Results 101 to 110 of about 1,081,004 (187)

S3153 Hypermobile Ehlers-Danlos Syndrome and Visceroptosis

American Journal of Gastroenterology, 2020
Will Takakura, Yaniv Raphael, Richard Sukov, Ali Rezaie   +3 more
openaire   +2 more sources

In-vivo force-length relationship of the medial gastrocnemius muscle in Hypermobile Ehlers-Danlos Syndrome and Hypermobility Spectrum Disorders

This article was originally published as: Golden, D.W., Oliemans, J.P., Ladell, A.J.M., Walls, K.D., Bennett, E.C., Skaper, S.J., Asmussen, M.J., Manocha, R.H.K., & Fletcher, J.R. (2026).
Manocha, Ranita H.K., Golden, Donald W., Asmussen, Michael J., Bennett, Eric C., Fletcher, Jared R., Oliemans, Jason P., Skaper, Spencer J., Ladell, Aera J.M., Walls, Kalindra D.   +8 more
core   +1 more source

A Nurse's Perspective Shaped by Illness: What Becoming the Zebra Revealed

Journal of Patient Experience
Hypermobile Ehlers-Danlos syndrome (hEDS) is a rare, multisystemic connective tissue disorder characterized by generalized joint hypermobility and pain with presence of other comorbidities affecting various organ systems.
Maci M. Burgener MS, Mikaela J. Kuenstler BSN, RN, Eric S. Graham MD   +2 more
doaj   +1 more source

Letter regarding “The usefulness of the genetic panel in the classification and refinement of diagnostic accuracy of Mexican patients with Marfan syndrome and other connective tissue disorders”

Biomolecules & Biomedicine
Dear Editor, We have read the article “The usefulness of the genetic panel in the classification and refinement of diagnostic accuracy of Mexican patients with Marfan syndrome and other connective tissue disorders”, recently published in your esteemed
Ana M. Serrano Ardila, Gilda S. Garza Mayén, Alejandro Gaviño-Vergara   +2 more
doaj   +1 more source

The Effect of Joint Hypermobility Syndrome on DOMS and Recovery Time

International Journal of Sports Physical Therapy
# Background Previous research has reported that people with Joint Hypermobility Syndrome (JHS) and Ehlers-Danlos Syndrome (EDS) generally experience a high rate of muscular injury and pain.
Nicole F Ostuni, Charles A Marinello, Taras Luzhnyy, Alexa Pawlikowski, Connor Vlasaty, Georgios Thomatos, Peter C Douris   +6 more
doaj   +1 more source

Healthcare Disparities among Hypermobile Spectrum Disorder and Hypermobile Ehlers-Danlos Syndrome Patients [PDF]

Hypermobile Ehlers-Danlos Syndrome (hEDS) is the most common subtype of rare connective tissue disorder called Ehlers-Danlos Syndrome (EDS). Hypermobile Spectrum Disorder (HSD) is a connective tissue disorder that presents itself similarly to hEDS.
Martinez, Brooke A
core  

Epidemiology of bleeding symptoms and hypermobile Ehlers‐Danlos syndrome in paediatrics [PDF]

Haemophilia, 2016
S E, Hickey, E A, Varga, B, Kerlin
openaire   +2 more sources

Type V and type III collagen modulate the expression and assembly of fibronectin extracellar matrix in classic and vascular Ehlers-Danlos syndrome fibroblasts, affecting cell survival and migration

, 2012
Extracellular matrix (ECM) regulates cell proliferation, migration, survival and gene expression, via signal transduction pathways differentially activated by ECM ligands interacting with specific integrins.
ZOPPI, Nicoletta, RITELLI, Marco Giuseppe, COLOMBI, Marina   +2 more
core  

Linking central sensitization to multisystemic manifestations in hypermobile Ehlers-Danlos syndrome. [PDF]

Front Pain Res (Lausanne)
Montemayor Zarazúa AP, Elizondo Solis CV, Ayala García C, Pacheco Estrella DJ, Ilizaliturri Guerra O, Arana Guajardo AC, Purón Gonzalez E, Silva Luna K, Lozano Plata LI, García Pompermayer MR, Garza Elizondo MA.   +10 more
europepmc   +1 more source

Ehlers-Danlos syndrome Type VI : Case report

, 1998
Ehlers-Danlos sendromu bağ dokusunun genetik geçiş gösteren bir hastalığıdır. Burada, eklem gevşekliği, deri bulguları gibi sendromun temel bulgularının yanısıra belirgin kifoskolyozunun da olması nedeniyle Ehlers-Danlos tip VI tanısı almış, anne ve ...
Ferda Özkınay, Galip Sarı, Özgür Çoğulu, Mahmut Çoker, Cihangir Özkınay, Ayşe Yenigün, Cumhur Gündüz   +6 more
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