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Nitric oxide synthase gene polymorphisms in children with minimal change nephrotic syndrome

Pediatrics international, 2009-02, Vol.51 (1), p.75-78

2009

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Significance of catechol-O-methyltransferase gene polymorphism in fibromyalgia syndrome

Rheumatology international, 2003-05, Vol.23 (3), p.104-107

2003

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Knowledge and Attitudes of Resident Physicians About Adverse Drug Reactions

Konuralp Tıp Dergisi, 2020-10, Vol.12 (3), p.498-502

2020

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Relationship between soluble intercellular adhesion molecules and attention-deficit/hyperactivity disorder

International journal of psychiatry in medicine, 2015-08, Vol.50 (2), p.238-247

2015

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Association of T102C polymorphism of the 5-HT2A receptor gene with pyschiatric status in fibromyalgia syndrome

Rheumatology international, 2001-10, Vol.21 (2), p.58-61

2001

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Evaluation of the attitudes of the nurses related to rational drug use in Gaziantep University Sahinbey Research and Practice Hospital in Turkey

Nurse education today, 2015-02, Vol.35 (2), p.395-401

2015

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Lack of Association Between the C276T Polymorphism of the Neuronal Nitric Oxide Synthase Gene and Migraine

International journal of neuroscience, 2013-01, Vol.123 (1), p.50-54

2013

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Evidence for elevated (LIMK2 and CFL1) and suppressed (ICAM1, EZR, MAP2K2, and NOS3) gene expressions in metabolic syndrome

Endocrine, 2016-08, Vol.53 (2), p.465-470

2016

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CYP gene expressions in obesity-associated metabolic syndrome

Obesity research & clinical practice, 2016-11, Vol.10 (6), p.719-723

2016

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Association between Rho-kinase ( ROCK2) gene polymorphisms and Behçet’s disease

Translational research : the journal of laboratory and clinical medicine, 2012-12, Vol.160 (6), p.428-434

2012

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Investigation of intercellular adhesion molecules (ICAMs) gene expressions in patients with Barrett's esophagus

Tumor biology, 2014-05, Vol.35 (5), p.4907-4912

2014

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Which genotype of MAO gene that the patients have are likely to be most susceptible to the symptoms of fibromyalgia?

Rheumatology international, 2008-02, Vol.28 (4), p.307-311

2008

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Significance of Serotonin Transporter Gene 5-HTTLPR and Variable Number of Tandem Repeat Polymorphism in Attention Deficit Hyperactivity Disorder

Neuropsychobiology, 2002-01, Vol.45 (4), p.176-181

2002

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No evidence for an association between the Glu298Asp polymorphism of the endothelial nitric oxide synthase gene and fibromyalgia syndrome

Rheumatology international, 2007-01, Vol.27 (3), p.275-280

2007

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Association of Rho-kinase 1 (ROCK1) Gene Polymorphisms with Behçet’s Disease

Molecular diagnosis & therapy, 2014-08, Vol.18 (4), p.419-426

2014

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Toward Novel Diagnostics for Primary Open-Angle Glaucoma? An Association Study of Polymorphic Variation in Ras Homolog Family Member (A, B, C, D) Genes RHOA, RHOB, RHOC, and RHOD

Omics (Larchmont, N.Y.), 2016-05, Vol.20 (5), p.290-295

2016

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Association between polymorphism of the angiotensin I converting enzyme gene and hypertension in Turkish type II diabetic patients

Acta medica Lékarskí fakulty Univerzity Karlovy v Hradci Králove, 2001, Vol.44 (1), p.29-32

2001

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DD Genotype of ACE Gene in Boys: May it be a Risk Factor for Minimal Change Nephrotic Syndrome?

