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Year Number of Results
1900 1
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1910 1
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1913 2
1914 2
1915 1
1916 1
1917 1
1919 1
1920 2
1921 2
1922 1
1923 2
1925 2
1927 1
1928 2
1929 2
1930 2
1932 1
1933 2
1934 1
1935 1
1937 1
1938 2
1939 1
1942 1
1943 2
1945 11
1946 23
1947 14
1948 26
1949 17
1950 22
1951 20
1952 26
1953 27
1954 17
1955 18
1956 24
1957 18
1958 10
1959 18
1960 16
1961 17
1962 20
1963 29
1964 31
1965 24
1966 29
1967 31
1968 42
1969 44
1970 35
1971 40
1972 37
1973 39
1974 46
1975 40
1976 34
1977 42
1978 42
1979 42
1980 47
1981 52
1982 56
1983 66
1984 67
1985 72
1986 100
1987 96
1988 132
1989 90
1990 97
1991 93
1992 112
1993 134
1994 138
1995 126
1996 129
1997 138
1998 148
1999 148
2000 136
2001 121
2002 108
2003 140
2004 136
2005 138
2006 139
2007 145
2008 162
2009 160
2010 290
2011 242
2012 249
2013 257
2014 258
2015 288
2016 288
2017 257
2018 289
2019 303
2020 332
2021 366
2022 377
2023 332
2024 323
2025 266

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8,448 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. ...There are four main types: epidermolysis bullosa simplex, dystrophic epiderm …
Epidermolysis bullosa (EB) is a group of rare congenital genetic conditions that result in painful blistering of the skin and mucous …
Epidermolysis Bullosa.
Khanna D, Bardhan A. Khanna D, et al. 2024 Jan 11. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. 2024 Jan 11. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. PMID: 38261681 Free Books & Documents.
Dystrophic Epidermolysis Bullosa (DEB) represents around 25% of all epidermolysis bullosa cases and may be autosomal dominant or recessive. ...Kindler Epidermolysis Bullosa (KEB) is the rarest of the 4 major epidermolysis bullosa types inherited in an …
Dystrophic Epidermolysis Bullosa (DEB) represents around 25% of all epidermolysis bullosa cases and may be autosomal dominant …
Epidermolysis bullosa in animals: a review.
Medeiros GX, Riet-Correa F. Medeiros GX, et al. Vet Dermatol. 2015 Feb;26(1):3-13, e1-2. doi: 10.1111/vde.12176. Epub 2014 Oct 30. Vet Dermatol. 2015. PMID: 25354580 Review.
Epidermolysis bullosa (EB) is a hereditary mechanobullous disease of animals and humans, characterized by an extreme fragility of the skin and mucous membranes. ...Based on the ultrastructural levels of tissue separation, EB is divided into the following three broad catego …
Epidermolysis bullosa (EB) is a hereditary mechanobullous disease of animals and humans, characterized by an extreme fragility of the …
The incidence of concha bullosa: a retrospective radiologic study.
Kar M, Altıntaş M. Kar M, et al. Eur Arch Otorhinolaryngol. 2023 Feb;280(2):731-735. doi: 10.1007/s00405-022-07552-y. Epub 2022 Jul 23. Eur Arch Otorhinolaryngol. 2023. PMID: 35870004
Of middle types of concha bullosa, lamellar type concha bullosa was detected in 575 (41.01%) patients, bulbous type in 363 (25.89%), and extensive type in 464 (33.09%). Of the cases with lamellar type middle concha bullosa, it was found that 130 (22.60%) had …
Of middle types of concha bullosa, lamellar type concha bullosa was detected in 575 (41.01%) patients, bulbous type in 363 (25 …
Folliculitis decalvans and dystrophic epidermolysis bullosa: a significant association.
Matard B, Bourrat E, Cavalié M, Chiaverini C, Reygagne P. Matard B, et al. Br J Dermatol. 2022 Dec;187(6):1026-1028. doi: 10.1111/bjd.21796. Epub 2022 Sep 6. Br J Dermatol. 2022. PMID: 35904062
This work reports 30 cases of folliculitis decalvans (FD) in patients with dystrophic epidermolysis bullosa (DEB) among a cohort of 125 DEB patients seen between 2010 and 2021 in 2 French expert centers for the management of inherited epidermolysis bullosa. ...Scarr …
This work reports 30 cases of folliculitis decalvans (FD) in patients with dystrophic epidermolysis bullosa (DEB) among a cohort of 1 …
Epidermolysis bullosa dystrophica pretibialis - Clinical snapshot and management of a rare orphan disease.
Will LM, Reichrath J, Vogt T. Will LM, et al. J Dtsch Dermatol Ges. 2021 Jul;19(7):983-986. doi: 10.1111/ddg.14446. Epub 2021 May 5. J Dtsch Dermatol Ges. 2021. PMID: 33951274 Review.
If blistering occurs in childhood, the possibility of hereditary epidermolysis bullosa should be considered even if the symptoms are mild. Besides clinical and histological examination, molecular genetic screening is diagnostically relevant. ...
If blistering occurs in childhood, the possibility of hereditary epidermolysis bullosa should be considered even if the symptoms are …
[Epidermolysis bullosa].
Firing C, Bygum A. Firing C, et al. Ugeskr Laeger. 2017 Nov 20;179(47):V07170568. Ugeskr Laeger. 2017. PMID: 29208193 Free article. Review. Danish.
Epidermolysis bullosa (EB) is a rare genodermatosis. A new classification system is presented, distinguishing the subtypes of EB, and this system is based on the phenotype, mode of inheritance, ultrastructure, immunofluorescence findings, and specific mutation(s) present. …
Epidermolysis bullosa (EB) is a rare genodermatosis. A new classification system is presented, distinguishing the subtypes of EB, and …
Epidermolysis bullosa: a case study in transport, treatment, and care.
Price-Douglas W, Diehl-Svrjcek B. Price-Douglas W, et al. Adv Neonatal Care. 2007 Dec;7(6):289-94. doi: 10.1097/01.ANC.0000304967.46708.ea. Adv Neonatal Care. 2007. PMID: 18097210 Review.
A neonate presented with epidermolysis bullosa and provided an opportunity for learning about this condition and various dermatologic resources, primarily DermAtlas. ...The resources available in the neonatal community, primarily DermAtlas, for the identification of epider …
A neonate presented with epidermolysis bullosa and provided an opportunity for learning about this condition and various dermatologic …
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. ...Here, we present a case of dystrophic epidermolysis bullosa in a 26-year-old male. Keywords: blister; dystrophic epidermolysis bullosa …
Dystrophic epidermolysis bullosa is a type of epidermolysis bullosa caused by mutation in type VII collagen, COL7A1. ...Here, …
Epidermolysis bullosa.
[No authors listed] [No authors listed] Nat Rev Dis Primers. 2020 Sep 24;6(1):79. doi: 10.1038/s41572-020-00220-7. Nat Rev Dis Primers. 2020. PMID: 32973138 No abstract available.
8,448 results