المؤلفون: Robert, Françoise, Chassagne, Aline, Pélissier, Aurore, Peyron, Christine, Béjean, Sophie, Cretin, Élodie, Gautier, Élodie, Salvi, Dominique, Kidri, Sarah, Godard, Aurélie, Thauvin-Robinet, Christel, Masurel, Alice, Lehalle, Daphné, Jean-Marçais, Nolwenn, Thevenon, Julien, Lesca, Gaëtan, Putoux, Audrey, Cordier, Marie-Pierre, Dupuis-Girod, Sophie, Till, Marianne, Duffourd, Yannis, Rivière, Jean-Baptiste, Joly, Lorraine, Juif, Christine, Putois, Olivier, Ancet, Pierre, Lapointe, Anne-Sophie, Morin, Paulette, Edery, Patrick, Rossi, Massimiliano, Sanlaville, Damien, Faivre, Laurence

المصدر: Maladies rares. 2023, p. 103-120.

الاتاحة: https://www.cairn.info/maladies-rares--9782749277707-page-103.htm

المؤلفون: DeMille, D., McDonald, Jamie, Bernabéu, Carmelo, Racher, H., Olivieri, Carla, Cantarini, Claudia, Sbalchiero, Anna, Thompson, Bryony A., Jovine, Luca, Shovlin, Claire L., Dupuis-Girod, Sophie, Lesca, Gaetan, Tusseau, Maud, Ganguly, A., Kasthuri, R. S., Jessen, J., Massink, Maarten P. G., Ichikawa, S., Bayrak-Toydemir, Pinar

المساهمون: NIHR Biomedical Research Centre (UK), Knut and Alice Wallenberg Foundation, Swedish Research Council, Consejo Superior de Investigaciones Científicas (España), Ministero dell'Università e della Ricerca, Banca d’Italia, National Human Genome Research Institute (US), National Cancer Institute (US), DeMille, D., McDonald, Jamie, Bernabéu, Carmelo, Racher, H., Olivieri, Carla, Cantarini, Claudia, Sbalchiero, Anna, Thompson, Bryony A., Jovine, Luca, Shovlin, Claire L., Dupuis-Girod, Sophie, Lesca, Gaetan, Tusseau, Maud, Ganguly, A., Kasthuri, R. S., Jessen, J., Massink, Maarten P. G., Ichikawa, S., Bayrak-Toydemir, Pinar

Relation: Publisher's version; https://doi.org/10.1155/2024/3043736; Sí; Human Mutation 2024: 3043736 (2024); http://hdl.handle.net/10261/359457

الاتاحة: http://hdl.handle.net/10261/359457
https://doi.org/10.1155/2024/3043736

المؤلفون: Caillot, Claire, Saurin, Jean-Christophe, Hervieu, Valérie, Faoucher, Marie, Reversat, Julie, Decullier, Evelyne, Poncet, Gilles, Bailly, Sabine, Giraud, Sophie, Dupuis-Girod, Sophie

مصطلحات موضوعية: Phenotypes

وصف الملف: text/html

Relation: http://jmg.bmj.com/cgi/content/short/61/8/734; http://dx.doi.org/10.1136/jmg-2023-109632

الاتاحة: http://jmg.bmj.com/cgi/content/short/61/8/734
https://doi.org/10.1136/jmg-2023-109632

المؤلفون: Viora-Dupont, Eléonore, Robert, Françoise, Chassagne, Aline, Pélissier, Aurore, Staraci, Stéphanie, Sanlaville, Damien, Edery, Patrick, Lesca, Gaetan, Putoux, Audrey, Pons, Linda, Cadenes, Amandine, Baurand, Amandine, Sawka, Caroline, Bertolone, Geoffrey, Spetchian, Myrtille, Yousfi, Meriem, Salvi, Dominique, Gautier, Elodie, Vitobello, Antonio, Denommé-Pichon, Anne-Sophie, Bruel, Ange-Line, Tran Mau-Them, Frédéric, Faudet, Anne, Keren, Boris, Labalme, Audrey, Chatron, Nicolas, Abel, Carine, Dupuis-Girod, Sophie, Poisson, Alice, Buratti, Julien, Mignot, Cyril, Afenjar, Alexandra, Whalen, Sandra, Charles, Perrine, Heide, Solveig, Mouthon, Linda, Moutton, Sébastien, Sorlin, Arthur, Nambot, Sophie, Briffaut, Anne-Sophie, Asensio, Marie-Laure, Philippe, Christophe, Thauvin-Robinet, Christel, Héron, Delphine, Rossi, Massimiliano, Meunier-Bellard, Nicolas, Gargiulo, Marcela, Peyron, Christine, Binquet, Christine, Faivre, Laurence

