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Year Number of Results
1929 2
1939 1
1946 2
1947 1
1948 2
1949 2
1951 1
1953 1
1956 1
1959 1
1962 2
1964 1
1965 1
1967 1
1968 1
1969 4
1970 3
1971 3
1972 2
1973 3
1974 1
1975 6
1976 3
1977 2
1978 9
1979 9
1980 7
1981 9
1982 10
1983 13
1984 9
1985 15
1986 22
1987 21
1988 28
1989 20
1990 21
1991 25
1992 35
1993 28
1994 28
1995 27
1996 26
1997 30
1998 31
1999 22
2000 18
2001 21
2002 29
2003 29
2004 22
2005 18
2006 22
2007 32
2008 22
2009 30
2010 43
2011 55
2012 38
2013 37
2014 31
2015 51
2016 48
2017 44
2018 55
2019 44
2020 34
2021 45
2022 44
2023 50
2024 26
2025 13

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1,294 results

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Page 1
Epidermolysis bullosa acquisita.
Miyamoto D, Gordilho JO, Santi CG, Porro AM. Miyamoto D, et al. An Bras Dermatol. 2022 Jul-Aug;97(4):409-423. doi: 10.1016/j.abd.2021.09.010. Epub 2022 Jun 11. An Bras Dermatol. 2022. PMID: 35701269 Free PMC article.
Epidermolysis bullosa acquisita is a rare autoimmune disease, characterized by the synthesis of anti-collagen VII autoantibodies, the main component of hemidesmosome anchoring fibrils. ...There is no specific therapy for epidermolysis bullosa …
Epidermolysis bullosa acquisita is a rare autoimmune disease, characterized by the synthesis of anti-collagen VII autoa …
Acquired epidermolysis bullosa in a pediatric patient.
Torres-Iberico R, Henostroza-Inga K, Pérez-Córdova R, Lipa-Chancolla R. Torres-Iberico R, et al. Bol Med Hosp Infant Mex. 2023;80(Supl 1):77-81. doi: 10.24875/BMHIM.22000118. Bol Med Hosp Infant Mex. 2023. PMID: 37490686 Free article. English.
BACKGROUND: Acquired epidermolysis bullosa is a rare and chronic autoimmune subepidermal bullous disease characterized by the formation of autoantibodies against type VII collagen. ...CONCLUSIONS: Acquired epidermolysis bullosa is unusual …
BACKGROUND: Acquired epidermolysis bullosa is a rare and chronic autoimmune subepidermal bullous disease characterized …
Vesiculobullous Lesions of the Oral Cavity.
Alramadhan SA, Islam MN. Alramadhan SA, et al. Oral Maxillofac Surg Clin North Am. 2023 May;35(2):203-217. doi: 10.1016/j.coms.2022.10.006. Oral Maxillofac Surg Clin North Am. 2023. PMID: 37019505 Review.
These diseases include pemphigus Vulgaris, benign mucous membrane pemphigoid, bullous pemphigoid, and epidermolysis bullosa acquisita. These diseases have a significant impact on the quality of life, as they can lead to serious complications, depending on the …
These diseases include pemphigus Vulgaris, benign mucous membrane pemphigoid, bullous pemphigoid, and epidermolysis bullosa …
Epidermolysis bullosa acquisita.
Cobos G, Mu E, Cohen J, Beasley J, Brinster N, Femia A. Cobos G, et al. Dermatol Online J. 2017 Dec 15;23(12):13030/qt4jk4333w. Dermatol Online J. 2017. PMID: 29447655 Free article. Review.
Epidermolysis bullosa acquisita (EBA) is a rare, acquired subepidermal blistering disease. ...
Epidermolysis bullosa acquisita (EBA) is a rare, acquired subepidermal blistering disease. ...
[Epidermolysis bullosa acquisita].
Hofmann SC, Weidinger A. Hofmann SC, et al. Hautarzt. 2019 Apr;70(4):265-270. doi: 10.1007/s00105-019-4387-7. Hautarzt. 2019. PMID: 30887080 Review. German.
Epidermolysis bullosa acquisita (EBA) is a rare acquired subepidermal bullous autoimmune dermatosis, associated with autoantibodies against collagen type VII, the most important component of dermal anchoring fibrils. ...
Epidermolysis bullosa acquisita (EBA) is a rare acquired subepidermal bullous autoimmune dermatosis, associated …
Epidermolysis bullosa acquisita.
Gupta R, Woodley DT, Chen M. Gupta R, et al. Clin Dermatol. 2012 Jan-Feb;30(1):60-9. doi: 10.1016/j.clindermatol.2011.03.011. Clin Dermatol. 2012. PMID: 22137228 Free PMC article. Review.
Epidermolysis bullosa acquisita (EBA) is a rare, acquired, chronic subepidermal bullous disease of the skin and mucosa characterized by autoantibodies to type VII collagen (C7) structures, a major component of anchoring fibrils, which attach the epider …
Epidermolysis bullosa acquisita (EBA) is a rare, acquired, chronic subepidermal bullous disease of the skin and …
Epidermolysis bullosa acquisita.
Kim JH, Kim SC. Kim JH, et al. J Eur Acad Dermatol Venereol. 2013 Oct;27(10):1204-13. doi: 10.1111/jdv.12096. Epub 2013 Feb 1. J Eur Acad Dermatol Venereol. 2013. PMID: 23368767 Review.
Epidermolysis bullosa acquisita (EBA) is a chronic autoimmune subepidermal bullous disease with clinical features similar to the genetic form of dystrophic epidermolysis bullosa. ...
Epidermolysis bullosa acquisita (EBA) is a chronic autoimmune subepidermal bullous disease with clinical features simil …
Epidermolysis bullosa acquisita mechanica.
Fordham S, O'Bryen J, Bricknell J, Huang J, Banney L. Fordham S, et al. Aust J Gen Pract. 2023 Mar;52(3):122-125. doi: 10.31128/AJGP-06-22-6474. Aust J Gen Pract. 2023. PMID: 36872089 Free article. No abstract available.
Coexistence of acquired hemophilia A and epidermolysis bullosa acquisita: Two case reports and published work review.
Yan TM, He CX, Hua BL, Li L, Jin HZ, Liu YH, Zuo YG. Yan TM, et al. J Dermatol. 2017 Jan;44(1):76-79. doi: 10.1111/1346-8138.13546. Epub 2016 Aug 11. J Dermatol. 2017. PMID: 27511892 Review.
Epidermolysis bullosa acquisita (EBA) is a rare chronic subepidermal bullous autoimmune disease. The occurrence of acquired hemophilia A (AHA) is low and so the coexistence of EBA and AHA is extremely rare. ...
Epidermolysis bullosa acquisita (EBA) is a rare chronic subepidermal bullous autoimmune disease. The occurrence of a …
Pediatric epidermolysis bullosa acquisita: A review.
Hignett E, Sami N. Hignett E, et al. Pediatr Dermatol. 2021 Sep;38(5):1047-1050. doi: 10.1111/pde.14722. Epub 2021 Aug 2. Pediatr Dermatol. 2021. PMID: 34339066 Review.
Epidermolysis bullosa acquisita (EBA) is an acquired autoimmune blistering skin disorder that is rare in adults and even rarer in childhood. ...Our literature review was conducted in MEDLINE() using the search terms related to juvenile epidermolysis …
Epidermolysis bullosa acquisita (EBA) is an acquired autoimmune blistering skin disorder that is rare in adults …
1,294 results