Zobrazeno 1 - 10
of 131
pro vyhledávání: '"Sylvie Brailly-Tabard"'
Autor:
Emmanuelle Motte-Signoret, Shivani Shankar-Aguilera, Sylvie Brailly-Tabard, Yohan Soreze, Valentina Dell Orto, Rafik Ben Ammar, Daniele De Luca, Pascal Boileau
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Objective: To investigate the impact of fetal growth restriction (FGR) on hormonal regulation of post-natal growth and glucose metabolism [via insulin and growth hormone (GH)/Insulin-like Growth factor 1 (IGF1) axis pathways] in small for gestational
Externí odkaz:
https://doaj.org/article/1ee86611b5c646ea851f20b04f3f6c00
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Background: In patients with pituitary stalk interruption syndrome (PSIS), long-term follow-up is necessary to address their gonadotrophic status. The objectives of this study were (1) to describe pubertal features of and (2) to assess the ability of
Externí odkaz:
https://doaj.org/article/56aab96229d845aa83f2b2725280add8
Autor:
Nasser Laouali, Sylvie Brailly-Tabard, Catherine Helmer, Marie-Laure Ancelin, Christophe Tzourio, Alexis Elbaz, Anne Guiochon-Mantel, Marianne Canonico
Publikováno v:
Epidemiology and Health, Vol 42 (2020)
OBJECTIVES Previous studies have reported controversial findings regarding the association of testosterone with mortality in older men. This heterogeneity might be partially explained by comorbidities and the presence of metabolic syndrome, as well a
Externí odkaz:
https://doaj.org/article/a9d1cd68996a4ca7b80454270c592216
Autor:
Catherine Le Stunff, Anne-Laure Castell, Nicolas Todd, Clémence Mille, Marie-Pierre Belot, Nathalie Frament, Sylvie Brailly-Tabard, Alexandra Benachi, Delphine Fradin, Pierre Bougnères
Publikováno v:
Clinical Epigenetics, Vol 10, Iss 1, Pp 1-7 (2018)
Abstract Background There are many reasons to think that epigenetics is a key determinant of fetal growth variability across the normal population. Since IGF1 and INS genes are major determinants of intrauterine growth, we examined the methylation of
Externí odkaz:
https://doaj.org/article/257338b79613435aa3252790022c792e
Autor:
Isabelle Stücker, Diane Martin, Monica Neri, Pierre Laurent-Puig, Hélène Blons, Martine Antoine, Anne Guiochon-Mantel, Sylvie Brailly-Tabard, Marianne Canonico, Marie Wislez, Jean Trédaniel, WELCA study group
Publikováno v:
BMC Public Health, Vol 17, Iss 1, Pp 1-8 (2017)
Abstract Background Lung cancer aetiology and clinical aspects have been mainly studied in men, although specific risk factors probably exist in women. Here we present the rationale, design and organization of the WELCA study (Women Epidemiology Lung
Externí odkaz:
https://doaj.org/article/c106edd8fbdc4a49925f0d6bde7f80ac
Publikováno v:
PLoS ONE, Vol 13, Iss 12, p e0205810 (2018)
OBJECTIVE:To compare the serum inhibin B, anti-Müllerian hormone (AMH) and leptin concentrations in girls with idiopathic central precocious puberty (CPP) to their concomitant characteristics and evaluate the capacity of each of these hormones to pr
Externí odkaz:
https://doaj.org/article/81f81415aca54686946710a4151a394f
Autor:
Anne-Sophie Lambert, Anya Rothenbuhler, Perrine Charles, Sylvie Brailly-Tabard, Séverine Trabado, Elisabeth Célestin, Emmanuel Durand, Isabelle Fontaine, Lotfi Miladi, Philippe Wicart, Nadia Bahi-Buisson, Agnès Linglart
Publikováno v:
PLoS ONE, Vol 12, Iss 10, p e0186941 (2017)
Classic Rett Syndrome (RS) is a disabling condition mainly caused by MECP2 mutations. Girls with RS are at risk of developing bone fragility and fractures at a young age which results in pain and may seriously impair quality of life.To retrospectivel
Externí odkaz:
https://doaj.org/article/fda0bfe6504547169618796b229aa24d
Autor:
Catherine Le Stunff, Anne-Laure Castell, Nicolas Todd, Clémence Mille, Marie-Pierre Belot, Nathalie Frament, Sylvie Brailly-Tabard, Alexandra Benachi, Delphine Fradin, Pierre Bougnères
Publikováno v:
Clinical Epigenetics, Vol 10, Iss 1, Pp 1-1 (2018)
After publication of the original article [1], it came to the publishers’ attention that the below author’s corrections provided at the proofing stage had been misinterpreted.
Externí odkaz:
https://doaj.org/article/2dfa2a22977e4f15a1920e070efc62f5
Autor:
Frédéric Brioude, Jérôme Bouligand, Bruno Francou, Jérôme Fagart, Ronan Roussel, Say Viengchareun, Laurent Combettes, Sylvie Brailly-Tabard, Marc Lombès, Jacques Young, Anne Guiochon-Mantel
Publikováno v:
PLoS ONE, Vol 8, Iss 1, p e53896 (2013)
CONTEXT: KISS1R mutations have been reported in few patients with normosmic congenital hypogonadotropic hypogonadism (nCHH) (OMIM #146110). OBJECTIVE: To describe in detail nCHH patients with biallelic KISS1R mutations belonging to 2 unrelated famili
Externí odkaz:
https://doaj.org/article/40b7198a37f6439d9dc1cd1d50c97c53
Autor:
Audrey Vizeneux, Aude Hilfiger, Jérôme Bouligand, Monique Pouillot, Sylvie Brailly-Tabard, Anu Bashamboo, Ken McElreavey, Raja Brauner
Publikováno v:
PLoS ONE, Vol 8, Iss 10, p e77827 (2013)
BACKGROUND:The majority of the patients reported with mutations in isolated hypogonadotropic hypogonadism (HH) are adults. We analysed the presentation and the plasma inhibin B and anti-müllerian hormone (AMH) concentrations during childhood and ado
Externí odkaz:
https://doaj.org/article/b124fc798b0447a1b1084b8502e24d68