المساهمون: Direction Générale de l'offre de Soins

المصدر: European Journal of Human Genetics ; ISSN 1018-4813 1476-5438

الاتاحة: http://dx.doi.org/10.1038/s41431-024-01616-9
https://www.nature.com/articles/s41431-024-01616-9.pdf
https://www.nature.com/articles/s41431-024-01616-9

المؤلفون: L’Huillier, Romain, Pagnoux, Gaële, Dupuis-Girod, Sophie, Stacoffe, Nicolas

المصدر: CVIR Endovascular ; volume 7, issue 1 ; ISSN 2520-8934

الاتاحة: http://dx.doi.org/10.1186/s42155-024-00444-8
https://link.springer.com/content/pdf/10.1186/s42155-024-00444-8.pdf
https://link.springer.com/article/10.1186/s42155-024-00444-8/fulltext.html

المؤلفون: Delpon, Jean-Etienne, Greffier, Joel, Lacombe, Hugo, Barbe, Apolline, Bouin, Morgane, De Oliveira, Fabien, Mansuy, Adeline, Delagrange, Laura, Fargeton, Anne-Emmanuelle, Beregi, Jean-Paul, Cottin, Vincent, Dupuis-Girod, Sophie, Si-Mohamed, Salim Aymeric

المصدر: Diagnostic and Interventional Imaging ; ISSN 2211-5684

الاتاحة: http://dx.doi.org/10.1016/j.diii.2024.03.006
https://api.elsevier.com/content/article/PII:S2211568424000822?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S2211568424000822?httpAccept=text/plain

المؤلفون: Zawerton, Ash, Mignot, Cyril, Sigafoos, Ashley, Blackburn, Patrick R, Haseeb, Abdul, McWalter, Kirsty, Ichikawa, Shoji, Nava, Caroline, Keren, Boris, Charles, Perrine, Marey, Isabelle, Tabet, Anne-Claude, Levy, Jonathan, Perrin, Laurence, Hartmann, Andreas, Lesca, Gaetan, Schluth-Bolard, Caroline, Monin, Pauline, Dupuis-Girod, Sophie, Guillen Sacoto, Maria J, Schnur, Rhonda E, Zhu, Zehua, Poisson, Alice, El Chehadeh, Salima, Alembik, Yves, Bruel, Ange-Line, Lehalle, Daphné, Nambot, Sophie, Moutton, Sébastien, Odent, Sylvie, Jaillard, Sylvie, Dubourg, Christèle, Hilhorst-Hofstee, Yvonne, Barbaro-Dieber, Tina, Ortega, Lucia, Bhoj, Elizabeth J, Masser-Frye, Diane, Bird, Lynne M, Lindstrom, Kristin, Ramsey, Keri M, Narayanan, Vinodh, Fassi, Emily, Willing, Marcia, Cole, Trevor, Salter, Claire G, Akilapa, Rhoda, Vandersteen, Anthony, Canham, Natalie, Rump, Patrick, Gerkes, Erica H, Klein Wassink-Ruiter, Jolien S, Bijlsma, Emilia, Hoffer, Mariëtte JV, Vargas, Marcelo, Wojcik, Antonina, Cherik, Florian, Francannet, Christine, Rosenfeld, Jill A, Machol, Keren, Scott, Daryl A, Bacino, Carlos A, Wang, Xia, Clark, Gary D, Bertoli, Marta, Zwolinski, Simon, Thomas, Rhys H, Akay, Ela, Chang, Richard C, Bressi, Rebekah, Sanchez Russo, Rossana, Srour, Myriam, Russell, Laura, Goyette, Anne-Marie E, Dupuis, Lucie, Mendoza-Londono, Roberto, Karimov, Catherine, Joseph, Maries, Nizon, Mathilde, Cogné, Benjamin, Kuechler, Alma, Piton, Amélie, Klee, Eric W, Lefebvre, Véronique, Clark, Karl J, Depienne, Christel

