نتایج جستجو برای: dystrophic epidermolysis

تعداد نتایج: 5839  

Journal: :journal of skin and stem cell 0
sona zare skin and stem cell research center, tehran university of medical sciences, tehran, ir iran reza ahmadi department of clinical biochemistry, faculty of medicine, iran university of medical sciences, tehran, ir iran ayoob rostamzadeh department of anatomical sciences, faculty of medicine, shahrekord university of medical sciences, shahrekord, ir iran soleiman kurd school of advanced technologies in medicine, shahid beheshti university of medical sciences, tehran, ir iran somayeh hejazi skin and stem cell research center, tehran university of medical sciences, tehran, ir iran maryam fard department of anatomical science, faculty of medicine, qazvin university of medical sciences, qazvin, ir iran

context connective tissue cells include fibroblasts, chondrocytes, adipocyte, and osteocytes. these cells are specialized for the secretion of collagenous extracellular matrix and are responsible for the architectural framework of the human body. evidence acquisition connective tissue cells play a central role in supporting as well as repairing tissues and organs. fibroblast cell therapy could ...

Journal: :Molecular medicine 1998
J L Arbiser J D Fine D Murrell A Paller S Connors K Keough E Marsh J Folkman

BACKGROUND Patients with recessive dystrophic epidermolysis bullosa (RDEB) have deficiencies of collagen type VII and have elevated levels of fibroblast collagenase, and a greatly increased risk of cutaneous squamous cell carcinoma. Patients with other genetic blistering disorders do not have elevated collagenase or an increased risk of squamous cell carcinoma, despite chronic wounding. The con...

Journal: :JAMA dermatology 2013
Sivanie Vivehanantha Richard A Carr John A McGrath Saleem M Taibjee Sharmila Madhogaria Andrew Ilchyshyn

IMPORTANCE Epidermolysis bullosa (EB) pruriginosa is a rare variant of dystrophic EB. It may manifest late in life and is characterized by intense pruritus, resulting in a phenotype resembling acquired inflammatory dermatoses. Dermatopathology textbooks include hereditary forms of EB among the "cell-poor" list of subepidermal blistering disorders. OBSERVATIONS We report a case of dominant dys...

2015
Cassandra Chaptini Genevieve Casey Adam G. Harris Dedee F. Murrell Lynne Gordon

Fig 1. Squamous cell carcinoma identified after multiple biopsy specimens of poorly healing area over left E pidermolysis bullosa (EB) consists of a heterogeneous group of autosomal dominant or recessive disorders, characterized by epithelial fragility. In dystrophic EB, patients have a genetic defect in the gene encoding collagen VII, COL7A1. Generalized severe recessive dystrophic EB (RDEB) i...

Journal: :Dermatologic clinics 2010
W F Yan Dédée F Murrell

Dystrophic epidermolysis bullosa (DEB) is a severe skin fragility disorder associated with trauma-induced blistering, progressive soft tissue scarring, and increased risk of skin cancer. DEB is caused by mutations in the COL7A1 gene which result in reduced, truncated, or absent type VII collagen, and anchoring fibrils at the dermal-epidermal junction (DEJ). Because no topical wound-healing agen...

Journal: :The Journal of investigative dermatology 2013
Clare P Morgan Danny S I Allen Sophia Millington-Ward Gareth E O'Dwyer Arpad Palfi G Jane Farrar

Julia Spoendlin, Johannes J. Voegel, Susan S. Jick and Christoph R. Meier Basel Pharmacoepidemiology Unit, Division of Clinical Pharmacy and Epidemiology, Department of Pharmaceutical Sciences, University of Basel, Basel, Switzerland; Hospital Pharmacy, University Hospital Basel, Basel, Switzerland; Galderma Research & Development, Sophia Antipolis, France and Boston Collaborative Drug Surveill...

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