Guimiot F - Search Results

1

Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene.

Delahaye A, Khung-Savatovsky S, Aboura A, Guimiot F, Drunat S, Alessandri JL, Gérard M, Bitoun P, Boumendil J, Robin S, Huel C, Guilherme R, Serero S, Gressens P, Elion J, Verloes A, Benzacken B, Delezoide AL, Pipiras E. Delahaye A, et al. Among authors: guimiot f. Am J Med Genet A. 2012 Oct;158A(10):2430-8. doi: 10.1002/ajmg.a.35548. Epub 2012 Aug 17. Am J Med Genet A. 2012. PMID: 22903608

2

Positive allosteric modulators of AMPA receptors are neuroprotective against lesions induced by an NMDA agonist in neonatal mouse brain.

Dicou E, Rangon CM, Guimiot F, Spedding M, Gressens P. Dicou E, et al. Among authors: guimiot f. Brain Res. 2003 Apr 25;970(1-2):221-5. doi: 10.1016/s0006-8993(03)02357-6. Brain Res. 2003. PMID: 12706264

3

Expression of the RSK2 gene during early human development.

Guimiot F, Delezoide AL, Hanauer A, Simonneau M. Guimiot F, et al. Gene Expr Patterns. 2004 Jan;4(1):111-4. doi: 10.1016/j.modgep.2003.06.001. Gene Expr Patterns. 2004. PMID: 14678837

4

Sodium/iodide symporter (NIS) gene expression is the limiting step for the onset of thyroid function in the human fetus.

Szinnai G, Lacroix L, Carré A, Guimiot F, Talbot M, Martinovic J, Delezoide AL, Vekemans M, Michiels S, Caillou B, Schlumberger M, Bidart JM, Polak M. Szinnai G, et al. Among authors: guimiot f. J Clin Endocrinol Metab. 2007 Jan;92(1):70-6. doi: 10.1210/jc.2006-1450. Epub 2006 Oct 31. J Clin Endocrinol Metab. 2007. PMID: 17077129

5

Comparison between magnetic resonance imaging and fetopathology in the evaluation of fetal posterior fossa non-cystic abnormalities.

Tilea B, Delezoide AL, Khung-Savatovski S, Guimiot F, Vuillard E, Oury JF, Garel C. Tilea B, et al. Among authors: guimiot f. Ultrasound Obstet Gynecol. 2007 Jun;29(6):651-9. doi: 10.1002/uog.4012. Ultrasound Obstet Gynecol. 2007. PMID: 17476704 Free article.

6

Quantitative evaluation of collagen type VI and SOD gene expression in the nuchal skin of human fetuses with trisomy 21.

Quarello E, Guimiot F, Moalic JM, Simoneau M, Ville Y, Delezoide AL. Quarello E, et al. Among authors: guimiot f. Prenat Diagn. 2007 Oct;27(10):926-31. doi: 10.1002/pd.1803. Prenat Diagn. 2007. PMID: 17602442

7

Contribution of diffusion-weighted imaging in the evaluation of diffuse white matter ischemic lesions in fetuses: correlations with fetopathologic findings.

Guimiot F, Garel C, Fallet-Bianco C, Menez F, Khung-Savatovsky S, Oury JF, Sebag G, Delezoide AL. Guimiot F, et al. AJNR Am J Neuroradiol. 2008 Jan;29(1):110-5. doi: 10.3174/ajnr.A0754. Epub 2007 Oct 18. AJNR Am J Neuroradiol. 2008. PMID: 17947368 Free PMC article.

8

Giant diencephalic harmartoma and related anomalies: a newly recognized entity distinct from the Pallister-Hall syndrome.

Guimiot F, Marcorelles P, Aboura A, Bonyhay G, Patrier S, Menez F, Drouin-Garraud V, Icowick V, Eurin D, Garel C, Moirot H, Verspyck E, Saugier-Veber P, Attie-Bitach T, Picone O, Oury JF, Verloes A, Delezoide AL, Laquerrière A. Guimiot F, et al. Am J Med Genet A. 2009 Jun;149A(6):1108-15. doi: 10.1002/ajmg.a.32859. Am J Med Genet A. 2009. PMID: 19449422

9

Very early twin-to-twin transfusion syndrome and discordant activation of the renin-angiotensin system.

Guilherme R, Patrier S, Gubler MC, Lemercier D, Guimiot F, Dommergues M. Guilherme R, et al. Among authors: guimiot f. Placenta. 2009 Aug;30(8):731-4. doi: 10.1016/j.placenta.2009.06.001. Epub 2009 Jul 3. Placenta. 2009. PMID: 19577294

10

Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations.

Passemard S, Titomanlio L, Elmaleh M, Afenjar A, Alessandri JL, Andria G, de Villemeur TB, Boespflug-Tanguy O, Burglen L, Del Giudice E, Guimiot F, Hyon C, Isidor B, Mégarbané A, Moog U, Odent S, Hernandez K, Pouvreau N, Scala I, Schaer M, Gressens P, Gerard B, Verloes A. Passemard S, et al. Among authors: guimiot f. Neurology. 2009 Sep 22;73(12):962-9. doi: 10.1212/WNL.0b013e3181b8799a. Neurology. 2009. PMID: 19770472

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