Guimiot F - Search Results

1

Finding vacuolated lymphocytes in fetal effusions improves the prenatal diagnosis of lysosomal storage diseases.

Taconet S, Dreux S, Guimiot F, Pettazzoni M, Allaf B, Spaggiari E, Rosenblatt J, Khung-Savatovsky S. Taconet S, et al. Among authors: guimiot f. Prenat Diagn. 2020 Apr;40(5):605-611. doi: 10.1002/pd.5657. Epub 2020 Feb 11. Prenat Diagn. 2020. PMID: 32003481

2

Biochemical analysis of ascites fluid as an aid to etiological diagnosis: a series of 100 cases of nonimmune fetal ascites.

Dreux S, Salomon LJ, Rosenblatt J, Favre R, Houfflin-Debarge V, Broussin B, Guimiot F, Fenaux H, Delezoide AL, Muller F. Dreux S, et al. Among authors: guimiot f. Prenat Diagn. 2015 Mar;35(3):214-20. doi: 10.1002/pd.4522. Epub 2014 Nov 26. Prenat Diagn. 2015. PMID: 25346315

3

Prognosis and outcome of pregnancies exposed to renin-angiotensin system blockers.

Spaggiari E, Heidet L, Grange G, Guimiot F, Dreux S, Delezoide AL; Renin-Angiotensin System Blockers Study Group; Muller F. Spaggiari E, et al. Among authors: guimiot f. Prenat Diagn. 2012 Nov;32(11):1071-6. doi: 10.1002/pd.3960. Epub 2012 Aug 18. Prenat Diagn. 2012. PMID: 22903358

4

Fetal serum α-1 microglobulin for renal function assessment: comparison with β2-microglobulin and cystatin C.

Nguyen C, Dreux S, Heidet L, Czerkiewicz I, Salomon LJ, Guimiot F, Schmitz T, Tsatsaris V, Boulot P, Rousseau T, Muller F. Nguyen C, et al. Among authors: guimiot f. Prenat Diagn. 2013 Aug;33(8):775-81. doi: 10.1002/pd.4128. Epub 2013 May 14. Prenat Diagn. 2013. PMID: 23592560

5

Prenatal diagnosis of inherited epidermolysis bullosa in a patient with no family history: a case report and literature review.

Azarian M, Dreux S, Vuillard E, Meneguzzi G, Haber S, Guimiot F, Muller F. Azarian M, et al. Among authors: guimiot f. Prenat Diagn. 2006 Jan;26(1):57-9. doi: 10.1002/pd.1349. Prenat Diagn. 2006. PMID: 16378325

6

Fetal urine biochemistry at 13-23 weeks of gestation in lower urinary tract obstruction: criteria for in-utero treatment.

Abdennadher W, Chalouhi G, Dreux S, Rosenblatt J, Favre R, Guimiot F, Salomon LJ, Oury JF, Ville Y, Muller F. Abdennadher W, et al. Among authors: guimiot f. Ultrasound Obstet Gynecol. 2015 Sep;46(3):306-11. doi: 10.1002/uog.14734. Epub 2015 Aug 10. Ultrasound Obstet Gynecol. 2015. PMID: 25412852 Free article.

7

Prenatal phenotype of congenital hyperparathyroidism.

Spaggiari E, Bucau M, Capri Y, Belarbi N, Bekmezian A, Briffa JM, Delezoide AL, Guimiot F. Spaggiari E, et al. Among authors: guimiot f. Prenat Diagn. 2012 Sep;32(9):906-8. doi: 10.1002/pd.3912. Epub 2012 Jun 5. Prenat Diagn. 2012. PMID: 22674768 No abstract available.

8

Specific biochemical amniotic fluid pattern of fetal isolated esophageal atresia.

Muller C, Czerkiewicz I, Guimiot F, Dreux S, Salomon LJ, Khen-Dunlop N, Bonnard A, Schmitz T, Oury JF, Muller F. Muller C, et al. Among authors: guimiot f. Pediatr Res. 2013 Nov;74(5):601-5. doi: 10.1038/pr.2013.131. Epub 2013 Sep 11. Pediatr Res. 2013. PMID: 23942557

9

Severe Phenotype of Cutis Laxa Type 1B with Antenatal Signs due to a Novel Homozygous Nonsense Mutation in EFEMP2.

Letard P, Schepers D, Albuisson J, Bruneval P, Spaggiari E, Van de Beek G, Khung-Savatovsky S, Belarbi N, Capri Y, Delezoide AL, Loeys B, Guimiot F. Letard P, et al. Among authors: guimiot f. Mol Syndromol. 2018 Jul;9(4):190-196. doi: 10.1159/000489838. Epub 2018 Jun 8. Mol Syndromol. 2018. PMID: 30140196 Free PMC article.

10

Duplicated distal phalanx of thumb or hallux in trisomy 13: A recurrent feature in a series of 42 fetuses.

Létard P, Guimiot F, Dupont C, Rosenblatt J, Delezoide AL, Khung-Savatovsky S. Létard P, et al. Among authors: guimiot f. Am J Med Genet A. 2018 Nov;176(11):2325-2330. doi: 10.1002/ajmg.a.40505. Epub 2018 Oct 17. Am J Med Genet A. 2018. PMID: 30328679

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