Fernandes S - Search Results

1

A novel Alu-mediated microdeletion at 11p13 removes WT1 in a patient with cryptorchidism and azoospermia.

Seabra CM, Quental S, Neto AP, Carvalho F, Gonçalves J, Oliveira JP, Fernandes S, Sousa M, Barros A, Amorim A, Lopes AM. Seabra CM, et al. Among authors: fernandes s. Reprod Biomed Online. 2014 Sep;29(3):388-91. doi: 10.1016/j.rbmo.2014.04.017. Epub 2014 May 16. Reprod Biomed Online. 2014. PMID: 24912414

2

Prognostic factors for successful testicle spermatid recover.

Sousa M, Fernandes S, Barros A. Sousa M, et al. Among authors: fernandes s. Mol Cell Endocrinol. 2000 Aug 15;166(1):37-43. doi: 10.1016/s0303-7207(00)00295-1. Mol Cell Endocrinol. 2000. PMID: 10989206 Review.

3

High deletion frequency of the complete AZFa sequence in men with Sertoli-cell-only syndrome.

Kamp C, Huellen K, Fernandes S, Sousa M, Schlegel PN, Mielnik A, Kleiman S, Yavetz H, Krause W, Küpker W, Johannisson R, Schulze W, Weidner W, Barros A, Vogt PH. Kamp C, et al. Among authors: fernandes s. Mol Hum Reprod. 2001 Oct;7(10):987-94. doi: 10.1093/molehr/7.10.987. Mol Hum Reprod. 2001. PMID: 11574668

4

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: fernandes s. Prenat Diagn. 2001 Dec;21(12):1093-9. doi: 10.1002/pd.250. Prenat Diagn. 2001. PMID: 11746170

5

High frequency of DAZ1/DAZ2 gene deletions in patients with severe oligozoospermia.

Fernandes S, Huellen K, Goncalves J, Dukal H, Zeisler J, Rajpert De Meyts E, Skakkebaek NE, Habermann B, Krause W, Sousa M, Barros A, Vogt PH. Fernandes S, et al. Mol Hum Reprod. 2002 Mar;8(3):286-98. doi: 10.1093/molehr/8.3.286. Mol Hum Reprod. 2002. PMID: 11870237

6

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

7

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: fernandes s. Mol Hum Reprod. 2004 Oct;10(10):755-61. doi: 10.1093/molehr/gah104. Epub 2004 Sep 3. Mol Hum Reprod. 2004. PMID: 15347736

8

Unique t(Y;1)(q12;q12) reciprocal translocation with loss of the heterochromatic region of chromosome 1 in a male with azoospermia due to meiotic arrest: a case report.

Pinho MJ, Neves R, Costa P, Ferrás C, Sousa M, Alves C, Almeida C, Fernandes S, Silva J, Ferrás L, Barros A. Pinho MJ, et al. Among authors: fernandes s. Hum Reprod. 2005 Mar;20(3):689-96. doi: 10.1093/humrep/deh653. Epub 2005 Jan 21. Hum Reprod. 2005. PMID: 15665019

9

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

10

DAZ gene copies: evidence of Y chromosome evolution.

Fernandes AT, Fernandes S, Gonçalves R, Sá R, Costa P, Rosa A, Ferrás C, Sousa M, Brehm A, Barros A. Fernandes AT, et al. Among authors: fernandes s. Mol Hum Reprod. 2006 Aug;12(8):519-23. doi: 10.1093/molehr/gal051. Epub 2006 Jun 15. Mol Hum Reprod. 2006. PMID: 16777954

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