Barros A - Search Results

1

Effect and in silico characterization of genetic variants associated with severe spermatogenic disorders in a large Iberian cohort.

Cerván-Martín M, Bossini-Castillo L, Rivera-Egea R, Garrido N, Luján S, Romeu G, Santos-Ribeiro S; IVIRMA Group, Lisbon Clinical Group; Castilla JA, Gonzalvo MDC, Clavero A, Vicente FJ, Guzmán-Jiménez A, Burgos M, Barrionuevo FJ, Jiménez R, Sánchez-Curbelo J, López-Rodrigo O, Peraza MF, Pereira-Caetano I, Marques PI, Carvalho F, Barros A, Bassas L, Seixas S, Gonçalves J, Larriba S, Lopes AM, Carmona FD, Palomino-Morales RJ. Cerván-Martín M, et al. Among authors: barros a. Andrology. 2021 Jul;9(4):1151-1165. doi: 10.1111/andr.13009. Epub 2021 Apr 20. Andrology. 2021. PMID: 33784440 Free article.

2

Preimplantation genetic diagnosis for familial amyloidotic polyneuropathy (FAP).

Carvalho F, Sousa M, Fernandes S, Silva J, Saraiva MJ, Barros A. Carvalho F, et al. Among authors: barros a. Prenat Diagn. 2001 Dec;21(12):1093-9. doi: 10.1002/pd.250. Prenat Diagn. 2001. PMID: 11746170

3

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: barros a. Eur J Hum Genet. 2002 Aug;10(8):467-74. doi: 10.1038/sj.ejhg.5200835. Eur J Hum Genet. 2002. PMID: 12111641

4

Genomic imprinting in disruptive spermatogenesis.

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

5

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: barros a. Hum Reprod. 2004 Nov;19(11):2502-8. doi: 10.1093/humrep/deh462. Epub 2004 Aug 27. Hum Reprod. 2004. PMID: 15333598

6

AZF and DAZ gene copy-specific deletion analysis in maturation arrest and Sertoli cell-only syndrome.

Ferrás C, Fernandes S, Marques CJ, Carvalho F, Alves C, Silva J, Sousa M, Barros A. Ferrás C, et al. Among authors: barros a. Mol Hum Reprod. 2004 Oct;10(10):755-61. doi: 10.1093/molehr/gah104. Epub 2004 Sep 3. Mol Hum Reprod. 2004. PMID: 15347736

7

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: barros a. Fertil Steril. 2005 Feb;83(2):448-51. doi: 10.1016/j.fertnstert.2004.07.967. Fertil Steril. 2005. PMID: 15705389 Free article.

8

Abnormal methylation of imprinted genes in human sperm is associated with oligozoospermia.

Marques CJ, Costa P, Vaz B, Carvalho F, Fernandes S, Barros A, Sousa M. Marques CJ, et al. Among authors: barros a. Mol Hum Reprod. 2008 Feb;14(2):67-74. doi: 10.1093/molehr/gam093. Epub 2008 Jan 4. Mol Hum Reprod. 2008. PMID: 18178607

9

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: barros a. 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.

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: barros a. 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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