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1دورية أكاديمية
المؤلفون: Régis Coutant, Marc Nicolino, Benoit Cammas, Valérie de Buyst, Maïthé Tauber, Jean-François Hamel
المصدر: Frontiers in Endocrinology, Vol 12 (2022)
مصطلحات موضوعية: recombinant human growth hormone, children, height gain, adherence, electronic device, growth hormone deficiency, Diseases of the endocrine glands. Clinical endocrinology, RC648-665
وصف الملف: electronic resource
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المؤلفون: Sabine Baron, Jacques Weill, Catherine Arnaud, Catie Cessans, Yline Capri, Benoit Cammas, Pascal Barat, Armelle Yart, Bruno Leheup, Jean-Pierre Salles, Didier Lacombe, Virginie Ehlinger, Régis Coutant, Marc Nicolino, Thomas Edouard, Hélène Cavé, Alain Verloes, Maithé Tauber, Albert David
المساهمون: Centre d'Endocrinologie, Maladies Osseuses, Génétique et Gynécologie Médicale, Hôpital des Enfants, CHU Toulouse [Toulouse]-CHU Toulouse [Toulouse], Epidémiologie et analyses en santé publique : risques, maladies chroniques et handicaps (LEASP), Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National de la Santé et de la Recherche Médicale (INSERM), Service d'épidémiologie [Toulouse], CHU Toulouse [Toulouse], Institut des Maladies Métaboliques et Cardiovasculaires (I2MC), Département de génétique [Robert Debré], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-AP-HP Hôpital universitaire Robert-Debré [Paris], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), CIC Bordeaux, Université Bordeaux Segalen - Bordeaux 2-Institut National de la Santé et de la Recherche Médicale (INSERM), Service de génétique médicale, Université de Bordeaux (UB)-CHU Bordeaux [Bordeaux]-Groupe hospitalier Pellegrin, Endocrinologie pédiatrique[CHU Angers], Centre Hospitalier Universitaire d'Angers (CHU Angers), PRES Université Nantes Angers Le Mans (UNAM)-PRES Université Nantes Angers Le Mans (UNAM)-Université d'Angers (UA), Service de génétique médicale - Unité de génétique clinique [Nantes], Université de Nantes (UN)-Centre hospitalier universitaire de Nantes (CHU Nantes), Service d'Endocrinologie Pédiatrique [CHU Nantes], Centre hospitalier universitaire de Nantes (CHU Nantes), Service d'endocrinologie pédiatrique [CHU Lille], Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille)-Hôpital Jeanne de Flandre [Lille], Service de Médecine Infantile III et Génétique Clinique [CHRU Nancy], Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy), Nutrition-Génétique et Exposition aux Risques Environnementaux (NGERE), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lorraine (UL), Service d'endocrinologie pédiatrique [CHU Lyon-Hospices Civils de Lyon], Hospices Civils de Lyon (HCL), Centre de Physiopathologie Toulouse Purpan (CPTP), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
المصدر: European Journal of Endocrinology
European Journal of Endocrinology, BioScientifica, 2016, 174 (5), pp.641-650. ⟨10.1530/EJE-15-0922⟩مصطلحات موضوعية: Male, 0301 basic medicine, Endocrinology, Diabetes and Metabolism, [SDV]Life Sciences [q-bio], medicine.disease_cause, Gastroenterology, Body Mass Index, 0302 clinical medicine, Endocrinology, Genotype, Birth Weight, Rescues, Young adult, Child, Leopard-Syndrome, 2. Zero hunger, education.field_of_study, Noonan Syndrome, Age Factors, General Medicine, Child, Preschool, Population study, Female, Defects, KRAS, Gestation, Adult, musculoskeletal diseases, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Standards, Born, Birth weight, Population, Activation, 030209 endocrinology & metabolism, Young Adult, 03 medical and health sciences, PTPN11 SHP2 Mutations, Internal medicine, medicine, Humans, education, business.industry, Body Weight, Infant, Newborn, medicine.disease, Body Height, 030104 developmental biology, Noonan syndrome, business, Body mass index, Pathway
