Biran-Mucignat V - Search Results

1

Assessment of dysphagia in infants with facial malformations.

Baudon JJ, Renault F, Goutet JM, Biran-Mucignat V, Morgant G, Garabedian EN, Vazquez MP. Baudon JJ, et al. Among authors: biran mucignat v. Eur J Pediatr. 2009 Feb;168(2):187-93. doi: 10.1007/s00431-008-0729-7. Epub 2008 May 22. Eur J Pediatr. 2009. PMID: 18496714

2

[Management of an intestinal stoma in neonatology].

Beucher S, Biran-Mucignat V, Baudon JJ, Gold F. Beucher S, et al. Among authors: biran mucignat v. Soins Pediatr Pueric. 2006 Feb-Mar;(228):37-9. Soins Pediatr Pueric. 2006. PMID: 16524212 French. No abstract available.

3

22q11.2 duplication syndrome: two new familial cases with some overlapping features with DiGeorge/velocardiofacial syndromes.

Portnoï MF, Lebas F, Gruchy N, Ardalan A, Biran-Mucignat V, Malan V, Finkel L, Roger G, Ducrocq S, Gold F, Taillemite JL, Marlin S. Portnoï MF, et al. Among authors: biran mucignat v. Am J Med Genet A. 2005 Aug 15;137(1):47-51. doi: 10.1002/ajmg.a.30847. Am J Med Genet A. 2005. PMID: 16007629 Review.

4

[Apnea of prematurity: risk factors and ambulatory treatment with caffeine citrate].

Ducrocq S, Biran-Mucignat V, Boelle PY, Lebas F, Baudon JJ, Gold F. Ducrocq S, et al. Among authors: biran mucignat v. Arch Pediatr. 2006 Oct;13(10):1299-304. doi: 10.1016/j.arcped.2006.06.016. Epub 2006 Aug 21. Arch Pediatr. 2006. PMID: 16919922 French.

5

[Determinants of diphemanil methylsulfate (Prantal) utilization: a survey of practice in the French neonatal and intensive care units].

Biran-Mucignat V, Flamant C, Lachtar M, Perrot C, Chauty A, Novakova J, Lavallée I, Mitanchez D, Aujard Y, Gold F. Biran-Mucignat V, et al. Arch Pediatr. 2007 Mar;14(3):254-8. doi: 10.1016/j.arcped.2006.11.017. Epub 2006 Dec 18. Arch Pediatr. 2007. PMID: 17175143 French.

6

[Caffeine citrate utilization for treatment of apnea in French neonatal units].

Ducrocq S, Biran-Mucignat V, Lebas F, Baudon JJ, Gold F. Ducrocq S, et al. Among authors: biran mucignat v. Arch Pediatr. 2006 Oct;13(10):1305-8. doi: 10.1016/j.arcped.2006.06.007. Epub 2006 Jul 26. Arch Pediatr. 2006. PMID: 16872813 French.

7

Splenogonadal fusion limb defect syndrome: report of five new cases and review.

Bonneau D, Roume J, Gonzalez M, Toutain A, Carles D, Maréchaud M, Biran-Mucignat V, Amati P, Moraine C. Bonneau D, et al. Am J Med Genet. 1999 Oct 8;86(4):347-58. doi: 10.1002/(sici)1096-8628(19991008)86:4<347::aid-ajmg9>3.0.co;2-a. Am J Med Genet. 1999. PMID: 10494091 Review.

8

[Indications for chromosome and DNA analysis for diagnosis of genetic diseases].

Bonneau D, Biran-Mucignat V. Bonneau D, et al. Among authors: biran mucignat v. Rev Prat. 2000 Jan 15;50(2):203-8. Rev Prat. 2000. PMID: 10737095 French. No abstract available.

9

X-linked lissencephaly with absent corpus callosum and ambiguous genitalia (XLAG): clinical, magnetic resonance imaging, and neuropathological findings.

Bonneau D, Toutain A, Laquerrière A, Marret S, Saugier-Veber P, Barthez MA, Radi S, Biran-Mucignat V, Rodriguez D, Gélot A. Bonneau D, et al. Among authors: biran mucignat v. Ann Neurol. 2002 Mar;51(3):340-9. doi: 10.1002/ana.10119. Ann Neurol. 2002. PMID: 11891829

10

Prenatal diagnosis of Gaucher's disease type 2. Ultrasonographic, biochemical and histological aspects.

Sarfati R, Hubert A, Dugué-Maréchaud M, Biran-Mucignat V, Pierre F, Bonneau D. Sarfati R, et al. Among authors: biran mucignat v. Prenat Diagn. 2000 Apr;20(4):340-3. doi: 10.1002/(sici)1097-0223(200004)20:4<340::aid-pd795>3.0.co;2-n. Prenat Diagn. 2000. PMID: 10740209

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