Erişim şekli için "info:eu-repo/semantics/closedAccess" Çocuk Sağlığı ve Hastalıkları Anabilim Dalı listeleme
Toplam kayıt 82, listelenen: 41-60
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Frequency of low serum immunoglobulin levels in children with allergic diseases
(Wiley-Blackwell, 2016)… -
Gastroesophageal reflux disease in children: How much we know?
(Bilimsel Tip Yayinevi, 2015)Objective: Gastroesophageal reflux disease (GERD) can manifest with various clinical presentations and accompany to several diseases. This study aimed to assess presenting complaints, clinical characteristics and comorbid ... -
Heart Rate Variability in Neonates with Hypoxic Ischemic Encephalopathy
(All India Inst Medical Sciences, 2012)Objective To evaluate the changes in heart rate variability (HRV) in newborns with hypoxic-ischemic encephalopathy (HIE). Methods Twenty-two newborns (14 boys, 8 girls) with moderate or severe HIE and 24 term neonates with ... -
Helicobacter pylori resistance to clarithromycin and fluoroquinolones in a pediatric population in Turkey: A cross-sectional study
(Wiley, 2019)BackgroundHelicobacter pylori antimicrobial resistance is gradually increasing around the world. However, there are a limited number of studies reporting on this issue in the pediatric population. In this study, we aimed ... -
Identification of three novel mutations in fourteen patients with citrullinemia type 1
(Pergamon-Elsevier Science Ltd, 2017)Objectives: Citrullinemia type 1 (CTLN1) is an autosomal recessive genetic disorder caused by mutations in the argininosuccinate synthetase 1 (ASST) gene, which encodes for the argininosuccinate synthetase enzyme. Here, ... -
Incidence of iodine deficiency in Turkish patients with congenital hypothyroidism
(Blackwell Publishing, 2008)Background: Turkey is located in an area of mild to moderate iodine deficiency. The aim of the present study was to investigate the incidence of iodine deficiency in patients with congenital hypothyroidism. Methods: Twenty ... -
Inherited coagulation disorders in Turkish children: A retrospective, single-center cohort study
(PERGAMON-ELSEVIER SCIENCE LTD, 2020)Objective: This study aims to investigate the distribution, clinical characteristics and outcome of inherited coagulation disorders (ICD) in Turkish children. Subjects and methods: Data from all children (age < 18 years) ... -
Initial Ophthalmic Findings in Turkish Children with Autism Spectrum Disorder
(Springer/Plenum Publishers, 2015)Children with autism spectrum disorders (ASD) frequently have ophthalmologic disorders. Due to poor cooperation with ophthalmological examination, ocular abnormalities in such children may be overlooked. We retrospectively ... -
Intrascrotal Extratesticular Neurofibroma as a Possible Cause of Failed Descent in Ipsilateral Testis
(All India Inst Medical Sciences, 2012)Intrascrotal extratesticular neurofibromas (IEN) often originate from genitofemoral nerve (GFN) and present as a paratesticular mass. Synchronous presence of IEN and undescended testis has not been reported previously. A ... -
Investigation of the effect of dorsal penile block to penile tissue
(Elsevier Sci Ltd, 2015)Background Dorsal penile block (DPB) is a frequently used technique for regional anesthesia, but the effect of DPB on penile tissue has not been reported so far. Objective An experimental study was conducted to evaluate ... -
Kırkıkkale ilinde adolesan sağlık durumunun ve etkileyen faktörlerin belirlenmesi
(Kırıkkale Üniversitesi, 2005)ÖZET Ağar Güven A., Kırıkkale ilinde adolesan sağlık durumunun ve etkileyen faktörlerin belirlenmesi, Kırıkkale Üniversitesi Tıp Fakültesi Çocuk Sağlığı ve Hastalıkları Anabilim Dalı Uzmanlık Tezi, Kırıkkale 2005. Adolesan, ... -
Kırıkkale ili matebolik hastalık durumu ve sistinüri prevalansının belirlenmesi
(Kırıkkale Üniversitesi, 2005)ÖZET Kalıtsal metabolik hastalıklar, nadir rastlanan ve değişik klinik bulgular göstermesi nedeniyle de tanısı zor olan hastalıklardır. Çoğunlukla otozomal resesif geçiş gösteren bu hastalıklara, akraba evliliklerinin sık ... -
Kırıkkale ilinde yaşayan 0-16 yaş grubu çocuklarda uyku özellikleri
(Kırıkkale Üniversitesi, 2005)ÖZET Bulduk R., Kırıkkale İlinde yaşayan 0-16 yaş grubu çocuklarda uyku özellikleri Kırıkkale Üniversitesi Tıp Fakültesi Çocuk Sağlığı Ye Hastalıkları Ânabilim Dalı Uzmanlık Tezi, Kırıkkale 2005. Uyku, kişinin herhangi bir ... -
Kırıkkale Üniversitesi Pediatri Polikliniğine baş ağrısı ile başvuran çocukların değerlendirilmesi
(Kırıkkale Üniversitesi, 2005)ÖZET Saygı S., Kırıkkale Üniversitesi Pediatri Polikliniğine Baş Ağrısı İle Başvuran Çocukların Değerlendirilmesi, Kırıkkale Üniversitesi Tıp Fakültesi Çocuk Sağlığı ve Hastalıkları Anabilim Dalı Uzmanlık Tezi, Kırıkkale ... -
Kırıkkale Üniversitesi Tıp Fakültesi'ne başvuran çocuklarda demir eksikliği anemisi sıklığı ve beslenme durumu ile ilişkisi
(2005)Amaç: Daha önce bu konu ile ilgili çalışma yapılmamış Kırıkkale ilinde demir eksikliği anemisinin sıklığı ve beslenme durumu ile ilişkisinin araştırılması. Yöntem: Ocak 2001-Temmuz 2001 tarihleri arasında herhangi bir ... -
MEFV gene mutations in Henoch- Schonlein purpura
(Wiley, 2013)AimCoexistence of familial Mediterranean fever (FMF) with various systemic vasculitides, including Henoch-Schonlein purpura (HSP) and other inflammatory disorders has been reported and the MEFV gene has been suggested to ... -
Novel approach for Newborn Errors in Metabolism Screening (NEMS) by NMR: Clinical NEMS-by-NMR Study in Turkey
(Pergamon-Elsevier Science Ltd, 2014)… -
A novel mutation which causes a frameshift in thePHOX2Bgene causes Haddad syndrome
(LIPPINCOTT WILLIAMS & WILKINS, 2020)[Özet Yok]