Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Inge, De Wandele"'
Autor:
Ellen Ewer, MSc, Hanadi Kazkaz, MD, Nelly Ninis, MD, Peter Rowe, MD, Robby De Pauw, PhD, Eudora Tang, MSc, Cathy Barrett, MPhtySt, Lies Rombaut, PhD, Inge De Wandele, PhD, Jane V. Simmonds, DProf
Publikováno v:
Journal of Pediatrics: Clinical Practice, Vol 12, Iss , Pp 200098- (2024)
Objectives: The multisystemic comorbid symptoms/conditions of hypermobility spectrum disorders (HSD) and hypermobile Ehlers-Danlos syndrome (hEDS) often significantly affect daily life. Many of these symptoms are under-recognized during diagnosis and
Externí odkaz:
https://doaj.org/article/de68429cf32a4521b94302fa593b551c
Autor:
Stijn De Baets, Marieke De Temmerman, Patrick Calders, Fransiska Malfait, Geert Van Hove, Guy Vanderstraeten, Inge De Wandele, Dominique Van de Velde
Publikováno v:
Frontiers in Rehabilitation Sciences, Vol 3 (2022)
BackgroundPeople with Ehlers-Danlos Syndromes and Hypermobility Spectrum Disorders are hampered in their social participation, especially in the social relationships they have.ObjectiveThe aim of this study is to research the impact of hypermobile Eh
Externí odkaz:
https://doaj.org/article/1f3366b93b0f48f9927f81fed91bb351
Autor:
Leslie L. Nicholson, Jane Simmonds, Verity Pacey, Inge De Wandele, Lies Rombaut, Cylie M. Williams, Cliffton Chan
Publikováno v:
JCR-JOURNAL OF CLINICAL RHEUMATOLOGY
There is exponential clinical and research interest in joint hypermobility due to recognition of the complexity of identification, assessment, and its appropriate referral pathways, ultimately impacting management. This state-of-the-science review pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d683f582578d9c34d1c204321b61f96f
https://doi.org/10.1097/rhu.0000000000001864
https://doi.org/10.1097/rhu.0000000000001864
Autor:
Kelly Berckmans, Valentien Spanhove, Fransiska Malfait, Inge De Wandele, Ann Cools, Patrick Calders, Tanneke Palmans
Publikováno v:
Arthritis Care & Research. 74:833-840
Objective To investigate differences in EMG muscle activity and scapular kinematics during elevation in the scapular plane between healthy controls, participants with multidirectional shoulder laxity (MDL), and patients with multidirectional shoulder
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5795139f344c8a26b70a329eda7cf237
https://doi.org/10.1002/acr.24525
https://doi.org/10.1002/acr.24525
Autor:
Marlies Colman, Delfien Syx, Inge de Wandele, Lies Rombaut, Deborah Wille, Zoë Malfait, Mira Meeus, Anne-Marie Malfait, Jessica Van Oosterwijck, Fransiska Malfait
Publikováno v:
medRxiv
Pain is one of the most important, yet poorly understood complaints in heritable connective tissue disorders (HCTD) caused by monogenic defects in extracellular matrix molecules. This is particularly the case for Ehlers-Danlos syndromes (EDS), paradi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5524c2f28424fd68cf1f653012c9cb2e
https://doi.org/10.1101/2023.02.24.23286404
https://doi.org/10.1101/2023.02.24.23286404
Autor:
null Marie Coussens, null Bruno Lapauw, null Charlotte Verroken, null Stefan Goemaere, null Inge De Wandele, null Fransiska Malfait, null Thiberiu Banica, null Patrick Calders
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7db05ab8fca2d0230d3915e0d3523789
https://doi.org/10.1002/jbmr.4722/v2/response1
https://doi.org/10.1002/jbmr.4722/v2/response1
Publikováno v:
Human Mutation. 42:1294-1306
Classical Ehlers-Danlos syndrome (cEDS) is a heritable connective tissue disorder mainly caused by pathogenic variants in COL5A1 or COL5A2, encoding type V collagen. Its diagnosis, based on clinical criteria and molecular confirmation, can be challen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::211c3b2b492e0ce070bf742713b2b611
https://doi.org/10.1002/humu.24258
https://doi.org/10.1002/humu.24258
Autor:
Bruno Lapauw, Inge De Wandele, Bert Celie, Patrick Calders, Thiberiu Banica, Verity Pacey, Marie Coussens, Fransiska Malfait, Lies Rombaut
Publikováno v:
Arthritis Care & Research. 73:1041-1048
Objective Reduced maximal muscle strength and strength endurance have been found in patients with hypermobile Ehlers-Danlos syndrome/hypermobility spectrum disorder (hEDS/HSD) and are recognized as common associated features of the disorder. However,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5c70005f5ebc5a808419354f29b4355
https://doi.org/10.1002/acr.24220
https://doi.org/10.1002/acr.24220
Autor:
Marie Coussens, Thiberiu Banica, Bruno Lapauw, Inge De Wandele, Lies Rombaut, Fransiska Malfait, Patrick Calders
Publikováno v:
Bone. 166
To compare bone parameters between individuals with hypermobile Ehlers-Danlos syndrome (hEDS) and generalized joint hypermobility spectrum disorder (G-HSD), both diagnosed according to the most recent diagnostic criteria, and with controls.Twenty fem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f3d902506bd317beea2b9593d90a839
https://pubmed.ncbi.nlm.nih.gov/36243401
https://pubmed.ncbi.nlm.nih.gov/36243401
Autor:
Inge De Wandele, Marlies Colman, Linda Hermans, Jessica Van Oosterwijck, Mira Meeus, Lies Rombaut, Griet Brusselmans, Delfien Syx, Patrick Calders, Fransiska Malfait
Publikováno v:
European journal of pain (London, England)REFERENCES. 26(6)
The hypermobile type of Ehlers-Danlos syndrome (hEDS) is a heritable connective tissue disorder, associated with joint hypermobility and prominent chronic pain. Because experimental pain testing in hEDS is scarce, the underlying mechanisms are still
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c83effa201ee9026937005f396e72e3
https://pubmed.ncbi.nlm.nih.gov/35442549
https://pubmed.ncbi.nlm.nih.gov/35442549