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

Year Number of Results
1981 1
1983 1
1985 1
1988 1
1990 1
1991 3
1992 3
1993 2
1994 2
1995 5
1996 4
1997 5
1998 4
1999 9
2000 2
2001 2
2002 1
2003 2
2004 4
2005 3
2006 6
2007 5
2008 7
2009 5
2010 5
2011 6
2012 7
2013 1
2014 6
2015 9
2016 5
2017 9
2018 8
2019 8
2020 10
2021 7
2022 10
2023 5
2024 1

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157 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.
We reviewed EB based on the following subheadings: epidemiology, diagnosis, therapy, prognosis, and clinical prediction guidelines. EB is due to mutation in a number of genes, some types are autosomal dominant while others are autosomal recessive. ...EB presents in …
We reviewed EB based on the following subheadings: epidemiology, diagnosis, therapy, prognosis, and clinical prediction guidel …
Epidermolysis bullosa. II. Type VII collagen mutations and phenotype-genotype correlations in the dystrophic subtypes.
Varki R, Sadowski S, Uitto J, Pfendner E. Varki R, et al. J Med Genet. 2007 Mar;44(3):181-92. doi: 10.1136/jmg.2006.045302. Epub 2006 Sep 13. J Med Genet. 2007. PMID: 16971478 Free PMC article.
DISCUSSION: Examination of the mutation database suggested phenotype-genotype correlations, contributing to the improved subclassification of DEB with prognostic implications. The mutation information also forms the basis for accurate genetic counselling and prenatal diagn …
DISCUSSION: Examination of the mutation database suggested phenotype-genotype correlations, contributing to the improved subclassification o …
Updated review of genetic reticulate pigmentary disorders.
Zhang J, Li M, Yao Z. Zhang J, et al. Br J Dermatol. 2017 Oct;177(4):945-959. doi: 10.1111/bjd.15575. Epub 2017 Sep 27. Br J Dermatol. 2017. PMID: 28407215 Review.
Although each condition possesses unique phenotypic characteristics and the prognosis for each is somewhat different, there is a large degree of overlap between the disorders and therefore they are difficult to differentiate in the clinical setting. ...
Although each condition possesses unique phenotypic characteristics and the prognosis for each is somewhat different, there is a larg …
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.
From the sample results, it can be concluded that the clinical manifestation of EB patients is highly variable and very different in prognosis. Oral health deeply influences the quality of life of EB patients. ...
From the sample results, it can be concluded that the clinical manifestation of EB patients is highly variable and very different in prog …
Epidermolysis bullosa with congenital absence of skin: Review of the literature.
Martinez-Moreno A, Ocampo-Candiani J, Alba-Rojas E. Martinez-Moreno A, et al. Pediatr Dermatol. 2020 Sep;37(5):821-826. doi: 10.1111/pde.14245. Epub 2020 Jul 20. Pediatr Dermatol. 2020. PMID: 32686866 Review.
Extracutaneous features were present in 29 patients; with pyloric atresia and ear malformations being the most common. The prognosis varied based on the subtype of EB and the presence of additional comorbidities; 50% of the patients with junctional EB with pyloric atresia …
Extracutaneous features were present in 29 patients; with pyloric atresia and ear malformations being the most common. The prognosis …
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.
In contrast to other variants of dystrophic epidermolysis bullosa, the inverse type has a more favorable prognosis. We present a case of a 45-year-old female patient with dystrophic epidermolysis bullosa inversa, diagnosed in adulthood based on typical clinical presentatio …
In contrast to other variants of dystrophic epidermolysis bullosa, the inverse type has a more favorable prognosis. We present a case …
Phenotype and genotype correlation of inherited epidermolysis bullosa in Indonesia.
Arline Diana I, Tan EC, Gondokaryono SP, Koh MJ, Dwiyana RF, Rahardja JI, Yogya Y, Rafi'ee K, Suwarsa O. Arline Diana I, et al. Australas J Dermatol. 2023 Nov;64(4):e327-e332. doi: 10.1111/ajd.14121. Epub 2023 Jul 14. Australas J Dermatol. 2023. PMID: 37452458
This demonstrated the importance of early genetic testing for accurate diagnosis, prognostication, management and genetic counselling....
This demonstrated the importance of early genetic testing for accurate diagnosis, prognostication, management and genetic counselling …
Transcriptome-Guided Drug Repurposing for Aggressive SCCs.
Zauner R, Wimmer M, Dorfer S, Ablinger M, Koller U, Piñón Hofbauer J, Guttmann-Gruber C, Bauer JW, Wally V. Zauner R, et al. Int J Mol Sci. 2022 Jan 17;23(2):1007. doi: 10.3390/ijms23021007. Int J Mol Sci. 2022. PMID: 35055192 Free PMC article.
However, against the background of pre-existing risk factors such as immunosuppression upon organ transplantation, or conditions such as recessive dystrophic epidermolysis bullosa (RDEB), SCCs arise more frequently and follow a particularly aggressive course. Notably, such …
However, against the background of pre-existing risk factors such as immunosuppression upon organ transplantation, or conditions such as rec …
ABCB5+ mesenchymal stromal cells facilitate complete and durable wound closure in recessive dystrophic epidermolysis bullosa.
Dieter K, Niebergall-Roth E, Daniele C, Fluhr S, Frank NY, Ganss C, Kiritsi D, McGrath JA, Tolar J, Frank MH, Kluth MA. Dieter K, et al. Cytotherapy. 2023 Jul;25(7):782-788. doi: 10.1016/j.jcyt.2023.01.015. Epub 2023 Mar 1. Cytotherapy. 2023. PMID: 36868990 Free article.
METHODS: Documentary photographs of the affected body regions taken on days 0, 17, 35 and at 12 weeks were evaluated regarding proportion, temporal course and durability of wound closure as well as development of new wounds. ...
METHODS: Documentary photographs of the affected body regions taken on days 0, 17, 35 and at 12 weeks were evaluated regarding proportion, t …
Epidermolysis bullosa pruriginosa: a systematic review exploring genotype-phenotype correlation.
Kim WB, Alavi A, Walsh S, Kim S, Pope E. Kim WB, et al. Am J Clin Dermatol. 2015 Apr;16(2):81-7. doi: 10.1007/s40257-015-0119-7. Am J Clin Dermatol. 2015. PMID: 25690953 Review.
In the case of potential diagnostic challenge, assessment for presence of common clinical findings as well as molecular testing may facilitate correct identification and prognostication....
In the case of potential diagnostic challenge, assessment for presence of common clinical findings as well as molecular testing may facilita …
157 results