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The Turkish Journal of Pediatrics

Original Articles
Pedirhythm 3
Pediatric Rhythm Congress
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Probiotics and prebiotics in pediatrics: where are we now?
Hania Szajewska
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Genetic factors in neonatal hyperbilirubinemia and kernicterus
S. Ümit Sarıcı, Mehmet Saldır
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Evaluation of clinical characteristics, diagnosis and management in childhood immune thrombocytopenic purpura: a single center’s experience
Ülker Koçak1, Yusuf Ziya Aral2, Zühre Kaya1, Gülyüz Öztürk3, Türkiz Gürsel1
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Demographic and clinical features of child abuse and neglect cases
Ebru Çengel-Kültür, Füsun Çuhadaroğlu-Çetin, Bahar Gökler
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Neurological soft signs in comorbid learning and attention deficit hyperactivity disorders
Runa Uslu1, Emine Gül Kapçı2, Didem Öztop3
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Association between mannose binding lectin polymorphisms and predisposition to bacterial meningitis
Fadıl Vardar1, Sacide Pehlivan2, Hüseyin Onay1, Füsun Atlıhan3, Nesrin Güliz3, Cihangir Özkınay4, Ferda Özkınay1
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Doxycycline in autoimmune central nervous system disorders in children: an in vitro study
Banu Anlar1, Nesrin Şenbil2, Alev Güven3
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Demographic status and prevalence of intestinal parasitic infections in schoolchildren in İzmir, Turkey
Ümit Aksoy, Çiler Akısü, Songül Bayram-Delibaş, Soykan Özkoç, Serap Şahin, Selma Usluca
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Nutritional status and risk factors of chronic malnutrition in children under five years of age in Aydın, a western city of Turkey
Filiz Ergin, Pınar Okyay, Gonca Atasoylu, Erdal Beşer
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Evaluation of risk factors in developmental dysplasia of the hip: results of infantile hip ultrasonography
Alp Akman1, Ayşe Korkmaz2, M. Cemalettin Aksoy1, Muharrem Yazıcı1, Murat Yurdakök2, Gülsevin Tekinalp2
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Atypical presentations of SSPE: a clinical study in four cases
Ercan Demir1, Ayşe Aksoy1, Banu Anlar2, Fatma Müjgan Sönmez1
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Hypocalcemic seizure due to congenital rickets in the first day of life
Ömer Erdeve1, Begüm Atasay1, Saadet Arsan1, Zeynep Şıklar2, Gönül Öcal2, Merih Berberoğlu2
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Severe graft versus host disease in a patient with globoid cell leukodystrophy following umbilical cord blood transplantation: resemblance to the twitcher mouse model
Maide Özen1, Duygu Uçkan1, Mualla Çetin1, İlhan Tezcan1, Murat Tuncer1, Banu Anlar2
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Successful treatment of retroperitoneal giant cell-type malignant fibrous histiocytoma in a 5-year-old boy
Kudret Çağlar1, