Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Huriez syndrome"'
Publikováno v:
JPRAS Open, Vol 43, Iss , Pp 180-186 (2025)
Context: Huriez syndrome is a rare de rmatological condition characterized by severe sclerotic and atrophic changes in the extremities (hands and feet) and an increased tendency to develop squamous cell carcinomas, with no established gold standard f
Externí odkaz:
https://doaj.org/article/43ce89c040134560b345bc8b2253fcc6
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Benjamin Klein, Claudia Günther
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Type I interferons (IFNs) as part of the innate immune system have an outstanding importance as antiviral defense cytokines that stimulate innate and adaptive immune responses. Upon sensing of pattern recognition particles (PRPs) such as nucleic acid
Externí odkaz:
https://doaj.org/article/c7235c194dc0481f8fb7b54f6f151ec9
Autor:
Klein, Benjamin, Günther, Claudia
Type I interferons (IFNs) as part of the innate immune system have an outstanding importance as antiviral defense cytokines that stimulate innate and adaptive immune responses. Upon sensing of pattern recognition particles (PRPs) such as nucleic acid
Externí odkaz:
https://ul.qucosa.de/id/qucosa%3A84306
https://ul.qucosa.de/api/qucosa%3A84306/attachment/ATT-0/
https://ul.qucosa.de/api/qucosa%3A84306/attachment/ATT-0/
Autor:
Yu-An Wei, Chieh-Shan Wu
Publikováno v:
Dermatologica Sinica, Vol 37, Iss 3, Pp 147-149 (2019)
Huriez syndrome is a rare genodermatosis, which is characterized by palmoplantar keratoderma, sclerodactyly, nail abnormalities, and an increasing risk of squamous cell carcinoma. The exact causative gene and pathogenesis of Huriez syndrome have not
Externí odkaz:
https://doaj.org/article/2e009937071c4fd9914a7dfe798c0ff8
Autor:
A P J J Bray, Bruno Reversade, S Muthiah, Neil Rajan, A Y T Loh, Byrappa Venkatesh, C M Ho, T J Carney, Simon Zwolinski
Publikováno v:
British journal of dermatology, 184(6), 1205-1207. Wiley-Blackwell
Huriez syndrome (HRZ ; MIM181600) is a rare autosomal dominant genodermatosis, which is characterised by scleroatrophy of the hands and feet, hypoplasia of the nails and palmoplantar keratoderma1,2 . Approximately 15% of HRZ patients are predisposed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87ff8f0b82bcc6561f535202cfe53e96
https://doi.org/10.1111/bjd.19799
https://doi.org/10.1111/bjd.19799
Autor:
Abigail Y. T. Loh, Sanja Špoljar, Granville Y. W. Neo, Nathalie Escande‐Beillard, Marc Leushacke, Monique N. H. Luijten, Byrappa Venkatesh, Carine Bonnard, Maurice A. M. Steensel, Henning Hamm, Andrew Carmichael, Neil Rajan, Thomas J. Carney, Bruno Reversade
Publikováno v:
American journal of medical genetics. Part AREFERENCES. 188(6)
Huriez syndrome (HRZ, OMIM181600) is a rare genodermatosis characterized by scleroatrophic hands and feet, hypoplastic nails, palmoplantar keratoderma, and predisposition to cutaneous squamous cell carcinoma (cSCC). We report herein three HRZ familie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3b11c5b93eba52bdcb8e0e64ed198d5
https://pubmed.ncbi.nlm.nih.gov/35212137
https://pubmed.ncbi.nlm.nih.gov/35212137
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Indian Dermatology Online Journal
Indian Dermatology Online Journal, Vol 6, Iss 1, Pp 27-30 (2015)
Indian Dermatology Online Journal, Vol 6, Iss 1, Pp 27-30 (2015)
Huriez syndrome is a rare autosomal dominant genodermatosis characterized by the triad of congenital scleroatrophy of the distal extremities, palmoplantar keratoderma (PPK) and hypoplastic nails. We report the case of a 25 year old male, with nonfami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c38f448b8d3ee34518264ce689db28c3
http://europepmc.org/articles/PMC4314883
http://europepmc.org/articles/PMC4314883
Huriez syndrome, also referred to as “sclerotylosis,” is a rare autosomal dominant genodermatosis characterized by the triad of congenital scleroatrophy of the distal extremities, palmoplantar keratoderma, and hypoplastic nails. The development o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d6d9e6456d9306af5989095a45934c0
https://europepmc.org/articles/PMC5939708/
https://europepmc.org/articles/PMC5939708/