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Browsing Çocuk Sağlığı ve Hastalıkları Anabilim Dalı by Submit Date

Browsing Çocuk Sağlığı ve Hastalıkları Anabilim Dalı by Submit Date

Now showing items 1-20 of 101

Heart rate variability in diabetic children: sensitivity of the time- and frequency-domain methods

Akıncı, Ayşehan; Çeliker, Alpay; Baykal, Engin; Teziç, Tahsin (Pediatric Cardiology, 2017)

Heart rate variability (HRV) is a noninvasive index of the neural activity of the heart. Although also influenced by the sympathetic activity of the heart, HRV is essentially determined by the vagal stimulation of the ...
Turner Syndrome and Associated Problems in Turkish Children A Multicenter Study

Yeşilkaya, Ediz; Bereket, Abdullah; Darendeliler, Feyza; Baş, Firdevs (Journal of Clinical Research in Pediatric Endocrinology, 2015)

Turner syndrome (TS) is a genetic disorder characterized by total or partial absence of one sex chromosome (1). It is one of the most common chromosomal disorder with an incidence of 1:2500 female live births (2,3). The ...
Growth curves for Turkish Girls with Turner Syndrome Results of the Turkish Turner Syndrome Study Group

Darendeliler, Feyza; Yeşilkaya, Ediz; Bereket, Abdullah; Baş, Firdevs (Journal of Clinical Research in Pediatric Endocrinology, 2015)

Turner syndrome (TS) is a common chromosomal disorder occurring in 1:2500 female live births. The most common presenting symptom in girls with TS is short stature which is mild during early childhood but becomes more ...
Rare Causes of Primary Adrenal Insufficiency Genetic and Clinical Characterization of a Large Nationwide Cohort

Guran, Tülay; Buonocore, Federica; Saka, Nurçin; Akıncı, Ayşehan (The Journal of Clinical Endocrinology & Metabolism, 2015)

Context: Primary adrenal insufficiency (PAI) is a life-threatening condition that is often due to monogenic causes in children. Although congenital adrenal hyperplasia occurs commonly, several other important molecular ...
Clinical characteristics and phenotype genotype analysis of Turkish patients with congenital hyperinsulinism

Demirbilek, Hüseyin; Özbek, Mehmet Nuri; Akıncı, Ayşehan; Arya, Bhushan (Eur J Endocrinol, 2014)

Objective: Congenital hyperinsulinism (CHI) is the commonest cause of hyperinsulinaemic hypoglycaemia in the neonatal, infancy and childhood periods. Its clinical presentation, histology and underlying molecular biology ...
Factors effecting platelet activation in children with poorly controlled type 1 diabetes mellşitus

Swartz, Jonathan M.; Akıncı, Ayşehan; Andrew, Shayne F.; Sığırcı, Ahmet; Andrew, Shayne F.; Hirschhorn, Joel N; Rosenfeld, Ron G.; Dauber, Andrew; Hwa, Vivian (HealthMED, 2013)

Background—Cockayne syndrome is an autosomal recessive, heterogeneous syndrome with classic features, including short stature, microcephaly, developmental delay, neuropathy, and photosensitivity. New genomic approaches ...
Association of cardiac changes with serum adiponectin and resistin levels in obese and overweight children

Akıncı, Ayşehan; Karakurt, Cemsit; Gürbüz, Sibel; Elkıran, Özlem; Nalbantoğlu, Özlem; Kocak, Gulendam; Güldür, Tayfun; Yoloğlu, Saim (Journal of Cardiovascular Medicine, 2013)

Objectives To investigate serum adiponectin and resistin levels in childhood obesity and their relationship with cardiac changes and insulin resistance. Methods Seventy-one obese and 24 overweight children and 40 healthy ...
A novel exonic GHR mutataion c 784G C in a patient with classical growth hormone insensitivity syndrome

Akıncı, Ayşehan (Hormon Reseach Paediatr, 2013)

Context: Undetectable circulating growth hormone-binding protein (GHBP) can be indicative of a GH receptor (GHR) defect and cause GH insensitivity (GHI) syndrome. Case Report: The proband, severely growth retarded from ...
Plasma kisspeptin levels in girls with premature thelarche

Akıncı, Ayşehan; Çetin, Dilek; İlhan, Nevin (J Clin Res Pediatr Endocrinol, 2012)

Ob jec ti ve: Premature thelarche (PT) is defined as isolated breast development without secondary sex characteristics in girls below the age of eight. We aimed to determine whether the level of kisspeptin, which plays ...
Plasma kisspeptin levels in girls with premature thelarche

Akıncı, Ayşehan; Çetin, Dilek; İlhan, Nevin (J Clin Res Pediatr Endocrinol, 2012)

Gonadotropin-releasing hormone analog (GnRHa) therapy is used in idiopathic central precocious puberty (ICPP) worldwide. It has also been shown that during this therapy, body mass index (BMI) increases slightly as a side ...
The effect of gonadotropin releasing hormone analog leuprolide treatment on body fat distribution in idiopathic central precocious puberty

