Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

50 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Missing Heritability in Albinism: Deep Characterization of a Hungarian Albinism Cohort Raises the Possibility of the Digenic Genetic Background of the Disease.
Nagy N, Pal M, Kun J, Galik B, Urban P, Medvecz M, Fabos B, Neller A, Abdolreza A, Danis J, Szabo V, Yang Z, Fenske S, Biel M, Gyenesei A, Adam E, Szell M. Nagy N, et al. Among authors: medvecz m. Int J Mol Sci. 2024 Jan 20;25(2):1271. doi: 10.3390/ijms25021271. Int J Mol Sci. 2024. PMID: 38279271 Free PMC article.
Nonlinear optical microscopy is a novel tool for the analysis of cutaneous alterations in pseudoxanthoma elasticum.
Kiss N, Fésűs L, Bozsányi S, Szeri F, Van Gils M, Szabó V, Nagy AI, Hidvégi B, Szipőcs R, Martin L, Vanakker O, Arányi T, Merkely B, Wikonkál NM, Medvecz M. Kiss N, et al. Among authors: medvecz m. Lasers Med Sci. 2020 Oct;35(8):1821-1830. doi: 10.1007/s10103-020-03027-w. Epub 2020 May 6. Lasers Med Sci. 2020. PMID: 32372237 Free PMC article.
[Multidisciplinary management of patients affected with pseudoxanthoma elasticum].
Farkas K, Kiss N, Szabó V, Resch M, Vámos R, Borbándy Á, Nagy A, Apor A, Arányi T, Szeri F, Wikonkál N, Nagy Z, Merkely B, Medvecz M. Farkas K, et al. Among authors: medvecz m. Orv Hetil. 2022 May 1;163(18):702-711. doi: 10.1556/650.2022.32438. Print 2022 May 1. Orv Hetil. 2022. PMID: 35490386 Hungarian.
Assessment of the Genetic Spectrum of Uncombable Hair Syndrome in a Cohort of 107 Individuals.
Basmanav FB, Cesarato N, Kumar S, Borisov O, Kokordelis P, Ralser DJ, Wehner M, Axt D, Xiong X, Thiele H, Dolgin V, Gossmann Y, Fricker N, Dewenter MK, Weller K, Suri M, Reichenbach H, Oji V, Addor MC, Ramirez K, Stewart H, Garcia Bartels N, Weibel L, Wagner N, George S, Kilic A, Tantcheva-Poor I, Stewart A, Dikow N, Blaumeiser B, Medvecz M, Blume-Peytavi U, Farrant P, Grimalt R, Bertok S, Bradley L, Eskin-Schwartz M, Birk OS, Bygum A, Simon M, Krawitz P, Fischer C, Hamm H, Fritz G, Betz RC. Basmanav FB, et al. Among authors: medvecz m. JAMA Dermatol. 2022 Nov 1;158(11):1245-1253. doi: 10.1001/jamadermatol.2022.2319. JAMA Dermatol. 2022. PMID: 36044230 Free PMC article.
Multiple bronchial carcinoids associated with Cowden syndrome.
Tömböl Z, Tőke J, Tóth G, Varga Z, Balázs E, Tóth E, Gergely L, Danihel Ľ, Medvecz M, Borka K, Tóth M. Tömböl Z, et al. Among authors: medvecz m. Endocrine. 2024 Feb 14. doi: 10.1007/s12020-024-03693-8. Online ahead of print. Endocrine. 2024. PMID: 38353885
50 results