المصدر: Genetics in Medicine. 22(3)

مصطلحات موضوعية: Intellectual and Developmental Disabilities (IDD), Pediatric, Genetics, Brain Disorders, Clinical Research, Rare Diseases, Human Genome, Aetiology, 2.1 Biological and endogenous factors, Adolescent, Adult, Animals, Child, Child, Preschool, DNA-Binding Proteins, Female, Genetic Predisposition to Disease, Haploinsufficiency, Humans, Infant, Intellectual Disability, Language Development Disorders, Male, Mutation, Missense, Neurodevelopmental Disorders, Pedigree, Phenotype, SOXD Transcription Factors, Young Adult, autism, developmental delay, intellectual disability, epilepsy, missense variants, Deciphering Developmental DisorderStudy, missense variants., Clinical Sciences, Genetics & Heredity

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/14x4x4wp

المؤلفون: DeMille, D., McDonald, Jamie, Bernabéu, Carmelo, Dupuis-Girod, Sophie, Ganguly, A., Giraud, S., Ichikawa, S., Jessen, J., Jovine, Luca, Kasthuri, R. S., Olivieri, Carla, Ploos van Amstel, Hans K., Racher, H., Shovlin, Claire L., Bayrak-Toydemir, Pinar

المساهمون: McDonald, Jamie, Bernabéu, Carmelo, Dupuis-Girod, Sophie, Jovine, Luca, Olivieri, Carla, Ploos van Amstel, Hans K., Shovlin, Claire L., Bayrak-Toydemir, Pinar

Relation: Publisher's version; https://doi.org/10.1007/s10456-023-09887-4; Sí; 14th HHT International Scientific Conference Abstracts 2022 Angiogenesis 26:18 (2023); http://hdl.handle.net/10261/355296

الاتاحة: http://hdl.handle.net/10261/355296
https://doi.org/10.1007/s10456-023-09887-4

المؤلفون: NIHR Biomedical Research Centre (UK), Knut and Alice Wallenberg Foundation, Swedish Research Council, Consejo Superior de Investigaciones Científicas (España), Ministero dell'Università e della Ricerca, Banca d’Italia, National Human Genome Research Institute (US), National Cancer Institute (US), DeMille, D. [0000-0001-7924-3379], McDonald, Jamie [0000-0001-9939-7922], Bernabéu, Carmelo [0000-0002-1563-6162], Racher, H. [0000-0002-2827-7824], Olivieri, Carla [0000-0001-5812-3175], Cantarini, Claudia [0000-0002-8960-2678], Sbalchiero, Anna [0000-0002-0010-0840], Thompson, Bryony A. [0000-0001-8655-1839], Jovine, Luca [0000-0002-2679-6946], Shovlin, Claire L. [0000-0001-9007-5775], Dupuis-Girod, Sophie [0000-0002-8834-5526], Lesca, Gaetan [0000-0001-7691-9492], Tusseau, Maud [0000-0003-0494-5530], Ganguly, A. [0000-0003-4527-3216], Kasthuri, R. S. [0000-0001-6672-3082], Jessen, J. [0009-0002-1886-3560], Massink, Maarten P. G. [0000-0002-7845-6038], Ichikawa, S. [0000-0001-6477-0520], Bayrak-Toydemir, Pinar [0000-0001-9381-2478], DeMille, D., McDonald, Jamie, Bernabéu, Carmelo, Racher, H., Olivieri, Carla, Cantarini, Claudia, Sbalchiero, Anna, Thompson, Bryony A., Jovine, Luca, Shovlin, Claire L., Dupuis-Girod, Sophie, Lesca, Gaetan, Tusseau, Maud, Ganguly, A., Kasthuri, R. S., Jessen, J., Massink, Maarten P. G., Ichikawa, S., Bayrak-Toydemir, Pinar

مصطلحات الفهرس: artículo

URL: http://hdl.handle.net/10261/359457
https://doi.org/10.1155/2024/3043736
Publisher's version
https://doi.org/10.1155/2024/3043736
Sí

المؤلفون: Sénémaud, Jean, Gaudry, Marine, Jouve, Elisabeth, Blanchard, Arnaud, Milleron, Olivier, Dulac, Yves, Olivier-Faivre, Laurence, Stephan, Dominique, Odent, Sylvie, Lanéelle, Damien, Dupuis-Girod, Sophie, Jondeau, Guillaume, Bal-Theoleyre, Laurence

المساهمون: AP-HP - Hôpital Bichat - Claude Bernard Paris, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), CHU Marseille, Laboratoire de Recherche Vasculaire Translationnelle (LVTS (UMR_S_1148 / U1148)), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité)-Université Sorbonne Paris Nord, Centre Hospitalier Universitaire de Toulouse (CHU Toulouse), Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon), Centre Hospitalier Universitaire Strasbourg (CHU Strasbourg), Les Hôpitaux Universitaires de Strasbourg (HUS), Centre Hospitalier Universitaire de Rennes CHU Rennes = Rennes University Hospital Ponchaillou, Institut de Génétique et Développement de Rennes (IGDR), Université de Rennes (UR)-Centre National de la Recherche Scientifique (CNRS)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique ), CHU Caen, Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN), Hôpital Louis Pradel CHU - HCL, Hospices Civils de Lyon (HCL), None

المصدر: ISSN: 2077-0383 ; Journal of Clinical Medicine ; https://hal.science/hal-04090194 ; Journal of Clinical Medicine, 2023, 12 (8), pp.10.3390. ⟨10.3390/jcm12082902⟩.

مصطلحات موضوعية: Marfan syndrome, aortic dissection, ectasia, non-aortic aneurysm, [SDV.GEN]Life Sciences [q-bio]/Genetics

Relation: info:eu-repo/semantics/altIdentifier/pmid/37109238; hal-04090194; https://hal.science/hal-04090194; https://hal.science/hal-04090194/document; https://hal.science/hal-04090194/file/jcm-12-02902.pdf; PUBMED: 37109238

الاتاحة: https://hal.science/hal-04090194
https://hal.science/hal-04090194/document
https://hal.science/hal-04090194/file/jcm-12-02902.pdf
https://doi.org/10.3390/jcm12082902

المؤلفون: Guilhem, Alexandre, Dupuis-Girod, Sophie, Espitia, Olivier, Rivière, Sophie, Seguier, Julie, Kerjouan, Mallorie, Lavigne, Christian, Maillard, Hélène, Magro, Pascal, Alric, Laurent, Lipsker, Dan, Parrot, Antoine, Leguy, Vanessa, Vanlemmens, Claire, Guibaud, Laurent, Vikkula, Miikka, Eyries, Melanie, Valette, Pierre-Jean, Giraud, Sophie

مصطلحات موضوعية: Phenotypes

وصف الملف: text/html

Relation: http://jmg.bmj.com/cgi/content/short/60/9/905; http://dx.doi.org/10.1136/jmg-2022-109107

الاتاحة: http://jmg.bmj.com/cgi/content/short/60/9/905
https://doi.org/10.1136/jmg-2022-109107

المؤلفون: Dupuis‐Girod, Sophie, Rivière, Sophie, Lavigne, Christian, Fargeton, Anne‐Emmanuelle, Gilbert‐Dussardier, Brigitte, Grobost, Vincent, Leguy‐Seguin, Vanessa, Maillard, Hélène, Mohamed, Shirine, Decullier, Evelyne, Roux, Adeline, Bernard, Lorraine, Saurin, Jean‐Christophe, Saroul, Nicolas, Faure, Frédéric, Cartier, Cesar, Altwegg, Romain, Laccourreye, Laurent, Oberti, Frédéric, Beaudoin, Marjolaine, Dhelens, Carole, Desvignes, Céline, Azzopardi, Nicolas, Paintaud, Gilles, Hermann, Ruben, Chinet, Thierry

المصدر: Journal of Internal Medicine ; volume 294, issue 6, page 761-774 ; ISSN 0954-6820 1365-2796

