المؤلفون: Nawelle Famelart, Gwenaelle Diene, Sophie Çabal-Berthoumieu, Mélanie Glattard, Catherine Molinas, Maithe Tauber, Michèle Guidetti

المصدر: Frontiers in Psychiatry, Vol 13 (2022)

مصطلحات موضوعية: emotion competencies, developmental model, Prader–Willi syndrome, training programme, integrative approach, children, Psychiatry, RC435-571

وصف الملف: electronic resource

العلاقة: https://www.frontiersin.org/articles/10.3389/fpsyt.2022.1038223/fullTest; https://doaj.org/toc/1664-0640Test

الوصول الحر: https://doaj.org/article/a7d747dede8b4437a86f379e8cd7c594Test

المؤلفون: Dibia Liz Pacoricona Alfaro, Gwenaelle Diene, Graziella Pinto, Jean-Pierre Salles, Isabelle Gennero, Sandy Faye, Catherine Molinas, Marion Valette, Catherine Arnaud, Maithé Tauber

المصدر: Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)

مصطلحات موضوعية: Prader–Willi syndrome, Early-onset scoliosis, Total ghrelin, Acylated ghrelin, Unacylated ghrelin, AG/UAG ratio, Medicine

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/1750-1172Test

الوصول الحر: https://doaj.org/article/85c4c50f7a6a445abadf58f6047bda63Test

المؤلفون: Nawelle Famelart, Gwenaelle Diene, Sophie Çabal-Berthoumieu, Mélanie Glattard, Catherine Molinas, Michèle Guidetti, Maithe Tauber

المصدر: Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-14 (2020)

مصطلحات موضوعية: Emotion expressions, Prader-Willi syndrome, Children, Social adaptation, Medicine

وصف الملف: electronic resource

العلاقة: http://link.springer.com/article/10.1186/s13023-020-1333-9Test; https://doaj.org/toc/1750-1172Test

الوصول الحر: https://doaj.org/article/cbc35dca9eb649fe9943bf61b5f1d9baTest

المؤلفون: Kuzma Strenilkov, Jimmy Debladis, Juliette Salles, Marion Valette, Carine Mantoulan, Denise Thuilleaux, Virginie Laurier, Catherine Molinas, Pascal Barone, Maïthé Tauber

المصدر: Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)

مصطلحات موضوعية: Prader-Willi syndrome, Voice processing, Social interactions, Autism spectrum disorder, Medicine

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/1750-1172Test

الوصول الحر: https://doaj.org/article/1f3b3d235f8d4386a0fa41da577da8a7Test

المؤلفون: Jimmy Debladis, Marion Valette, Kuzma Strenilkov, Carine Mantoulan, Denise Thuilleaux, Virginie Laurier, Catherine Molinas, Pascal Barone, Maïthé Tauber

المصدر: Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-13 (2019)

مصطلحات موضوعية: Prader-Willi syndrome, Face processing, Face exploration, Eye tracking, Social interactions, Autism spectrum disorder, Medicine

وصف الملف: electronic resource

العلاقة: http://link.springer.com/article/10.1186/s13023-019-1221-3Test; https://doaj.org/toc/1750-1172Test

الوصول الحر: https://doaj.org/article/120d85666e6c44a9aeff658126efa733Test

المؤلفون: Dibia Liz Pacoricona Alfaro, Perrine Lemoine, Virginie Ehlinger, Catherine Molinas, Gwénaëlle Diene, Marion Valette, Graziella Pinto, Muriel Coupaye, Christine Poitou-Bernert, Denise Thuilleaux, Catherine Arnaud, Maithé Tauber

المصدر: Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-10 (2019)

مصطلحات موضوعية: Prader-Willi syndrome, Epidemiology, Mortality, Respiratory complications, Sudden death, Medicine

وصف الملف: electronic resource

العلاقة: http://link.springer.com/article/10.1186/s13023-019-1214-2Test; https://doaj.org/toc/1750-1172Test

الوصول الحر: https://doaj.org/article/27ec6559798c4c7590374449af42f65dTest

المؤلفون: Sabrina Grolleau, Marine Delagrange, Melina Souquiere, Catherine Molinas, Gwenaëlle Diene, Marion Valette, Maithé Tauber

المصدر: Journal of Clinical Medicine, Vol 11, Iss 8, p 2255 (2022)

مصطلحات موضوعية: Prader–Willi syndrome, obesity, socioeconomic status, deprivation, Medicine

