Delezoide A - Search Results

1

Prenatal diagnosis of hydrocephalus-stenosis of the aqueduct of Sylvius by ultrasound in the first trimester of pregnancy. Report of two cases.

Senat MV, Bernard JP, Delezoide A, Saugier-Veber P, Hillion Y, Roume J, Ville Y. Senat MV, et al. Among authors: delezoide a. Prenat Diagn. 2001 Dec;21(13):1129-32. doi: 10.1002/pd.184. Prenat Diagn. 2001. PMID: 11787037

2

Outcome following prenatal diagnosis of severe bilateral renal hypoplasia.

Spaggiari E, Stirnemann JJ, Heidet L, Dreux S, Ville Y, Oury JF, Delezoide AL, Muller F. Spaggiari E, et al. Prenat Diagn. 2013 Dec;33(12):1167-72. doi: 10.1002/pd.4217. Epub 2013 Sep 1. Prenat Diagn. 2013. PMID: 23943585

3

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. Prenat Diagn. 2007 Oct;27(10):926-31. doi: 10.1002/pd.1803. Prenat Diagn. 2007. PMID: 17602442

4

Prenatal diagnosis of a rare skeletal dysplasia by ultrasound and scan tomography: atelosteogenesis III (AO III). Correlation with autopsy.

Cordier AG, Mabille M, Delezoide AL, Chambon G, Frydman R, Senat MV, Picone O. Cordier AG, et al. Among authors: delezoide al. Prenat Diagn. 2008 Oct;28(10):975-7. doi: 10.1002/pd.2093. Prenat Diagn. 2008. PMID: 18792994 No abstract available.

5

Neuropathological review of 138 cases genetically tested for X-linked hydrocephalus: evidence for closely related clinical entities of unknown molecular bases.

Adle-Biassette H, Saugier-Veber P, Fallet-Bianco C, Delezoide AL, Razavi F, Drouot N, Bazin A, Beaufrère AM, Bessières B, Blesson S, Bucourt M, Carles D, Devisme L, Dijoud F, Fabre B, Fernandez C, Gaillard D, Gonzales M, Jossic F, Joubert M, Laurent N, Leroy B, Loeuillet L, Loget P, Marcorelles P, Martinovic J, Perez MJ, Satge D, Sinico M, Tosi M, Benichou J, Gressens P, Frebourg T, Laquerrière A. Adle-Biassette H, et al. Among authors: delezoide al. Acta Neuropathol. 2013 Sep;126(3):427-42. doi: 10.1007/s00401-013-1146-1. Epub 2013 Jul 3. Acta Neuropathol. 2013. PMID: 23820807

6

Familial Blomstrand chondrodysplasia with advanced skeletal maturation: further delineation.

Loshkajian A, Roume J, Stanescu V, Delezoide AL, Stampf F, Maroteaux P. Loshkajian A, et al. Among authors: delezoide al. Am J Med Genet. 1997 Aug 22;71(3):283-8. doi: 10.1002/(sici)1096-8628(19970822)71:3<283::aid-ajmg7>3.0.co;2-v. Am J Med Genet. 1997. PMID: 9268097 Review.

7

Unusual variant of holoprosencephaly in monosomy 13q.

Marcorelles P, Loget P, Fallet-Bianco C, Roume J, Encha-Razavi F, Delezoide AL. Marcorelles P, et al. Pediatr Dev Pathol. 2002 Mar-Apr;5(2):170-8. doi: 10.1007/s10024001-0200-5. Pediatr Dev Pathol. 2002. PMID: 11910512

8

Outcome and etiologies of fetal megacystis according to the gestational age at diagnosis.

Bornes M, Spaggiari E, Schmitz T, Dreux S, Czerkiewicz I, Delezoide AL, El-Ghoneimi A, Oury JF, Muller F. Bornes M, et al. Among authors: delezoide al. Prenat Diagn. 2013 Dec;33(12):1162-6. doi: 10.1002/pd.4215. Epub 2013 Sep 3. Prenat Diagn. 2013. PMID: 23939878

9

Prenatal Marfan syndrome: report of one case and review of the literature.

Lopes KR, Delezoide AL, Baumann C, Vuillard E, Luton D, Chitrit Y, Azancot A. Lopes KR, et al. Among authors: delezoide al. Prenat Diagn. 2006 Aug;26(8):696-9. doi: 10.1002/pd.1482. Prenat Diagn. 2006. PMID: 16752434

10

Prenatal diagnosis of Juberg-Hayward syndrome.

Couvreur-Lionnais S, Rousseau T, Laurent N, Thauvin-Robinet C, Senet-Lacombe E, Delezoïde AL, Mugneret F, Durand C, Faivre L, Sagot P. Couvreur-Lionnais S, et al. Prenat Diagn. 2005 Feb;25(2):172-5. doi: 10.1002/pd.943. Prenat Diagn. 2005. PMID: 15712337

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