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
1975 1
1976 1
1982 1
1983 3
1984 1
1985 2
1986 4
1987 2
1988 3
1990 2
1991 7
1992 9
1993 9
1994 7
1995 10
1996 9
1997 15
1998 11
1999 12
2000 10
2001 14
2002 11
2003 11
2004 14
2005 9
2006 12
2007 7
2008 11
2009 16
2010 22
2011 20
2012 17
2013 25
2014 19
2015 21
2016 24
2017 26
2018 28
2019 28
2020 32
2021 35
2022 28
2023 21
2024 9

Text availability

Article attribute

Article type

Publication date

Search Results

519 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Abnormal blistering of the skin"
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.
Over 30 subtypes are recognized, grouped into four major categories, based predominantly on the plane of cleavage within the skin and reflecting the underlying molecular abnormality: EB simplex, junctional EB, dystrophic EB and Kindler EB. ...In the absence of curat …
Over 30 subtypes are recognized, grouped into four major categories, based predominantly on the plane of cleavage within the skin and …
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 diagnosis is suspected based on symptoms and confirmed by skin …
Epidermolysis bullosa (EB) is a group of rare congenital genetic conditions that result in painful blistering of the skin …
Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility.
Has C, Bauer JW, Bodemer C, Bolling MC, Bruckner-Tuderman L, Diem A, Fine JD, Heagerty A, Hovnanian A, Marinkovich MP, Martinez AE, McGrath JA, Moss C, Murrell DF, Palisson F, Schwieger-Briel A, Sprecher E, Tamai K, Uitto J, Woodley DT, Zambruno G, Mellerio JE. Has C, et al. Br J Dermatol. 2020 Oct;183(4):614-627. doi: 10.1111/bjd.18921. Epub 2020 Mar 11. Br J Dermatol. 2020. PMID: 32017015 Review.
RESULTS: In this latest consensus report, we introduce the concept of genetic disorders with skin fragility, of which classical EB represents the prototype. Other disorders with skin fragility, where blisters are a minor part of the clinical picture or are no …
RESULTS: In this latest consensus report, we introduce the concept of genetic disorders with skin fragility, of which classical EB re …
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. EB can be categorized into four classical subtypes, EB simplex, junctional EB, …
Epidermolysis bullosa (EB) is a heterogeneous group of rare inherited blistering skin disorders characterized by skin f …
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.
The antigen-antibody binding elicits a complex inflammatory response, which culminates in the loss of dermo-epidermal adhesion of the skin and/or mucous membranes. Skin fragility with bullae, erosions, and milia in areas of trauma characterizes the mechanobullous fo …
The antigen-antibody binding elicits a complex inflammatory response, which culminates in the loss of dermo-epidermal adhesion of the ski …
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 classif …
Inherited epidermolysis bullosa is a group of genetic diseases characterized by skin fragility and blistering on the skin …
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-skin syndroms are a group of genetic disorders with renal and cutaneous manifestations that target molecular components present in both organs. Inherited renal-skin syndromes are mainly associated with defects of cell-matrix adhesion. ...
Renal-skin syndroms are a group of genetic disorders with renal and cutaneous manifestations that target molecular components present …
Muscle-Related Plectinopathies.
Zrelski MM, Kustermann M, Winter L. Zrelski MM, et al. Cells. 2021 Sep 19;10(9):2480. doi: 10.3390/cells10092480. Cells. 2021. PMID: 34572129 Free PMC article. Review.
The most common disorder is autosomal recessive disease epidermolysis bullosa simplex with muscular dystrophy (EBS-MD), which is characterized by skin blistering and progressive muscle weakness. Besides EBS-MD, PLEC mutations lead to EBS with nail dystrophy, EBS-MD …
The most common disorder is autosomal recessive disease epidermolysis bullosa simplex with muscular dystrophy (EBS-MD), which is characteriz …
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.
The pathophysiology of each condition is incompletely understood but broadly involves the formation of autoantibodies targeting skin adhesion proteins, a process that relies on a complex interplay between a dysregulated immune system, genetic predisposition, and environmen …
The pathophysiology of each condition is incompletely understood but broadly involves the formation of autoantibodies targeting skin …
Efficacy and safety of Oleogel-S10 (birch triterpenes) for epidermolysis bullosa: results from the phase III randomized double-blind phase of the EASE study.
Kern JS, Sprecher E, Fernandez MF, Schauer F, Bodemer C, Cunningham T, Löwe S, Davis C, Sumeray M, Bruckner AL, Murrell DF; EASE investigators. Kern JS, et al. Br J Dermatol. 2023 Jan 23;188(1):12-21. doi: 10.1093/bjd/ljac001. Br J Dermatol. 2023. PMID: 36689495 Clinical Trial.
Patients with EB are affected by mechanical fragility of epithelial surfaces including the skin and, as a result, extensive recurrent blistering is a characteristic of the condition. ...
Patients with EB are affected by mechanical fragility of epithelial surfaces including the skin and, as a result, extensive recurrent …
519 results