Carvalho F - Search Results

1

Unique (Y;13) translocation in a male with oligozoospermia: cytogenetic and molecular studies.

Alves C, Carvalho F, Cremades N, Sousa M, Barros A. Alves C, et al. Among authors: carvalho f. Eur J Hum Genet. 2002 Aug;10(8):467-74. doi: 10.1038/sj.ejhg.5200835. Eur J Hum Genet. 2002. PMID: 12111641

2

Genomic imprinting in disruptive spermatogenesis.

Marques CJ, Carvalho F, Sousa M, Barros A. Marques CJ, et al. Among authors: carvalho f. Lancet. 2004 May 22;363(9422):1700-2. doi: 10.1016/S0140-6736(04)16256-9. Lancet. 2004. PMID: 15158633

3

Characterization of cystic fibrosis conductance transmembrane regulator gene mutations and IVS8 poly(T) variants in Portuguese patients with congenital absence of the vas deferens.

Grangeia A, Niel F, Carvalho F, Fernandes S, Ardalan A, Girodon E, Silva J, Ferrás L, Sousa M, Barros A. Grangeia A, et al. Among authors: carvalho f. Hum Reprod. 2004 Nov;19(11):2502-8. doi: 10.1093/humrep/deh462. Epub 2004 Aug 27. Hum Reprod. 2004. PMID: 15333598

4

A novel missense mutation P1290S at exon-20 of the CFTR gene in a Portuguese patient with congenital bilateral absence of the vas deferens.

Grangeia A, Carvalho F, Fernandes S, Silva J, Sousa M, Barros A. Grangeia A, et al. Among authors: carvalho f. Fertil Steril. 2005 Feb;83(2):448-51. doi: 10.1016/j.fertnstert.2004.07.967. Fertil Steril. 2005. PMID: 15705389 Free article.

5

Molecular characterization of the cystic fibrosis transmembrane conductance regulator gene in congenital absence of the vas deferens.

Grangeia A, Sá R, Carvalho F, Martin J, Girodon E, Silva J, Ferráz L, Barros A, Sousa M. Grangeia A, et al. Among authors: carvalho f. Genet Med. 2007 Mar;9(3):163-72. doi: 10.1097/gim.0b013e3180318aaf. Genet Med. 2007. PMID: 17413420 Free article. Clinical Trial.

6

Cytological and expression studies and quantitative analysis of the temporal and stage-specific effects of follicle-stimulating hormone and testosterone during cocultures of the normal human seminiferous epithelium.

Sá R, Neves R, Fernandes S, Alves C, Carvalho F, Silva J, Cremades N, Malheiro I, Barros A, Sousa M. Sá R, et al. Among authors: carvalho f. Biol Reprod. 2008 Nov;79(5):962-75. doi: 10.1095/biolreprod.107.067546. Epub 2008 Jul 30. Biol Reprod. 2008. PMID: 18667755

7

Molecular and functional characterization of CBAVD-causing mutations located in CFTR nucleotide-binding domains.

Grangeia A, Barro-Soria R, Carvalho F, Damas AM, Maurício AC, Kunzelmann K, Barros A, Sousa M. Grangeia A, et al. Among authors: carvalho f. Cell Physiol Biochem. 2008;22(1-4):79-92. doi: 10.1159/000149785. Epub 2008 Jul 25. Cell Physiol Biochem. 2008. PMID: 18769034

8

Methylation defects of imprinted genes in human testicular spermatozoa.

Marques CJ, Francisco T, Sousa S, Carvalho F, Barros A, Sousa M. Marques CJ, et al. Among authors: carvalho f. Fertil Steril. 2010 Jul;94(2):585-94. doi: 10.1016/j.fertnstert.2009.02.051. Epub 2009 Apr 1. Fertil Steril. 2010. PMID: 19338988 Free article.

9

An efficient protocol for the detection of chromosomal abnormalities in spontaneous miscarriages or foetal deaths.

Dória S, Carvalho F, Ramalho C, Lima V, Francisco T, Machado AP, Brandão O, Sousa M, Matias A, Barros A. Dória S, et al. Among authors: carvalho f. Eur J Obstet Gynecol Reprod Biol. 2009 Dec;147(2):144-50. doi: 10.1016/j.ejogrb.2009.07.023. Epub 2009 Sep 8. Eur J Obstet Gynecol Reprod Biol. 2009. PMID: 19740589

10

Association of cystic fibrosis genetic modifiers with congenital bilateral absence of the vas deferens.

Havasi V, Rowe SM, Kolettis PN, Dayangac D, Sahin A, Grangeia A, Carvalho F, Barros A, Sousa M, Bassas L, Casals T, Sorscher EJ. Havasi V, et al. Among authors: carvalho f. Fertil Steril. 2010 Nov;94(6):2122-7. doi: 10.1016/j.fertnstert.2009.11.044. Epub 2010 Jan 25. Fertil Steril. 2010. PMID: 20100616 Free PMC article.

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