Touraine RL - Search Results

1

Is the CAG repeat of mitochondrial DNA polymerase gamma (POLG) associated with male infertility? A multi-centre French study.

Aknin-Seifer IE, Touraine RL, Lejeune H, Jimenez C, Chouteau J, Siffroi JP, McElreavey K, Bienvenu T, Patrat C, Levy R. Aknin-Seifer IE, et al. Among authors: touraine rl. Hum Reprod. 2005 Mar;20(3):736-40. doi: 10.1093/humrep/deh666. Epub 2005 Jan 13. Hum Reprod. 2005. PMID: 15650046

2

A simple, low cost and non-invasive method for screening Y-chromosome microdeletions in infertile men.

Aknin-Seifer IE, Touraine RL, Lejeune H, Laurent JL, Lauras B, Levy R. Aknin-Seifer IE, et al. Among authors: touraine rl. Hum Reprod. 2003 Feb;18(2):257-61. doi: 10.1093/humrep/deg067. Hum Reprod. 2003. PMID: 12571158

3

Preliminary study on the role of the human IZUMO gene in oocyte-spermatozoa fusion failure.

Granados-Gonzalez V, Aknin-Seifer I, Touraine RL, Chouteau J, Wolf JP, Levy R. Granados-Gonzalez V, et al. Among authors: touraine rl. Fertil Steril. 2008 Oct;90(4):1246-8. doi: 10.1016/j.fertnstert.2007.09.008. Epub 2007 Dec 20. Fertil Steril. 2008. PMID: 18082733 Clinical Trial.

4

A de novo SOX10 mutation causing severe type 4 Waardenburg syndrome without Hirschsprung disease.

Sznajer Y, Coldéa C, Meire F, Delpierre I, Sekhara T, Touraine RL. Sznajer Y, et al. Among authors: touraine rl. Am J Med Genet A. 2008 Apr 15;146A(8):1038-41. doi: 10.1002/ajmg.a.32247. Am J Med Genet A. 2008. PMID: 18348267

5

Chronic neuromyotonia as a phenotypic variation associated with a new mutation in the KCNA1 gene.

Poujois A, Antoine JC, Combes A, Touraine RL. Poujois A, et al. Among authors: touraine rl. J Neurol. 2006 Jul;253(7):957-9. doi: 10.1007/s00415-006-0134-y. Epub 2006 Mar 6. J Neurol. 2006. PMID: 16511644 No abstract available.

6

Two fast methods for detection of Y-microdeletions.

Aknin-Seifer IE, Touraine RL, Faure AK, Fellmann F, Chouteau J, Levy R. Aknin-Seifer IE, et al. Among authors: touraine rl. Fertil Steril. 2005 Sep;84(3):740-2. doi: 10.1016/j.fertnstert.2005.03.050. Fertil Steril. 2005. PMID: 16169411 Free article.

7

Y chromosome microdeletion screening in infertile men in France: a survey of French practice based on 88 IVF centres.

Aknin-Seifer IE, Lejeune H, Touraine RL, Levy R; Societe d'Andrologie de Langue Francaise. Aknin-Seifer IE, et al. Among authors: touraine rl. Hum Reprod. 2004 Apr;19(4):788-93. doi: 10.1093/humrep/deh157. Epub 2004 Feb 12. Hum Reprod. 2004. PMID: 15033947 Review.

8

[A simple, low-cost and non-invasive method for screening Y microdeletions in infertile men].

Aknin-Seifer I, Touraine RL, Lejeune H, Laurent JL, Lauras B, Levy R. Aknin-Seifer I, et al. Among authors: touraine rl. Gynecol Obstet Fertil. 2004 Jan;32(1):34-41. doi: 10.1016/j.gyobfe.2002.11.001. Gynecol Obstet Fertil. 2004. PMID: 14736598 French.

9

A syndromic form of X-linked mental retardation: the Coffin-Lowry syndrome.

Touraine RL, Zeniou M, Hanauer A. Touraine RL, et al. Eur J Pediatr. 2002 Apr;161(4):179-87. doi: 10.1007/s00431-001-0904-6. Eur J Pediatr. 2002. PMID: 12014383 Review.

10

Impaired autonomic control of the heart by SOX10 mutation.

Korsch E, Steinkuhle J, Massin M, Lyonnet S, Touraine RL. Korsch E, et al. Among authors: touraine rl. Eur J Pediatr. 2001 Jan;160(1):68-9. doi: 10.1007/s004310000624. Eur J Pediatr. 2001. PMID: 11195028

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