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Quoted phrase not found in phrase index: "Epidermolysis bullosa simplex 1C, localized"
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.
We performed a review of existing literature in the English language on EB via PubMed Clinical Queries, using key words such as "epidermolysis bullosa", "congenital" and "children". We reviewed EB based on the following subheadings: epidemiology, diagnosis, therapy, …
We performed a review of existing literature in the English language on EB via PubMed Clinical Queries, using key words such as "epidermo …
Epidermolysis bullosa and cancer.
Mallipeddi R. Mallipeddi R. Clin Exp Dermatol. 2002 Nov;27(8):616-23. doi: 10.1046/j.1365-2230.2002.01130.x. Clin Exp Dermatol. 2002. PMID: 12472531 Review.
Epidermolysis bullosa (EB) encompasses a group of inherited blistering skin disorders classified into three main subtypes of simplex, junctional and dystrophic. ...The reason why dystrophic EB patients readily develop SCC with such a poor prognosis rem …
Epidermolysis bullosa (EB) encompasses a group of inherited blistering skin disorders classified into three main subtypes of …
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. There are four major classical heritable EB types, due to mutations in as many as 20 d …
Epidermolysis bullosa (EB) is a group of skin disorders with skin fragility characterized by blistering from minimal mechanica …
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
BACKGROUND: Inherited epidermolysis bullosa (EB) is a group of genodermatoses with considerable clinical and genetic heterogeneity. ...This demonstrated the importance of early genetic testing for accurate diagnosis, prognostication, management and genetic co …
BACKGROUND: Inherited epidermolysis bullosa (EB) is a group of genodermatoses with considerable clinical and genetic heterogen …
Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex.
Evtushenko NA, Beilin AK, Kosykh AV, Vorotelyak EA, Gurskaya NG. Evtushenko NA, et al. 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. ...ER stress also leads to the release of proinflammatory danger-associated molecular patt …
Epidermolysis bullosa simplex (EBS) is a group of inherited keratinopathies that, in most cases, arise due to mutations …
Lethal acantholytic epidermolysis bullosa.
McGrath JA, Bolling MC, Jonkman MF. McGrath JA, et al. Dermatol Clin. 2010 Jan;28(1):131-5. doi: 10.1016/j.det.2009.10.015. Dermatol Clin. 2010. PMID: 19945626 Review.
Lethal acantholytic epidermolysis bullosa (LAEB) is an autosomal recessive disorder caused by mutations in the gene encoding the desmosomal protein, desmoplakin (DSP). It is recognized as a distinct form of suprabasal epidermolysis bullosa simplex …
Lethal acantholytic epidermolysis bullosa (LAEB) is an autosomal recessive disorder caused by mutations in the gene encoding t …
Perioperative Management of Congenital Epidermolysis Bullosa.
Yukawa H, Makino T, Hayashi K, Date H, Honda N, Anami Y. Yukawa H, et al. Ann Thorac Surg. 2023 Jul;116(1):e1-e4. doi: 10.1016/j.athoracsur.2022.06.045. Epub 2022 Jul 19. Ann Thorac Surg. 2023. PMID: 35863401
We present the case of a patient with congenital epidermolysis bullosa simplex who underwent thoracoscopic surgery for pneumothorax. ...General anesthesia and skin management are critical in thoracoscopic surgery for patients with congenital epidermolysis …
We present the case of a patient with congenital epidermolysis bullosa simplex who underwent thoracoscopic surgery for …
Progress in epidermolysis bullosa: genetic classification and clinical implications.
Uitto J, Richard G. Uitto J, et al. Am J Med Genet C Semin Med Genet. 2004 Nov 15;131C(1):61-74. doi: 10.1002/ajmg.c.30035. Am J Med Genet C Semin Med Genet. 2004. PMID: 15468152 Review.
Epidermolysis bullosa (EB), a heterogenous group of genodermatoses, is characterized by fragility and blistering of the skin associated with extracutaneous manifestations. ...Elucidation of mutations in different forms of EB has direct translational applications for …
Epidermolysis bullosa (EB), a heterogenous group of genodermatoses, is characterized by fragility and blistering of the skin a …
Incidence of Vesicobullous and Erosive Disorders of Neonates: Where and How Much to Worry?
Goyal T, Varshney A, Bakshi SK. Goyal T, et al. Indian J Pediatr. 2021 Jun;88(6):574-578. doi: 10.1007/s12098-011-0592-9. Epub 2011 Oct 25. Indian J Pediatr. 2021. PMID: 22037857
Of the transient skin lesions, erythema toxicum neonatorum was commonest of all, being seen in 18 neonates (41%), followed by four cases (9%) of miliaria crystallina, three cases of neonatal acne (6.8%) and two cases of sucking blisters (4.5%) and one case each of transient neona …
Of the transient skin lesions, erythema toxicum neonatorum was commonest of all, being seen in 18 neonates (41%), followed by four cases (9% …
120 results