The Turkish Journal of Pediatrics
2009 , Vol 51 , Num 2
Molecular genetics of maple syrup urine disease in the Turkish population
Kerstin Gorzelany, Ali Dursun, Turgay Coşkun, Serap H. Kalkanoğlu-Sivri, Gülden Fatma Gökçay, Mübeccel Demirkol, Oliver Feyen, Udo Wendel
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Determinants of allergic signs and symptoms in 24-48-monthold Turkish children
Elif N. Özmert, Eren Kale-Çekinmez, Kadriye Yurdakök, Bülent Enis Şekerel
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Early and severe presentation of vitamin D deficiency and nutritional rickets among hospitalized infants and the effective factors
Hasan Tezer, Zeynep Şıklar, Yıldız Dallar, Şeyda Doğankoç
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Endovascular stent implantation for coarctation of the aorta in children and young adults: intermediate follow-up results from Turkey
Ali Baykan, Tevfik Karagöz, Alpay Çeliker
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Seroprevalence of hepatitis B infection in the Turkish population in Northern Cyprus
Zafer Kurugöl, Güldane Koturolu, Sadk Akit, Tijen Özacar, Northern Cyprus Study Teama
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Foreign body ingestion in Turkish children
Sema Aydoğdu, Çiğdem Arıkan, Murat Çakır, Maşallah Baran, Hasan Ali Yüksekkaya, Ulaş Eylem Saz, Mehmet Tayyip Arslan
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Comparison of acute bloody and watery diarrhea: a case control study
Bar Kukonmaz, Kadriye Yurdakök, S. Song¨¹l Yalçn, Elif Özmert
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Perinatal risk factors affecting the maternal and fetal asymmetric dimethylarginine levels
Mustafa Kul, Erkan Demirkaya, Osman Metin İpçioğlu, Rahmi Sinan Karadeniz, Turan Tunç, Sebahattin Vurucu, Fahri Gürkan Yeşil, Hasan Öztin, Erdinç Çakır
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Chronic constipation in Turkish children: clinical findings and applicability of classification criteria
Sema Aydoğdu, Murat Çakır, Hasan Ali Yüksekkaya, Çiğdem Arıkan, Gökhan Tümgör, Maşallah Baran, Raşit Vural Yağcı
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Validity and reliability of the Turkish translation of the Pediatric Asthma Quality of Life Questionnaire
Hasan Yüksel, Özge Yılmaz, Cengiz Kırmaz, Erhan Eser
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Pantothenate kinase-associated neurodegeneration (PKAN): molecular confirmation of a Turkish patient with a rare frameshift mutation in the coding region of the PANK2 gene
Hakan Cangül,, Özlem Özdemir, Tahsin Yakut, Mehmet Okan, Neil V Morgan, Birol Baytan, Manju A Kurian, Ronald Spiegel, Eamonn R Maher
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A novel mutation of the GLUT2 gene in a Turkish patient with Fanconi-Bickel syndrome
Enver Şimşek, Şenay Savaş-Erdeve, Osamu Sakamoto, Tümay Doğancı, Yıldız Dallar
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Early congenital syphilis with isolated bone involvement: a case report
Didem Armangil, Fuat Emre Canpolat, Şule Yiğit, Hacı Ahmet Demir, Mehmet Ceyhan
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Tick infestation of the eyelid: a case report in a child
Uğur Keklikçi, Kaan Ünlü, Alpay Çakmak, Sedat Akdeniz, Nezehat Akpolat
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A report of a patient with duplication of 7p13→pter and deletion of 2p23→pter due to a maternal 2p;7p translocation
B. Bilge Türköver, Ceyhan Sayar, Güven Toksoy, Nursel Elçioğlu
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Neonatal suppurative submandibular sialadenitis
Anl Tapsz, Nuren Belet, Ergin Çiftçi, Suat Fitöz, Erdal nce, Ülker Doru
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Type 1 diabetes mellitus associated with autoimmune thyroid disease, celiac disease and familial Mediterranean fever: case report
Firdevs Ba, Sema Kabata-Erylmaz, Hlya Gnz, Feyza Darendeliler, Banu Kkemre, Rveyde Bundak, Nurin Saka
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A rare cause of mental motor retardation: recessive congenital methemoglobinemia type II
Deniz Yüksel, Nesrin Şenbil, Deniz Yılmaz, Neşe Yaralı, Y.K. Yavuz Gürer
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Incontinentia pigmenti: a case report and literature review
Sinan Emre, Yezdan Frat, Serdal Gngr, Ahmet Kemal Frat, Yelda Karncaolu
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An unusual presentation of gastrointestinal obstruction in a three-year-old boy
Özlem Boybeyi, Arbay Özden Çiftçi, Haluk Topaloğlu
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