Search Results - "Korkmaz, Huseyin Anıl"

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    Hypoparathyroidism in children and adolescents by Korkmaz, Hüseyin Anıl, Ozkan, Behzat

    “…Hypoparathyroidism is characterized by insufficient parathyroid hormone (PTH) release from the parathyroid glands to maintain serum calcium level within normal…”
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    Genetic diagnosis of congenital hypopituitarism in Turkish patients by a target gene panel: novel pathogenic variants in GHRHR, GLI2, LHX4 and POU1F1 genes by Kırkgöz, Tarık, Gürsoy, Semra, Acar, Sezer, Nalbantoğlu, Özlem, Özkaya, Beyhan, Anıl Korkmaz, Hüseyin, Hazan, Filiz, Özkan, Behzat

    Published in Archives of Endocrinology and Metabolism (10-11-2023)
    “…Congenital hypopituitarism (CH) is a rare disease characterized by one or more hormone deficiencies of the pituitary gland. To date, many genes have been…”
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    Detection of SHOX Gene Variations in Patients with Skeletal Abnormalities with or without Short Stature by Gürsoy, Semra, Hazan, Filiz, Aykut, Ayça, Nalbantoğlu, Özlem, Korkmaz, Hüseyin Anıl, Demir, Korcan, Özkan, Behzat, Çoğulu, Özgür

    “…Objective: SHOX gene mutations constitute one of the genetic causes of short stature. The clinical phenotype includes variable degrees of growth impairment,…”
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    The effect of antiepileptic drugs on thyroid function in children by Yılmaz, Ünsal, Yılmaz, Tuba Sevim, Akıncı, Gülçin, Korkmaz, Hüseyin Anıl, Tekgül, Hasan

    Published in Seizure (London, England) (01-01-2014)
    “…Abstract Background Limited and conflicting data exist for the influence of antiepileptic drugs on thyroid function in children. Objective The aim of this…”
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    A case of immune-mediated type 1 diabetes mellitus due to congenital rubella ınfection by Korkmaz, Hüseyin Anıl, Ermiş, Çağatay

    “…Congenital rubella infection is a transplacental infection that can cause intrauterine growth retardation, cataracts, patent ductus arteriosus, hearing loss,…”
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    Neonatal seizure as a manifestation of unrecognized maternal hyperparathyroidism by Korkmaz, Hüseyin Anıl, Ozkan, Behzat, Terek, Demet, Dizdarer, Ceyhun, Arslanoğlu, Sertaç

    “…Maternal hypercalcemia suppresses parathyroid activity in the fetus resulting in impaired parathyroid responsiveness to hypocalcemia after birth. Resultant…”
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    Can neutrophil/lymphocyte ratio be a novel biomarker of inflammation in children with asthma? by Nacaroglu, Hikmet Tekin, İsgüder, Rana, Bent, Sultan, Erdem Bahceci, Semiha, Ceylan, Gökhan, Korkmaz, Hüseyin Anıl, Karaman, Sait, Unsal Karkıner, Canan Sule, Can, Demet

    Published in European journal of inflammation (01-08-2016)
    “…Neutrophils are known to play a role in airway inflammation and are activated in inflammatory lung diseases such as asthma. In adult studies the…”
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    Approach to nutritional rickets by Korkmaz, Hüseyin Anıl, Padidela, Raja, Ozkan, Behzat

    “…Rickets is the disease of a growing skeleton and results from impaired apoptosis of hypertrophic chondrocytes and mineralization of the growth plate…”
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    Oxytocin alleviates cisplatin-induced renal damage in rats by Erbas, Oytun, Anil Korkmaz, Huseyin, Oltulu, Fatih, Aktug, Hüeyin, Yavasoglu, Altug, Akman, Levent, Solmaz, Volkan, Taskiran, Dilek

    Published in Iranian journal of basic medical sciences (01-10-2014)
    “…The purpose of the present study was to investigate the protective effect of oxytocin on cisplatin (CP)-induced renal damage in rats. Fourteen adult Sprague…”
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    The Association between Vitamin D Deficiency and Hepatosteatosis in Children and Adolescents with Obesity by Korkmaz, Hüseyin Anıl, Arya, Ved Bhushan, Barisik, Vatan, Atila, Dincer, Coskunol, Fulya, Alci, Serra, Cekdemir, Yasin Ertug, Torlak, Derun, Özkan, Behzat

    Published in Hormone research in paediatrics (2024)
    “…Increasingly, research groups have been studying the association of serum vitamin D and metabolic health indicators, especially in patients with obesity. We…”
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    A case of Turner syndrome with concomitant transient hypogammaglobulinaemia of infancy and central diabetes insipidus by Korkmaz, Hüseyin Anıl, Özkan, Behzat, Hazan, Filiz, Büyükinan, Muammer, Çelik, Tanju

    “…Turner syndrome (TS) is a genetic disorder that affects development in females and is characterized by the complete or partial absence of the second sex…”
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