Results 31 to 40 of about 1,088 (130)
, 2020 International Wound Journal, Volume 17, Issue 2, Page 519-521, April 2020.
Alessia Paganelli +5 more
wiley +1 more source
Elements of morphology: Standard terminology for the teeth and classifying genetic dental disorders
American Journal of Medical Genetics Part A, Volume 179, Issue 10, Page 1913-1981, October 2019., 2019 Abstract Dental anomalies occur frequently in a number of genetic disorders and act as major signs in diagnosing these disorders. We present definitions of the most common dental signs and propose a classification usable as a diagnostic tool by dentists, clinical geneticists, and other health care providers.
Muriel de La Dure‐Molla +24 more
wiley +1 more source
Anais Brasileiros de Dermatologia, 2011 As lesões melanocíticas adquiridas podem apresentar aspecto clínico não-usual em pacientes portadores de epidermólise bolhosa hereditária. Essas lesões são conhecidas como "nevos EB" e, muitas vezes, constituem um desafio diagnóstico ao dermatologista ...
Juliana Nakano de Melo +5 more
doaj +1 more source
Complexity, Volume 2019, Issue 1, 2019., 2019 In the big data era, sequencing technology has produced a large number of biological sequencing data. Different views of the cancer genome data provide sufficient complementary information to explore genetic activity. The identification of differentially expressed genes from multiview cancer gene data is of great importance in cancer diagnosis and ...
Yue Hu +5 more
wiley +1 more source
Anais Brasileiros de DermatologiaBackground Epidermolysis bullosa (EB) is a group of rare hereditary diseases, characterized by fragility of the skin and mucous membranes. Epidemiological data on EB in Brazil are scarce.
Chan I. Thien +5 more
doaj +1 more source
Suprathel®‐assisted surgical treatment of the hand in a dystrophic epidermolysis bullosa patient
International Wound Journal, Volume 11, Issue 5, Page 472-475, October 2014., 2014 Abstract Epidermolysis bullosa (EB) is a progressive familial disorder composed of dermal mucosal blisters, flexion contractures and pseudosyndactylies. Flexion contractures and pseudosyndactyly can be treated with surgery but usually require skin grafting. Because of poor wound healing, skin graft harvesting is a challenge in these patients.
Elif Sari +4 more
wiley +1 more source
Anais Brasileiros de Dermatologia, 2012 Pasini's albopapuloid epidermolysis bullosa is a very rare subtype of generalized dystrophic dominant epidermolyis bullosa. A 30 year-old white female patient presented since her childhood disseminated small blisters and papules.
Hiram Larangeira de Almeida Jr +3 more
doaj +1 more source
BioMed Research International, Volume 2013, Issue 1, 2013., 2013 Epidermolysis bullosa (EB) is a group of inherited skin disorders characterized by blistering following mechanical trauma. Chronic wounds of EB patients often lead to tumors such as squamous cell carcinoma (SCC). Early diagnosis may prevent its invasive growth—frequently the reason of premature mortality of EB‐patients.
Patrick Larisch +4 more
wiley +1 more source
Clinical Presentation, Pathogenesis, Diagnosis, and Treatment of Epidermolysis Bullosa Acquisita
International Scholarly Research Notices, Volume 2013, Issue 1, 2013., 2013 Epidermolysis bullosa acquisita (EBA) is a chronic mucocutaneous autoimmune skin blistering disease. The pathogenic relevance of autoantibodies targeting type VII collagen (COL7) has been well‐documented. Therefore, EBA is a prototypical autoimmune disease with a well‐characterized pathogenic relevance of autoantibody binding to the target antigen. EBA
Ralf J. Ludwig +4 more
wiley +1 more source
Anais Brasileiros de Dermatologia, 2012 In dystrophic epidermolysis bullosa, the genetic defect of anchoring fibrils leads to cleavage beneath the basement membrane and its consequent loss.
Hiram Larangeira de Almeida Jr +4 more
doaj +1 more source