Search Results - "Akcan, Mehmet"

Physical–Mechanical and Mineralogical Properties of Fired Bricks of the Archaeological Site of Harran, Turkey by Binici, Hanifi, Binici, Fatih, Akcan, Mehmet, Yardim, Yavuz, Mustafaraj, Enea, Corradi, Marco

“…In this study, the physical–mechanical and mineralogical properties of bricks used in historical structures of the site of Harran, Turkey have been…”
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Exploring genetic variants in congenital monosaccharide‐disaccharide metabolism: Carrier ratios and phenotypic insights by Akcan, Mehmet Berkay, Silan, Fatma

“…Objectives Adverse food reactions, often underestimated, encompass congenital monosaccharide‐disaccharide metabolism disorders, yielding diverse outcomes such…”
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A case report of a patient with neurodevelopmental disorder with impaired speech and hyperkinetic movements: A biallelic variant in the ZNF142 gene by Kaya, Derya, Ceylan Köse, Canan, Akcan, Mehmet Berkay, Silan, Fatma

“…Biallelic pathogenic variations in the zinc finger protein 142 (ZNF142) gene are associated with neurodevelopmental disorder with impaired speech and…”
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Anemia and thrombocytopenia due to a novel BRPF1 variant in a family from Çanakkale with intellectual disability and dysmorphic facies: Case report and review of the literature by Kose, Canan Ceylan, Kaya, Derya, Akcan, Mehmet Berkay, Silan, Fatma

“…Intellectual developmental disorder with dysmorphic facies and ptosis (IDDDFP) (MIM#617333) is an autosomal dominant disorder characterized by delayed…”
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Evaluating of colchicine use patterns and attack frequency of familial Mediterranean fever patients in the COVID‐19 pandemic by Akcan, Mehmet Berkay, Albuz, Burcu, Ozdemir, Ozturk, Silan, Fatma

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A New Case of Rare Microdeletion 10q22.3q23 along with Mosaic Klinefelter Syndrome Associated with Facial Dysmorphic Finding, Atrial Ventricular Septal Defect, and Motor Retardation by Dincsoy Bir, Firdevs, Silan, Fatma, Velickovic, Jelena, Berkay Akcan, Mehmet, Ozdemir, Ozturk

“…The chromosome 10q22.3q23.2 deletion syndrome is characterized by craniofacial dysmorphic features, developmental delay, congenital heart defect, and hand/foot…”
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Familial intragenic X-linked OPHN1 gene deletion in a newborn male infant with low birth weight and distinctive facial appearance that diagnosed by advanced microarray-CGH method by AYLANC, Hakan, SILAN, Fatma, ÇOKYAMAN, Turgay, AKCAN, Mehmet Berkay, ÖZDEMİR, Öztürk

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Hi̇stami̇n’iIndorsal Kök Gangli̇on Nöronlarinda HCN Kanallarina Etki̇si̇ by Akcan, Mehmet Hakan

“…Santral Sinir Sistemi, insan ve diğer hayvanların yaşamsal tüm faaliyetleri kontrol eder. Yaşamsal faaliyetler duyu organlarımızla algılanıp sinir sistemi ile…”
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A New Case of Rare Microdeletion 10q22.3q23 along with Mosaic Klinefelter Syndrome Associated with Facial Dysmorphic Finding, Atrial Ventricular Septal Defect, and Motor Retardation by Dincsoy Bir, Firdevs, Silan, Fatma, Velickovic, Jelena, Berkay Akcan, Mehmet, Ozdemir, Ozturk

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Yapay zeka algoritmalarının mimari şematik plan oluşturmak için kullanımı by Akçan, Zeki Mehmet

“…Günümüzde bir çok sektörde verimi oldukça yüksek yapay zeka teknolojisi ile donatılmış yazılımlar ve robotlar yerini almaya başlamıştır. Yapay zeka…”
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