Bilimsel çalışmalar
Prof. Dr. Hamdi Cihan Emeksiz
67 yayın. Her yayının yanında bilginin kaynağı yazar.
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Assessment of bone turnover markers and bone mineral density in normal short boys
Journal of Pediatric Endocrinology and Metabolism, 2015
DOI 10.1515/jpem-2014-0099 PMID 26197459 5 atıf (Europe PMC) Kaynak: OpenAlex
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Risk factors for cisplatin-induced long-term nephrotoxicity in pediatric cancer survivors
Pediatrics International, 2015
DOI 10.1111/ped.12542 PMID 25441241 12 atıf (Europe PMC) Kaynak: ORCID
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The Relationship of Metabolic Parameters with Serum Uric Acid and Percentage of Body Fat in Obese Adolescents
Turkish Journal of Pediatric Disease, 2015
DOI 10.12956/tjpd.2015.188 Kaynak: OpenAlex
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Turner Sendromlu Çocukların Başvuru Özellikleri ve Eşlik Eden Patolojiler: 842 Vakanın Ulusal Veritabanında Değerlendirme Sonuçları
AYBU AVESIS, 2014
Kaynak: OpenAlex
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Cardio-Facio-Cutaneous Syndrome with Precocious Puberty, Growth Hormone Deficiency and Hyperprolactinemia
Journal of Clinical Research in Pediatric Endocrinology, 2014
DOI 10.4274/jcrpe.1151 PMID 24637312 11 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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Extensive Middle Cranial Fossa Arachnoid Cysts and Different Clinical Presentation in Two Patients
Journal of Clinical Research in Pediatric Endocrinology, 2014
DOI 10.4274/jcrpe.1381 PMID 25241612 2 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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Evaluation of Subclinical Atherosclerosis by Non-Invasive Radiological Methods and its Relation with Endoglin and Nitric Oxide Levels
ESPE 2014, 2014
Kaynak: OpenAlex
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Leukocyte Populations and C-Reactive Protein as Predictors of Bacterial Infections in Febrile Outpatient Children
The Turkish Journal of Hematology, 2014
DOI 10.4274/tjh.2013.0057 PMID 24764729 5 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID
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Octreotide-Induced Long QT Syndrome in a Child with Congenital Hyperinsulinemia and a Novel Missense Mutation (p.Met115Val) in the ABCC8 Gene
Hormone Research in Paediatrics, 2013
DOI 10.1159/000354666 PMID 24080777 12 atıf (Europe PMC) Kaynak: OpenAlex
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The Prevalence of Metabolic Syndrome and Its Relation to Leptin Levels in Obese Children and Adolescents
Turkiye Klinikleri Journal of Medical Sciences, 2013
DOI 10.5336/medsci.2012-30524 Açık erişimli tam metinKaynak: OpenAlex
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Front & Back Matter
Hormone Research in Paediatrics, 2013
DOI 10.1159/000356566 Kaynak: OpenAlex
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Assessment of atherosclerosis risk due to the homocysteine-asymmetric dimethylarginine-nitric oxide cascade in children taking antiepileptic drugs
Seizure: European Journal of Epilepsy, 2013
DOI 10.1016/j.seizure.2012.11.007 PMID 23266348 16 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID
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Familial Hemophagocytic Lymphohistiocytosis with A665G Perforin Gene Mutation: A Case Report
The Turkish Journal of Hematology, 2012
DOI 10.5505/tjh.2012.62134 PMID 24744671 1 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID
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Iatrogenic water intoxication during pelvic ultrasonography in a patient with diabetes insipidus
Turkish Journal of Pediatrics, 2012
PMID 23692728 1 atıf (OpenAlex) Kaynak: ORCID
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Use of Physostigmine for Cyclopentolate Overdose in an Infant
Pediatrics, 2012
DOI 10.1542/peds.2011-3038 PMID 22908101 6 atıf (Europe PMC) Kaynak: ORCID
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Acute adrenal crisis mimicking familial Mediterranean fever attack in a renal transplant FMF patient with amyloid goiter
Rheumatology International, 2010
DOI 10.1007/s00296-009-1115-0 PMID 19711078 9 atıf (Europe PMC) Kaynak: ORCID
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Unresponsiveness to Colchicine Therapy in Patients with Familial Mediterranean Fever Homozygous for the M694V Mutation
The Journal of Rheumatology, 2010
DOI 10.3899/jrheum.090273 PMID 20008920 45 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID