المؤلفون: Muhammad Kassim Javaid, Alison Boyce, Natasha Appelman-Dijkstra, Juling Ong, Patrizia Defabianis, Amaka Offiah, Paul Arundel, Nick Shaw, Valter Dal Pos, Ann Underhil, Deanna Portero, Lisa Heral, Anne-Marie Heegaard, Laura Masi, Fergal Monsell, Robert Stanton, Pieter Durk Sander Dijkstra, Maria Luisa Brandi, Roland Chapurlat, Neveen Agnes Therese Hamdy, Michael Terrence Collins

المصدر: Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-17 (2019)

مصطلحات موضوعية: Fibrous dysplasia, McCune Albright syndrome, Guidelines, Diagnosis, Management, Medicine

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s13023-019-1102-9; https://doaj.org/toc/1750-1172

URL الوصول: https://doaj.org/article/bbcbbee103a0444987b518c3f8cf2459

المؤلفون: Muhammad Kassim Javaid, Alison Boyce, Natasha Appelman-Dijkstra, Juling Ong, Patrizia Defabianis, Amaka Offiah, Paul Arundel, Nick Shaw, Valter Dal Pos, Ann Underhil, Deanna Portero, Lisa Heral, Anne-Marie Heegaard, Laura Masi, Fergal Monsell, Robert Stanton, Pieter Durk Sander Dijkstra, Maria Luisa Brandi, Roland Chapurlat, Neveen Agnes Therese Hamdy, Michael Terrence Collins

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

مصطلحات موضوعية: Medicine

Relation: http://link.springer.com/article/10.1186/s13023-019-1255-6; https://doaj.org/toc/1750-1172; https://doaj.org/article/03b8bed7003b41bc9e87d962f107425f

الاتاحة: https://doi.org/10.1186/s13023-019-1255-6
https://doaj.org/article/03b8bed7003b41bc9e87d962f107425f

المؤلفون: Lomash, Richa Madan, Shchelochkov, Oleg, Chandler, Randy J., Venditti, Charles P., Pariser, Anne R., Ottinger, Elizabeth A., Gilberto V., Averion, Krishna, Balakrishnan, Carsten G., Bönnemann, Philip J., Brooks, Steven J., Burden, Eggerton, Campbell, Catherine, Chen, Eun-Young, Choi, Claire, Driscoll, Oksana, Dukhanina, Susan, Ferry, A. Reghan, Foley, Janelle Geist, Hauserman, Lina, Li, Donald C., Lo, Venkata, Mangalampalli, Irini, Manoli, Christopher, Mendoza, Julien, Oury, Forbes D., Porter, Deanna, Portero, Lili, Portilla, Jachinta, Rooney, Dimah, Saade, Jennifer L., Sloan, Mitali, Tambe, Pramod, Terse, Joshua, Todd, London, Toney, Carol, Van Ryzin, Rodica, Stan, Sury, Vepa, Erik, Wagner, Amy, Wang, Xin, Xu, Yaqun, Zou

المصدر: Human Gene Therapy ; volume 34, issue 5-6, page 217-227 ; ISSN 1043-0342 1557-7422

الاتاحة: http://dx.doi.org/10.1089/hum.2022.232
https://www.liebertpub.com/doi/full-xml/10.1089/hum.2022.232
https://www.liebertpub.com/doi/pdf/10.1089/hum.2022.232

المؤلفون: Elizabeth A. Ottinger, Anne Pariser, Philip J. Brooks, Asaf Alimardanov, Christopher P. Austin, Richa Madan Lomash, Eric Esposito, Pramod S. Terse, Carsten G. Bönnemann, Xin Xu, Deanna Portero, Randy J. Chandler, Janelle Geist Hauserman, Charles P. Venditti, Donald C. Lo

المصدر: Human Gene Therapy

مصطلحات موضوعية: Clinical Trials as Topic, business.industry, Genetic enhancement, Genetic Vectors, Genetic Therapy, Dependovirus, medicine.disease_cause, Bioinformatics, Clinical trial, Rare Diseases, Genetics, medicine, Humans, Molecular Medicine, Vector (molecular biology), business, Special Report, Molecular Biology, Gene, Adeno-associated virus

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5baa4221778a870fb9ecaeeecfde7506
https://doi.org/10.1089/hum.2020.259