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Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium.
Funct Integr Genomics. 2022 Jun;22(3):291-315. doi: 10.1007/s10142-021-00819-3. Epub 2022 Jan 31.
Funct Integr Genomics. 2022.
PMID: 35098403
Autosomal recessive hypophosphatemic rickets type 2; a novel mutation in the ENPP1 gene.
Bitkin EÇ, Aymelek HS.
Bitkin EÇ, et al. Among authors: aymelek hs.
Turk J Pediatr. 2022;64(3):585-591. doi: 10.24953/turkjped.2021.829.
Turk J Pediatr. 2022.
PMID: 35899574
Free article.
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Identification of three novel pathogenic ITGA2B and one novel pathogenic ITGB3 mutations in patients with hereditary Glanzmann's thrombasthenia living in Eastern Turkey.
Karaman K, Yürektürk E, Geylan H, Yaşar AŞ, Karaman S, Aymelek HS, Çetin M, Oner AF.
Karaman K, et al. Among authors: aymelek hs.
Platelets. 2021 Feb 17;32(2):238-242. doi: 10.1080/09537104.2020.1732331. Epub 2020 Feb 22.
Platelets. 2021.
PMID: 32089034
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Evaluation of pubertal and pathological gynaecomastia in children: A single-center experience.
Celebi Bitkin E, Aymelek HS, Karaman S.
Celebi Bitkin E, et al. Among authors: aymelek hs.
Andrologia. 2021 Apr;53(3):e13992. doi: 10.1111/and.13992. Epub 2021 Feb 2.
Andrologia. 2021.
PMID: 33533035
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Genetic Burden and Outcome of Cystic Hygromas Detected Antenatally: Results of 93 Pregnancies from a Single Center in the Northern Region of Turkey.
Aymelek HS, Oğur G, Tosun M, Abur Ü, Altundağ E, Çelik H, Kurtoğlu E, Malatyalıoğlu E, Akar ÖS, Alper T.
Aymelek HS, et al.
J Med Ultrasound. 2019 Apr 10;27(4):181-186. doi: 10.4103/JMU.JMU_114_18. eCollection 2019 Oct-Dec.
J Med Ultrasound. 2019.
PMID: 31867191
Free PMC article.
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Impact of Fluorescent In Situ Hybridization Aberrations and CLLU1 Expression on the Prognosis of Chronic Lymphocytic Leukemia: Presentation of 156 Patients from Turkey.
Abur Ü, Oğur G, Akar ÖS, Altundağ E, Aymelek HS, Özatlı D, Turgut M.
Abur Ü, et al. Among authors: aymelek hs.
Turk J Haematol. 2018 Mar 1;35(1):61-65. doi: 10.4274/tjh.2017.0112. Epub 2017 Nov 13.
Turk J Haematol. 2018.
PMID: 29129824
Free PMC article.
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Muir-Torre Syndrome with Novel Mutation in the MSH2 Gene.
Ustaoglu E, Agirgol S, Aymelek HS, Turhan EI.
Ustaoglu E, et al. Among authors: aymelek hs.
Acta Dermatovenerol Croat. 2023 Dec;31(3):144-147.
Acta Dermatovenerol Croat. 2023.
PMID: 38439724
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