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

Year Number of Results
1978 1
1979 2
1984 1
1987 2
1989 2
1992 1
1994 1
1995 1
1996 1
1999 1
2000 2
2001 1
2002 1
2003 2
2004 6
2005 5
2006 4
2007 2
2008 5
2009 11
2010 6
2011 5
2012 4
2013 7
2014 12
2015 12
2016 5
2017 4
2018 11
2019 8
2020 8
2021 12
2022 7
2023 5
2024 3

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142 results

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Page 1
Therapeutic Options for the Treatment of Darier's Disease: A Comprehensive Review of the Literature.
Hanna N, Lam M, Fleming P, Lynde CW. Hanna N, et al. J Cutan Med Surg. 2022 May-Jun;26(3):280-290. doi: 10.1177/12034754211058405. Epub 2021 Nov 28. J Cutan Med Surg. 2022. PMID: 34841914 Free PMC article. Review.
Considering the quality and quantity of evidence, clinicians may consider initiating a trial of select topical or oral retinoids first in patients with localized or generalized DD, respectively....
Considering the quality and quantity of evidence, clinicians may consider initiating a trial of select topical or oral retinoids firs …
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). ...B-VEC restored C7 expression in RDEB ker …
Recessive dystrophic epidermolysis bullosa (RDEB) is a lifelong genodermatosis associated with blistering, wounding, and scarring cau …
Emerging therapies in genodermatoses.
Silverberg N. Silverberg N. Clin Dermatol. 2020 Jul-Aug;38(4):462-466. doi: 10.1016/j.clindermatol.2020.03.006. Epub 2020 Mar 24. Clin Dermatol. 2020. PMID: 32972604 Review.
The next generation of genetics has investigated how these genes interact in the development of disease, identifying pathways of illness and end organ tissue abnormal development. From the knowledge of single genes and pathways of genodermatosis development arises the oppo …
The next generation of genetics has investigated how these genes interact in the development of disease, identifying pathways of illness and …
RNA-based therapies for genodermatoses.
Bornert O, Peking P, Bremer J, Koller U, van den Akker PC, Aartsma-Rus A, Pasmooij AM, Murauer EM, Nyström A. Bornert O, et al. Exp Dermatol. 2017 Jan;26(1):3-10. doi: 10.1111/exd.13141. Exp Dermatol. 2017. PMID: 27376675 Free PMC article. Review.
The aim of this review was to set the stage for the development of new and better therapies to improve the lives of patients and families affected by a genodermatosis....
The aim of this review was to set the stage for the development of new and better therapies to improve the lives of patients and families af …
Cutaneous gene delivery.
Kikuchi Y, Tamai K, Kaneda Y. Kikuchi Y, et al. J Dermatol Sci. 2008 May;50(2):87-98. doi: 10.1016/j.jdermsci.2007.07.006. Epub 2007 Aug 31. J Dermatol Sci. 2008. PMID: 17765482 Review.
However, most such approaches have been specifically aimed against genodermatosis, and have not produced sufficient results. The goal of such research is to develop a method in which genes are transferred easily, efficiently and stably into keratinocytes, especially into k …
However, most such approaches have been specifically aimed against genodermatosis, and have not produced sufficient results. The goal …
European Guidelines (S3) on diagnosis and management of mucous membrane pemphigoid, initiated by the European Academy of Dermatology and Venereology - Part II.
