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Neonatal Diabetes, Congenital Hypothyroidism, and Congenital Glaucoma Coexistence: A Case of GLIS3 Mutation

Journal of clinical research in pediatric endocrinology, 2023-12, Vol.15 (4), p.426-430

2023

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Current and Future Therapeutic Strategies for Limb Girdle Muscular Dystrophy Type R1: Clinical and Experimental Approaches

Pathophysiology (Amsterdam), 2021-05, Vol.28 (2), p.238-249

2021

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Comparing expression levels of PERIOD genes PER1, PER2 and PER3 in chronic insomnia patients and medical staff working in the night shift

Sleep medicine, 2020-09, Vol.73, p.101-105

2020

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Frequency of RPE65 Gene Mutation in Patients with Hereditary Retinal Dystrophy

Turk oftalmoloji gazetesi, 2022-08, Vol.52 (4), p.270-275

2022

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A Rare Cause of Hypotonia: 49,XXXXX (Pentasomy X): A Rare Cause of Hypotonia: 49,XXXXX (Pentasomy X)

Journal of pediatric academy, 2023-12, Vol.4 (4), p.149-151

2023

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Congenital Myasthenic Syndromes in Turkey: Clinical and Molecular Characterization of 16 Cases With Three Novel Mutations

Pediatric neurology, 2022-11, Vol.136, p.43-49

2022

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ABCA4 variant screening in a Turkish cohort with Stargardt disease

Ophthalmic genetics, 2024-04, Vol.45 (2), p.133-139

2024

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Current Advances in Breast Cancer: Implications for Developing New Treatment Strategies Through Epi-Drugs on the Road to Modifying the Epigenome

Journal of Clinical Practice & Research, 2023-09, Vol.45 (5), p.427-434

Kenanoğlu, Sercan

2023

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Loss of Dermatan-4-Sulfotransferase 1 Function Results in Adducted Thumb-Clubfoot Syndrome

American journal of human genetics, 2009-12, Vol.85 (6), p.873-882

2009

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Ameliorative effects of pentoxifylline on NOS induced by diabetes in rat kidney

Renal failure, 2016-04, Vol.38 (4), p.605-613

2016

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A retrospective study on the clinical and molecular outcomes of calpainopathy in a Turkish patient cohort

Turkish journal of medical sciences, 2024-01, Vol.54 (1), p.86-98

2024

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The frequencies of Y chromosome microdeletions in infertile males

Turkish journal of urology, 2018-09, Vol.44 (5), p.389-392

2018

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The effect of cytokine leukemia-inhibitory factor (LIF) and interleukin-11 (IL-11) gene expression on the primary infertility related to polycystic ovary syndrome, Tubal factor, and Unexplained infertility in Turkish women

The Egyptian journal of medical human genetics, 2021-12, Vol.22 (1), p.85

2021

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Nitric oxide synthase in diabetic rat testicular tissue and the effects of pentoxifylline therapy

Systems biology in reproductive medicine, 2016-01, Vol.62 (1), p.22-30

2016

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Loss of dermatan-4-sulfotransferase 1 (D4ST1/CHST14) function represents the first dermatan sulfate biosynthesis defect, "dermatan sulfate-deficient adducted thumb-clubfoot syndrome"

Human mutation, 2011-04, Vol.32 (4), p.484-485

2011

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The Association of Brain-Derived Neurotrophic Factor Gene Polymorphism with Obstructive Sleep Apnea Syndrome and Obesity

Lung, 2016-10, Vol.194 (5), p.839-846

2016

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A rare cause of membranoproliferative patterns of injury in siblings with steroid-resistant nephrotic syndrome: Answers

Pediatric nephrology (Berlin, West), 2021-12, Vol.36 (12), p.4029-4032

2021

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A rare cause of membranoproliferative patterns of injury in siblings with steroid-resistant nephrotic syndrome: Questions

Pediatric nephrology (Berlin, West), 2021-12, Vol.36 (12), p.4027-4028

2021

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Evaluation of aortic intima-media thickness in newborns with Down syndrome