الاتاحة: http://dx.doi.org/10.1111/joim.13714
https://onlinelibrary.wiley.com/doi/pdf/10.1111/joim.13714

المؤلفون: Grobost, Vincent, Hammi, Sami, Pereira, Bruno, Guilhem, Alexandre, Duffau, Pierre, Seguier, Julie, Parrot, Antoine, Gautier, Giovanni, Alric, Laurent, Kerjouan, Mallorie, Le Guillou, Xavier, Simon, Delphine, Chaussavoine, Laurent, Rondeau-Lutz, Murielle, Leguy-Seguin, Vanessa, Delagrange, Laura, Lavigne, Christian, Maillard, Hélène, Dupuis-Girod, Sophie

المصدر: Thrombosis Research ; volume 229, page 107-113 ; ISSN 0049-3848

الاتاحة: http://dx.doi.org/10.1016/j.thromres.2023.07.001
https://api.elsevier.com/content/article/PII:S004938482300213X?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S004938482300213X?httpAccept=text/plain

المؤلفون: Martinent, Guillaume, Carrot, Manon, Chirac, Anne, Dupuis-Girod, Sophie, Fargeton, Anne-Emmanuelle, Da Conceição, Stéphanie Blois, Fourdrinoy, Sylvie

المصدر: Quality of Life Research, 2020 May 01. 29(5), 1291-1299.

URL الوصول: https://www.jstor.org/stable/48733942

المؤلفون: Senemaud, Jean, Gaudry, Marine, Blanchard, Arnaud, Milleron, Olivier, Dulac, Yves, Olivier-Faivre, Laurence, Stephan, Dominique, Odent, Sylvie, Lanéelle, Damien, Dupuis-Girod, Sophie, Jondeau, Guillaume, Bal, Laurence

المصدر: AORTA ; 70th International Congress of the European Society for Cardiovascular and Endovascular Surgery and 7th International Meeting on Aortic Diseases ; ISSN 2325-4637

الاتاحة: http://dx.doi.org/10.1055/s-0042-1750912
http://www.thieme-connect.de/products/ejournals/html/10.1055/s-0042-1750912

المؤلفون: Muller, Marie, Baldysiak, Etienne, Benech, Nicolas, Pioche, Mathieu, Hervieu, Valérie, Calavas, Laura, Tusseau, Maud, Dupuis-Girod, Sophie, Saurin, Jean-Christophe

المصدر: Gastrointestinal Endoscopy; Nov2024, Vol. 100 Issue 5, p867-877, 11p

المؤلفون: Soukarieh, Omar, Deiber, Clémence, Meguerditchian, Caroline, Proust, Carole, Tusseau, Maud, Guilhem, Alexandre, Mohamed, Shirine, Jaspard-Vinassa, Béatrice, Goyenvalle, Aurélie, Dupuis-Girod, Sophie, Trégouët, David Alexandre

المساهمون: Bordeaux population health (BPH), Université de Bordeaux (UB)-Institut de Santé Publique, d'Épidémiologie et de Développement (ISPED)-Institut National de la Santé et de la Recherche Médicale (INSERM), ESHG, ANR-23-CE17-0042,ENDOMORF,Etude du caractère pathogène de variants créant des cadres de lecture ouverts en amont de la séquence codante de l'endogline - Nouvelles perspectives thérapeutiques pour la maladie du Rendu-Osler(2023)

المصدر: European Human Genetics Conference ; https://hal.science/hal-04613172 ; European Human Genetics Conference, ESHG, Jun 2024, Berlin, Germany

مصطلحات موضوعية: [SDV]Life Sciences [q-bio]

جغرافية الموضوع: Berlin, Germany

Relation: hal-04613172; https://hal.science/hal-04613172

الاتاحة: https://hal.science/hal-04613172

المؤلفون: Genetica, Genetica Sectie Genoomdiagnostiek, Demille, Desiree, McDonald, Jamie, Bernabeu, Carmelo, Racher, Hilary, Olivieri, Carla, Cantarini, Claudia, Sbalchiero, Anna, Thompson, Bryony A., Jovine, Luca, Shovlin, Claire L., Dupuis-Girod, Sophie, Lesca, Gaetan, Tusseau, Maud, Ganguly, Arupa, Kasthuri, Raj S., Jessen, Jaime, Massink, Maarten P.G., Ichikawa, Shoji, Bayrak-Toydemir, Pinar

