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A rare giant congenital left atrial appendage aneurysm in a 1‐day‐old newborn

Echocardiography (Mount Kisco, N.Y.), 2018-05, Vol.35 (5), p.757-759

2018

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A rare case in literature: Isochromosome Xq in Klinefelter syndrome

Andrologia, 2019-06, Vol.51 (5), p.e13253-n/a

2019

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A girl with metopic synostosis and trisomy 13 mosaicism: Case report and review of the literature

American journal of medical genetics. Part A, 2011-03, Vol.155 (3), p.638-641

2011

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Cerebral creatine deficiency syndrome with a novel missense variant in SLC6A8 gene

Neurology and clinical neuroscience, 2023-09, Vol.11 (5), p.286-288

2023

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A Turkish Family with Loeys-dietz Syndrome and a Report of a Homozygous Patient with SMAD3 Pathogenic Variation

Haseki tıp bülteni, 2022-01, Vol.60 (1), p.84-88

2022

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Evaluation of immunological abnormalities in patients with rare syndromes

Central-European journal of immunology, 2022-01, Vol.47 (4), p.299-307

2022

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Relationship between Glutathione S-transferase gene polymorphisms and clinical features of psoriasis: A case-control study in the Turkish population

Türkderm, 2024-10, Vol.58 (3), p.75-82

2024

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Generalized aggressive periodontitis in a child with 92, XXYY / 46,XY mosaicism: report of a second case

Turkish journal of pediatrics, 2010-01, Vol.52 (1), p.94-96

2010

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Exploring Methylphenidate-Induced Intraocular Pressure: A Cautionary Tale in Pediatric ADHD Management

Clinical neuropharmacology, 2024-09, Vol.47 (5), p.141-142

2024

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Psychometric properties of Turkish Orthorexia Nervosa Inventory in a clinical adolescent sample

Eating and weight disorders, 2023-09, Vol.28 (1), p.70-70, Article 70

2023

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Investigation of the relationship between ischemic stroke and endothelial nitric oxide synthase gene polymorphisms [G894T, intron 4 VNTR and T786C]

TURKISH JOURNAL OF MEDICAL SCIENCES, 2019-04, Vol.49 (2), p.589-594

2019

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Examination of symptoms related to cognitive disengagement syndrome in a clinical cohort of school-aged children

Düşünen adam (Bakırköy Ruh ve Sinir Hastalıkları Hastanesi), 2023-12, p.201-207

Yildirim, Selman

2023

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Electromyographic analysis of an ergonomic risk factor: overhead work

Journal of Physical Therapy Science, 2016, Vol.28(6), pp.1924-1927

2016

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The XRCC1 and TP53 gene polymorphisms are associated with advanced-stage disease and early distant metastasis at diagnosis in non-small cell lung cancer

Journal of cancer research and therapeutics, 2023-07, Vol.19 (5), p.1248-1254

2023

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Case Report: Seizures in a Child Caused by a Large Venous Angioma

Journal of child neurology, 2007-06, Vol.22 (6), p.787-789

2007

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Duplicate Mitral Valve in an Infant With Shone's Anomaly

The Annals of thoracic surgery, 2009-11, Vol.88 (5), p.1683-1685

2009

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Whole exome sequencing identifies three novel mutations in ANTXR1 in families with GAPO syndrome

American journal of medical genetics. Part A, 2014-09, Vol.164A (9), p.2328-2334

2014

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Interchromosomal effect: Report of a father and son, bearing different translocations of the same chromosome, and a review of the current literature

Andrologia, 2021-02, Vol.53 (1), p.e13805-n/a

2021

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Recurrent proximal 18p monosomy and 18q trisomy in a family due to a pericentric inversion

American journal of medical genetics. Part A, 2014-05, Vol.164A (5), p.1239-1244

2014

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Assessment of left ventricular diastolic function by Doppler tissue imaging in children with end-stage renal disease

Acta pædiatrica (Oslo), 2005-08, Vol.94 (8), p.1055-1059

2005

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Congenital Pulmonary Venous Stenosis Combined with Valvular Aortic Stenosis: A Very Rare Case

Congenital heart disease, 2008-05, Vol.3 (3), p.223-225

2008

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Comparison of MicroRNA Levels of 18-60-month-old Autistic Children with Those of Their Siblings and Controls

Clinical Psychopharmacology and Neuroscience, 2024, 22(2), , pp.322-332

2024

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NAT2 Gene Polymorphisms in Turkish Patients with Psoriasis Vulgaris

BioMed research international, 2018-01, Vol.2018 (2018), p.1-14

2018

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Changes in adolescent mental health during the Covid pandemic

Minerva Pediatrics, 2021-04, Vol.76 (5)

2021

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The Genetic Analysis of Cystic Fibrosis Patients With Seven Novel Mutations in the CFTR Gene in the Central Anatolian Region of Turkey

Balkan Medical Journal, 2021-11, Vol.38 (6), p.357-364

2021

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A rare giant congenital left atrial appendage aneurysm in a 1‐day‐old newborn

A rare case in literature: Isochromosome Xq in Klinefelter syndrome

A girl with metopic synostosis and trisomy 13 mosaicism: Case report and review of the literature

Cerebral creatine deficiency syndrome with a novel missense variant in SLC6A8 gene

A Turkish Family with Loeys-dietz Syndrome and a Report of a Homozygous Patient with SMAD3 Pathogenic Variation

Evaluation of immunological abnormalities in patients with rare syndromes

Relationship between Glutathione S-transferase gene polymorphisms and clinical features of psoriasis: A case-control study in the Turkish population

Generalized aggressive periodontitis in a child with 92, XXYY / 46,XY mosaicism: report of a second case

Exploring Methylphenidate-Induced Intraocular Pressure: A Cautionary Tale in Pediatric ADHD Management

Psychometric properties of Turkish Orthorexia Nervosa Inventory in a clinical adolescent sample

Investigation of the relationship between ischemic stroke and endothelial nitric oxide synthase gene polymorphisms [G894T, intron 4 VNTR and T786C]

Examination of symptoms related to cognitive disengagement syndrome in a clinical cohort of school-aged children

Electromyographic analysis of an ergonomic risk factor: overhead work

The XRCC1 and TP53 gene polymorphisms are associated with advanced-stage disease and early distant metastasis at diagnosis in non-small cell lung cancer

Case Report: Seizures in a Child Caused by a Large Venous Angioma

Duplicate Mitral Valve in an Infant With Shone's Anomaly

Whole exome sequencing identifies three novel mutations in ANTXR1 in families with GAPO syndrome

Interchromosomal effect: Report of a father and son, bearing different translocations of the same chromosome, and a review of the current literature

Recurrent proximal 18p monosomy and 18q trisomy in a family due to a pericentric inversion

Assessment of left ventricular diastolic function by Doppler tissue imaging in children with end-stage renal disease

Congenital Pulmonary Venous Stenosis Combined with Valvular Aortic Stenosis: A Very Rare Case

Comparison of MicroRNA Levels of 18-60-month-old Autistic Children with Those of Their Siblings and Controls

NAT2 Gene Polymorphisms in Turkish Patients with Psoriasis Vulgaris

Changes in adolescent mental health during the Covid pandemic

The Genetic Analysis of Cystic Fibrosis Patients With Seven Novel Mutations in the CFTR Gene in the Central Anatolian Region of Turkey

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