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Material Type: Artigo
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Homozygous Mutation in the Insulin Receptor Gene Associated with Mild Type A Insulin Resistance Syndrome: A Case ReportHacıhamdioğlu, Bülent ; Baş, Elif Gülşah ; Delil, Kenan Darendeliler,Fatma FeyzaJournal of clinical research in pediatric endocrinology, 2021-03, Vol.13 (1), p.100-103 [Periódico revisado por pares]Turkey: Galenos Yayinevi Tic. LtdTexto completo disponível |
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Material Type: Artigo
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Two cases of acute myocarditis with multiple intracardiac thrombi: the role of hypercoagulable StatesAtas, Halil ; Samadov, Fuad ; Sunbul, Murat ; Cincin, Altug ; Delil, Kenan ; Mutlu, BulentHeart views, 2014-01, Vol.15 (1), p.22-25 [Periódico revisado por pares]India: Medknow Publications and Media Pvt. LtdTexto completo disponível |
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Material Type: Artigo
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Challenges in the treatment of fibrodysplasia ossificans progressivaGencer-Atalay, Kardelen ; Ozturk, Ekim Can ; Yagci, Ilker ; Ata, Pinar ; Delil, Kenan ; Ozgen, Zerrin ; Akyuz, GulserenRheumatology international, 2019-03, Vol.39 (3), p.569-576 [Periódico revisado por pares]Berlin/Heidelberg: Springer Berlin HeidelbergTexto completo disponível |
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Material Type: Artigo
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22q11 deletion syndrome: current perspectiveHacıhamdioğlu, Bülent ; Hacıhamdioğlu, Duygu ; Delil, KenanApplication of clinical genetics, 2015-01, Vol.8 (default), p.123-132 [Periódico revisado por pares]New Zealand: Dove Medical Press LimitedTexto completo disponível |
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Material Type: Artigo
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Biallelic Mutations in DNAJB11 are Associated with Prenatal Polycystic Kidney Disease in a Turkish FamilyAteş, Esra Arslan ; Turkyilmaz, Ayberk ; Delil, Kenan ; Alavanda, Ceren ; Söylemez, Mehmet Ali ; Geçkinli, Bilgen Bilge ; Ata, Pinar ; Arman, AhmetMolecular syndromology, 2021-06, Vol.12 (3), p.179-185 [Periódico revisado por pares]Allschwilerstrasse 10, P.O. Box · Postfach · Case postale, CH–4009, Basel, Switzerland · Schweiz · Suisse, Phone: +41 61 306 11 11, Fax: +41 61 306 12 34, karger@karger.com: S. Karger AGTexto completo disponível |
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Material Type: Artigo
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Biallelic Mutations in DNAJB11are Associated with Prenatal Polycystic Kidney Disease in a Turkish FamilyAteş, Esra Arslan ; Turkyilmaz, Ayberk ; Delil, Kenan ; Alavanda, Ceren ; Söylemez, Mehmet Ali ; Geçkinli, Bilgen Bilge ; Ata, Pinar ; Arman, AhmetMolecular syndromology, 2021-06, Vol.12 (3), p.179-185 [Periódico revisado por pares]Basel, SwitzerlandTexto completo disponível |
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Material Type: Artigo
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Vitamin D receptor gene polymorphisms in children with kidney stone diseaseSubaşı, Berivan ; Gökçe, İbrahim ; Delil, Kenan ; Alpay, HarikaTurkish journal of pediatrics, 2017, Vol.59 (4), p.404-409 [Periódico revisado por pares]Turkey: Hacettepe University Faculty of MedicineTexto completo disponível |
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Material Type: Artigo
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Case of fatal heart failure with biventricular noncompaction, genital skeletal abnormalities and mental retardationAtaş, Halil ; Samadov, Fuad ; Sarı, İbrahim ; Delil, KenanAnadolu kardiyoloji dergisi : AKD, 2015-01, Vol.15 (1), p.71-72 [Periódico revisado por pares]Turkey: Kare PublishingTexto completo disponível |
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Material Type: Artigo
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Authors ReplyAtaş, Halil ; Samadov, Fuad ; Sarı, İbrahim ; Delil, KenanAnatolian journal of cardiology, 2015-05, Vol.15 (5), p.434-434 [Periódico revisado por pares]Turkey: Kare PublishingTexto completo disponível |
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Material Type: Artigo
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Functionally stable plasminogen activator inhibitor-1 in a family with cardiovascular disease and vitiligoAgirbasli, Mehmet ; Eren, Mesut ; Yasar, Songul ; Delil, Kenan ; Goktay, Fatih ; Oner, Ebru Toksoy ; Vaughan, Douglas E.Journal of thrombosis and thrombolysis, 2014-07, Vol.38 (1), p.50-56 [Periódico revisado por pares]Boston: Springer USTexto completo disponível |