J B Savary
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Explore the profile of J B Savary including associated specialties, affiliations and a list of published articles.
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46
Citations
66
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Recent Articles
1.
Brun L, Dufour P, Savary J, Valat A, Boute O, Subtil D, et al.
Presse Med
. 2001 Jan;
29(38):2082-6.
PMID: 11147045
Objective: We describe the different ultrasound findings suggestive of trisomy 18. Patients And Methods: We conducted a retrospective study in 40 cases of trisomy 18 diagnosed in the department of...
2.
Vasseur F, Delaporte E, Zabot M, Sturque M, Barrut D, Savary J, et al.
Acta Derm Venereol
. 1999 May;
79(2):150-2.
PMID: 10228638
Rothmund Thomson syndrome is a rare autosomal recessive skin disorder. The main clinical feature is poikiloderma appearing in early childhood associated with skeletal abnormalities. Early occurrence of malignancies is another...
3.
Dufour P, Berard J, Vinatier D, Savary J, Dubreucq S, MONNIER J, et al.
Eur J Obstet Gynecol Reprod Biol
. 1997 Apr;
72(2):159-64.
PMID: 9134395
Myotonic dystrophy is a rare disease (1/8000), that is rarely associated with pregnancy, due to the fact that parents carrying the disease often encounter hypogonadism. Myotonic dystrophy is a neuro-endocrinian...
4.
Vanderstichele S, Savary J, Dufour P, Berard J, Tordjeman N, Vinatier D, et al.
J Gynecol Obstet Biol Reprod (Paris)
. 1997 Jan;
26(6):630-2.
PMID: 9453981
The prenatal diagnosis of trisomy for the distal half of the short arm of n(o) 9 chromosome (partial trisomy 9p) has been realized from a morphologic ultrasound. A genetic investigation...
5.
Benzacken B, Savary J, Manouvrier S, Bucourt M, Gonzales J
Prenat Diagn
. 1996 Feb;
16(2):125-30.
PMID: 8650122
We report two fetuses with typical anomalies of Roberts syndrome. Prenatal diagnosis was confirmed by the characteristic disjunction of centromeres in amniocytes. We compare these cases with a child who...
6.
Delaporte E, Janin A, Savary J, Vasseur F, FEINGOLD N, Piette F, et al.
Br J Dermatol
. 1995 Sep;
133(3):409-16.
PMID: 8546996
Keratoderma with scleroatrophy of the extremities, also referred to as Huriez syndrome, is a rare, autosomal dominant condition, first described in 42 of 132 members of two families from northern...
7.
Deminatti M, RIBET M, Gosselin B, Bauters F, Mencier E, Savary J, et al.
Ann Genet
. 1994 Jan;
37(2):72-4.
PMID: 7985981
A familial lympho-epithelial thymoma with constitutional chromosomal translocation t (14;20) (q24;p13) is presented: the thymoma and its particular translocation are present in the mother and the two sons of her...
8.
Houfflin V, Dufour P, Vinatier D, Bernardi C, Lefebvre C, Depret S, et al.
J Gynecol Obstet Biol Reprod (Paris)
. 1993 Jan;
22(6):625-9.
PMID: 8263292
The authors present a case of partial trisomy 12q associated with chylothorax, diagnosed at 30 weeks of pregnancy. Cordocentesis for the karyotype as well as thoracocentesis were carried out. In...
9.
Savary J, Vasseur F, Vinatier D, Manouvrier S, Deminatti M
Prenat Diagn
. 1992 Nov;
12(11):969-71.
PMID: 1494551
No abstract available.
10.
Savary J, Daudignon A, Vasseur F, Deminatti M
Ann Genet
. 1992 Jan;
35(1):27-32.
PMID: 1610116
Pulse 5-bromodeoxyuridine (5-BrdU) incorporation during the last S-phase is known to produce R- or G-banded chromosomes after photolysis-plus-Giemsa (FPG) staining. The authors applied an immunological staining with monoclonal anti-BrdU antibody...