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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1946 2
1948 1
1949 2
1951 1
1953 1
1959 1
1962 1
1964 1
1965 1
1967 1
1969 2
1970 1
1971 1
1972 2
1973 2
1975 4
1976 2
1977 1
1978 6
1979 6
1980 5
1981 8
1982 9
1983 7
1984 7
1985 10
1986 17
1987 18
1988 26
1989 17
1990 20
1991 25
1992 30
1993 22
1994 21
1995 25
1996 24
1997 28
1998 27
1999 20
2000 16
2001 20
2002 25
2003 21
2004 19
2005 13
2006 20
2007 27
2008 16
2009 25
2010 37
2011 47
2012 35
2013 35
2014 27
2015 40
2016 42
2017 40
2018 49
2019 39
2020 30
2021 40
2022 43
2023 48
2024 25
2025 25
2026 4

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1,124 results

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Page 1
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: A comprehensive review.
Kridin K, Kneiber D, Kowalski EH, Valdebran M, Amber KT. Kridin K, et al. Autoimmun Rev. 2019 Aug;18(8):786-795. doi: 10.1016/j.autrev.2019.06.007. Epub 2019 Jun 7. Autoimmun Rev. 2019. PMID: 31181325 Review.
Epidermolysis bullosa acquisita is a rare autoimmune blistering disease which results in vesicle and bullae formation on the skin and erosions on the mucous membranes. ...
Epidermolysis bullosa acquisita is a rare autoimmune blistering disease which results in vesicle and bullae formation o …
[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 with au …
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 and eve …
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 …
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 epidermis to …
Epidermolysis bullosa acquisita (EBA) is a rare, acquired, chronic subepidermal bullous disease of the skin and mucosa …
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.
Epidermolysis bullosa acquisita involving the vulva.
Kassels A, Chuba N, Kraus CN. Kassels A, et al. Am J Obstet Gynecol. 2024 Jan;230(1):99-100. doi: 10.1016/j.ajog.2023.07.045. Epub 2023 Jul 27. Am J Obstet Gynecol. 2024. PMID: 37506750 Free article. No abstract available.
[Epidermolysis bullosa acquisita].
Kobayashi M, Amagai M. Kobayashi M, et al. Ryoikibetsu Shokogun Shirizu. 2000;(31):279-81. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11269080 Review. Japanese. No abstract available.
1,124 results