Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Emmanuelle, Caldagues"'
Autor:
Morgane Marion, Sylvie Lacroix, Marylène Caquard, Laurence Dreno, Pauline Scherdel, Christèle Gras Le Guen, Emmanuelle Caldagues, Elise Launay
Publikováno v:
Journal of Eating Disorders, Vol 8, Iss 1, Pp 1-9 (2020)
Abstract Background A better understanding of the healthcare pathway of children and adolescents with anorexia nervosa (AN) may contribute to earlier detection and better disease management. Here we measured and compared the symptomatic time to diagn
Externí odkaz:
https://doaj.org/article/bddd4ccab19645a29be4155f93ebfe07
Autor:
Lucie Levaillant, Natacha Bouhours-Nouet, Frédéric Illouz, Jessica Amsellem Jager, Anne Bachelot, Pascal Barat, Sabine Baron, Candace Bensignor, Aude Brac De La Perriere, Yasmine Braik Djellas, Morgane Caillot, Emmanuelle Caldagues, Marie-Neige Campas, Marylène Caquard, Audrey Cartault, Julie Cheignon, Anne Decrequy, Brigitte Delemer, Katherine Dieckmann, Aurélie Donzeau, Emilie Doye, Mélanie Fradin, Mélanie Gaudillière, Frédérique Gatelais, Magali Gorce, Isabelle Hazart, Nada Houcinat, Laure Houdon, Marielle Ister-Salome, Lucie Jozwiak, Patrick Jeannoel, Francois Labarthe, Didier Lacombe, Anne-Sophie Lambert, Christine Lefevre, Bruno Leheup, Clara Leroy, Benedicte Maisonneuve, Isis Marchand, Emeline Marquant, Matthias Muszlak, Letitia Pantalone, Sandra Pochelu, Chloé Quelin, Catherine Radet, Peggy Renoult-Pierre, Rachel Reynaud, Stéphanie Rouleau, Cécile Teinturier, Julien Thevenon, Caroline Turlotte, Aline Valle, Melody Vierge, Carine Villanueva, Alban Ziegler, Xavier Dieu, Nathalie Bouzamondo, Patrice Rodien, Delphine Prunier-Mirebeau, Régis Coutant
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism.
IntroductionCongenital hypothyroidism with gland-in-situ (CH-GIS) is usually attributed to mutations in the genes involved in thyroid hormone production. The diagnostic yield of targeted next-generation sequencing (NGS) varied widely between studies.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d44025035eff7bb02449322219792ee2
https://doi.org/10.1210/clinem/dgad119
https://doi.org/10.1210/clinem/dgad119
Autor:
Mathilde Louvigne, Stephanie Rouleau, Emmanuelle Caldagues, Isabelle Souto, Yanis Montcho, Audrey Migraine Bouvagnet, Olivier Baud, Jean Claude Carel, Geraldine Gascoin, Regis Coutant
Publikováno v:
PLoS ONE, Vol 13, Iss 5, p e0195383 (2018)
The objective was to determine whether maternal nutritional factors are associated with transient neonatal hyperinsulinism (HI).Case control study in 4 French tertiary Obstetrics and Neonatology Departments between 2008 and 2015.Sixty-seven mothers o
Externí odkaz:
https://doaj.org/article/a82587ba1408426b8bfafd374ca11da5
Autor:
Claire Rochette, Nicolas Jullien, Alexandru Saveanu, Emmanuelle Caldagues, Ignacio Bergada, Debora Braslavsky, Marija Pfeifer, Rachel Reynaud, Jean-Paul Herman, Anne Barlier, Thierry Brue, Alain Enjalbert, Frederic Castinetti
Publikováno v:
PLoS ONE, Vol 10, Iss 5, p e0126648 (2015)
LHX4 is a LIM homeodomain transcription factor involved in the early steps of pituitary ontogenesis. To date, 8 heterozygous LHX4 mutations have been reported as responsible of combined pituitary hormone deficiency (CPHD) in Humans. We identified 4 n
Externí odkaz:
https://doaj.org/article/cc9aa415b3a5416ca27db31833e7f380
Autor:
Laurence Perrin, Marjolaine Willems, Sylvie Rossignol, Hélène Bony-Trifunovic, Cécile Brachet, Catherine Naud-Saudreau, Frédéric Brioude, Claire Sechter, Domitille Thomas, Walid Abi Habib, Georges Gelwane, Elise Brischoux-Boucher, Laurence Berard, Virginie Steunou, Claire Jeandel, Yves Le Bouc, Muriel Houang, Irène Netchine, Eloise Giabicani, Sandra Chantot-Bastaraud, Bertrand Isidor, Salah Azzi, James Lespinasse, Isabelle Guemas, Monique Jesuran-Perelroizen, Emmanuelle Caldagues, Pierre-François Souchon, Juliette Piard, Nathalie Thibaud, Marie-Laure Cuvelier, Bich Lam, Régis Coutant, Caroline Storey
Publikováno v:
Journal of Medical Genetics
Journal of Medical Genetics, In press, ⟨10.1136/jmedgenet-2019-106328⟩
Journal of Medical Genetics, BMJ Publishing Group, In press, ⟨10.1136/jmedgenet-2019-106328⟩
Journal of Medical Genetics, In press, ⟨10.1136/jmedgenet-2019-106328⟩
Journal of Medical Genetics, BMJ Publishing Group, In press, ⟨10.1136/jmedgenet-2019-106328⟩
BackgroundThe type 1 insulin-like growth factor receptor (IGF1R) is a keystone of fetal growth regulation by mediating the effects of IGF-I and IGF-II. Recently, a cohort of patients carrying an IGF1R defect was described, from which a clinical score
