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Mermer Ocak İşletmeciliğinde Yastıklama Uygulamasının Üretim Verimine Etkisinin Araştırılması

Süleyman Demirel Üniversitesi Fen Bilimleri Enstitüsü dergisi, 2022-04, Vol.26 (1), p.132-140

2022

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Shortcomings & Spares/A quantitative Overview of Architectural Education in Turkey

Mimarlık, 2015-01 (381), p.35-40

2015

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Vienna-Chicago: Discussions on Architecture and Metropolis

Mimarlık, 2008-09 (343), p.84-97

2008

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Contemporary Tendencies in the Organization of Public Life and the Production of the City

Toplum ve bilim, 2006-01 (105), p.166-177

Bilgin, Ihsan

2006

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The relationship between politics and design

A|Z ITU Journal of Faculty of Architecture, 2004-03, Vol.1 (1), p.47-59

Bilgin, Ihsan

2004

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Right subclavian artery true aneurysm: A rare cause of dyspnea

Turkish Journal of Vascular Surgery, 2023-11, Vol.32 (3), p.181-183

2023

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Fatal Disseminated Multiple Intracranial Juvenile Xanthogranuloma without Cutaneous and Other Organ Involvement: A Rare Case Report

Pediatric neurosurgery, 2021-04, Vol.56 (2), p.166-170

2021

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Incidentally detected asymptomatic splenic artery aneurysm

Turkish Journal of Vascular Surgery, 2024-07, Vol.33 (2), p.112-114

2024

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The Authors' Reply: In systemic pseudohypoaldosteronism type 1 skin manifestations are not rare and the disease is not transient

Clinical endocrinology (Oxford), 2018-08, Vol.89 (2), p.241-242

2018

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Comparison of cardiovascular, cancer and herpes zoster risk of tofacitinib versus etanercept: Single Centre Observational Study

Rheumatology (Oxford, England), 2022-08, Vol.61 (9), p.e267-e269

2022

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A novel homozygous nonsense NDNF variant in Kallmann syndrome

American journal of medical genetics. Part A, 2023-03, Vol.191 (3), p.831-834

2023

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DLG2 Mutations in the Etiology of Pubertal Delay and Idiopathic Hypogonadotropic Hypogonadism

Hormone research in paediatrics, 2022-02, Vol.94 (9-10), p.364-368

2022

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Inactivating NHLH2 variants cause idiopathic hypogonadotropic hypogonadism and obesity in humans

Human genetics, 2022-02, Vol.141 (2), p.295-304

2022

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Differences and similarities of proliferative and non-proliferative forms of biopsy-proven lupus nephritis: Single centre, cross-disciplinary experience

Lupus, 2022-08, Vol.31 (9), p.1147-1156

2022

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Molecular genetic studies in a case series of isolated hypoaldosteronism due to biosynthesis defects or aldosterone resistance

Clinical endocrinology (Oxford), 2018-06, Vol.88 (6), p.799-805

2018

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The Comparison of scoring systems: SOFA, APACHE-II, LODS, MODS, and SAPS-II in critically ill elderly sepsis patients

Journal of infection in developing countries, 2024-01, Vol.18 (1), p.122-130

2024

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What Does COVID-19 Have to Do With Flying Cats?

The Pediatric infectious disease journal, 2023-07, Vol.42 (7), p.e254-e254

2023

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Post-operative pain management for single-level lumbar disc herniation surgery: A comparison of betamethasone, ibuprofen, and pregabalin

Aǧrı, 2021-04, Vol.33 (2), p.89-95

2021

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Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism

Genetics in medicine, 2021-06, Vol.23 (6), p.1008-1016

2021

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Prevalence and associated phenotypes of PLXNA1 variants in normosmic and anosmic idiopathic hypogonadotropic hypogonadism

Clinical genetics, 2019-02, Vol.95 (2), p.320-324

2019

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CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism

The journal of clinical endocrinology and metabolism, 2017-06, Vol.102 (6), p.1816-1825

2017

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Proposal of a new nomenclature for the underlying pathogenetic mechanism of severe Coronavirus Disease-19: “Inflammatory Thrombosis with Immune Endotheliitis—ITIE”

Rheumatology international, 2021-03, Vol.41 (3), p.679-680

2021

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Agomelatine modulates calcium signaling through protein kinase C and phospholipase C‐mediated mechanisms in rat sensory neurons

Journal of cellular physiology, 2019-07, Vol.234 (7), p.10741-10746

2019

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21-Hydroxylase deficiency: Mutational spectrum and Genotype–Phenotype relations analyses by next-generation sequencing and multiplex ligation-dependent probe amplification

European journal of medical genetics, 2020-04, Vol.63 (4), p.103782-103782, Article 103782

2020

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Mermer Ocak İşletmeciliğinde Yastıklama Uygulamasının Üretim Verimine Etkisinin Araştırılması

Shortcomings & Spares/A quantitative Overview of Architectural Education in Turkey

Vienna-Chicago: Discussions on Architecture and Metropolis

Contemporary Tendencies in the Organization of Public Life and the Production of the City

The relationship between politics and design

Right subclavian artery true aneurysm: A rare cause of dyspnea

Fatal Disseminated Multiple Intracranial Juvenile Xanthogranuloma without Cutaneous and Other Organ Involvement: A Rare Case Report

Incidentally detected asymptomatic splenic artery aneurysm

The Authors' Reply: In systemic pseudohypoaldosteronism type 1 skin manifestations are not rare and the disease is not transient

Comparison of cardiovascular, cancer and herpes zoster risk of tofacitinib versus etanercept: Single Centre Observational Study

A novel homozygous nonsense NDNF variant in Kallmann syndrome

DLG2 Mutations in the Etiology of Pubertal Delay and Idiopathic Hypogonadotropic Hypogonadism

Inactivating NHLH2 variants cause idiopathic hypogonadotropic hypogonadism and obesity in humans

Differences and similarities of proliferative and non-proliferative forms of biopsy-proven lupus nephritis: Single centre, cross-disciplinary experience

Molecular genetic studies in a case series of isolated hypoaldosteronism due to biosynthesis defects or aldosterone resistance

The Comparison of scoring systems: SOFA, APACHE-II, LODS, MODS, and SAPS-II in critically ill elderly sepsis patients

What Does COVID-19 Have to Do With Flying Cats?

Post-operative pain management for single-level lumbar disc herniation surgery: A comparison of betamethasone, ibuprofen, and pregabalin

Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism

Prevalence and associated phenotypes of PLXNA1 variants in normosmic and anosmic idiopathic hypogonadotropic hypogonadism

CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism

Proposal of a new nomenclature for the underlying pathogenetic mechanism of severe Coronavirus Disease-19: “Inflammatory Thrombosis with Immune Endotheliitis—ITIE”

Agomelatine modulates calcium signaling through protein kinase C and phospholipase C‐mediated mechanisms in rat sensory neurons

21-Hydroxylase deficiency: Mutational spectrum and Genotype–Phenotype relations analyses by next-generation sequencing and multiplex ligation-dependent probe amplification

17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort

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