Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1963 1
1974 1
1979 1
1983 1
1985 1
1988 3
1991 2
1992 4
1993 3
1994 3
1995 5
1996 5
1997 2
1998 3
1999 8
2000 2
2001 1
2003 1
2004 4
2005 3
2006 1
2007 4
2008 5
2009 2
2010 12
2011 4
2012 1
2013 4
2014 4
2015 10
2016 4
2017 7
2018 4
2019 5
2020 7
2021 10
2022 9
2023 4
2024 5

Text availability

Article attribute

Article type

Publication date

Search Results

149 results

Results by year

Filters applied: . Clear all
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
Beremagene Geperpavec: First Approval.
Dhillon S. Dhillon S. Drugs. 2023 Aug;83(12):1131-1135. doi: 10.1007/s40265-023-01921-5. Drugs. 2023. PMID: 37432558 Review.
In May 2023, beremagene geperpavec received its first approval in the US for the treatment of wounds in patients 6 months of age with dystrophic epidermolysis bullosa with mutation(s) in the COL7A1 gene. A Marketing Authorization Application for beremagene geperpave …
In May 2023, beremagene geperpavec received its first approval in the US for the treatment of wounds in patients 6 months of age with dystro …
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 …
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 …
Oral Alterations in Heritable Epidermolysis Bullosa: A Clinical Study and Literature Review.
Polizzi A, Santonocito S, Patini R, Quinzi V, Mummolo S, Leonardi R, Bianchi A, Isola G. Polizzi A, et al. Biomed Res Int. 2022 May 31;2022:6493156. doi: 10.1155/2022/6493156. eCollection 2022. Biomed Res Int. 2022. PMID: 35686231 Free PMC article. Review.
Epidermolysis bullosa (EB) is a group of skin disorders with skin fragility characterized by blistering from minimal mechanical trauma with rupture at the dermoepidermal junction. ...
Epidermolysis bullosa (EB) is a group of skin disorders with skin fragility characterized by blistering from minimal mechanica
Nutritional aspects of children and adolescents with epidermolysis bullosa: literature review.
Zidorio AP, Dutra ES, Leão DO, Costa IM. Zidorio AP, et al. An Bras Dermatol. 2015 Mar-Apr;90(2):217-23. doi: 10.1590/abd1806-4841.20153206. An Bras Dermatol. 2015. PMID: 25830992 Free PMC article. Review.
Epidermolysis Bullosa is a genetic disorder that affects mainly the skin, however, all others systems are influenced. ...This literature review discusses the latest knowledge on energy and specific nutrient requirements to the dietary treatment and monitoring of chi
Epidermolysis Bullosa is a genetic disorder that affects mainly the skin, however, all others systems are influenced. ...This
Dystrophic Epidermolysis Bullosa Inversa - Case Report and Review of the Literature.
Merzel Šabović EK, Luzar B, Wechtersbach K, Dolenc-Voljč M. Merzel Šabović EK, et al. Acta Dermatovenerol Croat. 2022 Nov;30(3):151-156. Acta Dermatovenerol Croat. 2022. PMID: 36812272 Review.
Dystrophic epidermolysis bullosa inversa is a very rare subtype of inherited dystrophic epidermolysis bullosa with a unique clinical manifestation. ...We present a case of a 45-year-old female patient with dystrophic epidermolysis bullosa
Dystrophic epidermolysis bullosa inversa is a very rare subtype of inherited dystrophic epidermolysis bullosa wi …
Epidermolysis bullosa dystrophica pretibialis - Clinical snapshot and management of a rare orphan disease.
Will LM, Reichrath J, Vogt T. Will LM, et al. J Dtsch Dermatol Ges. 2021 Jul;19(7):983-986. doi: 10.1111/ddg.14446. Epub 2021 May 5. J Dtsch Dermatol Ges. 2021. PMID: 33951274 Review.
If blistering occurs in childhood, the possibility of hereditary epidermolysis bullosa should be considered even if the symptoms are mild. ...
If blistering occurs in childhood, the possibility of hereditary epidermolysis bullosa should be considered even if the sympto …
Inherited epidermolysis bullosa: epidemiology and patient care in Slovenia with a review of the updated classification.
Štublar A, Dragoš V, Dolenc-Voljč M. Štublar A, et al. Acta Dermatovenerol Alp Pannonica Adriat. 2021 Jun;30(2):63-66. Acta Dermatovenerol Alp Pannonica Adriat. 2021. PMID: 34169701 Free article. Review.
INTRODUCTION: Inherited epidermolysis bullosa (EB) is a heterogeneous group of rare genetic skin disorders characterized by fragility of the skin and mucous membranes. The prevalence of all types of EB is estimated at approximately 11 per million, based on recent da …
INTRODUCTION: Inherited epidermolysis bullosa (EB) is a heterogeneous group of rare genetic skin disorders characterized by fr …
Eye Involvement and Management in Inherited Epidermolysis Bullosa.
Bachir Y, Daruich A, Marie C, Robert MP, Bremond-Gignac D. Bachir Y, et al. Drugs. 2022 Aug;82(12):1277-1285. doi: 10.1007/s40265-022-01770-8. Epub 2022 Sep 8. Drugs. 2022. PMID: 36074321 Review.
Inherited epidermolysis bullosa (EB) is a group of genetic rare diseases associated with skin fragility, which leads to the formation of blisters, erosions, and scars on the skin and mucous membranes. Epidermolysis bullosa includes four main types and …
Inherited epidermolysis bullosa (EB) is a group of genetic rare diseases associated with skin fragility, which leads to the fo …
149 results