Bilir, Pelin; Akıncı, Ayşehan (Turkish Journal of Pediatrics, 2011)

Gonadotropin-releasing hormone analog (GnRHa) therapy is used in idiopathic central precocious puberty (ICPP) worldwide. It has also been shown that during this therapy, body mass index (BMI) increases slightly as a side ...
GLP 1 and GLP 2 levels indiabetic ketoacidosis

Akıncı, Ayşehan; Aydın, Özgür; Özerol, Halil İbrahim (JCRPE, 2009)

Objective: The aim of this study was to investigate whether insulin deficiency and increased catabolism may have a role in the regulation of plasma glucagon-like peptide (GLP)-1 and GLP- 2 levels in children with diabetic ...
Neuroimaging Findings in Hyperargininemia

Güngör, Serdal; Akıncı, Ayşehan; Fırat, Ahmet Kemal; Tabel, Yılmaz; Alkan, Alper (Journal of Neuroimaging, 2008)

In hyperarginenemia, there is a defect in argininase enzyme, which is a catalyzer of urea cycle. Though the pathogenesis of neuronal damage in hyperargininemia is not clear, high serum and cerebrospinal fluid arginine ...
Brain metabolite changes on proton magnetic resonance spectroscopy in children with poorly controlled type1 diabetes mellitus

Saraç, Kaya; Akıncı, Ayşehan; Alkan, Alpay; Aslan, Mehmet; Baysal, Tamer; Özcan, Abdulcemal (NEURORADIOLOGY, 2005)

The metabolite changes in the brains of children with poorly controlled type 1 diabetes mellitus (DM) were investigated by proton magnetic resonance spectroscopy (MRS). A total of 30 subjects and 14 age-matched healthy ...
Strain and strain rate echocardiography in children with Wilson s disease

Karakurt, Cemşit; Çelik, Serkan Fazlı; Selimoğlu, Mukadder Ayşe; Varol, İlknur; Karabiber, Hamza; Yoloğlu, Saim (Cardiovascular Journal of Africa, 2016)

Objective: This study aimed to evaluate strain and strain rate echocardiography in children with Wilson’s disease to detect early cardiac dysfunction. Methods: In this study, 21 patients with Wilson’s disease and a ...
Huge left atrial pseudoaneurysm in a 5 month old baby presented with supraventricular tachycardia

Karakurt, Cemşit; Türköz, Rıza; Sarıtaş, Bülent; Çelik, Serkan; Elkıran, Özlem (Acta Cardiologica Sinica, 2016)

Cardiac pseudoaneurysm is an extremely rare condition in children. It can be congenital or acquired and has been primarily described in the left side of the heart. The congenital form of pseudoaneurysm is thought to be ...
A rare variant of type I truncus arteriosus truncus arteriosus with anterior origin of a main pulmonary artery

Çelik, Serkan Fazlı; Karakurt, Cemşit; Elkıran, Özlem; Öztürk, Mehmet; Görmeli, Cemile Ayşe (Echocardiography, 2015)

Truncus arteriosus (TA) is an uncommon congenital cardiovascular anomaly that is characterized by a single arterial trunk arising from the normally formed ventricles by means of a single semilunar valve. The anomaly ...
Possible association between fluconazole administration and acute hyperkalemia in a critically ill cyanotic infant

Elkıran, Özlem; Karakurt, Cemşit; Koçak, Gülendam; Tabel, Yılmaz; Güngör, Serdal (Arch Med Sci, 2015)

Fluconazole, an azole antifungal agent, inhibits the fungal cytochrome P450 enzyme. Although in vitro data show that fluconazole is not a potent inhibitor of mammalian P450 enzymes, hyperkalemia secondary to adrenal ...
Brucella myocarditis in a 3 month old probable transplacental transmission

Elkıran, Özlem; Koçak, Gülendam; Karakurt, Cemşit; Kuzucu, C. (Ann Trop Paediatr, 2014)

A 3-month-old girl presented with myocarditis owing to brucellosis. Her mother had been diagnosed with brucellosis at 28 weeks gestation but did not receive treatment until after delivery. The infant had intrauterine ...
Report of seven children with hepatopulmonary syndrome

Erge, Duygu; Selimoğlu, Mukadder Ayşe; Karakurt, Cemşit; Karabiber, Hamza; Elkıran, Özlem; Çatal, Ferhat; Köroğlu, Reyhan (Turk J Gastroenterol, 2014)

Hepatopulmonary syndrome is an important pulmonary vascular complication of liver disease. Its diagnosis is based on the presence of hypoxaemia and the demonstration of intrapulmonary shunting by contrast-enhanced echo ...

Now showing items 1-20 of 101

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Browsing Çocuk Sağlığı ve Hastalıkları Anabilim Dalı by Submit Date

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