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

Year Number of Results
1963 1
1964 1
1965 1
1969 1
1971 2
1974 4
1975 3
1976 1
1978 1
1979 1
1980 3
1981 7
1982 2
1983 7
1984 4
1985 6
1986 7
1987 4
1988 12
1989 5
1990 10
1991 10
1992 19
1993 18
1994 21
1995 18
1996 19
1997 24
1998 21
1999 24
2000 24
2001 17
2002 19
2003 22
2004 21
2005 20
2006 29
2007 23
2008 30
2009 28
2010 50
2011 54
2012 43
2013 48
2014 38
2015 39
2016 52
2017 45
2018 53
2019 60
2020 58
2021 67
2022 57
2023 58
2024 16

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1,104 results

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Page 1
Epidermolysis bullosa.
Bardhan A, Bruckner-Tuderman L, Chapple ILC, Fine JD, Harper N, Has C, Magin TM, Marinkovich MP, Marshall JF, McGrath JA, Mellerio JE, Polson R, Heagerty AH. Bardhan A, et al. Nat Rev Dis Primers. 2020 Sep 24;6(1):78. doi: 10.1038/s41572-020-0210-0. Nat Rev Dis Primers. 2020. PMID: 32973163 Review.
Epidermolysis bullosa (EB) is an inherited, heterogeneous group of rare genetic dermatoses characterized by mucocutaneous fragility and blister formation, inducible by often minimal trauma. ...
Epidermolysis bullosa (EB) is an inherited, heterogeneous group of rare genetic dermatoses characterized by mucocutaneous frag …
Epidermolysis Bullosa: Pediatric Perspectives.
Hon KL, Chu S, Leung AKC. Hon KL, et al. Curr Pediatr Rev. 2022;18(3):182-190. doi: 10.2174/1573396317666210525161252. Curr Pediatr Rev. 2022. PMID: 34036913 Review.
Epidermolysis bullosa (EB) is a group of rare congenital genetic conditions that result in painful blistering of the skin and mucous membranes, which occur with minor trauma or friction. ...The underlying mechanism is a defect in attachment between or within the epi …
Epidermolysis bullosa (EB) is a group of rare congenital genetic conditions that result in painful blistering of the skin and …
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 acquisita …
Epidermolysis bullosa acquisita is a rare autoimmune disease, characterized by the synthesis of anti-collagen VII autoantibodi …
Inherited epidermolysis bullosa: update on the clinical and genetic aspects.
Mariath LM, Santin JT, Schuler-Faccini L, Kiszewski AE. Mariath LM, et al. An Bras Dermatol. 2020 Sep-Oct;95(5):551-569. doi: 10.1016/j.abd.2020.05.001. Epub 2020 Jul 8. An Bras Dermatol. 2020. PMID: 32732072 Free PMC article. Review.
Inherited epidermolysis bullosa is a group of genetic diseases characterized by skin fragility and blistering on the skin and mucous membranes in response to minimal trauma. Epidermolysis bullosa is clinically and genetically very heterogeneous, being …
Inherited epidermolysis bullosa is a group of genetic diseases characterized by skin fragility and blistering on the skin and …
Investigational Treatments for Epidermolysis Bullosa.
Hou PC, Wang HT, Abhee S, Tu WT, McGrath JA, Hsu CK. Hou PC, et al. Am J Clin Dermatol. 2021 Nov;22(6):801-817. doi: 10.1007/s40257-021-00626-3. Epub 2021 Jul 22. Am J Clin Dermatol. 2021. PMID: 34292508 Review.
Epidermolysis bullosa (EB) is a heterogeneous group of rare inherited blistering skin disorders characterized by skin fragility following minor trauma, usually present since birth. ...
Epidermolysis bullosa (EB) is a heterogeneous group of rare inherited blistering skin disorders characterized by skin fragilit …
Renal-skin syndromes.
Has C, He Y. Has C, et al. Cell Tissue Res. 2017 Jul;369(1):63-73. doi: 10.1007/s00441-017-2623-y. Epub 2017 Apr 22. Cell Tissue Res. 2017. PMID: 28432467 Review.
Renal and urinary tract involvement is described in all four major epidermolysis bullosa types and, in particular, in junctional subtypes and in recessive dystrophic epidermolysis bullosa. ...
Renal and urinary tract involvement is described in all four major epidermolysis bullosa types and, in particular, in junction …
Nutrition and bullous diseases.
Stoj V, Lu J. Stoj V, et al. Clin Dermatol. 2022 Mar-Apr;40(2):156-165. doi: 10.1016/j.clindermatol.2021.10.009. Epub 2021 Nov 19. Clin Dermatol. 2022. PMID: 34808244 Review.
This group of diseases is broad and encompasses subepidermal conditions such as bullous pemphigoid, cicatricial pemphigoid, epidermolysis bullosa acquisita, dermatitis herpetiformis, and linear IgA bullous dermatosis, as well as intraepidermal conditions such as pem …
This group of diseases is broad and encompasses subepidermal conditions such as bullous pemphigoid, cicatricial pemphigoid, epidermolysis …
Hereditary epidermolysis bullosa.
Laimer M, Prodinger C, Bauer JW. Laimer M, et al. J Dtsch Dermatol Ges. 2015 Nov;13(11):1125-33. doi: 10.1111/ddg.12774. J Dtsch Dermatol Ges. 2015. PMID: 26513070 Review.
The term epidermolysis bullosa (EB) includes a group of rare genodermatoses characterized by mutational impairment of the structural and functional integrity of intraepidermal adhesion and dermoepidermal anchorage. ...
The term epidermolysis bullosa (EB) includes a group of rare genodermatoses characterized by mutational impairment of the stru …
Diagnosis and Care of the Newborn with Epidermolysis Bullosa.
Lucky AW, Whalen J, Rowe S, Marathe KS, Gorell E. Lucky AW, et al. Neoreviews. 2021 Jul;22(7):e438-e451. doi: 10.1542/neo.22-7-e438. Epub 2021 Jul 1. Neoreviews. 2021. PMID: 34210808 Review.
Epidermolysis bullosa (EB) is a group of rare genetic disorders that are characterized by fragile skin. ...
Epidermolysis bullosa (EB) is a group of rare genetic disorders that are characterized by fragile skin. ...
Inherited epidermolysis bullosa.
El Hachem M, Giancristoforo S, Diociaiuti A. El Hachem M, et al. G Ital Dermatol Venereol. 2014 Dec;149(6):651-62. Epub 2014 Oct 3. G Ital Dermatol Venereol. 2014. PMID: 25279494 Review.
Inherited epidermolysis bullosa (EB) refers to a clinically and genetically heterogeneous group of rare disorders characterized by fragility of the skin and mucous membranes. ...
Inherited epidermolysis bullosa (EB) refers to a clinically and genetically heterogeneous group of rare disorders characterize …
1,104 results