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Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in Central Anatolia

Annals of Saudi medicine, 2019-11, Vol.39 (6), p.382-387

2019

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CCR2 Polymorphism in Chronic Renal Failure Patients Requiring Long-Term Hemodialysis

Internal Medicine, 2011, Vol.50(21), pp.2457-2461

2011

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Associations of fractalkine receptor (CX3CR1) and CCR5 gene variants with hypertension, diabetes and atherosclerosis in chronic renal failure patients undergoing hemodialysis

International urology and nephrology, 2016-07, Vol.48 (7), p.1163-1170

2016

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Frequency of familial Mediterranean fever (MEFV) gene mutations in patients with biopsy-proven primary glomerulonephritis

Clinical rheumatology, 2017-11, Vol.36 (11), p.2589-2594

2017

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The protective effect of MCP-1 -2518 A>G promoter polymorphism in Turkish chronic renal failure patients requiring long-term hemodialysis

International urology and nephrology, 2015-03, Vol.47 (3), p.551-556

2015

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The type and prevalence of chromosomal abnormalities in couples with recurrent first trimester abortions: A Turkish retrospective study

Journal of gynecology obstetrics and human reproduction, 2019-09, Vol.48 (7), p.521-525

2019

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The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas

The journal of international advanced otology, 2019-12, Vol.15 (3), p.373-378

2019

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A comparison of acoustic radiation force impulse imaging and scintigraphy in the functional evaluation of the major salivary glands

Nuclear medicine communications, 2015-12, Vol.36 (12), p.1220-1226

2015

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The effect of the time interval between the last breastfeeding and Tc-99m MIBI injection on the intensity of Tc-99m MIBI uptake in breast tissue

Medical Science and Discovery, 2015-10, Vol.3 (1)

2015

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8Q22.3-Q24.23 Duplication: A Case Report

Journal of clinical research in pediatric endocrinology, 2017-06, Vol.9 (2), p.1

2017

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Analysis of PKD1 and PKD2 Gene Mutations for Autosomal Dominant Polycystic Kidney Disease Cases in Turkish Population

Turkish journal of nephrology, 2020-10, Vol.29 (4), p.304-309

2020

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The Role of the CCR2 Gene Polymorphism in Abdominal Aortic Aneurysms

Angiology, 2011-02, Vol.62 (2), p.140-143

2011

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Prevalence of known mutations in the MEFV gene in a population screening with high rate of carriers

Molecular biology reports, 2011-06, Vol.38 (5), p.3195-3200

2011

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Recombinant chromosome with partial 14 q trisomy due to maternal pericentric inversion

Molecular cytogenetics, 2015-11, Vol.8 (92), p.92, Article 92

2015

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Complete Androgen Insensitivity Syndrome with 45, XY, t(13q; 14q) Translocation (Two cases)

CYTOLOGIA, 2002, Vol.67(2), pp.135-137

2002

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Dental Findings in Cornelia De Lange Syndrome

Yonsei medical journal, 2009-04, p.289-292

2009

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Analysis of HumFABP2 as a polymorphic human genetic marker in the Turkish population

Saudi medical journal, 2007-10, Vol.28 (10), p.1493

2007

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8Q22.3-Q24.23 Duplication: A Case Report

Journal of clinical research in pediatric endocrinology, 2017-06, Vol.9 (1), p.1

2017

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Karyotype Analysis in Alburnus heckeli (Battalgil, 1943) from Lake Hazer

Turkish Journal of Veterinary and Animal Sciences; Year: 2004 Volume: 28 Issue: 2; 309-314, 2004-01, Vol.28 (2), p.309-314

GÜL, Süleyman

2004

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Effect of the reverse redistribution pattern on the left ventricular ejection fraction in the Tc-99m MIBI SPECT myocardial perfusion scintigraphy

Journal of clinical and experimental investigations, 2015-10, Vol.6 (3), p.286

2015

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Adult height in Turkish patients with Turner syndrome without growth hormone treatment

Turkish journal of pediatrics, 2008-09, Vol.50 (5), p.415-417

2008

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Meckel-gruber syndrome associated with gastrointestinal tractus anomaly

Turkish journal of pediatrics, 2004-10, Vol.46 (4), p.388-392

2004

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Comparison of thyroid scintigraphy and ARFI-elastography in autoimmune thyroid diseases

Journal of health sciences and medicine : (Turkey), 2022-03, Vol.5 (2), p.504-509

2022

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Mesoaxial complete syndactyly and synostosis with hypoplastic thumbs: an unusual combination or homozygous expression of syndactyly type I?

Journal of medical genetics, 1998-10, Vol.35 (10), p.868-874

1998

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Van Gölüne endemik olan inci kefali (Chalcalburnus tarichi Pallas 1811) kromozomlarının C,G ve restriksiyon endonükleazlar (Alu I, Nhe III,Hae III, Mbo I, Hinf I) ile bantlanması

Turkish journal of veterinary & animal sciences, 2003, Vol.27 (6), p.1293-1298

2003

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Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in Central Anatolia

CCR2 Polymorphism in Chronic Renal Failure Patients Requiring Long-Term Hemodialysis

Associations of fractalkine receptor (CX3CR1) and CCR5 gene variants with hypertension, diabetes and atherosclerosis in chronic renal failure patients undergoing hemodialysis

Frequency of familial Mediterranean fever (MEFV) gene mutations in patients with biopsy-proven primary glomerulonephritis

The protective effect of MCP-1 -2518 A>G promoter polymorphism in Turkish chronic renal failure patients requiring long-term hemodialysis

The type and prevalence of chromosomal abnormalities in couples with recurrent first trimester abortions: A Turkish retrospective study

The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas

A comparison of acoustic radiation force impulse imaging and scintigraphy in the functional evaluation of the major salivary glands

The effect of the time interval between the last breastfeeding and Tc-99m MIBI injection on the intensity of Tc-99m MIBI uptake in breast tissue

8Q22.3-Q24.23 Duplication: A Case Report

Analysis of PKD1 and PKD2 Gene Mutations for Autosomal Dominant Polycystic Kidney Disease Cases in Turkish Population

The Role of the CCR2 Gene Polymorphism in Abdominal Aortic Aneurysms

Prevalence of known mutations in the MEFV gene in a population screening with high rate of carriers

Recombinant chromosome with partial 14 q trisomy due to maternal pericentric inversion

Complete Androgen Insensitivity Syndrome with 45, XY, t(13q; 14q) Translocation (Two cases)

Dental Findings in Cornelia De Lange Syndrome

Analysis of HumFABP2 as a polymorphic human genetic marker in the Turkish population

8Q22.3-Q24.23 Duplication: A Case Report

Karyotype Analysis in Alburnus heckeli (Battalgil, 1943) from Lake Hazer

Effect of the reverse redistribution pattern on the left ventricular ejection fraction in the Tc-99m MIBI SPECT myocardial perfusion scintigraphy

Adult height in Turkish patients with Turner syndrome without growth hormone treatment

Meckel-gruber syndrome associated with gastrointestinal tractus anomaly

Comparison of thyroid scintigraphy and ARFI-elastography in autoimmune thyroid diseases

Mesoaxial complete syndactyly and synostosis with hypoplastic thumbs: an unusual combination or homozygous expression of syndactyly type I?

Van Gölüne endemik olan inci kefali (Chalcalburnus tarichi Pallas 1811) kromozomlarının C,G ve restriksiyon endonükleazlar (Alu I, Nhe III,Hae III, Mbo I, Hinf I) ile bantlanması

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