Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Dacre R. T. Knight"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-9 (2024)
Abstract Background The Ehlers-Danlos Syndromes (EDS) are a group of connective tissue disorders that are hereditary in nature and characterized by joint hypermobility and tissue fragility. The complex nature of this unique patient population require
Externí odkaz:
https://doaj.org/article/4277de450cc64d21a164d93af46a235a
Publikováno v:
Frontiers in Public Health, Vol 12 (2024)
IntroductionPatients with Ehlers-Danlos syndromes (EDS) and hypermobility spectrum disorders (HSD) have significant health challenges that are well-documented, however their impact in terms of cost is not known. Our research objective was to examine
Externí odkaz:
https://doaj.org/article/2ab02b17b1074c0695391d334a80a738
Autor:
Dacre R. T. Knight, Katelyn A. Bruno, Ayush Singh, Bala Munipalli, Shilpa Gajarawala, Mahima Solomon, S. Christian Kocsis, Ashley A. Darakjian, Angita Jain, Emily R. Whelan, Archana Kotha, David J. Gorelov, Sabrina D. Phillips, DeLisa Fairweather
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 11 (2024)
BackgroundDefective connective tissue structure may cause individuals with hypermobile Ehlers-Danlos syndrome (hEDS) or hypermobility spectrum disorders (HSD) to develop cardiac defects.MethodsWe conducted a retrospective chart review of adult patien
Externí odkaz:
https://doaj.org/article/191b349a345f47d08a3977898b563d03
Autor:
DeLisa Fairweather, Katelyn A. Bruno, Ashley A. Darakjian, Barbara K. Bruce, Jessica M. Gehin, Archana Kotha, Angita Jain, Zhongwei Peng, David O. Hodge, Todd D. Rozen, Bala Munipalli, Fernando A. Rivera, Pedro A. Malavet, Dacre R. T. Knight
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
BackgroundJoint pain is a common symptom in patients with hypermobile Ehlers-Danlos Syndrome (hEDS), hypermobility spectrum disorders (HSD) and fibromyalgia. The goal of this study was to determine whether symptoms and comorbidities overlap in patien
Externí odkaz:
https://doaj.org/article/9a38cc6f5b624b20a5b7c3be90f83883
Publikováno v:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8eb496efc34678a5759a5435474bcdf6
https://doi.org/10.1002/ajmg.c.32038
https://doi.org/10.1002/ajmg.c.32038
Autor:
Dacre R T, Knight, Sunnie M, Confiado, Katelyn A, Bruno, DeLisa, Fairweather, Andrea M, Seymour-Sonnier, Angita, Jain, Jessica M, Gehin, Emily R, Whelan, Joshua H, Culberson, Bala, Munipalli, Nancy L, Dawson, Todd D, Rozen, Joseph J, Wick, Archana, Kotha
Publikováno v:
SN Comprehensive Clinical Medicine. 4
In a large academic medical center, patient requests from the community and internal referrals for evaluation of suspected hypermobility conditions were being denied consultation because services specific to this condition were not available. We iden
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10e0a000c4be7ef1a47dd5230217c38e
https://doi.org/10.1007/s42399-022-01218-w
https://doi.org/10.1007/s42399-022-01218-w