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Quoted phrase not found in phrase index: "Junctional epidermolysis bullosa gravis of Herlitz"
Page 1
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 …
Quality of life in people with epidermolysis bullosa: a systematic review.
Togo CCG, Zidorio APC, Gonçalves VSS, Hubbard L, de Carvalho KMB, Dutra ES. Togo CCG, et al. Qual Life Res. 2020 Jul;29(7):1731-1745. doi: 10.1007/s11136-020-02495-5. Epub 2020 Apr 3. Qual Life Res. 2020. PMID: 32246433
PURPOSE: Individuals with epidermolysis bullosa (EB) present with various clinical manifestations of different severities that affect quality of life (QoL). ...More than half of the articles observed lower QoL in individuals with recessive dystrophic EB (RDEB) or …
PURPOSE: Individuals with epidermolysis bullosa (EB) present with various clinical manifestations of different severities that …
Clinical practice guidelines: Oral health care for children and adults living with epidermolysis bullosa.
Krämer S, Lucas J, Gamboa F, Peñarrocha Diago M, Peñarrocha Oltra D, Guzmán-Letelier M, Paul S, Molina G, Sepúlveda L, Araya I, Soto R, Arriagada C, Lucky AW, Mellerio JE, Cornwall R, Alsayer F, Schilke R, Antal MA, Castrillón F, Paredes C, Serrano MC, Clark V. Krämer S, et al. Spec Care Dentist. 2020 Nov;40 Suppl 1(Suppl 1):3-81. doi: 10.1111/scd.12511. Spec Care Dentist. 2020. PMID: 33202040 Free PMC article.
BACKGROUND: Inherited epidermolysis bullosa (EB) is a genetic disorder characterized by skin fragility and unique oral features. ...
BACKGROUND: Inherited epidermolysis bullosa (EB) is a genetic disorder characterized by skin fragility and unique oral feature …
(New) antenatal ultrasound signs of fetal junctional epidermolysis bullosa: A case report and systematic review of literature.
Tosto V, Herrero B, Illescas T, De la Calle Fernandez-Miranda M, Moreno-Sanz B, de Lucas R, Bartha JL, Antolin E. Tosto V, et al. Eur J Obstet Gynecol Reprod Biol. 2023 Nov;290:43-50. doi: 10.1016/j.ejogrb.2023.08.379. Epub 2023 Aug 24. Eur J Obstet Gynecol Reprod Biol. 2023. PMID: 37717401 Review.
Epidermolysis bullosa is a rare hereditary autosomal disease that is included in the heterogeneous group of genodermatosis. ...Prognosis is often poor, and death can occur in neonatal period due to severe sepsis. We present a case of fetal junctional epide
Epidermolysis bullosa is a rare hereditary autosomal disease that is included in the heterogeneous group of genodermatosis. ..
Clinical outcomes and molecular profile of patients with Carmi syndrome: A systematic review and evidence quality assessment.
Mylonas KS, Hayes M, Ko LN, Griggs CL, Kroshinsky D, Masiakos PT. Mylonas KS, et al. J Pediatr Surg. 2019 Jul;54(7):1351-1358. doi: 10.1016/j.jpedsurg.2018.05.019. Epub 2018 May 29. J Pediatr Surg. 2019. PMID: 29935895
PURPOSE: Carmi syndrome is a rare genetic disorder characterized by junctional epidermolysis bullosa (JEB) and pyloric atresia (PA). We reviewed the clinicopathologic and molecular features of patients with Carmi syndrome to identify predictors of clinical ou …
PURPOSE: Carmi syndrome is a rare genetic disorder characterized by junctional epidermolysis bullosa (JEB) and pyloric …
Donor skin allograft survival after bone marrow transplantation: Case report and systematic review of the literature☆.
Nunez-Villaveiran T, Feasel P, Keenan S, Aliotta R, Bosler D, Stearns D, Bergfeld W, Gurunluoglu R. Nunez-Villaveiran T, et al. J Plast Reconstr Aesthet Surg. 2019 Jan;72(1):23-34. doi: 10.1016/j.bjps.2018.05.018. Epub 2018 Jun 9. J Plast Reconstr Aesthet Surg. 2019. PMID: 29983364
Skin allografts were used to treat graft-versus-host-disease, Herlitz junctional epidermolysis bullosa, and to test tolerance before a kidney transplantation from the same donor. ...
Skin allografts were used to treat graft-versus-host-disease, Herlitz junctional epidermolysis bullosa, and to t …