1881-5. doi: 10.1056/NEJM199806253382604. N Engl J Med. 1998. PMID: 9637807 Free article.

5

Pseudoaminopterin syndrome: clinical report with new characteristics.

Sobreira N, Cernach M, Batista D, Brunoni D, Perez A. Sobreira N, et al. Among authors: brunoni d. Am J Med Genet A. 2009 Dec;149A(12):2843-8. doi: 10.1002/ajmg.a.33125. Am J Med Genet A. 2009. PMID: 19938091

6

Finlay-Marks (SEN) syndrome: a sporadic case and the delineation of the syndrome.

Sobreira NL, Brunoni D, Cernach MC, Perez AB. Sobreira NL, et al. Among authors: brunoni d. Am J Med Genet A. 2006 Feb 1;140(3):300-2. doi: 10.1002/ajmg.a.31063. Am J Med Genet A. 2006. PMID: 16411189 No abstract available.

7

Sclerocornea in a patient with van den Ende-Gupta syndrome homozygous for a SCARF2 microdeletion.

Migliavacca MP, Sobreira NL, Antonialli GP, Oliveira MM, Melaragno MI, Casteels I, de Ravel T, Brunoni D, Valle D, Perez AB. Migliavacca MP, et al. Among authors: brunoni d. Am J Med Genet A. 2014 May;164A(5):1170-4. doi: 10.1002/ajmg.a.36425. Epub 2014 Jan 29. Am J Med Genet A. 2014. PMID: 24478002 Free PMC article.

8

Identification of 8 new mutations in Brazilian families with Marfan syndrome. Mutations in brief no. 211. Online.

Perez AB, Pereira LV, Brunoni D, Zatz M, Passos-Bueno MR. Perez AB, et al. Among authors: brunoni d. Hum Mutat. 1999;13(1):84. doi: 10.1002/(SICI)1098-1004(1999)13:1<84::AID-HUMU15>3.0.CO;2-U. Hum Mutat. 1999. PMID: 10189222

9

Methylenetetrahydrofolate reductase (MTHFR): incidence of mutations C677T and A1298C in Brazilian population and its correlation with plasma homocysteine levels in spina bifida.

Perez AB, D'Almeida V, Vergani N, de Oliveira AC, de Lima FT, Brunoni D. Perez AB, et al. Among authors: brunoni d, d almeida v. Am J Med Genet A. 2003 May 15;119A(1):20-5. doi: 10.1002/ajmg.a.10059. Am J Med Genet A. 2003. PMID: 12707953

10

Novel mutations in the TBX5 gene in patients with Holt-Oram Syndrome.

Porto MP, Vergani N, Carvalho AC, Cernach MC, Brunoni D, Perez AB. Porto MP, et al. Among authors: brunoni d. Genet Mol Biol. 2010 Apr;33(2):232-6. doi: 10.1590/S1415-47572010005000051. Epub 2010 Jun 1. Genet Mol Biol. 2010. PMID: 21637475 Free PMC article.

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