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Heybet Tüzün

Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations
2015 · Huseyin Demirbilek, Ved Bhushan Arya, et al. · European Journal of Endocrinology · 65
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Serum leptin levels in asthmatic children treated with an inhaled corticosteroid
2004 · Fuat Gurkan, Yildiz Atamer, et al. · Annals of Allergy Asthma & Immunology · 60
Multicenter randomized controlled trial of therapeutic hypothermia plus magnesium sulfate versus therapeutic hypothermia plus placebo in the management of term and near-term infants with hypoxic ischemic encephalopathy (The Mag Cool study): A pilot study
2015 · SajjadUr Rahman, FuatEmre Canpolat, et al. · Journal of Clinical Neonatology · 37
Mutations in BTD gene causing biotinidase deficiency: a regional report
2014 · Çiğdem Seher Kasapkara, Melek Akar, et al. · Journal of Pediatric Endocrinology and Metabolism · 17
Relationship Among Serum Selenium Levels, Lipid Peroxidation, and Acute Bronchiolitis in Infancy
2004 · Fuat Gurkan, Yildiz Atamer, et al. · Biological Trace Element Research · 17
Sirolimus-Induced Hepatitis in Two Patients with Hyperinsulinemic Hypoglycemia
2017 · Belma Haliloğlu, Heybet Tüzün, et al. · Journal of Clinical Research in Pediatric Endocrinology · 15
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Severe renal failure and hyperammonemia in a newborn with propionic acidemia: effects of treatment on the clinical course
2013 · Çiğdem Seher Kasapkara, Melek Akar, et al. · Renal Failure · 9
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Microangiopathic Hemolytic Anemia, Thrombocytopenia and Acute Renal Failure Associated with Acute Brucellosis
2001 · Murat Söker, Celal Devecioğlu, et al. · 9
Problems of the neonates with congenital heart disease requiring early interventions: a regional report
2015 · Muhittin Celik, Bedri Aldudak, et al. · Türk Pediatri Arşivi · 6
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Transient nephrogenic diabetes insipidus caused by fetal exposure to haloperidol
2014 · Melek Akar, Çiğdem Seher Kasapkara, et al. · Renal Failure · 6
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Folate deficiency in patients with classical galactosemia: A novel finding that needs to be considered for dietary treatments
2018 · Muhittin Çelik, Nezir Özgün, et al. · The Turkish Journal of Pediatrics · 3
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Mutational analysis of the galactose-1-phosphate uridyltransferase (GALT) gene in southeast part of Turkey: a regional report.
2015 · M Akar, M Celik, et al. · PubMed · 3
Clinical Diagnosis, Biochemical Findings, Genetics and Incidence of Zellweger Syndrome
2017 · Muhittin Celik, Mehmet Sah Ipek, et al. · Iranian Journal of Pediatrics · 2
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Unusual Presentation of Congenital Plasmodium Vivax Malaria in a Neonate From Turkey
2004 · Fuat Gürkan, Meki Bilici, et al. · Electronic Journal of General Medicine · 1
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The role of metabolic diseases in neonatal convulsions.
2023 · S Samanci, M Celik, et al. · PubMed
The Effectiveness of Sirolimus in a Newborn with Hyperinsulinaemic Hypoglycaemia
2015 · Belma Haliloğlu, Heybet Tüzün, et al. · 54th Annual ESPE
Mutations in BTD gene causing biotinidase deficiency a regional report
2014 · TANYALÇIN, TİJEN, AKAR, MELEK, et al. · AYBU AVESIS
When a common symptom of a neonate becomes an unusual diagnosis A case report of HMG CoA lyase deficiency
2014 · ÖZBEK, MEHMET NURİ, TÜZÜN, HEYBET, et al. · AYBU AVESIS
Variety of critical congenital heart diseases and referral centers followed up in neonatal intensive care unit: regional report
2013 · Melek Akar, Bedri Aldudak, et al. · The Anatolian Journal of Cardiology
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Güneydoğu Anadolu Bölgesinde tanı alan klasik galaktozemili hastaların klinik bulguları ve mutasyon sonuçları
2013 · BARAN, RIZA TANER, KASAPKARA, ÇİĞDEM SEHER, et al. · AYBU AVESIS
A cross sectional study of autoantibodies in children with hepatitis A infection
2011 · PIRINCCIOGLU, Ayfer Gözü, YALCIN, Kendal, et al. · DergiPark (Istanbul University)
Works count: 21
Citation count: 250
H-index: 8
I10-index: 6
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