وصف الملف: electronic resource

العلاقة: https://www.mdpi.com/2077-0383/11/8/2255Test; https://doaj.org/toc/2077-0383Test

الوصول الحر: https://doaj.org/article/1d3254e8f7244d9bad733e5117c89856Test

المؤلفون: Céline Bar, Gwenaelle Diene, Catherine Molinas, Eric Bieth, Charlotte Casper, Maithé Tauber

المصدر: Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-6 (2017)

مصطلحات موضوعية: Prader-Willi syndrome, Neonatal care, Birth incidence, Early diagnosis, Prenatal diagnosis, Delayed diagnosis, Medicine

وصف الملف: electronic resource

العلاقة: http://link.springer.com/article/10.1186/s13023-017-0673-6Test; https://doaj.org/toc/1750-1172Test

الوصول الحر: https://doaj.org/article/6204eb1919ad48bebf22a701788ab321Test

المؤلفون: Lisa Cole Burnett, Françoise Conte Auriol, Eric Bieth, Jean Pierre Salles, Juliette Salles, Maithé Tauber, Gwenaelle Diene, Catherine Molinas, Rudolph L. Leibel, Boris V. Skryabin, Isabelle Gennero, Timofey S. Rozhdestvensky, Sanaa Eddiry

المساهمون: Centre d'investigation clinique de Toulouse (CIC 1436), 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)-Pôle Santé publique et médecine publique [CHU Toulouse], Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)-Centre Hospitalier Universitaire de Toulouse (CHU Toulouse), Institut Toulousain des Maladies Infectieuses et Inflammatoires (Infinity), 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), Centre de Référence du Syndrome de Prader-Willi, Pôle Enfants [CHU Toulouse], Service Psychiatrie et psychologie médicale [CHU Toulouse], Pôle Psychiatrie [CHU Toulouse], Institut Fédératif de Biologie (IFB), Centre Hospitalier Universitaire de Toulouse (CHU Toulouse), University Hospital Münster - Universitaetsklinikum Muenster [Germany] (UKM), University of Illinois [Chicago] (UIC), University of Illinois System, Columbia University [New York], Pistre, Karine

المصدر: Genetics in Medicine
Genetics in Medicine, 2021, 23 (9), pp.1664-1672. ⟨10.1038/s41436-021-01185-y⟩

مصطلحات موضوعية: 0301 basic medicine, MESH: Prader-Willi Syndrome* / genetics, medicine.medical_specialty, MESH: RNA, Small Nucleolar, congenital, hereditary, and neonatal diseases and abnormalities, IGFBP7, [SDV]Life Sciences [q-bio], Induced Pluripotent Stem Cells, MESH: Neurons, MESH: Induced Pluripotent Stem Cells, Article, MESH: Prader-Willi Syndrome* / drug therapy, 03 medical and health sciences, Mice, 0302 clinical medicine, Neurodevelopmental disorder, Downregulation and upregulation, Internal medicine, medicine, Animals, Humans, RNA, Small Nucleolar, MESH: Animals, MESH: Mice, Genetics (clinical), Neurons, MESH: Humans, [SDV.MHEP] Life Sciences [q-bio]/Human health and pathology, business.industry, Dopaminergic, nutritional and metabolic diseases, medicine.disease, Phenotype, Pathophysiology, nervous system diseases, [SDV] Life Sciences [q-bio], 030104 developmental biology, Endocrinology, MESH: Growth Hormone, Growth Hormone, Knockout mouse, business, Genomic imprinting, Prader-Willi Syndrome, 030217 neurology & neurosurgery, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e0080d05680200cd3deb6cb1061f247Test
http://europepmc.org/articles/PMC8460435Test

المؤلفون: Gaëlle Nannette, Céline Bar, Gwenaëlle Diene, Catherine Pienkowski, Isabelle Oliver-Petit, Béatrice Jouret, Audrey Cartault, Valérie Porquet-Bordes, Jean-Pierre Salles, Solange Grunenwald, Thomas Edouard, Catherine Molinas, Maithé Tauber

المصدر: The Journal of clinical endocrinology and metabolism.

مصطلحات موضوعية: Endocrinology, Endocrinology, Diabetes and Metabolism, Biochemistry (medical), Clinical Biochemistry, Biochemistry

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a4f19d3a273d39f8c60a91d86418c25Test
https://pubmed.ncbi.nlm.nih.gov/36201475Test