نتائج البحث - "Léger, Juliane"

1

دورية أكاديمية

Diagnosis and management of congenital hypopituitarism in children

المؤلفون: Castets, Sarah, Thomas-Teinturier, Cécile, Villanueva, Carine, Amsellem, Jessica, Barat, Pascal, Brun, Gilles, Quoc, Emmanuel Bui, Carel, Jean-Claude, De Filippo, Gian Paolo, Kipnis, Clara, Martinerie, Laetitia, Vergier, Julia, Saveanu, Alexandru, Teissier, Natacha, Coutant, Régis, Léger, Juliane, Reynaud, Rachel

المصدر: Archives de Pédiatrie ; volume 31, issue 3, page 165-171 ; ISSN 0929-693X

مصطلحات موضوعية: Pediatrics, Perinatology and Child Health

الإتاحة: https://doi.org/10.1016/j.arcped.2024.01.003Test
https://api.elsevier.com/content/article/PII:S0929693X24000186?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0929693X24000186?httpAccept=text/plainTest

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2

دورية أكاديمية

Human type I IFN deficiency does not impair B cell response to SARS-CoV-2 mRNA vaccination

المؤلفون: Sokal, Aurélien, Bastard, Paul, Chappert, Pascal, Barba-Spaeth, Giovanna, Fourati, Slim, Vanderberghe, Alexis, Lagouge-Roussey, Pauline, Meyts, Isabelle, Gervais, Adrian, Bouvier-Alias, Magali, Azzaoui, Imane, Fernández, Ignacio, de la Selle, Andréa, Zhang, Qian, Bizien, Lucy, Pellier, Isabelle, Linglart, Agnès, Rothenbuhler, Anya, Marcoux, Estelle, Anxionnat, Raphael, Cheikh, Nathalie, Léger, Juliane, Amador-Borrero, Blanca, Fouyssac, Fanny, Menut, Vanessa, Goffard, Jean-Christophe, Storey, Caroline, Demily, Caroline, Mallebranche, Coralie, Troya, Jesus, Pujol, Aurora, Zins, Marie, Tiberghien, Pierre, Gray, Paul, Mcnaughton, Peter, Sullivan, Anna, Peake, Jane, Levy, Romain, Languille, Laetitia, Rodiguez-Gallego, Carlos, Boisson, Bertrand, Gallien, Sébastien, Neven, Bénédicte, Michel, Marc, Godeau, Bertrand, Abel, Laurent, Rey, Felix, Weill, Jean-Claude, Reynaud, Claude-Agnès, Tangye, Stuart, Casanova, Jean-Laurent, Mahévas, Matthieu

