Epidermolysis bullosa simplex: localized (Weber-Cockayne type).
Dermatol Nurs. 2004.
PMID: 15690931
No abstract available.
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1,053 results
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Citations
9
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found by citation matching
Localized epidermolysis bullosa simplex (Weber-Cockayne type).
J Pediatr Adolesc Gynecol. 2011.
PMID: 22206097
No abstract available.
Ultrastructure of blister formation in epidermolysis bullosa hereditaria: V. Epidermolysis bullosa simplex localisata type Weber-Cockayne.
J Invest Dermatol. 1982.
PMID: 7057054
Search results
Page 1
Epidermolysis bullosa simplex.
Dermatol Clin. 2010 Jan;28(1):23-32. doi: 10.1016/j.det.2009.10.003.
Dermatol Clin. 2010.
PMID: 19945613
Review.
The prevalence of epidermolysis bullosa simplex (EBS) is estimated to be approximately 6 to 30 per 1 million live births. ...
The prevalence of epidermolysis bullosa simplex (EBS) is estimated to be approximately 6 to 30 per 1 million live birth …
Keratins and epidermolysis bullosa simplex.
J Cell Physiol. 2018 Jan;234(1):289-297. doi: 10.1002/jcp.26898. Epub 2018 Aug 4.
J Cell Physiol. 2018.
PMID: 30078200
Review.
Understanding the importance of this subject is possible with the investigation of keratin defects in epidermolysis bullosa simplex (EBS). Nowadays, in addition to clinical criteria, new molecular diagnostic methods, such as next generation sequencing, can he …
Understanding the importance of this subject is possible with the investigation of keratin defects in epidermolysis bullosa …
Muscle-Related Plectinopathies.
Cells. 2021 Sep 19;10(9):2480. doi: 10.3390/cells10092480.
Cells. 2021.
PMID: 34572129
Free PMC article.
Review.
Mutations in the human plectin gene (PLEC) cause several rare diseases that are grouped under the term plectinopathies. The most common disorder is autosomal recessive disease epidermolysis bullosa simplex with muscular dystrophy (EBS-MD), which is characteri …
Mutations in the human plectin gene (PLEC) cause several rare diseases that are grouped under the term plectinopathies. The most common diso …
Malignant melanoma and epidermolysis bullosa simplex.
JAMA Dermatol. 2013 Oct;149(10):1148-9. doi: 10.1001/jamadermatol.2013.5628.
JAMA Dermatol. 2013.
PMID: 23966137
No abstract available.
Topical Diacerein Ointment for Epidermolysis Bullosa Simplex: A Review.
Skin Therapy Lett. 2019 May;24(3):7-9.
Skin Therapy Lett. 2019.
PMID: 31095348
Free article.
Review.
Epidermolysis bullosa (EB) is a group of rare mucocutaneous fragility disorders often presenting in infancy and early childhood with painful blistering of the skin and mucous membranes. ...Studies have shown that patients with generalized severe epidermolysis …
Epidermolysis bullosa (EB) is a group of rare mucocutaneous fragility disorders often presenting in infancy and early childhoo …
Epidermolysis bullosa simplex.
Semin Dermatol. 1993 Sep;12(3):173-90.
Semin Dermatol. 1993.
PMID: 7692916
Review.
Epidermolysis Bullosa Simplex (EBS) is a genetic disorder usually characterized by an autosomal dominant mode of transmission in which the skin blisters in response to trivial mechanical trauma. ...
Epidermolysis Bullosa Simplex (EBS) is a genetic disorder usually characterized by an autosomal dominant mode of transm …
Epidermolysis bullosa simplex with muscular dystrophy.
Dermatol Clin. 2010 Apr;28(2):245-55, viii. doi: 10.1016/j.det.2010.01.001.
Dermatol Clin. 2010.
PMID: 20447487
Review.
Epidermolysis bullosa simplex (EBS) is an inherited skin disorder characterized by separation of the epidermis from the underlying dermis, with the cleavage plane lying within the basal-cell layer of the epithelium. ...
Epidermolysis bullosa simplex (EBS) is an inherited skin disorder characterized by separation of the epidermis from the …
Plectin-related skin diseases.
J Dermatol Sci. 2015 Mar;77(3):139-45. doi: 10.1016/j.jdermsci.2014.11.005. Epub 2014 Nov 28.
J Dermatol Sci. 2015.
PMID: 25530118
Review.
Plectin has been characterized as a linker protein that is expressed in many cell types and is distinctive in various isoforms in the N-terminus and around the rod domain due to complicated alternative splicing of PLEC, the gene encoding plectin. Plectin deficiency causes autosom …
Plectin has been characterized as a linker protein that is expressed in many cell types and is distinctive in various isoforms in the N-term …
Diacerein 1% Ointment for the Treatment of Epidermolysis Bullosa Simplex: A Randomized, Controlled Trial.
J Drugs Dermatol. 2023 Jun 1;22(6):599-604. doi: 10.36849/JDD.7108.
J Drugs Dermatol. 2023.
PMID: 37276163
Clinical Trial.
BACKGROUND: In epidermolysis bullosa simplex (EBS), epithelial structural fragility results in blisters and erosions. ...Teng J, Paller AS, Bruckner AL, et al. Diacerein 1% ointment for the treatment of epidermolysis bullosa simplex: a ra …
BACKGROUND: In epidermolysis bullosa simplex (EBS), epithelial structural fragility results in blisters and erosions. . …
Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex.
Int J Mol Sci. 2021 Nov 18;22(22):12446. doi: 10.3390/ijms222212446.
Int J Mol Sci. 2021.
PMID: 34830328
Free PMC article.
Review.
Epidermolysis bullosa simplex (EBS) is a group of inherited keratinopathies that, in most cases, arise due to mutations in keratins and lead to intraepidermal ruptures. ...
Epidermolysis bullosa simplex (EBS) is a group of inherited keratinopathies that, in most cases, arise due to mutations …
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