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

Year Number of Results
1935 1
1945 1
1946 2
1952 1
1953 2
1954 1
1957 2
1963 2
1964 1
1965 1
1966 1
1969 1
1970 1
1971 3
1972 1
1973 1
1974 3
1975 2
1976 1
1977 2
1979 3
1980 5
1981 3
1982 6
1983 7
1984 6
1985 9
1986 11
1987 5
1988 12
1989 12
1990 14
1991 16
1992 24
1993 31
1994 31
1995 21
1996 24
1997 25
1998 20
1999 29
2000 22
2001 18
2002 21
2003 28
2004 33
2005 25
2006 24
2007 17
2008 17
2009 25
2010 41
2011 34
2012 32
2013 28
2014 39
2015 43
2016 34
2017 39
2018 29
2019 35
2020 44
2021 58
2022 57
2023 51
2024 25

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1,058 results

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Page 1
Epidermolysis bullosa simplex.
Sprecher E. Sprecher E. Dermatol Clin. 2010 Jan;28(1):23-32. doi: 10.1016/j.det.2009.10.003. Dermatol Clin. 2010. PMID: 19945613 Review.
The prevalence of epidermolysis bullosa simplex (EBS) is estimated to be approximately 6 to 30 per 1 million live births. ...
The prevalence of epidermolysis bullosa simplex (EBS) is estimated to be approximately 6 to 30 per 1 million live birth …
Keratins and epidermolysis bullosa simplex.
Khani P, Ghazi F, Zekri A, Nasri F, Behrangi E, Aghdam AM, Mirzaei H. Khani P, et al. J Cell Physiol. 2018 Jan;234(1):289-297. doi: 10.1002/jcp.26898. Epub 2018 Aug 4. J Cell Physiol. 2018. PMID: 30078200 Review.
Understanding the importance of this subject is possible with the investigation of keratin defects in epidermolysis bullosa simplex (EBS). Nowadays, in addition to clinical criteria, new molecular diagnostic methods, such as next generation sequencing, can he …
Understanding the importance of this subject is possible with the investigation of keratin defects in epidermolysis bullosa
Epidermolysis bullosa simplex.
Coulombe PA, Fuchs E. Coulombe PA, et al. Semin Dermatol. 1993 Sep;12(3):173-90. Semin Dermatol. 1993. PMID: 7692916 Review.
Epidermolysis Bullosa Simplex (EBS) is a genetic disorder usually characterized by an autosomal dominant mode of transmission in which the skin blisters in response to trivial mechanical trauma. ...
Epidermolysis Bullosa Simplex (EBS) is a genetic disorder usually characterized by an autosomal dominant mode of transm
Topical Diacerein Ointment for Epidermolysis Bullosa Simplex: A Review.
Limmer AL, Nwannunu CE, Shah R, Coleman K, Patel RR, Mui UN, Tyring SK. Limmer AL, et al. Skin Therapy Lett. 2019 May;24(3):7-9. Skin Therapy Lett. 2019. PMID: 31095348 Free article. Review.
Epidermolysis bullosa (EB) is a group of rare mucocutaneous fragility disorders often presenting in infancy and early childhood with painful blistering of the skin and mucous membranes. ...Studies have shown that patients with generalized severe epidermolysis
Epidermolysis bullosa (EB) is a group of rare mucocutaneous fragility disorders often presenting in infancy and early childhoo
Epidermolysis bullosa simplex with muscular dystrophy.
Chiavérini C, Charlesworth A, Meneguzzi G, Lacour JP, Ortonne JP. Chiavérini C, et al. Dermatol Clin. 2010 Apr;28(2):245-55, viii. doi: 10.1016/j.det.2010.01.001. Dermatol Clin. 2010. PMID: 20447487 Review.
Epidermolysis bullosa simplex (EBS) is an inherited skin disorder characterized by separation of the epidermis from the underlying dermis, with the cleavage plane lying within the basal-cell layer of the epithelium. ...
Epidermolysis bullosa simplex (EBS) is an inherited skin disorder characterized by separation of the epidermis from the
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. ...
Epidermolysis bullosa simplex (EBS) is a group of inherited keratinopathies that, in most cases, arise due to mutations
Epidermolysis bullosa simplex due to bi-allelic DST mutations: Case series and review of the literature.
Ganani D, Malovitski K, Sarig O, Gat A, Sprecher E, Samuelov L. Ganani D, et al. Pediatr Dermatol. 2021 Mar;38(2):436-441. doi: 10.1111/pde.14477. Epub 2021 Jan 20. Pediatr Dermatol. 2021. PMID: 33471381 Review.
BACKGROUND: Epidermolysis bullosa simplex (EBS) is a heterogeneous group of inherited disorders characterized by skin fragility due to intraepidermal separation. ...
BACKGROUND: Epidermolysis bullosa simplex (EBS) is a heterogeneous group of inherited disorders characterized by skin f …
Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility.
Coulombe PA, Kerns ML, Fuchs E. Coulombe PA, et al. J Clin Invest. 2009 Jul;119(7):1784-93. doi: 10.1172/JCI38177. Epub 2009 Jul 1. J Clin Invest. 2009. PMID: 19587453 Free PMC article. Review.
Epidermolysis bullosa (EB) simplex is a rare genetic condition typified by superficial bullous lesions that result from frictional trauma to the skin. ...Here we review how laboratory investigations centered on keratin biology have deepened our understanding
Epidermolysis bullosa (EB) simplex is a rare genetic condition typified by superficial bullous lesions that result from
1,058 results