المساهمون: Institut Necker Enfants-Malades (INEM - UM 111 (UMR 8253 / U1151)), Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité), Imagine - Institut des maladies génétiques (IHU) (Imagine - U1163), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité), Rockefeller University New York, Institut Mondor de Recherche Biomédicale (IMRB), Institut National de la Santé et de la Recherche Médicale (INSERM)-IFR10-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12), Virologie Structurale - Structural Virology, Institut Pasteur Paris (IP)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité), CHU Henri Mondor Créteil, Catholic University of Leuven = Katholieke Universiteit Leuven (KU Leuven), INSERM U955, team 2. Mondor Biomedical Research Institute, Paris-Est Créteil University, Créteil, France. Departement of Internal Medicine, Henri Mondor University Hospital, Assistance Publique-Hôpitaux de Paris, Paris-Est Créteil University, Créteil, France, Centre Hospitalier Universitaire d'Angers (CHU Angers), PRES Université Nantes Angers Le Mans (UNAM), Université d'Angers (UA), Hôpital Bicêtre AP-HP, Le Kremlin-Bicêtre, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Université Paris-Saclay, Hôpital Nord Franche-Comté Hôpital de Trévenans (HNFC), Service de pédiatrie CHRU Besançon, Centre Hospitalier Régional Universitaire de Besançon (CHRU Besançon), GHU AP-HP Nord - Université Paris Cité, Hôpital Lariboisière-Fernand-Widal APHP, Centre Hospitalier Universitaire de Nancy (CHU Nancy), Hôpital Mère-Enfant Hôpital Hôtel Dieu, Nantes, Centre Hospitalier Universitaire de Nantes = Nantes University Hospital (CHU Nantes), Université libre de Bruxelles (ULB), Hôpital Robert Debré, Centre Hospitalier le Vinatier Bron, Hospital Universitario Infanta Leonor Madrid, Institut d'Investigació Biomèdica de Bellvitge = Bellvitge Biomedical Research Institute (IDIBELL), Université Paris Cité (UPCité), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Etablissement Français du Sang La Plaine Saint-Denis (EFS), Sydney Children's hospital, University of New South Wales Sydney (UNSW), Children’s Health Queensland Brisbane (CHQ), Hôpital Necker - Enfants Malades AP-HP, Universidad Fernando Pessoa Canarias Las Palmas de Gran Canaria, Spain, Garvan Institute of medical research, Howard Hughes Medical Institute New York (HHMI), Howard Hughes Medical Institute (HHMI)-New York University School of Medicine, NYU System (NYU)-NYU System (NYU)-Rockefeller University New York -Columbia University Irving Medical Center (CUIMC), Funder(s): Agence Nationale de la Recherche Award Id(s): ANR-21-RHUS-0008, ANR-10-IAHU-01, ANR-10-LABX-62-IBEID , ANR-20-CE93-003Funder(s): Fondation pour la Recherche MédicaleAward Id(s): MEMO-COV-2-FRMFunder(s): Institut PasteurFunder(s): Agence Nationale de Recherches sur le Sida et les Hépatites ViralesFunder(s): Howard Hughes Medical InstituteFunder(s): Rockefeller UniversityFunder(s): St. Giles FoundationFunder(s): National Institutes of Health Award Id(s): R01AI088364, R01AI163029, UL1TR001866Funder(s): National Center for Advancing Translational SciencesFunder(s): Fisher Center for Alzheimer’s Research FoundationFunder(s): Meyer FoundationFunder(s): JPB FoundationFunder(s): French Foundation for Medical Research Award Id(s): EQU201903007798, EA20170638020Funder(s): European Union’s Horizon 2020 Award Id(s): 824110Funder(s): Square FoundationFunder(s): Fondation du SouffleFunder(s): French Ministry of Higher Education, Research, and Innovation Award Id(s): MESRI-COVID-19Funder(s): Institut National de la Santé et de la Recherche MédicaleFunder(s): Fondation Bettencourt SchuellerFunder(s): CSL BehringFunder(s): KU Leuven Award Id(s): C16/18/007Funder(s): http://dx.doi.org/10.13039/501100003130Test Award Id(s): G0C8517N, G0B5120N, G0E8420NFunder(s): Jeffrey Modell FoundationFunder(s): National Health and Medical Research Council Award Id(s): 1176665Funder(s): Allergy and Immunology Foundation of AustraliaFunder(s): John Brown Cook FoundationFunder(s): Fondation Princesse GraceFunder(s): Comité ad-hoc de pilotage national des essais thérapeutiques et autres recherchesFunder(s): Assistance Publique—Hôpitaux de Paris Award Id(s): MEMO-COV-2Funder(s): Société Nationale de Médecine InterneFunder(s): ANRS Nord-Sud Award Id(s): ANRS-COV05Funder(s): ANR-RHU Award Id(s): ANR-21-RHUS-08 (COVIFERON)Funder(s): HORIZON-HLTH-2021-DISEASE-04 Award Id(s): 01057100Funder(s): Grandir - Fonds de solidarité pour l’enfanceFunder(s): SCOR Corporate Foundation for ScienceFunder(s): REACTing-INSERMFunder(s): University of Paris CitéFunder(s): Imagine InstituteFunder(s): VIB GC PIDFunder(s): European Research Council Award Id(s): ERC-StG MORE2ADA2, ANR-21-RHUS-0008,COVIFERON,Covid-19 and interferons: from discovery to therapy(2021), ANR-10-IAHU-0001,Imagine,Institut Hospitalo-Universitaire Imagine(2010), ANR-10-LABX-0062,IBEID,Integrative Biology of Emerging Infectious Diseases(2010), ANR-20-CE93-0003,GENVIR,Analyse multi-omique de l'immunité anti-virale: de l'identification des circuits biologiques pertinents à la découverte de défauts monogéniques héréditaires de l'immunité chez les patients avec infections virales sévères(2020), European Project: 824110,H2020-INFRAIA-2018-1,EASI-Genomics(2019), European Project: 948959,ERC-2020-STG,MORE2ADA2(2021)

المصدر: ISSN: 0022-1007.

