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A novel mutation of sgk-1 gene in central serous chorioretinopathy.
Akyol M, Erol MK, Ozdemir O, Coban DT, Bilgin AB, Sari ES, Turkoglu EB. Akyol M, et al. Int J Ophthalmol. 2015 Feb 18;8(1):23-8. doi: 10.3980/j.issn.2222-3959.2015.01.04. eCollection 2015. Int J Ophthalmol. 2015. PMID: 25709902 Free PMC article.
Keratoconus presenting with bilateral simultaneous acute corneal hydrops.
Bilgin B, Unal B, Unal M, Doğan E, Cetinkaya A, Akyol M, Yücel I, Akar Y, Apaydın C, Ilhan D. Bilgin B, et al. Among authors: akyol m. Cont Lens Anterior Eye. 2013 Apr;36(2):98-100. doi: 10.1016/j.clae.2012.10.080. Epub 2012 Nov 2. Cont Lens Anterior Eye. 2013. PMID: 23123434
The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG).
Sinner MF, Pfeufer A, Akyol M, Beckmann BM, Hinterseer M, Wacker A, Perz S, Sauter W, Illig T, Näbauer M, Schmitt C, Wichmann HE, Schömig A, Steinbeck G, Meitinger T, Kääb S. Sinner MF, et al. Among authors: akyol m. Eur Heart J. 2008 Apr;29(7):907-14. doi: 10.1093/eurheartj/ehm619. Epub 2008 Jan 25. Eur Heart J. 2008. PMID: 18222980
Common variants in myocardial ion channel genes modify the QT interval in the general population: results from the KORA study.
Pfeufer A, Jalilzadeh S, Perz S, Mueller JC, Hinterseer M, Illig T, Akyol M, Huth C, Schöpfer-Wendels A, Kuch B, Steinbeck G, Holle R, Näbauer M, Wichmann HE, Meitinger T, Kääb S. Pfeufer A, et al. Among authors: akyol m. Circ Res. 2005 Apr 1;96(6):693-701. doi: 10.1161/01.RES.0000161077.53751.e6. Epub 2005 Mar 3. Circ Res. 2005. PMID: 15746444
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization.
Arking DE, Pfeufer A, Post W, Kao WH, Newton-Cheh C, Ikeda M, West K, Kashuk C, Akyol M, Perz S, Jalilzadeh S, Illig T, Gieger C, Guo CY, Larson MG, Wichmann HE, Marbán E, O'Donnell CJ, Hirschhorn JN, Kääb S, Spooner PM, Meitinger T, Chakravarti A. Arking DE, et al. Among authors: akyol m. Nat Genet. 2006 Jun;38(6):644-51. doi: 10.1038/ng1790. Epub 2006 Apr 30. Nat Genet. 2006. PMID: 16648850
CLOCK gene variants associate with sleep duration in two independent populations.
Allebrandt KV, Teder-Laving M, Akyol M, Pichler I, Müller-Myhsok B, Pramstaller P, Merrow M, Meitinger T, Metspalu A, Roenneberg T. Allebrandt KV, et al. Among authors: akyol m. Biol Psychiatry. 2010 Jun 1;67(11):1040-7. doi: 10.1016/j.biopsych.2009.12.026. Epub 2010 Feb 10. Biol Psychiatry. 2010. PMID: 20149345 Free article.
Evaluation of the Factors Influencing Mortality in Patients with Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis: A Multicenter Study of 166 Patients.
Erduran F, Adışen E, Emre S, Hayran Y, Başkan EB, Yazıcı S, Bilgiç A, Alpsoy E, Günaydın SD, Elmas L, Akyol M, Güner R, Arıca DA, Aypek Y, Ergun T, Karavelioğlu D, Yazıcı AC, Aydoğan K, Bayramgürler D, Kıran R, Erdoğan HK, Acer E, Aktaş A. Erduran F, et al. Among authors: akyol m. Dermatol Ther (Heidelb). 2024 May 17. doi: 10.1007/s13555-024-01180-6. Online ahead of print. Dermatol Ther (Heidelb). 2024. PMID: 38758423
Analysis of clinical characteristics and factors affecting treatment responses in patients with pyoderma gangrenosum: a multicenter study of 239 patients☆.
Erduran F, Adışen E, Hayran Y, Aksoy GG, Alpsoy E, Selçuk LB, Günaydın SD, Yazıcı AC, Öktem A, Güngör M, Afacan E, Kuşçu DD, Elmas L, Aydoğan K, Bayramgürler D, Demirsoy EO, Akyol M, Güner RY, Erdoğan HK, Acer E, Ergun T, Yaylı S, Bulut F, Saraç E, Aktaş A. Erduran F, et al. Among authors: akyol m. An Bras Dermatol. 2024 May 11:S0365-0596(24)00079-5. doi: 10.1016/j.abd.2024.02.002. Online ahead of print. An Bras Dermatol. 2024. PMID: 38735817 Free article.
291 results