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

Year Number of Results
1963 1
1974 1
1979 1
1983 1
1984 2
1985 1
1987 2
1988 4
1989 1
1990 2
1991 2
1992 4
1993 6
1994 6
1995 6
1996 5
1997 2
1998 3
1999 8
2000 2
2001 1
2002 2
2003 2
2004 8
2005 4
2006 1
2007 4
2008 7
2009 3
2010 15
2011 5
2012 2
2013 5
2014 6
2015 11
2016 6
2017 8
2018 6
2019 7
2020 10
2021 11
2022 9
2023 4
2024 5

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192 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, d …
Epidermolysis bullosa (EB) is a group of rare congenital genetic conditions that result in painful blistering of the skin and …
Beremagene Geperpavec: First Approval.
Dhillon S. Dhillon S. Drugs. 2023 Aug;83(12):1131-1135. doi: 10.1007/s40265-023-01921-5. Drugs. 2023. PMID: 37432558 Review.
Beremagene geperpavec-svdt (VYJUVEK) is a topically applied, redosable, live, replication defective herpes simplex virus-1 (HSV-1) vector -based gene therapy that is being developed by Krystal Biotech to deliver functional human collagen type VII alpha 1 chain (COL7A1) genes in p …
Beremagene geperpavec-svdt (VYJUVEK) is a topically applied, redosable, live, replication defective herpes simplex virus-1 (HSV-1) vector -b …
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 …
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 junction …
Muscle-Related Plectinopathies.
Zrelski MM, Kustermann M, Winter L. Zrelski MM, et al. Cells. 2021 Sep 19;10(9):2480. doi: 10.3390/cells10092480. Cells. 2021. PMID: 34572129 Free PMC article. Review.
Mutations in the human plectin gene (PLEC) cause several rare diseases that are grouped under the term plectinopathies. The most common disorder is autosomal recessive disease epidermolysis bullosa simplex with muscular dystrophy (EBS-MD), which is characteri …
Mutations in the human plectin gene (PLEC) cause several rare diseases that are grouped under the term plectinopathies. The most common diso …
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 …
Recessive dystrophic epidermolysis bullosa is a disorder marked by skin and mucosal blistering after minimal tra …
Type VII Collagen Replacement Therapy in Recessive Dystrophic Epidermolysis Bullosa-How Much, How Often?
South AP, Uitto J. South AP, et al. J Invest Dermatol. 2016 Jun;136(6):1079-1081. doi: 10.1016/j.jid.2016.03.005. J Invest Dermatol. 2016. PMID: 27212645 Free article. Review.
Recessive dystrophic epidermolysis bullosa is a devastating blistering disease caused by mutations in the COL7A1 gene, which encodes type VII collagen, the major component of anchoring fibrils. The anchoring fibrils in patients with recessive …
Recessive dystrophic epidermolysis bullosa is a devastating blistering disease caused by mutations in the COL7A1 …
Impaired Wound Healing, Fibrosis, and Cancer: The Paradigm of Recessive Dystrophic Epidermolysis Bullosa.
Tartaglia G, Cao Q, Padron ZM, South AP. Tartaglia G, et al. Int J Mol Sci. 2021 May 12;22(10):5104. doi: 10.3390/ijms22105104. Int J Mol Sci. 2021. PMID: 34065916 Free PMC article. Review.
Recessive Dystrophic Epidermolysis Bullosa (RDEB) is a devastating skin blistering disease caused by mutations in the gene encoding type VII collagen (C7), leading to epidermal fragility, trauma-induced blistering, and long term, hard-to-heal wounds. . …
Recessive Dystrophic Epidermolysis Bullosa (RDEB) is a devastating skin blistering disease caused by mutations i …
Kindler syndrome.
Lai-Cheong JE, McGrath JA. Lai-Cheong JE, et al. Dermatol Clin. 2010 Jan;28(1):119-24. doi: 10.1016/j.det.2009.10.013. Dermatol Clin. 2010. PMID: 19945624 Review.
Kindler syndrome (MIM173650) is an autosomal recessive genodermatosis characterized by poikiloderma, trauma-induced skin blistering, mucosal inflammation, and photosensitivity. Loss-of-function mutations in the FERMT1 gene are the cause of Kindler syndrome. Kindler syndrom …
Kindler syndrome (MIM173650) is an autosomal recessive genodermatosis characterized by poikiloderma, trauma-induced skin blistering, …
Patent landscape of molecular and cellular targeted therapies for recessive dystrophic epidermolysis bullosa.
Dourado Alcorte M, Sogayar MC, Demasi MA. Dourado Alcorte M, et al. Expert Opin Ther Pat. 2019 May;29(5):327-337. doi: 10.1080/13543776.2019.1608181. Epub 2019 Apr 24. Expert Opin Ther Pat. 2019. PMID: 31017019 Review.
INTRODUCTION: Recessive Dystrophic Epidermolysis Bullosa (RDEB) is a monogenetic inherited genodermatosis associated with deleterious mutations in the gene encoding type VII collagen (COL7A1). ...
INTRODUCTION: Recessive Dystrophic Epidermolysis Bullosa (RDEB) is a monogenetic inherited genodermatosis associ …
192 results