Sousa M - Search Results

1

The mutational spectrum of WT1 in male infertility.

Seabra CM, Quental S, Lima AC, Carvalho F, Gonçalves J, Fernandes S, Pereira I, Silva J, Marques PI, Sousa M, Barros A, Seixas S, Amorim A, Lopes AM. Seabra CM, et al. Among authors: sousa m. J Urol. 2015 May;193(5):1709-15. doi: 10.1016/j.juro.2014.11.004. Epub 2014 Nov 11. J Urol. 2015. PMID: 25451826

2

Developmental potential of human spermatogenic cells co-cultured with Sertoli cells.

Sousa M, Cremades N, Alves C, Silva J, Barros A. Sousa M, et al. Hum Reprod. 2002 Jan;17(1):161-72. doi: 10.1093/humrep/17.1.161. Hum Reprod. 2002. PMID: 11756382

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

4

Preimplantation genetic diagnosis using FISH for carriers of Robertsonian translocations: the Portuguese experience.

Alves C, Sousa M, Silva J, Barros A. Alves C, et al. Among authors: sousa m. Prenat Diagn. 2002 Dec;22(12):1153-62. doi: 10.1002/pd.503. Prenat Diagn. 2002. PMID: 12454975

5

Genomic imprinting in disruptive spermatogenesis.

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

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

7

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: sousa m. Hum Reprod. 2005 Mar;20(3):689-96. doi: 10.1093/humrep/deh653. Epub 2005 Jan 21. Hum Reprod. 2005. PMID: 15665019

8

A moral case study for discussion: designer babies and tissue typing.

Sousa M, Barros A. Sousa M, et al. Reprod Biomed Online. 2004 Dec;9(6):596-7. doi: 10.1016/s1472-6483(10)61764-6. Reprod Biomed Online. 2004. PMID: 15670399 No abstract available.

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

10

Quantitative study of caspase-3 activity in semen and after swim-up preparation in relation to sperm quality.

Almeida C, Cardoso MF, Sousa M, Viana P, Gonçalves A, Silva J, Barros A. Almeida C, et al. Among authors: sousa m. Hum Reprod. 2005 May;20(5):1307-13. doi: 10.1093/humrep/deh727. Epub 2005 Mar 10. Hum Reprod. 2005. PMID: 15760967

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

2,956 results

Search Page

Filters