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

Year Number of Results
1951 1
1953 1
1954 1
1960 1
1964 1
1975 2
1976 4
1977 1
1979 2
1980 1
1981 2
1982 3
1983 6
1984 8
1985 8
1986 13
1987 14
1988 15
1989 13
1990 17
1991 10
1992 23
1993 15
1994 30
1995 29
1996 27
1997 32
1998 41
1999 30
2000 30
2001 26
2002 12
2003 22
2004 22
2005 30
2006 27
2007 22
2008 25
2009 15
2010 30
2011 25
2012 26
2013 25
2014 37
2015 32
2016 28
2017 24
2018 41
2019 23
2020 48
2021 62
2022 51
2023 53
2024 29

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1,022 results

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Page 1
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 …
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 …
Herlitz junctional epidermolysis bullosa.
Laimer M, Lanschuetzer CM, Diem A, Bauer JW. Laimer M, et al. Dermatol Clin. 2010 Jan;28(1):55-60. doi: 10.1016/j.det.2009.10.006. Dermatol Clin. 2010. PMID: 19945616 Review.
Junctional epidermolysis bullosa type Herlitz (JEB-H) is the autosomal recessively inherited, more severe variant of "lucidolytic" JEB. ...
Junctional epidermolysis bullosa type Herlitz (JEB-H) is the autosomal recessively inherited, more severe variant of "l …
Non-herlitz junctional epidermolysis bullosa.
Yancey KB, Hintner H. Yancey KB, et al. Dermatol Clin. 2010 Jan;28(1):67-77. doi: 10.1016/j.det.2009.10.008. Dermatol Clin. 2010. PMID: 19945618 Review.
Non-Herlitz junctional epidermolysis bullosa (nH JEB) is characterized by generalized blisters that predominate in sites exposed to friction, trauma, or heat. ...
Non-Herlitz junctional epidermolysis bullosa (nH JEB) is characterized by generalized blisters that predominate in site …
Neonatal junctional epidermolysis bullosa: treatment conundrums and ethical decision making.
Yang CS, Kroshinksy D, Cummings BM. Yang CS, et al. Am J Clin Dermatol. 2014 Oct;15(5):445-50. doi: 10.1007/s40257-014-0091-7. Am J Clin Dermatol. 2014. PMID: 25117154 Review.
Junctional epidermolysis bullosa (JEB), generalized severe (previously called JEB, Herlitz-type) has an extremely poor prognosis, with a mean age of death at 5 months old and most dead before age 3 years. ...We review the literature as well as discuss the eth …
Junctional epidermolysis bullosa (JEB), generalized severe (previously called JEB, Herlitz-type) has an extremely poor …
Junctional epidermolysis bullosa.
Kao CH, Chen SJ, Hwang B, Yang AH, Hsu CY, Huang CH. Kao CH, et al. J Chin Med Assoc. 2006 Oct;69(10):503-6. doi: 10.1016/S1726-4901(09)70318-1. J Chin Med Assoc. 2006. PMID: 17098678 Free article.
Epidermolysis bullosa (EB) encompasses a heterogeneous group of genodermatoses, characterized by fragility and blistering of the skin, often associated with extracutaneous manifestations. ...Electron microscopy confirmed the cleavage of epidermis from dermis within …
Epidermolysis bullosa (EB) encompasses a heterogeneous group of genodermatoses, characterized by fragility and blistering of t …
Laminin 332 in junctional epidermolysis bullosa.
Kiritsi D, Has C, Bruckner-Tuderman L. Kiritsi D, et al. Cell Adh Migr. 2013 Jan-Feb;7(1):135-41. doi: 10.4161/cam.22418. Epub 2012 Oct 17. Cell Adh Migr. 2013. PMID: 23076207 Free PMC article. Review.
The phenotypic consequences are diminished dermal-epidermal adhesion and, as clinical symptoms, skin fragility and mechanically induced blistering. The disorder is designated as junctional epidermolysis bullosa (JEB). This article delineates the signs and sym …
The phenotypic consequences are diminished dermal-epidermal adhesion and, as clinical symptoms, skin fragility and mechanically induced blis …
A case of junctional epidermolysis bullosa intermediate with collagen XVII deficiency treated with dupilumab.
Zhang L, Wang S, Chen Q, Xiang L. Zhang L, et al. J Dermatolog Treat. 2023 Dec;34(1):2253943. doi: 10.1080/09546634.2023.2253943. Epub 2023 Nov 15. J Dermatolog Treat. 2023. PMID: 37968922 Free article.
Junctional epidermolysis bullosa is associated with mutations in genes expressing proteins of the dermo-epidermal junction. Dupilumab, an antibody that directly targets interleukin (IL)-4 receptor alpha, may be an effective treatment for dystrophic epiderm …
Junctional epidermolysis bullosa is associated with mutations in genes expressing proteins of the dermo-epidermal junct …
Leading edge: emerging drug, cell, and gene therapies for junctional epidermolysis bullosa.
Keith AR, Twaroski K, Ebens CL, Tolar J. Keith AR, et al. Expert Opin Biol Ther. 2020 Aug;20(8):911-923. doi: 10.1080/14712598.2020.1740678. Epub 2020 Mar 20. Expert Opin Biol Ther. 2020. PMID: 32178539 Free PMC article. Review.
INTRODUCTION: Junctional epidermolysis bullosa (JEB) is a rare inherited genetic disorder with limited treatments beyond palliative care. ...
INTRODUCTION: Junctional epidermolysis bullosa (JEB) is a rare inherited genetic disorder with limited treatments beyon …
Cicatricial junctional epidermolysis bullosa.
Jonkman MF, de Jong MC, van der Meer JB. Jonkman MF, et al. J Am Acad Dermatol. 1994 Aug;31(2 Pt 1):286-8. doi: 10.1016/s0190-9622(08)81983-4. J Am Acad Dermatol. 1994. PMID: 8040421 Review. No abstract available.
1,022 results