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IL-17A, MCP-1, CCR-2, and ABCA1 polymorphisms in children with non-alcoholic fatty liver disease

Jornal de pediatria, 2019-05, Vol.95 (3), p.350-357

2019

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Importance and usage of chromosomal microarray analysis in diagnosing intellectual disability, global developmental delay, and autism; and discovering new loci for these disorders

Molecular cytogenetics, 2018-09, Vol.11 (1), p.54-54, Article 54

2018

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IL‐17A, MCP‐1, CCR‐2, and ABCA1 polymorphisms in children with non‐alcoholic fatty liver disease

Jornal de Pediatria (Versão em Português), 2019-05, Vol.95 (3), p.350-357

2019

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Geç Tanı Almış Komplet Virilize Bir 46,XX 11-Beta Hidroksilaz Eksikliği Olgusu

Gazi tıp dergisi, 2016-03, Vol.27 (3)

2016

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Combination treatment of bortezomib and epirubicin increases the expression of TNFRSF10 A/B, and induces TRAIL-mediated cell death in colorectal cancer cells

Biochemical and biophysical research communications, 2023-10, Vol.675, p.33-40

2023

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A novel INPP4A mutation with pontocerebellar hypoplasia, myoclonic epilepsy, microcephaly, and severe developmental delay

Brain & development (Tokyo. 1979), 2023-05, Vol.45 (5), p.300-305

2023

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Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients

Clinical immunology (Orlando, Fla.), 2023-10, Vol.255, p.109757-109757, Article 109757

2023

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Corrigendum to “Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients” [Clinical Immunology 255 (2023) 109757]

Clinical immunology (Orlando, Fla.), 2023-11, Vol.256, p.109799-109799, Article 109799

2023

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An Alternative Perspective to the FMF Clinic: MCP-1 (A-2518G) and CCR2 (G190A) Polymorphisms and MCP1 Expression

Çağdaş tıp dergisi, 2022-09, Vol.12 (5), p.804-810

2022

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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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ASD with the Bor Syndrome: A Case Report

Psychopharmacology bulletin, 2020-05, Vol.50 (2), p.45-50

2020

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Maternal Germline Mosaicism of a de Novo TUBB2B Mutation Leads to Complex Cortical Dysplasia in Two Siblings

Fetal and pediatric pathology, 2022-02, Vol.41 (1), p.155-165

2022

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A novel INPP4A mutation with pontocerebellar hypoplasia, myoclonic epilepsy, microcephaly, and severe developmental delay

Brain & development, 2023, Vol.45 (5), p.300-305

2023

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Investigation of sub‐chromosomal changes in males with idiopathic azoospermia by chromosomal microarray analysis

Andrologia, 2022-10, Vol.54 (9), p.e14489-n/a

2022

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Akut Koroner Sendromlu Genç Hastalarda Monosit Kemoatraktan Protein-1 ve CC Kemokin Reseptörü Tip 2 Gen Polimorfizmlerinin Klinik Önemi

Harran Üniversitesi Tıp Fakültesi Dergisi, 2022-08, Vol.19 (2), p.272-276

2022

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ASD with the Bor Syndrome: A Case Report

Psychopharmacology bulletin, 2020, Vol.50 (2), p.45-50

2020

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IL-1β, IL-18 and Caspase-1 Levels in Serum as an Early Marker in Familial Mediterranean Fever Patients with Attack and Attack-free Period

Çağdaş tıp dergisi, 2021-07, Vol.11 (4), p.494-499

2021

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IL-1β, IL-18 and Caspase-1 Levels in Serum as an Early Marker in Familial Mediterranean Fever Patients with Attack and Attack-free Period

Çağdaş tıp dergisi, 2021-07, Vol.11 (4), p.494-499

2021

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Faktör V Leiden ve Mthfr İkili Mutasyonu Bulunan Renal Ven Trombozlu Yenidoğan Olgusu

Çağdaş tıp dergisi, 2015, Vol.5 (2)

2015

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Maternal Germline Mosaicism of a de Novo TUBB2B Mutation Leads to Complex Cortical Dysplasia in Two Siblings

Fetal and Pediatric Pathology, 2022, Vol.41 (1), p.155-165

2022

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IL-17A, MCP-1, CCR-2, and ABCA1 polymorphisms in children with non-alcoholic fatty liver disease

Importance and usage of chromosomal microarray analysis in diagnosing intellectual disability, global developmental delay, and autism; and discovering new loci for these disorders

IL‐17A, MCP‐1, CCR‐2, and ABCA1 polymorphisms in children with non‐alcoholic fatty liver disease

Geç Tanı Almış Komplet Virilize Bir 46,XX 11-Beta Hidroksilaz Eksikliği Olgusu

Combination treatment of bortezomib and epirubicin increases the expression of TNFRSF10 A/B, and induces TRAIL-mediated cell death in colorectal cancer cells

A novel INPP4A mutation with pontocerebellar hypoplasia, myoclonic epilepsy, microcephaly, and severe developmental delay

Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients

Corrigendum to “Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients” [Clinical Immunology 255 (2023) 109757]

An Alternative Perspective to the FMF Clinic: MCP-1 (A-2518G) and CCR2 (G190A) Polymorphisms and MCP1 Expression

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

ASD with the Bor Syndrome: A Case Report

Maternal Germline Mosaicism of a de Novo TUBB2B Mutation Leads to Complex Cortical Dysplasia in Two Siblings

A novel INPP4A mutation with pontocerebellar hypoplasia, myoclonic epilepsy, microcephaly, and severe developmental delay

Investigation of sub‐chromosomal changes in males with idiopathic azoospermia by chromosomal microarray analysis

Akut Koroner Sendromlu Genç Hastalarda Monosit Kemoatraktan Protein-1 ve CC Kemokin Reseptörü Tip 2 Gen Polimorfizmlerinin Klinik Önemi

ASD with the Bor Syndrome: A Case Report

IL-1β, IL-18 and Caspase-1 Levels in Serum as an Early Marker in Familial Mediterranean Fever Patients with Attack and Attack-free Period

IL-1β, IL-18 and Caspase-1 Levels in Serum as an Early Marker in Familial Mediterranean Fever Patients with Attack and Attack-free Period

Faktör V Leiden ve Mthfr İkili Mutasyonu Bulunan Renal Ven Trombozlu Yenidoğan Olgusu

Maternal Germline Mosaicism of a de Novo TUBB2B Mutation Leads to Complex Cortical Dysplasia in Two Siblings

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