Renal failure, 2012-02, Vol.34 (1), p.19-23

2012

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Lack of Association between the Thr431Asn and Arg83Lys Polymorphisms of the ROCK2 Gene and Diabetic Retinopathy

Current eye research, 2010-12, Vol.35 (12), p.1128-1134

2010

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Investigation of the Esophageal Rho-kinase Expression in Patients with Barrett's Esophagus

Ultrastructural pathology, 2013-08, Vol.37 (4), p.284-289

2013

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Nitric Oxide Synthase Gene Polymorphisms in Children with Primary Nocturnal Enuresis: A Preliminary Study

Renal failure, 2007, Vol.29 (1), p.79-83

2007

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Taqı polymorphism of the vitamin-D receptor gene and quality of life in postmenopausal Turkish women

Turkish journal of medical sciences, 2008-02, Vol.38 (1), p.21-26

2008

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Evaluation of Antibiotic Prophylaxis in the University of Gaziantep Medical Faculty Research Hospital Surgical Departments

European journal of therapeutics, 2011-01, Vol.17 (1), p.11-14

2011

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Angiotensin converting enzyme gene insertion/deletion polymorphism in migraine patients

Türk nöroloji dergisi, 2009-01, Vol.15 (4), p.161-165

2009

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High dose of caffeine administered to pregnant rats causes histopathological changes in the cornea of newborn pups

Medical science monitor, 2003-05, Vol.9 (5), p.BR168

2003

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Nitric oxide synthase gene polymorphisms in children with minimal change nephrotic syndrome

Significance of catechol-O-methyltransferase gene polymorphism in fibromyalgia syndrome

Knowledge and Attitudes of Resident Physicians About Adverse Drug Reactions

Relationship between soluble intercellular adhesion molecules and attention-deficit/hyperactivity disorder

Association of T102C polymorphism of the 5-HT2A receptor gene with pyschiatric status in fibromyalgia syndrome

Evaluation of the attitudes of the nurses related to rational drug use in Gaziantep University Sahinbey Research and Practice Hospital in Turkey

Lack of Association Between the C276T Polymorphism of the Neuronal Nitric Oxide Synthase Gene and Migraine

Evidence for elevated (LIMK2 and CFL1) and suppressed (ICAM1, EZR, MAP2K2, and NOS3) gene expressions in metabolic syndrome

CYP gene expressions in obesity-associated metabolic syndrome

Association between Rho-kinase ( ROCK2) gene polymorphisms and Behçet’s disease

Investigation of intercellular adhesion molecules (ICAMs) gene expressions in patients with Barrett's esophagus

Which genotype of MAO gene that the patients have are likely to be most susceptible to the symptoms of fibromyalgia?

Significance of Serotonin Transporter Gene 5-HTTLPR and Variable Number of Tandem Repeat Polymorphism in Attention Deficit Hyperactivity Disorder

No evidence for an association between the Glu298Asp polymorphism of the endothelial nitric oxide synthase gene and fibromyalgia syndrome

Association of Rho-kinase 1 (ROCK1) Gene Polymorphisms with Behçet’s Disease

Toward Novel Diagnostics for Primary Open-Angle Glaucoma? An Association Study of Polymorphic Variation in Ras Homolog Family Member (A, B, C, D) Genes RHOA, RHOB, RHOC, and RHOD

Association between polymorphism of the angiotensin I converting enzyme gene and hypertension in Turkish type II diabetic patients

DD Genotype of ACE Gene in Boys: May it be a Risk Factor for Minimal Change Nephrotic Syndrome?

Lack of Association between the Thr431Asn and Arg83Lys Polymorphisms of the ROCK2 Gene and Diabetic Retinopathy

Investigation of the Esophageal Rho-kinase Expression in Patients with Barrett's Esophagus

Nitric Oxide Synthase Gene Polymorphisms in Children with Primary Nocturnal Enuresis: A Preliminary Study

Taqı polymorphism of the vitamin-D receptor gene and quality of life in postmenopausal Turkish women

Evaluation of Antibiotic Prophylaxis in the University of Gaziantep Medical Faculty Research Hospital Surgical Departments

Angiotensin converting enzyme gene insertion/deletion polymorphism in migraine patients

High dose of caffeine administered to pregnant rats causes histopathological changes in the cornea of newborn pups

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