Results 91 to 100 of about 1,259,935 (185)

Carotid artery dissection linked to intermittent apnoeic swimming: A case–control study

Experimental Physiology, Volume 111, Issue 11, Page 4966-4978, 1 November 2026.
Abstract Internal carotid artery (ICA) dissection is a rare and potentially devastating cause of cerebral ischaemia, initiated by an intimal tear or rupture of the vasa vasorum, that can lead to an intraluminal thrombus, vascular stenosis, occlusion, or dissecting aneurysm formation.
Damian M. Bailey, Richard G. Davies, Brenig L. Gwilym, Benjamin S. Stacey, Danny Walmsley, Michael H. Lewis, Josip Butkovic, Ivan Mumlek, Brad Perry, Zvonomir Vrselja, Shigehiko Ogoh, James A. Pawelczyk, Mohamad Bashir, Richard D. White, Ian M. Williams   +14 more
wiley   +1 more source

Ehlers-Danlos Sendromu

, 2021
Ehlers-Danlos Syndrome (EDS) is a heterogeneous group of inherited diseases with jointhypermobility, skin hyperextensibility and tissue fragility. There is no specific treatment for EDS.
Giray Bozkaya, Özlem
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Ehlers-Danlos syndrome

, 2016
Ehlers-Danlos syndromeEhlers-Danlos syndrome (EDS) comprises a group of diseases characterized by connective tissue fragility. The clinical symptoms primarily involve the skin, joints, blood vessels and internal organs.
Farholt, Stense, Leganger, Julie, Burcharth, Jakob, Søborg, Marie-Louise Kulas, Rosenberg, Jacob, Lund, Allan Meldgaard   +5 more
core   +1 more source

Vascular-type Ehlers-Danlos syndrome caused by a hitherto unknown genetic mutation: a case report

Journal of Medical Case Reports, 2013
Introduction Vascular-type Ehlers-Danlos syndrome is an autosomal dominant disease that causes arterial spurting, intestinal perforation, uterine rupture and hemopneumothorax due to decreased production of type III collagen.
Kashizaki Fumihiro, Hatamochi Atsushi, Kamiya Kazunori, Yoshizu Akira, Okamoto Hiroaki   +4 more
doaj   +1 more source

Ehlers-Danlos syndrome and neurological features: a review

, 2011
Ehlers-Danlos Syndrome is a term that comprises a variety of inherited connective tissue disorders characterized primarily by skin hyperextensibility, joints hypermobility and excessive dislocations, easy bruisability, generalized fragility.
Merli P, Savasta S, Bianchi L, Ruggieri M, Spartà MV   +4 more
core   +1 more source

Multiple perforation of small-intestine diverticula in a patient with Ehlers-Danlos syndrome. [PDF]

, 2017
Ehlers-Danlos syndrome represents a group of hereditary connective tissue disorders characterized by ligamentous hyperlaxity, fragile skin and joint hypermobility.
Palacios Lázaro, Elena, Burgos García, Aurora, Honrubia Lopez, Raúl   +2 more
core   +1 more source

Walsh & Hoyt: Ehlers-Danlos Syndrome, Marafan\u27s Syndrome, and Pseudoxanthoma Elasticum

, 2005
Ehlers-Danlos syndrome encompasses a group of inherited disorders of connective tissue, all of which have abnormalities of collagen ...
Steven A. Newman, MD
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Familial gigantiform cementoma with Ehlers- Danlos syndrome: A report of 2 cases

, 2015
Ehlers-Danlos syndrome is an autosomal dominant hereditary disorder of connective tissue, while familial gigantiform cementoma is a condition that usually manifests as multiple radiopaque cementum-like masses throughout the jaws.
Olcay Şakar, Sakar, Olcay, Unalan, Fatma, Aksakalli, Nihan, Mumcu, Zeynep, Fatma Ünalan, Aren, Gamze, Tolgay, Ceren Guney, Gamze Aren, Nihan Aksakallı, Ceren Güney Tolgay, Zeynep Mumcu   +11 more
core   +1 more source

Retrospective descriptive study of prevalence of symptoms of suspected connective tissue disease: focus on Ehlers-Danlos syndrome

openLo studio analizzerà la prevalenza di sintomi nella Sindrome di Ehlers Danlos cercando di descrivere eventuali sintomi maggiormente significativi per la ...
CALLEGARI, DAVIDE
core  

Fibromyalgia: an unrecognized Ehlers-Danlos syndrome hypermobile type? [PDF]

, 2013
peer reviewedSome patients suffering from fibromyalgia present with clinical signs and alterations in the histopathology, immunohistochemistry and ultrastructure of the dermis similar to the Ehlers-Danlos syndrome, hypermobile type (EDSH).
PIERARD, Gérald, Hermanns-Lê, Trinh, Angenot, Ph   +2 more
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