مصطلحات موضوعية: [SDV.IMM]Life Sciences [q-bio]/Immunology, [SDV.IMM.VAC]Life Sciences [q-bio]/Immunology/Vaccinology

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/36342455; info:eu-repo/grantAgreement//824110/EU/European Advanced infraStructure for Innovative Genomics/EASI-Genomics; info:eu-repo/grantAgreement//948959/EU/Multi-omics research applied to Human ADA2 deficiency and beyond/MORE2ADA2; pasteur-03847416; https://pasteur.hal.science/pasteur-03847416Test; https://pasteur.hal.science/pasteur-03847416/documentTest; https://pasteur.hal.science/pasteur-03847416/file/jem_20220258.pdfTest; PUBMED: 36342455

الإتاحة: https://doi.org/10.1084/jem.20220258Test
https://pasteur.hal.science/pasteur-03847416Test
https://pasteur.hal.science/pasteur-03847416/documentTest
https://pasteur.hal.science/pasteur-03847416/file/jem_20220258.pdfTest

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3

دورية أكاديمية

Exploring the values, preferences, and information needs of patients with NKX2-1-related disorders: A qualitative study protocol

المؤلفون: Martín Gómez, Carmen, Ortigoza Escobar, Juan Darío, Nou Fontanet, Laia, Molina Linde, Juan M., Bachoud Lévi, Anne Catherine, Léger, Juliane

مصطلحات موضوعية: 32 Ciencias Médicas

العلاقة: Publisher’s version; Martín-Gómez, C., Ortigoza-Escobar, J. D., Nou-Fontanet, L., Molina-Linde, J. M., Bachoud-Lévi, A.-C., Léger, J., & Blasco-Amaro, J. A. (2023). Exploring the values, preferences, and information needs of patients with NKX2-1-related disorders: A qualitative study protocol. In P. Moreno-Peral (Ed.), PLOS ONE (Vol. 18, Issue 2, p. e0281573). Public Library of Science (PLoS). https://doi.org/10.1371/journal.pone.0281573Test; 1932-6203 (electrónico); https://hdl.handle.net/10272/22265Test

الإتاحة: https://doi.org/10.1371/journal.pone.0281573Test
https://hdl.handle.net/10272/22265Test

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4

دورية أكاديمية

Gonadotropin administration to mimic mini-puberty in hypogonadotropic males: pump or injections?

المؤلفون: Avril, Tristan, Hennocq, Quentin, Lambert, Anne-Sophie, Leger, Juliane, Simon, Dominique, Martinerie, Laetitia, Bouvattier, Claire

المصدر: Endocrine Connections ; volume 12, issue 4 ; ISSN 2049-3614

الإتاحة: https://doi.org/10.1530/ec-22-0252Test
https://ec.bioscientifica.com/view/journals/ec/12/4/EC-22-0252.xmlTest
https://ec.bioscientifica.com/downloadpdf/journals/ec/12/4/EC-22-0252.xmlTest

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5

دورية أكاديمية

Hormone Therapy During Infancy or Early Childhood for Patients with Hypogonadotropic Hypogonadism, Klinefelter or Turner Syndrome

المؤلفون: Fiot, Elodie, Léger, Juliane, Martinerie, Laetitia

المصدر: Endocrinology and Metabolism Clinics of North America ; ISSN 0889-8529

مصطلحات موضوعية: Endocrinology, Endocrinology, Diabetes and Metabolism

الإتاحة: https://doi.org/10.1016/j.ecl.2024.02.003Test
https://api.elsevier.com/content/article/PII:S0889852924000148?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0889852924000148?httpAccept=text/plainTest

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6

دورية أكاديمية

2022 European Thyroid Association Guideline for the management of pediatric Graves’ disease

المؤلفون: Mooij, Christiaan F., Cheetham, Timothy D., Verburg, Frederik A., Eckstein, Anja, Pearce, Simon H., Léger, Juliane, van Trotsenburg, A. S. Paul

المصدر: Mooij , C F , Cheetham , T D , Verburg , F A , Eckstein , A , Pearce , S H , Léger , J & van Trotsenburg , A S P 2022 , ' 2022 European Thyroid Association Guideline for the management of pediatric Graves’ disease ' , EUROPEAN THYROID JOURNAL , vol. 11 , no. 1 , e210073 . https://doi.org/10.1530/ETJ-21-0073Test

العلاقة: https://research.vumc.nl/en/publications/5fe4a838-db56-4c11-91b8-f3962bcfdb87Test