Advances in clinical and experimental medicine : official organ Wroclaw Medical University, 2017-11, Vol.26 (8), p.1253-1256

2017

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European Biotechnology Congress 2022

The eurobiotech journal, 2023-01, Vol.7 (1), p.1-3

2023

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Recurrent symptomatic urolithiasis in a patient with cystic fibrosis

Pediatric nephrology (Berlin, West), 2024-06

2024

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Impacts of Biotechnologically Developed Microorganisms on Ecosystems

The eurobiotech journal, 2023-10, Vol.7 (4), p.196-205

2023

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Loss of dermatan sulfate epimerase (DSE) function results in musculocontractural Ehlers-Danlos syndrome

Human molecular genetics, 2013-09, Vol.22 (18), p.3761-3772

2013

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The Age Structure, Stringency Policy, Income, and Spread of Coronavirus Disease 2019: Evidence From 209 Countries

Frontiers in psychology, 2021-02, Vol.11, p.632192-632192

2021

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A Case Series of Three Patients with Cleidocranial Dysplasia: Clinical Presentation and Diagnostic Considerations

The Cleft palate-craniofacial journal, 2024-02, p.10556656241234742-10556656241234742

2024

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Neonatal Diabetes, Congenital Hypothyroidism, and Congenital Glaucoma Coexistence: A Case of GLIS3 Mutation

Current and Future Therapeutic Strategies for Limb Girdle Muscular Dystrophy Type R1: Clinical and Experimental Approaches

Comparing expression levels of PERIOD genes PER1, PER2 and PER3 in chronic insomnia patients and medical staff working in the night shift

Frequency of RPE65 Gene Mutation in Patients with Hereditary Retinal Dystrophy

A Rare Cause of Hypotonia: 49,XXXXX (Pentasomy X): A Rare Cause of Hypotonia: 49,XXXXX (Pentasomy X)

Congenital Myasthenic Syndromes in Turkey: Clinical and Molecular Characterization of 16 Cases With Three Novel Mutations

ABCA4 variant screening in a Turkish cohort with Stargardt disease

Current Advances in Breast Cancer: Implications for Developing New Treatment Strategies Through Epi-Drugs on the Road to Modifying the Epigenome

Loss of Dermatan-4-Sulfotransferase 1 Function Results in Adducted Thumb-Clubfoot Syndrome

Ameliorative effects of pentoxifylline on NOS induced by diabetes in rat kidney

A retrospective study on the clinical and molecular outcomes of calpainopathy in a Turkish patient cohort

The frequencies of Y chromosome microdeletions in infertile males

The effect of cytokine leukemia-inhibitory factor (LIF) and interleukin-11 (IL-11) gene expression on the primary infertility related to polycystic ovary syndrome, Tubal factor, and Unexplained infertility in Turkish women

Nitric oxide synthase in diabetic rat testicular tissue and the effects of pentoxifylline therapy

Loss of dermatan-4-sulfotransferase 1 (D4ST1/CHST14) function represents the first dermatan sulfate biosynthesis defect, "dermatan sulfate-deficient adducted thumb-clubfoot syndrome"

The Association of Brain-Derived Neurotrophic Factor Gene Polymorphism with Obstructive Sleep Apnea Syndrome and Obesity

A rare cause of membranoproliferative patterns of injury in siblings with steroid-resistant nephrotic syndrome: Answers

A rare cause of membranoproliferative patterns of injury in siblings with steroid-resistant nephrotic syndrome: Questions

Evaluation of aortic intima-media thickness in newborns with Down syndrome

European Biotechnology Congress 2022

Recurrent symptomatic urolithiasis in a patient with cystic fibrosis

Impacts of Biotechnologically Developed Microorganisms on Ecosystems

Loss of dermatan sulfate epimerase (DSE) function results in musculocontractural Ehlers-Danlos syndrome

The Age Structure, Stringency Policy, Income, and Spread of Coronavirus Disease 2019: Evidence From 209 Countries

A Case Series of Three Patients with Cleidocranial Dysplasia: Clinical Presentation and Diagnostic Considerations

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