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BMJ, 2019
### What you need to know Awareness of the Ehlers-Danlos syndromes (EDS) in the UK has risen over the past decade, in part due to high profile of EDS patient organisations and the EDS National Diagnostic Service commissioned in 2009. Significant advances in genetic testing have culminated in the publication of a new international classification in ...
Neeti, Ghali +2 more
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### What you need to know Awareness of the Ehlers-Danlos syndromes (EDS) in the UK has risen over the past decade, in part due to high profile of EDS patient organisations and the EDS National Diagnostic Service commissioned in 2009. Significant advances in genetic testing have culminated in the publication of a new international classification in ...
Neeti, Ghali +2 more
openaire +2 more sources
2013
The Ehlers-Danlos Syndromes comprise a heterogeneous group of diseases, which are characterized by fragility of the soft connective tissues and widespread manifestations in skin, ligaments and joints, blood vessels and internal organs. The clinical spectrum varies from mild skin and joint hyperlaxity to severe physical disability and life-threatening ...
Fransiska, Malfait, Anne, De Paepe
openaire +2 more sources
The Ehlers-Danlos Syndromes comprise a heterogeneous group of diseases, which are characterized by fragility of the soft connective tissues and widespread manifestations in skin, ligaments and joints, blood vessels and internal organs. The clinical spectrum varies from mild skin and joint hyperlaxity to severe physical disability and life-threatening ...
Fransiska, Malfait, Anne, De Paepe
openaire +2 more sources
Southern Medical Journal, 1981
We have described a patient with type 4 Ehlers-Danlos syndrome who died of a ruptured pulmonary artery. Of the six subtypes of Ehlers-Danlos syndrome, which can usually be clinically differentiated, only types 1 and 4 appear to be associated with a substantial risk of arterial rupture.
W, Pearl, M, Spicer
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We have described a patient with type 4 Ehlers-Danlos syndrome who died of a ruptured pulmonary artery. Of the six subtypes of Ehlers-Danlos syndrome, which can usually be clinically differentiated, only types 1 and 4 appear to be associated with a substantial risk of arterial rupture.
W, Pearl, M, Spicer
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Archives of Pediatrics & Adolescent Medicine, 1950
The syndrome of Ehlers and Danlos apparently is a constitutional dyscrasia of the mesenchyma, characterized by specific manifestations in the skin, joints and subcutaneous tissue, often associated with other congenital defects. Its history was initiated in 1899 when Ehlers reported on a patient to the Danish Dermatologic Society.1With the turn of the ...
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The syndrome of Ehlers and Danlos apparently is a constitutional dyscrasia of the mesenchyma, characterized by specific manifestations in the skin, joints and subcutaneous tissue, often associated with other congenital defects. Its history was initiated in 1899 when Ehlers reported on a patient to the Danish Dermatologic Society.1With the turn of the ...
openaire +2 more sources
Der Hautarzt, 1999
The Ehlers-Danlos syndrome (EDS) comprises a heterogenous group of nine hereditary connective tissue disorders, characterized by hyperelasticity of skin and hypermobility of joints to differing extents. The skin is easily injured and wound healing is delayed. The majority of EDS patients belong to EDS-types I-III. The pathogenesis in these cases is not
J, Brinckmann +5 more
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The Ehlers-Danlos syndrome (EDS) comprises a heterogenous group of nine hereditary connective tissue disorders, characterized by hyperelasticity of skin and hypermobility of joints to differing extents. The skin is easily injured and wound healing is delayed. The majority of EDS patients belong to EDS-types I-III. The pathogenesis in these cases is not
J, Brinckmann +5 more
openaire +2 more sources