Yayınlar & Eserler

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Congenital erythropoietic porphyria with erythrodontia: A case report

INTERNATIONAL JOURNAL OF PAEDIATRIC DENTISTRY, cilt.29, ss.542-548, 2019 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Successful Treatment of Tardive Oculogyric Crisis with Bornaprine

ISRAEL JOURNAL OF PSYCHIATRY AND RELATED SCIENCES, cilt.56, ss.53-56, 2019 (SCI İndekslerine Giren Dergi) identifier identifier

CLINIC AND GENETIC PRESENTATION OF CHILDREN WITH CYSTINURIA

PEDIATRIC NEPHROLOGY, cilt.33, ss.1912, 2018 (SCI İndekslerine Giren Dergi) identifier

Ataxia-Telangiectasia Clinical and Laboratory Features: Single Center Results

PEDIATRIC ALLERGY IMMUNOLOGY AND PULMONOLOGY, cilt.31, ss.9-14, 2018 (SCI İndekslerine Giren Dergi) identifier identifier

karyotyping of patients with psychomotor retardation and epilepsy

MOLECULAR CYTOGENETICS, cilt.10, 2017 (SCI İndekslerine Giren Dergi) identifier

Systemic levels of ceruloplasmin oxidase activity in allergic asthma and allergic rhinitis

IMMUNOPHARMACOLOGY AND IMMUNOTOXICOLOGY, cilt.34, ss.1047-1053, 2012 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Diğer Dergilerde Yayınlanan Makaleler

A family with two different dystrophies

CUKUROVA MEDICAL JOURNAL, cilt.44, ss.36-40, 2019 (ESCI İndekslerine Giren Dergi) identifier

Molecular diagnosis and diagnosis rate of facio-scapulo-humeral-muscular dystrophy

CUKUROVA MEDICAL JOURNAL, cilt.44, ss.8-12, 2019 (ESCI İndekslerine Giren Dergi) identifier

MELAS family

CUKUROVA MEDICAL JOURNAL, cilt.44, ss.47-51, 2019 (ESCI İndekslerine Giren Dergi) identifier

Mechanisms and diagnostic methods in neurogenetic disease

CUKUROVA MEDICAL JOURNAL, cilt.44, ss.13-16, 2019 (ESCI İndekslerine Giren Dergi) identifier

CADASIL: clinic and genetic corelation

CUKUROVA MEDICAL JOURNAL, cilt.44, ss.41-46, 2019 (ESCI İndekslerine Giren Dergi) identifier

Autosomal-Recessive Spastic Ataxia of Charlevoix-Saguenay: A Turkish Child

JOURNAL OF PEDIATRIC NEUROSCIENCES, cilt.13, ss.355-357, 2018 (ESCI İndekslerine Giren Dergi) identifier identifier identifier

LEPR Deficiency: Prevalence and Importance of a Novel Mutation and Significant Genetic Variants, Usually Underestimated

TURKISH JOURNAL OF ENDOCRINOLOGY AND METABOLISM, cilt.22, ss.85-90, 2018 (ESCI İndekslerine Giren Dergi) Creative Commons License identifier identifier

Clinical utility of of molecular karyotyping

CUKUROVA MEDICAL JOURNAL, cilt.43, ss.44-49, 2018 (ESCI İndekslerine Giren Dergi) identifier identifier

A novel mutation in congenital glucose galactose malabsorption syndrome

CUKUROVA MEDICAL JOURNAL, cilt.43, ss.1062-1064, 2018 (ESCI İndekslerine Giren Dergi) identifier

A Rare Double Aneuploidy Case (Down-Klinefelter)

JOURNAL OF PEDIATRIC GENETICS, cilt.6, ss.241-243, 2017 (ESCI İndekslerine Giren Dergi) identifier identifier

Familial hypertrophic cardiomyopathy: A case with a new mutation in the MYBPC3 gene.

Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir, cilt.45, ss.450-453, 2017 (ESCI İndekslerine Giren Dergi) identifier identifier identifier

What is your diagnosis?

JOURNAL OF THE TURKISH-GERMAN GYNECOLOGICAL ASSOCIATION, cilt.16, ss.121-122, 2015 (ESCI İndekslerine Giren Dergi) identifier identifier identifier

Nörogenetik Hastalıklarda Yaşam Kalitesi: Moleküler Tanı ve Dahası

TURKISH JOURNAL OF NEUROLOGY, no.1, ss.87-91, 2014 (Diğer Kurumların Hakemli Dergileri)

Hemoglobinopatilerde Genetik Modifiye Hematopoetik Kök Hücre Tedavisinde Son Gelişmeler

Archives Medical Review Journal, no.1, ss.14-25, 2014 (Hakemli Üniversite Dergisi)

The Incidence of the Epidemiological Markers of Allergy in Adults

JOURNAL OF CLINICAL AND ANALYTICAL MEDICINE, no.2, ss.138-143, 2014 (Diğer Kurumların Hakemli Dergileri)

Progress of Gene-Modified Hematopoietic Stem Cell Therapy For Hemoglobinopathies

Archives Medical Review Journal, no.1, ss.14-25, 2014 (Hakemli Üniversite Dergisi)

Integrating the bioinformatics into cancer research

International Journal of Cancer Research & Diagnosis, no.1, ss.1-2, 2013 (Diğer Kurumların Hakemli Dergileri)

Omalizumab: Anti-IgE Therapy in Severe Allergic Conditions

Journal of Allergy and Therapy, no.120, ss.1-6, 2012 (Diğer Kurumların Hakemli Dergileri)

Trimetazidine effect on burn-induced intestinal mucosal injury and kidney damage in rats

International Journal of Burn and Trauma, no.2, ss.110-117, 2012 (Diğer Kurumların Hakemli Dergileri)

Immunosenescence

Erciyes Tıp Dergisi, no.3, ss.229-234, 2011 (Diğer Kurumların Hakemli Dergileri)

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

CADASIL: klinik-genetik korelasyon

5. Adana Genetik Günleri Nörogenetik Sempozyumu, Türkiye, 23 - 24 Mart 2019, ss.41-46

MELAS ailesi

5. Adana Genetik Günleri Nörogenetik Sempozyumu, Türkiye, 23 - 24 Mart 2019, ss.47-51

İki farklı distrofili bir aile

5. ADANA GENETİK GÜNLERİ NÖROGENETİK SEMPOZYUMU, Türkiye, 23 - 24 Mart 2019

Liquid biopsy profiles of lung cancer patients

Turk Toraks Derneği Kongresi, Türkiye, 11 - 15 Nisan 2018

Charcot Marie Tooth Disease Type 2n: A Case Report

13 th Meeting of the Mediterranean Society of Myology, 27 - 29 Haziran 2018

FSHMD Moleküler Tanısı ve Tanı Oranı: Çukurova Üniversitesi Tecrübesi

1. ulusal nöromusküler hastalıklar kongresi, Türkiye, 18 - 20 Mayıs 2017

A new mutation in congenital glucose galactose malabsorption syndrome.

4th International Conference on Nutrition & Growth, Amsterdam, Hollanda, 2 - 04 Mart 2017, ss.335

A new mutation in congenital glucose galactose malabsorption syndrome.

4th International Conference on Nutrition & Growth, Amsterdam, Hollanda, 2 - 04 Mart 2017, ss.335

Interaction of CD200 overexpression on tumor cells with CD200R1 overexpression on stromal cells: An escape from the host immune response in rectal cancer patients

105th Annual Meeting of the American-Association-for-Cancer-Research (AACR), California, Amerika Birleşik Devletleri, 5 - 09 Nisan 2014, cilt.74