C Molinas
Overview
Explore the profile of C Molinas including associated specialties, affiliations and a list of published articles.
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27
Citations
1076
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Recent Articles
1.
Kuppens R, Diene G, Bakker N, Molinas C, Faye S, Nicolino M, et al.
Endocrine
. 2015 May;
50(3):633-42.
PMID: 25989955
Prader-Willi syndrome (PWS) is characterized by a switch from failure to thrive to excessive weight gain and hyperphagia in early childhood. Hyperghrelinemia may be involved in the underlying mechanisms of...
2.
Laurier V, Lapeyrade A, Copet P, Demeer G, Silvie M, Bieth E, et al.
J Intellect Disabil Res
. 2014 Jun;
59(5):411-21.
PMID: 24947991
Background: Prader-Willi syndrome (PWS) is a developmental genetic disorder characterised by a variable expression of medical, cognitive and behavioural symptoms. In adulthood, the prevalence and severity of these symptoms determine...
3.
Cadoudal T, Buleon M, Sengenes C, Diene G, Desneulin F, Molinas C, et al.
Int J Obes (Lond)
. 2014 Jan;
38(9):1234-40.
PMID: 24406482
Background: Prader-Willi syndrome (PWS) results from abnormalities in the genomic imprinting process leading to hypothalamic dysfunction with an alteration of growth hormone (GH) secretion. PWS is associated with early morbid...
4.
de Graaff L, Clark A, Tauber M, Ranke M, Johnston L, Caliebe J, et al.
Horm Res Paediatr
. 2013 Nov;
80(6):466-76.
PMID: 24280783
Background: Fetal growth failure has been associated with an increased risk of hypertension, cardiovascular disease and diabetes in adulthood. Exploring the mechanisms underlying this association should improve our understanding of...
5.
Jouret B, Dulac Y, Bassil Eter R, Taktak A, Cristini C, Lounis N, et al.
Horm Res Paediatr
. 2011 Sep;
76(4):240-7.
PMID: 21912079
Background: Early cardiovascular events preceding atherosclerosis have been reported in children born small for gestational age (SGA). Aims: To describe in detail the mechanical and functional arterial properties of SGA...
6.
Cochen De Cock V, Diene G, Molinas C, Dauriac-Le Masson V, Kieffer I, Mimoun E, et al.
Am J Med Genet A
. 2011 Jun;
155A(7):1552-7.
PMID: 21671379
Excessive daytime sleepiness is a frequent and a highly disruptive symptom to the daily routine of children with Prader-Willi Syndrome (PWS) and their families. The objective of the study was...
7.
Diene G, Mimoun E, Feigerlova E, Caula S, Molinas C, Grandjean H, et al.
Horm Res Paediatr
. 2010 Apr;
74(2):121-8.
PMID: 20395666
Aim: The first results from the French National Prader-Willi pediatric database in a cohort of 142 children aged 0.2-18.8 years are reported. This database gathers information about the endocrine dysfunctions...
8.
Copet P, Jauregi J, Laurier V, Ehlinger V, Arnaud C, Cobo A, et al.
J Intellect Disabil Res
. 2010 Feb;
54(3):204-15.
PMID: 20136683
Background: Prader-Willi syndrome (PWS) is a rare genetic disorder characterised by developmental abnormalities leading to somatic and psychological symptoms. These include dysmorphic features, impaired growth and sexual maturation, hyperphagia, intellectual...
9.
Tauber M, Diene G, Molinas C, Hebert M
Am J Med Genet A
. 2008 Mar;
146A(7):881-7.
PMID: 18324685
Several deaths have been reported in children with Prader-Willi syndrome (PWS) following treatment with growth hormone (GH). We collected all of the reports of deaths in PWS children, both in...
10.
Bachere N, Diene G, Delagnes V, Molinas C, Moulin P, Tauber M
Horm Res
. 2007 Dec;
69(1):45-52.
PMID: 18059083
Background/aims: To describe and evaluate the impact of very early diagnosis and multidisciplinary care on the evolution and care of infants presenting with Prader-Willi syndrome (PWS). Methods: 19 infants diagnosed...