الإتاحة: https://doi.org/10.1530/ETJ-21-0073Test
https://research.vumc.nl/en/publications/5fe4a838-db56-4c11-91b8-f3962bcfdb87Test
http://www.scopus.com/inward/record.url?scp=85130870300&partnerID=8YFLogxKTest

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7

دورية أكاديمية

Turner syndrome: French National Diagnosis and Care Protocol (NDCP; National Diagnosis and Care Protocol)

المؤلفون: Fiot, Elodie, Alauze, Bertille, Donadille, Bruno, Samara-Boustani, Dinane, Houang, Muriel, de Filippo, Gianpaolo, Bachelot, Anne, Delcour, Clemence, Beyler, Constance, Bois, Emilie, Bourrat, Emmanuelle, Bui Quoc, Emmanuel, Bourcigaux, Nathalie, Chaussain, Catherine, Cohen, Ariel, Cohen-Solal, Martine, da Costa, Sabrina, Dossier, Claire, Ederhy, Stephane, Elmaleh, Monique, Iserin, Laurence, Lengliné, Hélène, Poujol-Robert, Armelle, Roulot, Dominique, Viala, Jerome, Albarel, Frederique, Bismuth, Elise, Bernard, Valérie, Bouvattier, Claire, Brac, Aude, Bretones, Patricia, Chabbert-Buffet, Nathalie, Chanson, Philippe, Coutant, Regis, de Warren, Marguerite, Demaret, Béatrice, Duranteau, Lise, Eustache, Florence, Gautheret, Lydie, Gelwane, Georges, Gourbesville, Claire, Grynberg, Mickaël, Gueniche, Karinne, Jorgensen, Carina, Kerlan, Veronique, Lebrun, Charlotte, Lefevre, Christine, Lorenzini, Françoise, Manouvrier, Sylvie, Pienkowski, Catherine, Reynaud, Rachel, Reznik, Yves, Siffroi, Jean-Pierre, Tabet, Anne-Claude, Tauber, Maïthé, Netchine, Irène, Vautier, Vanessa, Tauveron, Igor, Wambre, Sebastien, Zenaty, Delphine, Polak, Michel, Touraine, Philippe, Carel, Jean-Claude, Christin-Maitre, Sophie, Léger, Juliane

المساهمون: Centre de Référence des Maladies Endocriniennes Rares de la Croissance APHP Robert Debré, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Robert Debré-Université Paris Cité (UPCité), Maladies neurodéveloppementales et neurovasculaires (NeuroDiderot (UMR_S_1141 / U1141)), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité), CHU Saint-Antoine AP-HP, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Service d'endocrinologie, gynécologie et diabétologie pédiatriques CHU Necker, Hôpital Necker - Enfants Malades AP-HP, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), CHU Trousseau APHP, CHU Pitié-Salpêtrière AP-HP, Département d'obstétrique et de gynécologie Hôpital Robert Debré, Université Paris Diderot - Paris 7 (UPD7)-AP-HP Hôpital universitaire Robert-Debré Paris, AP-HP Hôpital universitaire Robert-Debré Paris, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), CHU Charles Foix AP-HP, Service de Rhumatologie CHU Lariboisière, Hôpital Lariboisière-Fernand-Widal APHP, Hôpital Européen Georges Pompidou APHP (HEGP), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpitaux Universitaires Paris Ouest - Hôpitaux Universitaires Île de France Ouest (HUPO), Hôpital Avicenne AP-HP, Service d'endocrinologie, diabète, maladies métaboliques Hôpital de la Conception - APHM, Aix Marseille Université (AMU), CHU de Bordeaux Pellegrin Bordeaux, Hôpital Bicêtre AP-HP, Le Kremlin-Bicêtre, Hospices Civils de Lyon (HCL), CHU Tenon AP-HP, Endocrinologie pédiatrique CHU Angers, Université d'Angers (UA)-Centre Hospitalier Universitaire d'Angers (CHU Angers), PRES Université Nantes Angers Le Mans (UNAM)-PRES Université Nantes Angers Le Mans (UNAM), Hôpital Jean Verdier AP-HP, Service Endocrinologie - Diabétologie CHU Caen, Université de Caen Normandie (UNICAEN), Normandie Université (NU)-Normandie Université (NU)-CHU Caen, Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)-Tumorothèque de Caen Basse-Normandie (TCBN), AP-HP - Hôpital Antoine Béclère Clamart, Centre Hospitalier Régional Universitaire de Brest (CHRU Brest), Hôpital Jeanne de Flandre Lille, Service Endocrinologie, génétique et gynécologie médicale pédiatrique CHU Toulouse, Pôle Enfants CHU Toulouse, Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)-Centre Hospitalier Universitaire de Toulouse (CHU Toulouse), Service de pédiatrie multidisciplinaire Hôpital de la Timone Enfants - APHM, Hôpital de la Timone CHU - APHM (TIMONE), CHU Caen, Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN), Maladies génétiques d'expression pédiatrique (U933), Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Trousseau APHP, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Département de génétique Robert Debré, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-AP-HP Hôpital universitaire Robert-Debré Paris, Centre de Recherche Saint-Antoine (CRSA), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU), CHU Clermont-Ferrand, Ministère de la Santé

