A Philippe
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Explore the profile of A Philippe including associated specialties, affiliations and a list of published articles.
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67
Citations
1107
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Recent Articles
11.
Philippe A, Ruivard M, Auclair C, Accoceberry M, Bonnin M, Pouly J, et al.
Gynecol Obstet Fertil
. 2015 Feb;
43(3):187-90.
PMID: 25708848
Objective: To compare peripartum management of anticoagulated patients concerning locoregional analgesia, post-partum hemorrhage and thrombotic events according to planified interruption or not of antithrombotic therapy. Patients And Methods: We conducted...
12.
Leroy C, Jacquemont M, Doray B, Lamblin D, Cormier-Daire V, Philippe A, et al.
Clin Genet
. 2015 Feb;
89(1):68-73.
PMID: 25677961
The Xq25 duplications syndrome has recently emerged as a distinct clinical entity. We report here on six new patients belonging to two unrelated families and harbouring an Xq25 microduplication detected...
13.
Beqqal K, Horellou M, Philippe A, Alhene Gelas M, Flaujac C, Gorin I, et al.
J Wound Care
. 2014 Feb;
23(2 Suppl):S16-9.
PMID: 24526169
In the setting of protein C deficiency, skin necrosis, which occurs most often at the initial phase of oral anticoagulants therapy, is a rare side effect. Six cases have previously...
14.
Clery H, Andersson F, Bonnet-Brilhault F, Philippe A, Wicker B, Gomot M
Neuroimage Clin
. 2013 Nov;
2:303-12.
PMID: 24179785
People with autism spectrum disorders (ASD) may show unusual reactions to unexpected changes that appear in their environment. Although several studies have highlighted atypical auditory change processing in ASD, little...
15.
Giral M, Foucher Y, Dufay A, Duong van Huyen J, Renaudin K, Moreau A, et al.
Am J Transplant
. 2013 Aug;
13(10):2567-76.
PMID: 23919486
The angiotensin II type 1 receptor (AT1R) is an emerging target of functional non-HLA antibodies (Ab). We examined the potential of determining the degree of presensitization against AT1R as a...
16.
Philippe A, Curinier S, Piquier-Perret G, Delabaere A, Acoccebery M, Velemir L, et al.
J Gynecol Obstet Biol Reprod (Paris)
. 2011 Sep;
41(2):194-7.
PMID: 21880437
No abstract available.
17.
Bonnet C, Andrieux J, Beri-Dexheimer M, Leheup B, Boute O, Manouvrier S, et al.
J Med Genet
. 2010 Jun;
47(6):377-84.
PMID: 20522426
BACKGROUND Genome-wide screening of large patient cohorts with mental retardation using microarray-based comparative genomic hybridisation (array-CGH) has recently led to identification several novel microdeletion and microduplication syndromes. METHODS Owing to...
18.
Walters R, Jacquemont S, Valsesia A, de Smith A, Martinet D, Andersson J, et al.
Nature
. 2010 Feb;
463(7281):671-5.
PMID: 20130649
Obesity has become a major worldwide challenge to public health, owing to an interaction between the Western 'obesogenic' environment and a strong genetic contribution. Recent extensive genome-wide association studies (GWASs)...
19.
Casadebaig F, Philippe A, Guillaud-Bataille J, Gausset M, Quemada N, Terra J
Eur Psychiatry
. 2009 Aug;
12(6):289-93.
PMID: 19698538
This study concerns the state of physical health and the availability of somatic care for 3,470 adult patients diagnosed as schizophrenic according to the research criteria established by the International...
20.
Philippe A, Weber S, Esquivel E, Houbron C, Hamard G, Ratelade J, et al.
Kidney Int
. 2008 Feb;
73(9):1038-47.
PMID: 18288100
Mutations in the NPHS2 gene, encoding podocin, are responsible for familial autosomal recessive and sporadic cases of steroid-resistant nephrotic syndrome. We have successfully generated a mouse model in which the...