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

591 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Childhood headaches and brain magnetic resonance imaging findings.
Yılmaz Ü, Çeleğen M, Yılmaz TS, Gürçınar M, Ünalp A. Yılmaz Ü, et al. Among authors: yilmaz ts. Eur J Paediatr Neurol. 2014 Mar;18(2):163-70. doi: 10.1016/j.ejpn.2013.11.003. Epub 2013 Nov 9. Eur J Paediatr Neurol. 2014. PMID: 24268890
SURF1 related Leigh syndrome: Clinical and molecular findings of 16 patients from Turkey.
Kose M, Canda E, Kagnici M, Aykut A, Adebali O, Durmaz A, Bircan A, Diniz G, Eraslan C, Kose E, Ünalp A, Yılmaz Ü, Ozyilmaz B, Özdemir TR, Atik T, Uçar SK, McFarland R, Taylor RW, Brown GK, Çoker M, Özkınay F. Kose M, et al. Among authors: yilmaz u. Mol Genet Metab Rep. 2020 Oct 23;25:100657. doi: 10.1016/j.ymgmr.2020.100657. eCollection 2020 Dec. Mol Genet Metab Rep. 2020. PMID: 33134083 Free PMC article.
Evaluation of clinical findings and neurofibromatosis type 1 bright objects on brain magnetic resonance images of 60 Turkish patients with NF1 gene variants.
Hazan F, Gürsoy S, Unalp A, Yılmaz U, Demirağ B, Aydin Köker S, Ozyılmaz B, Erdogan KM, Kalenderer Ö, Erkuş S, Gürçınar M, Tükün A. Hazan F, et al. Among authors: yilmaz u. Neurol Sci. 2021 May;42(5):2045-2057. doi: 10.1007/s10072-020-04988-0. Epub 2021 Jan 14. Neurol Sci. 2021. PMID: 33443663
The utility of next-generation sequencing technologies in diagnosis of Mendelian mitochondrial diseases and reflections on clinical spectrum.
Kose M, Isik E, Aykut A, Durmaz A, Kose E, Ersoy M, Diniz G, Adebali O, Ünalp A, Yilmaz Ü, Karaoğlu P, Edizer S, Tekin HG, Özdemir TR, Atik T, Onay H, Özkınay F. Kose M, et al. Among authors: yilmaz u. J Pediatr Endocrinol Metab. 2021 Feb 24;34(4):417-430. doi: 10.1515/jpem-2020-0410. Print 2021 Apr 27. J Pediatr Endocrinol Metab. 2021. PMID: 33629572
591 results