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfbbe9790935b74c803d353d0b0a023d
https://hal.univ-lorraine.fr/hal-01662610 -
3
المؤلفون: Maryse Cartigny, Charles Sultan, C. Heinrich, Francois Kurtz, Catherine Pienkowski, Laurent Maïmoun, Benoit Cammas, Pascal Philibert, Françoise Audran
المصدر: International Journal of Andrology. 33:841-847
مصطلحات موضوعية: Genetics, Urology, Endocrinology, Diabetes and Metabolism, 5α-Reductase deficiency, Biology, Gene mutation, medicine.disease, Compound heterozygosity, Undervirilization, Exon, Reproductive Medicine, SRD5A2, medicine, Androgen insensitivity syndrome, Partial androgen insensitivity syndrome
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المؤلفون: Fabienne Nacka, Vanessa Vautier, Pascal Barat, Aurélie Lacoste, Jérôme Harambat, Benoit Cammas, Jean-Benoît Corcuff
المساهمون: Nutrition et Neurobiologie intégrée (NutriNeuro), Institut National de la Recherche Agronomique (INRA)-Université Sciences et Technologies - Bordeaux 1-Centre National de la Recherche Scientifique (CNRS), CHU Bordeaux [Bordeaux]
المصدر: Diabetes Care
Diabetes Care, American Diabetes Association, 2012, 35 (1), pp.e1. ⟨10.2337/dc11-1398⟩مصطلحات موضوعية: Blood Glucose, Glycation End Products, Advanced, Male, medicine.medical_specialty, Percentile, Diabetes Care Electronic Pages, Endocrinology, Diabetes and Metabolism, [SDV]Life Sciences [q-bio], 030209 endocrinology & metabolism, Fluorescence, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Glycation, Interquartile range, Internal medicine, Diabetes mellitus, Internal Medicine, medicine, Humans, Online Letters: Observations, Sibling, Child, ComputingMilieux_MISCELLANEOUS, 030304 developmental biology, Skin, Advanced and Specialized Nursing, Glycated Hemoglobin, 0303 health sciences, Type 1 diabetes, business.industry, Siblings, fungi, medicine.disease, 3. Good health, Endocrinology, Diabetes Mellitus, Type 1, chemistry, Advanced glycation end-product, Female, Glycated hemoglobin, business
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المؤلفون: Marc de Kerdanet, Benoit Cammas, Michel Polak, Nicos Skordis, M. Eunice, Nadège Servant, Dominique Simon, Sylvie Tenoutasse, Françoise Audran, Philippe Bouchard, Bruno Leheup, Patrick Fénichel, Clarisse Baumann, Mona M. Hafez, Zeev Hochberg, Guy Van Vliet, Maryse Cartigny, Gönül Öcal, Horia H. Al Mawlawi, Laurent Maïmoun, Sylvia S. Einaudi, Françoise Paris, Annette Grüters, Serge Lumbroso, Cristóbal C.J. Del Valle Nuñez, Rachel Reynaud, Catherine Pienkowski, Ariachery C. Ammini, Merih Berberoğlu, Sylvie Cabrol, Charles Sultan, Claudine Heinrichs, Inas Mazen, Kabangu K. Kayemba-Kay's, Francois Kurtz, Pascal Philibert
المصدر: The Journal of clinical endocrinology and metabolism. 96(2)
مصطلحات موضوعية: Male, medicine.medical_specialty, Heterozygote, Adolescent, Genotype, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, 5α-Reductase deficiency, Disorders of Sex Development, Consanguinity, Biology, Genitalia, Male, Biochemistry, Cohort Studies, Young Adult, Endocrinology, 3-Oxo-5-alpha-Steroid 4-Dehydrogenase, Internal medicine, medicine, Humans, Testosterone, Allele, Child, Alleles, Genetics, Polymorphism, Genetic, Biochemistry (medical), Infant, Membrane Proteins, Heterozygote advantage, Dihydrotestosterone, DNA, Exons, Genitalia, Female, Androgen-Insensitivity Syndrome, medicine.disease, Phenotype, Amino Acid Substitution, Child, Preschool, Cohort, Mutation, Female, Cohort study
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd289be9940fd8139a9402d15797f793
https://pubmed.ncbi.nlm.nih.gov/21147889