Zobrazeno 1 - 10
of 6 137
pro vyhledávání: '"Ehlers–Danlos syndromes"'
Autor:
Dijk MD, PhD, Fleur S. van1 (AUTHOR) Fleur.dijk@nhs.net, Angwin, Chloe2 (AUTHOR) chloeangwin@nhs.net, Ghali MBChB, MRCPCH, MD, Neeti3 (AUTHOR) neeti.ghali@nhs.net, Zschocke Ph.D., Johannes4 (AUTHOR) Johannes.Zschocke@i-med.ac.at, Wagner, Bart5 (AUTHOR) bart.wagner@nhs.net
Publikováno v:
Medizinische Genetik. Dec2024, Vol. 36 Issue 4, p247-254. 8p.
Autor:
van Dijk MD, PhD, Fleur S.1 (AUTHOR) Fleur.dijk@nhs.net, Angwin, Chloe2 (AUTHOR) chloeangwin@nhs.net, Demirdas MD, Ph.D., Serwet3 (AUTHOR) s.demirdas@erasmusmc.nl, Ghali MBChB, MRCPCH, MD, Neeti4 (AUTHOR) neeti.ghali@nhs.net, Zschocke Ph.D., Johannes5 (AUTHOR) Johannes.Zschocke@i-med.ac.at
Publikováno v:
Medizinische Genetik. Dec2024, Vol. 36 Issue 4, p225-234. 10p.
Autor:
Kexin Xu, Guozhuang Li, Zhihong Wu, Terry Jianguo Zhang, Nan Wu, On behalf of the Chinese Multi-Disciplinary Working Group on the Ehlers-Danlos Syndromes
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-6 (2024)
Abstract Background The Ehlers-Danlos syndromes (EDS) are a group of rare hereditary connective tissue disorders. EDS is clinically and genetically heterogeneous and usually involves multiple systems. There are 14 subtypes of EDS with hallmark featur
Externí odkaz:
https://doaj.org/article/82db6927b78a4b63bcf58092e75dd8dc
Autor:
Xu, Kexin1,2,3,4 (AUTHOR), Li, Guozhuang1,2,3,4 (AUTHOR), Wu, Zhihong2,3,4,5 (AUTHOR), Zhang, Terry Jianguo1,2,3,4 (AUTHOR) jgzhang_pumch@yahoo.com, Wu, Nan1,2,3,4 (AUTHOR) dr.wunan@pumch.cn
Publikováno v:
Orphanet Journal of Rare Diseases. 5/13/2024, Vol. 19 Issue 1, p1-6. 6p.
Autor:
Zschocke Ph.D., Johannes1 (AUTHOR) Johannes.Zschocke@i-med.ac.at, Demirdas MD, Ph.D., Serwet2 (AUTHOR) s.demirdas@erasmusmc.nl, van Dijk MD, PhD, Fleur S.3 (AUTHOR) Fleur.dijk@nhs.net
Publikováno v:
Medizinische Genetik. Dec2024, Vol. 36 Issue 4, p235-245. 11p.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
XU Kexin, LI Guozhuang, LI Qing, YIN Xiangjie, FANG Kun, WU Zhihong, ZHANG Jianguo, DISCO (Deciphering Disorders Involving Scoliosis ＆ COmorbidities) Study Group, WU Nan
Publikováno v:
罕见病研究, Vol 3, Iss 3, Pp 295-303 (2024)
The Ehlers-Danlos syndromes (EDS) are a group of rare hereditary connective tissue disorders characterized by joint hypermobility, skin hyperextensibility, and tissue fragility. The clinical and genetic hetero- geneity of EDS frequently leads to unde
Externí odkaz:
https://doaj.org/article/db6025bccc7742379bb0fdaab73a2b71
Publikováno v:
罕见病研究, Vol 2, Iss 4, Pp 554-588 (2023)
The Ehlers-Danlos syndromes (EDS) are a group of rare hereditary connective tissue disorders. EDS is clinically and genetically heterogeneous and usually involves multiple systems. EDS has 14 subtypes, the common features of which include joint hyper
Externí odkaz:
https://doaj.org/article/94a1b09b9e4d421b99b0e5352ec2c403
Autor:
Schubart, Jane R.1 (AUTHOR) jschubart@pennstatehealth.psu.edu, Mills, Susan E.1 (AUTHOR), Rodeo, Scott A.2 (AUTHOR), Francomano, Clair A.3 (AUTHOR)
Publikováno v:
BMC Musculoskeletal Disorders. 10/24/2024, Vol. 25 Issue 1, p1-19. 19p.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.