A Vergnaud
Overview
Explore the profile of A Vergnaud including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
23
Citations
34
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Gerard-Blanluet M, Pipiras E, Levaillant J, Joye N, Koubi V, Kanafani S, et al.
Prenat Diagn
. 2007 Aug;
27(11):1062-3.
PMID: 17705236
No abstract available.
2.
Delahaye A, Pipiras E, Kanafani S, Touboul C, Vergnaud A, Encha-Razavi F, et al.
Fetal Diagn Ther
. 2007 Mar;
22(4):306-12.
PMID: 17361086
Objective: We describe the analysis of an apparently balanced inherited reciprocal translocation in a fetus presenting with multiple congenital abnormalities, characterize the structural chromosome rearrangement, and report an unexpected additional...
3.
Sinico M, Levaillant J, Vergnaud A, Blondeau J, Encha-Razavi F, Mornet E, et al.
Prenat Diagn
. 2007 Jan;
27(3):222-7.
PMID: 17238218
Background: Hypophosphatasia is an osseous dysplasia with highly variable clinical expression, ranging from a recessive lethal prenatal type to late onset dominant short stature with premature shedding of teeth. Lethal...
4.
Levaillant J, Touboul C, Sinico M, Vergnaud A, Serero S, Druart L, et al.
Prenat Diagn
. 2005 Nov;
25(12):1150-5.
PMID: 16258951
Objectives: Deletion of short arm of chromosome 4 is difficult to ascertain prenatally, and can be missed. Methods: A prenatal suspicion of 4p- syndrome was thoroughly investigated by using two-dimensional...
5.
Mangione R, Guyon F, Taine L, Wen Z, Roux D, Vergnaud A, et al.
Fetal Diagn Ther
. 2001 Nov;
16(6):360-3.
PMID: 11694739
Objective: One of the concerns of prenatal diagnosis is to find sensitive markers to screen for chromosome abnormalities, such as serum assays or nuchal translucency (NT). This study reports our...
6.
Mangione R, Guyon F, Vergnaud A, Jimenez M, Saura R, Horovitz J
Eur J Obstet Gynecol Reprod Biol
. 1999 Sep;
86(1):105-7.
PMID: 10471151
We report the case of a fetus with supraventricular tachycardia complicated by congestive heart failure and ascites. After failure of initial transplacental treatment, the injection of amiodarone into the umbilical...
7.
Saura R, Roux D, Taine L, Wen Z, Vergnaud A, Horovitz J
Prenat Diagn
. 1998 Sep;
18(8):866-7.
PMID: 9742583
No abstract available.
8.
Saura R, Traore W, Taine L, Wen Z, Roux D, Maugey-Laulom B, et al.
Prenat Diagn
. 1995 Jul;
15(7):609-14.
PMID: 8532619
Six prenatally diagnosed cases of trisomy 9 are reported and 22 previously reported cases are reviewed; the difficulty of genetic counselling for such cases and the variation in the percentage...
9.
Brun J, Saura R, Horovitz J, Maugey B, Taine L, Roux D, et al.
Fetal Diagn Ther
. 1994 Jul;
9(4):246-51.
PMID: 7945905
During a 4-year period, 29 fetal nuchal edemas were observed, associated with other ultrasound abnormalities in 7 cases (24%). Fetal karyotypes were abnormal in 10 cases: 6 trisomy 21; 3...
10.
Saura R, Gauthier B, Taine L, Wen Z, Horovitz J, Roux D, et al.
Prenat Diagn
. 1994 Jan;
14(1):70-1.
PMID: 8183841
No abstract available.