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

Year Number of Results
1934 1
1937 1
1945 2
1946 2
1947 1
1948 4
1949 3
1950 7
1951 4
1952 6
1953 6
1954 3
1955 3
1956 8
1957 2
1958 2
1959 2
1960 1
1961 4
1962 3
1963 5
1964 7
1965 6
1966 5
1967 4
1968 10
1969 10
1970 4
1971 7
1972 9
1973 7
1974 7
1975 14
1976 8
1977 16
1978 8
1979 14
1980 9
1981 11
1982 19
1983 25
1984 26
1985 24
1986 25
1987 18
1988 41
1989 29
1990 32
1991 30
1992 42
1993 49
1994 39
1995 36
1996 36
1997 37
1998 40
1999 50
2000 29
2001 27
2002 32
2003 40
2004 41
2005 36
2006 44
2007 35
2008 53
2009 55
2010 76
2011 79
2012 68
2013 79
2014 88
2015 90
2016 81
2017 69
2018 99
2019 104
2020 121
2021 131
2022 147
2023 118
2024 63

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2,391 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.
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
In vivo topical gene therapy for recessive dystrophic epidermolysis bullosa: a phase 1 and 2 trial.
Gurevich I, Agarwal P, Zhang P, Dolorito JA, Oliver S, Liu H, Reitze N, Sarma N, Bagci IS, Sridhar K, Kakarla V, Yenamandra VK, O'Malley M, Prisco M, Tufa SF, Keene DR, South AP, Krishnan SM, Marinkovich MP. Gurevich I, et al. Nat Med. 2022 Apr;28(4):780-788. doi: 10.1038/s41591-022-01737-y. Epub 2022 Mar 28. Nat Med. 2022. PMID: 35347281 Free PMC article. Clinical Trial.
Recessive dystrophic epidermolysis bullosa (RDEB) is a lifelong genodermatosis associated with blistering, wounding, and scarring caused by mutations in COL7A1, the gene encoding the anchoring fibril component, collagen VII (C7). ...
Recessive dystrophic epidermolysis bullosa (RDEB) is a lifelong genodermatosis associated with blistering, wounding, an …
Herpes simplex virus gene therapy for dystrophic epidermolysis bullosa (DEB).
Epstein AL, Haag-Molkenteller C. Epstein AL, et al. Cell. 2023 Aug 17;186(17):3523-3523.e1. doi: 10.1016/j.cell.2023.07.031. Cell. 2023. PMID: 37595560
The FDA has recently approved Krystal biotech's beremagene geperpavec (B-VEC, Vyjuvek) to treat the wounds of dystrophic epidermolysis bullosa (DEB) patients. This represents a giant step, not only toward the treatment of this devastating disease, but also fo …
The FDA has recently approved Krystal biotech's beremagene geperpavec (B-VEC, Vyjuvek) to treat the wounds of dystrophic epidermol
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.
Dystrophic epidermolysis bullosa inversa is a very rare subtype of inherited dystrophic epidermolysis bullosa with a unique clinical manifestation. ...We present a case of a 45-year-old female patient with dystrophic epidermolys
Dystrophic epidermolysis bullosa inversa is a very rare subtype of inherited dystrophic epidermolysis
Dystrophic Epidermolysis Bullosa.
Yadav RS, Jayswal A, Shrestha S, Gupta SK, Paudel U. Yadav RS, et al. JNMA J Nepal Med Assoc. 2018 Sep-Oct;56(213):879-882. doi: 10.31729/jnma.3791. JNMA J Nepal Med Assoc. 2018. PMID: 31065125 Free PMC article.
Dystrophic epidermolysis bullosa is a type of epidermolysis bullosa caused by mutation in type VII collagen, COL7A1. ...Preventing possible skin and mucosal injury in patients requiring surgery should be worked on. Here, we present a case of
Dystrophic epidermolysis bullosa is a type of epidermolysis bullosa caused by mutation in type VII collag
Dystrophic epidermolysis bullosa.
Das BB, Sahoo S. Das BB, et al. J Perinatol. 2004 Jan;24(1):41-7. doi: 10.1038/sj.jp.7211019. J Perinatol. 2004. PMID: 14726937 Review. No abstract available.
The potential of gene therapy for recessive dystrophic epidermolysis bullosa.
Subramaniam KS, Antoniou MN, McGrath JA, Lwin SM. Subramaniam KS, et al. Br J Dermatol. 2022 Apr;186(4):609-619. doi: 10.1111/bjd.20910. Epub 2022 Apr 1. Br J Dermatol. 2022. PMID: 34862606 Review.
Epidermolysis bullosa (EB) encompasses a heterogeneous group of inherited skin fragility disorders, with mutations in genes encoding the basement membrane zone (BMZ) proteins that normally ensure dermal-epidermal integrity. ...Furthermore, the past decade has witnes
Epidermolysis bullosa (EB) encompasses a heterogeneous group of inherited skin fragility disorders, with mutations in genes en
Inpatient management of children with recessive dystrophic epidermolysis bullosa: A review.
Li AW, Prindaville B, Bateman ST, Gibson TE, Wiss K. Li AW, et al. Pediatr Dermatol. 2017 Nov;34(6):647-655. doi: 10.1111/pde.13276. Epub 2017 Sep 25. Pediatr Dermatol. 2017. PMID: 28944966 Review.
Recessive dystrophic epidermolysis bullosa is a disorder marked by skin and mucosal blistering after minimal trauma. ...To minimize discomfort for patients with recessive dystrophic epidermolysis bullosa during the hospital stay, inpatien …
Recessive dystrophic epidermolysis bullosa is a disorder marked by skin and mucosal blistering after minimal trauma. .. …
2,391 results