المصدر: ISSN: 1750-1172 ; Orphanet Journal of Rare Diseases ; https://inserm.hal.science/inserm-04031866Test ; Orphanet Journal of Rare Diseases, 2022, 17 (S1), pp.261. ⟨10.1186/s13023-022-02423-5⟩.

مصطلحات موضوعية: Adulthood, Childhood, Diagnosis, Management, Recommendation, Turner’s syndrome, [SDV.MHEP.EM]Life Sciences [q-bio]/Human health and pathology/Endocrinology and metabolism, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/35821070; inserm-04031866; https://inserm.hal.science/inserm-04031866Test; https://inserm.hal.science/inserm-04031866/documentTest; https://inserm.hal.science/inserm-04031866/file/13023_2022_Article_2423.pdfTest; PUBMED: 35821070; PUBMEDCENTRAL: PMC9277788; WOS: 000824881800001

الإتاحة: https://doi.org/10.1186/s13023-022-02423-5Test
https://inserm.hal.science/inserm-04031866Test
https://inserm.hal.science/inserm-04031866/documentTest
https://inserm.hal.science/inserm-04031866/file/13023_2022_Article_2423.pdfTest

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8

دورية أكاديمية

Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe

المؤلفون: Nowotny, Hanna, Neumann, Uta, Tardy-Guidollet, Véronique, Ahmed, S Faisal, Baronio, Federico, Battelino, Tadej, Bertherat, Jérôme, Blankenstein, Oliver, Bonomi, Marco, Bouvattier, Claire, Brac de la Perrière, Aude, Brucker, Sara, Cappa, Marco, Chanson, Philippe, Claahsen-van der Grinten, Hedi L, Colao, Annamaria, Cools, Martin, Davies, Justin H, Doerr, Helmuth-Guenther, Fenske, Wiebke K, Ghigo, Ezio, Giordano, Roberta, Gravholt, Claus H, Huebner, Angela, Husebye, Eystein Sverre, Igbokwe, Rebecca, Juul, Anders, Kiefer, Florian W, Leger, Juliane, Menassa, Rita, Meyer, Gesine, Neocleous, Vassos, Phylactou, Leonidas A, Rohayem, Julia, Russo, Gianni, Scaroni, Carla, Touraine, Philippe, Unger, Nicole, Vojtkova, Jarmila, Yeste, Diego, Lajic, Svetlana, Reisch, Nicole

المساهمون: H. Nowotny, U. Neumann, V. Tardy-Guidollet, S.F. Ahmed, F. Baronio, T. Battelino, J. Bertherat, O. Blankenstein, M. Bonomi, C. Bouvattier, A. Brac de la Perrière, S. Brucker, M. Cappa, P. Chanson, H.L. Claahsen-van der Grinten, A. Colao, M. Cool, J.H. Davie, H. Doerr, W.K. Fenske, E. Ghigo, R. Giordano, C.H. Gravholt, A. Huebner, E.S. Husebye, R. Igbokwe, A. Juul, F.W. Kiefer, J. Leger, R. Menassa, G. Meyer, V. Neocleou, L.A. Phylactou, J. Rohayem, G. Russo, C. Scaroni, P. Touraine, N. Unger, J. Vojtkova, D. Yeste, S. Lajic, N. Reisch

مصطلحات موضوعية: Settore MED/13 - Endocrinologia, Settore MED/38 - Pediatria Generale e Specialistica

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/35235536; info:eu-repo/semantics/altIdentifier/wos/WOS:000802046600004; volume:186; issue:5; firstpage:K17; lastpage:K24; numberofpages:8; journal:EUROPEAN JOURNAL OF ENDOCRINOLOGY; http://hdl.handle.net/2434/914404Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85128000223

الإتاحة: https://doi.org/10.1530/EJE-21-0554Test
http://hdl.handle.net/2434/914404Test

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