Schmidt E, Rashid H, Marzano AV, Lamberts A, Di Zenzo G, Diercks GFH, Alberti-Violetti S, Barry RJ, Borradori L, Caproni M, Carey B, Carrozzo M, Cianchini G, Corrà A, Dikkers FG, Feliciani C, Geerling G, Genovese G, Hertl M, Joly P, Meijer JM, Mercadante V, Murrell DF, Ormond M, Pas HH, Patsatsi A, Rauz S, van Rhijn BD, Roth M, Setterfield J, Zillikens D, C Prost, Zambruno G, Horváth B, Caux F. Schmidt E, et al. J Eur Acad Dermatol Venereol. 2021 Oct;35(10):1926-1948. doi: 10.1111/jdv.17395. Epub 2021 Jul 26. J Eur Acad Dermatol Venereol. 2021. PMID: 34309078 Free PMC article.
While the first part of this guideline addressed methodology, as well as epidemiology, terminology, aetiology, clinical presentation and outcome measures in MMP, the second part presents the diagnostics and management of MMP. ...Treatment recommendations are limited by the …
While the first part of this guideline addressed methodology, as well as epidemiology, terminology, aetiology, clinical presentation …
Hailey-Hailey disease and review of management.
Chiaravalloti A, Payette M. Chiaravalloti A, et al. J Drugs Dermatol. 2014 Oct;13(10):1254-7. J Drugs Dermatol. 2014. PMID: 25607561 Review.
IMPORTANCE: Hailey-Hailey disease, or familial benign chronic pemphigus, is a rare genodermatosis that can be challenging for both patients and dermatologists as the disease can significantly impact patients' quality of life and is often difficult to control. ...
IMPORTANCE: Hailey-Hailey disease, or familial benign chronic pemphigus, is a rare genodermatosis that can be challenging for both pa …
Long-term safety and efficacy of gene-corrected autologous keratinocyte grafts for recessive dystrophic epidermolysis bullosa.
So JY, Nazaroff J, Iwummadu CV, Harris N, Gorell ES, Fulchand S, Bailey I, McCarthy D, Siprashvili Z, Marinkovich MP, Tang JY, Chiou AS. So JY, et al. Orphanet J Rare Dis. 2022 Oct 17;17(1):377. doi: 10.1186/s13023-022-02546-9. Orphanet J Rare Dis. 2022. PMID: 36253825 Free PMC article. Clinical Trial.
BACKGROUND: Recessive dystrophic epidermolysis bullosa (RDEB) is a rare, devastating blistering genodermatosis caused by mutations in the COL7A1 gene, which encodes for type VII collagen and is necessary for dermal-epidermal adhesion and integrity. ...CONCLUSIONS: Treatmen …
BACKGROUND: Recessive dystrophic epidermolysis bullosa (RDEB) is a rare, devastating blistering genodermatosis caused by mutations in …
A novel approach to the classification of epidermodysplasia verruciformis.
Huang S, Wu JH, Lewis DJ, Rady PL, Tyring SK. Huang S, et al. Int J Dermatol. 2018 Nov;57(11):1344-1350. doi: 10.1111/ijd.14196. Epub 2018 Aug 29. Int J Dermatol. 2018. PMID: 30156265 Review.
BACKGROUND: Epidermodysplasia verruciformis (EV) is a rare genodermatosis that causes disseminated eruptions of hypo- or hyperpigmented macules and wart-like papules that can coalesce and scale. ...
BACKGROUND: Epidermodysplasia verruciformis (EV) is a rare genodermatosis that causes disseminated eruptions of hypo- or hyperpigment …
The PER3rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria.
Chen H, Yang P, Yang D, Wang D, Lu M, Li Y, Zhong Z, Zhang J, Zeng Z, Liu Z, Zeng X, Jia X, Xing Q, Zhou D. Chen H, et al. J Mol Med (Berl). 2023 Mar;101(3):279-294. doi: 10.1007/s00109-023-02288-6. Epub 2023 Feb 15. J Mol Med (Berl). 2023. PMID: 36790533
Dyschromatosis universalis hereditaria (DUH) is a pigmentary genodermatosis characterized by a mixture of hyperpigmented and hypopigmented macules distributed randomly over the body. ...
Dyschromatosis universalis hereditaria (DUH) is a pigmentary genodermatosis characterized by a mixture of hyperpigmented and hypopigm …
142 results