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30ee6d49255a92d9a87bc5b4b19c1735
https://hal.sorbonne-universite.fr/hal-02435128
https://hal.sorbonne-universite.fr/hal-02435128
Autor:
L. Dreno, Nathalie Vabres, Emmanuelle Caldagues, L. Cohen, Georges Picherot, C. Gras-Le Guen, J. Fleury
Publikováno v:
Archives de Pédiatrie. 24:1214-1219
Resume Introduction Les adolescents admis dans les services d’accueil des urgences pediatriques (SAUP) pour agitation sont de plus en plus nombreux. Leur agitation, multifactorielle, survient dans un parcours souvent « complexe ». Ils mettent en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98271f2e02429a6c88a5f2407824297e
https://doi.org/10.1016/j.arcped.2017.10.001
https://doi.org/10.1016/j.arcped.2017.10.001
Autor:
Eloïse, Giabicani, Marjolaine, Willems, Virginie, Steunou, Sandra, Chantot-Bastaraud, Nathalie, Thibaud, Walid, Abi Habib, Salah, Azzi, Bich, Lam, Laurence, Bérard, Hélène, Bony-Trifunovic, Cécile, Brachet, Elise, Brischoux-Boucher, Emmanuelle, Caldagues, Regis, Coutant, Marie-Laure, Cuvelier, Georges, Gelwane, Isabelle, Guemas, Muriel, Houang, Bertrand, Isidor, Claire, Jeandel, James, Lespinasse, Catherine, Naud-Saudreau, Monique, Jesuran-Perelroizen, Laurence, Perrin, Juliette, Piard, Claire, Sechter, Pierre-François, Souchon, Caroline, Storey, Domitille, Thomas, Yves, Le Bouc, Sylvie, Rossignol, Irène, Netchine, Frédéric, Brioude
Publikováno v:
Journal of medical genetics. 57(3)
The type 1 insulin-like growth factor receptor (IGF1R) is a keystone of fetal growth regulation by mediating the effects of IGF-I and IGF-II. Recently, a cohort of patients carrying anDNA was tested for either deletions or single nucleotide variant (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::884176ec4ad9bcfb4577ed8a72968606
https://pubmed.ncbi.nlm.nih.gov/31586944
https://pubmed.ncbi.nlm.nih.gov/31586944
Publikováno v:
La Presse Médicale. 45:e51-e58
Child abuse represents a contributing factor to develop various psychopathological disorders, such as somatoform disorders. OBJECTIVES: Improving the detection of child abuse, based on the analysis of somatoform disorders and the comparison between n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d85d08467639b5b0ef39ee0a8b3e5d4a
https://doi.org/10.1016/j.lpm.2015.10.023
https://doi.org/10.1016/j.lpm.2015.10.023
Autor:
Jean Claude Carel, Yanis Montcho, Mathilde Louvigne, Isabelle Souto, Géraldine Gascoin, Olivier Baud, Emmanuelle Caldagues, Stéphanie Rouleau, Audrey Migraine Bouvagnet, Régis Coutant
Publikováno v:
Plos One 5 (13), e0195383. (2018)
PLOS ONE, Vol. 13, No 5 (2018) P. e0195383
PLoS ONE, Vol 13, Iss 5, p e0195383 (2018)
PLoS ONE
PLoS ONE, Public Library of Science, 2018, 13 (5), pp.e0195383. ⟨10.1371/journal.pone.0195383⟩
PLOS ONE, Vol. 13, No 5 (2018) P. e0195383
PLoS ONE, Vol 13, Iss 5, p e0195383 (2018)
PLoS ONE
PLoS ONE, Public Library of Science, 2018, 13 (5), pp.e0195383. ⟨10.1371/journal.pone.0195383⟩
International audience; OBJECTIVE: The objective was to determine whether maternal nutritional factors are associated with transient neonatal hyperinsulinism (HI).DESIGN AND SETTING: Case control study in 4 French tertiary Obstetrics and Neonatology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95faf4d70a8572b2f8871cb6f1abe13b
http://prodinra.inra.fr/record/495104
http://prodinra.inra.fr/record/495104
Autor:
Frederic Castinetti, Alain Enjalbert, Alexandru Saveanu, Marija Pfeifer, Claire Rochette, Emmanuelle Caldagues, Thierry Brue, Debora Braslavsky, Nicolas Jullien, James P. Herman, Ignacio Bergadá, Anne Barlier, Rachel Reynaud
Publikováno v:
PLoS ONE
PLoS ONE, 2015, 10 (e0126648), ⟨10.1371/journal.pone.0126648⟩
PLoS ONE, Public Library of Science, 2015, 10 (e0126648), ⟨10.1371/journal.pone.0126648⟩
PLoS ONE, Vol 10, Iss 5, p e0126648 (2015)
PLoS ONE, 2015, 10 (e0126648), ⟨10.1371/journal.pone.0126648⟩
PLoS ONE, Public Library of Science, 2015, 10 (e0126648), ⟨10.1371/journal.pone.0126648⟩
PLoS ONE, Vol 10, Iss 5, p e0126648 (2015)
International audience; LHX4 is a LIM homeodomain transcription factor involved in the early steps of pituitary ontogenesis. To date, 8 heterozygous LHX4 mutations have been reported as responsible of combined pituitary hormone deficiency (CPHD) in H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a4cb196cdcfe4f9031d63929b17f1c4
https://hal-amu.archives-ouvertes.fr/hal-01211758
https://hal-amu.archives-ouvertes.fr/hal-01211758