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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
Gene Therapy for Epidermolysis Bullosa.
Marinkovich MP, Tang JY. Marinkovich MP, et al. J Invest Dermatol. 2019 Jun;139(6):1221-1226. doi: 10.1016/j.jid.2018.11.036. Epub 2019 May 5. J Invest Dermatol. 2019. PMID: 31068252 Free article. Review.
Epidermolysis bullosa is a family of diseases characterized by blistering and fragility of the skin in response to mechanical trauma. Advances in our understanding of epidermolysis bullosa pathophysiology have provided the necessary foundation for the
Epidermolysis bullosa is a family of diseases characterized by blistering and fragility of the skin in response to mechanical
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 …
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
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
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
Inherited epidermolysis bullosa and squamous cell carcinoma: a systematic review of 117 cases.
Montaudié H, Chiaverini C, Sbidian E, Charlesworth A, Lacour JP. Montaudié H, et al. Orphanet J Rare Dis. 2016 Aug 20;11(1):117. doi: 10.1186/s13023-016-0489-9. Orphanet J Rare Dis. 2016. PMID: 27544590 Free PMC article. Review.
BACKGROUND: Inherited epidermolysis bullosa (EB) comprises a highly heterogeneous group of rare diseases characterized by exacerbated skin and/or mucosal fragility and blister formation after minor mechanical trauma. ...Interestingly, the cSCC duration, before its d …
BACKGROUND: Inherited epidermolysis bullosa (EB) comprises a highly heterogeneous group of rare diseases characterized by exac …
Neonatal junctional epidermolysis bullosa: treatment conundrums and ethical decision making.
Yang CS, Kroshinksy D, Cummings BM. Yang CS, et al. Am J Clin Dermatol. 2014 Oct;15(5):445-50. doi: 10.1007/s40257-014-0091-7. Am J Clin Dermatol. 2014. PMID: 25117154 Review.
Junctional epidermolysis bullosa (JEB), generalized severe (previously called JEB, Herlitz-type) has an extremely poor prognosis, with a mean age of death at 5 months old and most dead before age 3 years. ...We review the literature as well as discuss the eth
Junctional epidermolysis bullosa (JEB), generalized severe (previously called JEB, Herlitz-type) has an extremely poor
Inherited epidermolysis bullosa: epidemiology and patient care in Slovenia with a review of the updated classification.
Štublar A, Dragoš V, Dolenc-Voljč M. Štublar A, et al. Acta Dermatovenerol Alp Pannonica Adriat. 2021 Jun;30(2):63-66. Acta Dermatovenerol Alp Pannonica Adriat. 2021. PMID: 34169701 Free article. Review.
INTRODUCTION: Inherited epidermolysis bullosa (EB) is a heterogeneous group of rare genetic skin disorders characterized by fragility of the skin and mucous membranes. The prevalence of all types of EB is estimated at approximately 11 per million, based on recent da …
INTRODUCTION: Inherited epidermolysis bullosa (EB) is a heterogeneous group of rare genetic skin disorders characterized by fr …
139 results