Joint hypermobility syndrome (JHS) and Ehlers-Danlos syndrome, hypermobility type (EDS-HT) are two clinically overlapping heritable connective tissue disorders strongly associating with pain, fatigue and other secondary aspects. No specific treatment exist for this syndrome and rehabilitation play a role in the management of these patients. The aim of this paper is to evaluate what are the evidence in literature about rehabilitation. Research was done using database PUBMED and consist in a revision of the studies published in the last 15 years. All studies agree to the beneficial role of the rehabilitative treatment and physical therapy but it’s necessary to add more further studies to establish a high quality, evidence-based physical thera...
Original article can be found at : http://www.sciencedirect.com/ Copyright Elsevier [Full text of th...
Generalized joint hypermobility (GJH) is highly prevalent among patients diagnosed with chronic pain...
Full text of this book is not available in the UHRAThis book investigates and catalogues the traits ...
This issue of the American Journal of Medical Genetics Seminar Series Part C is dedicated to general...
New insights into the phenotype of Joint Hypermobility Syndrome (JHS) and Ehlers‐Danlos Syndrome‐hyp...
Joint hypermobility syndrome (JHS), or Ehlers-Danlos syndrome (EDS) hypermobility type (EDS-HT), is ...
Disability in children diagnosed with hypermobility syndrome (HMS) and Ehlers-Danlos (hypermobility ...
Chronic widespread pain is a common complaint among individuals affected by generalised joint hyperm...
Joint hypermobility syndrome (JHS), also known as Ehlers-Danlos III, is an inherited disorder of con...
Generalized joint hypermobility (GJH) is highly prevalent among patients diagnosed with chronic pain...
Joint hypermobility syndrome (JHS) and Ehlers-Danlos syndrome, hypermobility type (EDS-HT) are two c...
Background. In this study we aimed to identify and review publications relating to the diagnosis of ...
© 2019, © 2019 Informa UK Limited, trading as Taylor & Francis Group. Background: Joint Hypermobil...
Background: In this study we aimed to identify and review publications relating to the diagnosis of ...
Ehlers-Danlos Syndrome (EDS) is a heritable connective tissue disorder with many subtypes. Hypermobi...
Original article can be found at : http://www.sciencedirect.com/ Copyright Elsevier [Full text of th...
Generalized joint hypermobility (GJH) is highly prevalent among patients diagnosed with chronic pain...
Full text of this book is not available in the UHRAThis book investigates and catalogues the traits ...
This issue of the American Journal of Medical Genetics Seminar Series Part C is dedicated to general...
New insights into the phenotype of Joint Hypermobility Syndrome (JHS) and Ehlers‐Danlos Syndrome‐hyp...
Joint hypermobility syndrome (JHS), or Ehlers-Danlos syndrome (EDS) hypermobility type (EDS-HT), is ...
Disability in children diagnosed with hypermobility syndrome (HMS) and Ehlers-Danlos (hypermobility ...
Chronic widespread pain is a common complaint among individuals affected by generalised joint hyperm...
Joint hypermobility syndrome (JHS), also known as Ehlers-Danlos III, is an inherited disorder of con...
Generalized joint hypermobility (GJH) is highly prevalent among patients diagnosed with chronic pain...
Joint hypermobility syndrome (JHS) and Ehlers-Danlos syndrome, hypermobility type (EDS-HT) are two c...
Background. In this study we aimed to identify and review publications relating to the diagnosis of ...
© 2019, © 2019 Informa UK Limited, trading as Taylor & Francis Group. Background: Joint Hypermobil...
Background: In this study we aimed to identify and review publications relating to the diagnosis of ...
Ehlers-Danlos Syndrome (EDS) is a heritable connective tissue disorder with many subtypes. Hypermobi...
Original article can be found at : http://www.sciencedirect.com/ Copyright Elsevier [Full text of th...
Generalized joint hypermobility (GJH) is highly prevalent among patients diagnosed with chronic pain...
Full text of this book is not available in the UHRAThis book investigates and catalogues the traits ...