URL: https://doi.org/10.1155/2024/3043736
http://hdl.handle.net/1874/455400
https://dspace.library.uu.nl/handle/1874/455400
http://www.scopus.com/inward/record.url?scp=85194373910&partnerID=8YFLogxK
1059-7794
Human mutation
2024
3043736

المؤلفون: Si-Mohamed, Salim, Cierco, Alexandra, Gamondes, Delphine, Restier, Lauria Marie, Delagrange, Laura, Cottin, Vincent, Dupuis-Girod, Sophie, Revel, Didier

المساهمون: Hospices Civils de Lyon (HCL), Centre de Recherche en Acquisition et Traitement de l'Image pour la Santé (CREATIS), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National des Sciences Appliquées de Lyon (INSA Lyon), Université de Lyon-Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Université Jean Monnet - Saint-Étienne (UJM)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Université de Lyon, Hôpital Femme Mère Enfant CHU - HCL (HFME), Infections Virales et Pathologie Comparée - UMR 754 (IVPC), École Pratique des Hautes Études (EPHE), Université Paris Sciences et Lettres (PSL)-Université Paris Sciences et Lettres (PSL)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)

المصدر: ISSN: 2075-4426 ; Journal of Personalized Medicine ; https://hal.inrae.fr/hal-03839407 ; Journal of Personalized Medicine, 2022, 12 (7), pp.1091. ⟨10.3390/jpm12071091⟩.

مصطلحات موضوعية: hereditary hemorrhagic telangiectasia, Rendu-Osler-Weber disease, thorax, arteriovenous malformations, embolization, [SDV.MHEP.PSR]Life Sciences [q-bio]/Human health and pathology/Pulmonology and respiratory tract

Relation: info:eu-repo/semantics/altIdentifier/pmid/35887588; hal-03839407; https://hal.inrae.fr/hal-03839407; https://hal.inrae.fr/hal-03839407/document; https://hal.inrae.fr/hal-03839407/file/2022_Si-Mohamed_J_Person_Med.pdf; PUBMED: 35887588; WOS: 000832027800001

الاتاحة: https://hal.inrae.fr/hal-03839407
https://hal.inrae.fr/hal-03839407/document
https://hal.inrae.fr/hal-03839407/file/2022_Si-Mohamed_J_Person_Med.pdf
https://doi.org/10.3390/jpm12071091

المؤلفون: Dupuis-Girod, Sophie, Shovlin, Claire L, Kjeldsen, Anette D, Mager, Hans-Jurgen, Sabba, Carlo, Droege, Freya, Fargeton, Anne-Emmanuelle, Fialla, Annette D, Gandolfi, Silvia, Hermann, Ruben, Lenato, Gennaro M, Manfredi, Guido, Post, Marco C, Rennie, Catherine, Suppressa, Patrizia, Sure, Ulrich, Buscarini, Elisabetta

المصدر: Dupuis-Girod , S , Shovlin , C L , Kjeldsen , A D , Mager , H-J , Sabba , C , Droege , F , Fargeton , A-E , Fialla , A D , Gandolfi , S , Hermann , R , Lenato , G M , Manfredi , G , Post , M C , Rennie , C , Suppressa , P , Sure , U , Buscarini , E & ePag group 2022 , ' European reference network for rare vascular diseases (VASCERN) : When and how to use intravenous bevacizumab in Hereditary Haemorrhagic Telangiectasia (HHT)? ....

مصطلحات موضوعية: Arteriovenous Malformations, Bevacizumab/therapeutic use, Epistaxis/drug therapy, Humans, Rare Diseases, Telangiectasia, Hereditary Hemorrhagic/drug therapy

وصف الملف: application/pdf

الاتاحة: https://portal.findresearcher.sdu.dk/da/publications/17b6293a-59c1-41e9-9509-0872f9f16bfe
https://doi.org/10.1016/j.ejmg.2022.104575
https://findresearcher.sdu.dk/ws/files/220355440/1_s2.0_S1769721222001562_main.pdf