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Year Number of Results
1983 1
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139 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. ...Over 30 subtypes are recognized, grouped into four major categories, base …
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 …
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 fragilit …
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 junct …
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 varian …
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. ...Mild (or severe) disease early in life may be characterized by the opposite phenotype in a …
Non-Herlitz junctional epidermolysis bullosa (nH JEB) is characterized by generalized blisters that predominate …
Autoimmunity against laminin 332.
Patzelt S, Schmidt E. Patzelt S, et al. Front Immunol. 2023 Aug 10;14:1250115. doi: 10.3389/fimmu.2023.1250115. eCollection 2023. Front Immunol. 2023. PMID: 37638011 Free PMC article. Review.
The importance of laminin 332 for the structural integrity of the BMZ is demonstrated by mutations in any of the three genes encoding for its three chains causing variants of junctional epidermolysis bullosa. Autoimmunity against laminin 332 is observed in mu …
The importance of laminin 332 for the structural integrity of the BMZ is demonstrated by mutations in any of the three genes encoding for it …
Birch Bark Extract: A Review in Epidermolysis Bullosa.
Heo YA. Heo YA. Drugs. 2023 Sep;83(14):1309-1314. doi: 10.1007/s40265-023-01935-z. Epub 2023 Sep 2. Drugs. 2023. PMID: 37658982 Review.
Birch bark extract (Filsuvez(); also known as the developmental name Oleogel-S10), a topical gel consisting of 10% dry birch bark extract and 90% sunflower oil, is the first therapy approved in the EU and UK for the treatment of partial thickness wounds associated with dystrophic …
Birch bark extract (Filsuvez(); also known as the developmental name Oleogel-S10), a topical gel consisting of 10% dry birch bark extract an …
Laryngo-onycho-cutaneous syndrome.
Cohn HI, Murrell DF. Cohn HI, et al. Dermatol Clin. 2010 Jan;28(1):89-92. doi: 10.1016/j.det.2009.10.010. Dermatol Clin. 2010. PMID: 19945620 Review.
Laryngo-onycho-cutaneous (LOC) syndrome was reclassified as a subtype of junctional epidermolysis bullosa (JEB) based on clinical features similar to JEB and its association, in the majority of patients from the Punjab, with a unique mutation affecting the N …
Laryngo-onycho-cutaneous (LOC) syndrome was reclassified as a subtype of junctional epidermolysis bullosa (JEB) based o …
139 results