Search Results - "Aydi̇n, Halil İbrahim"
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Kur’ân’da Yeryüzü Merkezli Doğal Afetlerle İlgili Olarak Zikredilen Bazı Kavramların Bağlamsal Açıdan Değerlendirilmesi
Published in Artuklu Akademi (30-06-2024)“…Kur’ân’da deprem başta olmak üzere kuraklık, kıtlık, sel, su taşkını, erozyon ve obruk gibi yeryüzünde gerçekleşen jeolojik, klimatik ve biyolojik afetlerle…”
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2
Muhtevâ ve Üslup Açısından Kur’an’da Secde Âyetleri
Published in Düzce İlahiyat Dergisi (30-06-2023)“…Kur’an, hem üslubu hem de muhtevâsı itibarıyla mu´ciz bir yapıda vahiy edilmiştir. Bu yapı tilâvet secdesi ile ilgili âyetlerde de kendini göstermektedir…”
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3
Chronic enteropathy associated with SLCO2A1 gene and hereditary fructose intolerance: A coincidence of two rare diseases
Published in Arab journal of gastroenterology (01-11-2022)“…Chronic enteropathy associated with SLCO2A1 gene (CEAS) is a rare disorder characterized by multiple small intestine ulcers. Patients with CEAS typically…”
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4
Ekonomi güvenliği üzerine ekonomi- politik bir çözümleme
Published in Journal of Finance Letters / Maliye Finans Yazıları Dergisi (01-04-2022)“…Soğuk Savaş’ın sona ermesi ile ivme kazanan küreselleşme süreci geleneksel güvenlik anlayışında bir takım değişimlere neden olmuştur. Küreselleşme süreci…”
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5
Hearing Loss in Biotinidase Deficiency: Genotype-Phenotype Correlation
Published in The Journal of pediatrics (01-04-2007)“…Children with symptoms of profound biotinidase deficiency with null mutations are more likely to have hearing loss develop than those with missense mutations,…”
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Türkiye’de vergi gelirleri ile ekonomik kalkınma arasındaki ilişki: Frekans alanı nedensellik analizi
Published in Doğuş Üniversitesi dergisi (01-01-2018)“…Çalışmanın amacı, Türkiye’de 1975-2013 dönemine ait yıllık verilerle vergi gelirleri ile kalkınma arasındaki ilişkinin varlığını araştırmakla beraber söz…”
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7
Bi-allelic loss-of-function OBSCN variants predispose individuals to severe recurrent rhabdomyolysis
Published in Brain (London, England : 1878) (21-11-2022)“…Rhabdomyolysis is the acute breakdown of skeletal myofibres in response to an initiating factor, most commonly toxins and over exertion. A variety of genetic…”
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HDR Syndrome (Hypoparathyroidism, Sensorineural Deafness and Renal Disease) Accompanied by Renal Tubular Acidosis and Endocrine Abnormalities
Published in Internal Medicine (01-01-2008)“…Type 1 (distal) and type 2 (proximal) renal tubular acidosis (RTA) are uncommon disorders, particularly in adults. HDR syndrome (hypoparathyroidism,…”
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9
The Relationship between Daily Fructose Consumption and Oxidized Low-Density Lipoprotein and Low-Density Lipoprotein Particle Size in Children with Obesity
Published in Pediatric gastroenterology, hepatology & nutrition (01-09-2021)“…Obesity has become a very significant health problem in childhood. Fructose taken in an uncontrolled manner and consumed in excessive amounts is rapidly…”
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10
Coexistence of guanidinoacetate methyltransferase (GAMT) deficiency and neuroleptic malignant syndrome without creatine kinase elevation
Published in Brain & development (Tokyo. 1979) (01-05-2020)“…We describe the first child with guanidinoacetate methyltransferase (GAMT) deficiency who developed neuroleptic malignant syndrome (NMS) after the treatment of…”
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11
Association between coronary artery disease severity and overactive bladder in geriatric patients
Published in World journal of urology (2018)“…Purpose To investigate the association between overactive bladder (OAB) and coronary artery disease (CAD) as demonstrated on coronary angiography in…”
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PARA POLİTİKASI TASARIMLARINDA FİYAT VE FİNANSAL İSTİKRAR İLİŞKİSİ: EURO ALANINDAN KANITLAR (1999:01-2020:12)
Published in Mehmet Akif Ersoy Üniversitesi İktisadi ve İdari Bilimler Fakültesi dergisi (23-03-2022)“…Bu çalışmada, para politikası tasarımlarının fiyat istikrarı ile finansal istikrar arasındaki ilişkileri açıklamakta 1990’lardan buyana Geleneksel Bilgelik ve…”
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13
Banka darbe tekniği: Şeyh Dr. A. Es Sufi; çeviren, Halil İbrahim Aydın
Published 2018“…1532 yılında Machiavelli'nin kitabı Il Principe basıldı. Niyeti kâfir yöneticiler için gerekli liderlik bilgisini ortaya koymaktı. Eser, 'Ferdî Yönetim' ilkesi…”
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14
Cerebral creatine deficiency syndrome with a novel missense variant in SLC6A8 gene
Published in Neurology and clinical neuroscience (01-09-2023)“…Cerebral creatine deficiency syndromes (CCDS) are three metabolic diseases characterized by loss of function in three proteins (GATM, GAMT, and SLC6A8) that…”
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A novel mutation in TRMT5 associated with idiopathic non-cirrhotic portal hypertension and hepatopulmonary syndrome: Case report of two siblings
Published in Clinics and research in hepatology and gastroenterology (01-10-2022)“…Non-cirrhotic portal hypertension (NCPH) is a rare clinical entity in children. Familial clusters of idiopathic non-cirrhotic portal hypertension (INCPH) were…”
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Three-Country Snapshot of Ornithine Transcarbamylase Deficiency
Published in Life (Basel, Switzerland) (27-10-2022)“…X-linked ornithine transcarbamylase deficiency (OTCD) is the most common urea cycle defect. The disease severity ranges from asymptomatic carrier state to…”
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Morbidity and mortality characteristics of infants hospitalized in the Pediatrics Department of the largest Turkish military hospital in 2001
Published in Military medicine (01-01-2005)“…A descriptive study was conducted in the pediatric inpatient unit of Gulhane Military Medical Academy, to investigate the morbidity and mortality…”
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18
ed-Dirâsâtü’s-Savtiyye İ‘nde U‘lemâi’t-Tecvîd, Yazar Gânim Kaddûrî Hamed (Ammân: Dâr-u Ammâr, 2007)
Published in BEÜ İlahiyat Fakültesi Dergisi (01-02-2019)“…Kur’ân’ın doğru bir şekilde okunmasını temin eden tecvid ilminin, ilk vahiyden itibaren nasıl devam edegeldiği, sistemli bir ilim haline gelmesinden önceki…”
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19
Retrospective evaluation of patients with X-linked adrenoleukodystrophy with a wide range of clinical presentations: a single center experience
Published in Journal of pediatric endocrinology & metabolism : JPEM (27-09-2021)“…X-linked adrenoleukodystrophy (X-ALD), is a peroxisomal inborn error of metabolism caused due to the loss of function variants of gene that leads to…”
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Preliminary study on DNA damage in non breast-fed infants
Published in Pediatrics international (01-04-2002)“…Background : There are many advantages of human milk for infants, including protection against cancer development and the advantages have been emphasized in…”
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