Results 111 to 120 of about 3,078 (199)
S3153 Hypermobile Ehlers-Danlos Syndrome and Visceroptosis
Will Takakura +3 more
openaire +2 more sources
UEG Week 2025 Moderated Posters
United European Gastroenterology Journal, Volume 13, Issue S8, Page S189-S802, October 2025.
wiley +1 more source
UEG Week 2025 Poster Presentations
United European Gastroenterology Journal, Volume 13, Issue S8, Page S803-S1476, October 2025.
wiley +1 more source
A Nurse's Perspective Shaped by Illness: What Becoming the Zebra Revealed
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 +2 more
doaj +1 more source
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 +2 more
doaj +1 more source
The Effect of Joint Hypermobility Syndrome on DOMS and Recovery Time
# 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 +6 more
doaj +1 more source
The Physical and Psychological Impacts of Exercise on hypermobile Ehlers-Danlos Syndrome: A Case Study [PDF]
Hypermobile Ehlers-Danlos Syndrome (hEDS) is a subtype of a series of connective tissue disorders identified by joint hypermobility and multisystemic symptoms.
Posey, Savannah
core +1 more source
Oral health in prevalent types of Ehlers-Danlos syndromes [PDF]
Ainamo J +47 more
core +2 more sources
Epidemiology of bleeding symptoms and hypermobile Ehlers‐Danlos syndrome in paediatrics [PDF]
S E, Hickey, E A, Varga, B, Kerlin
openaire +2 more sources

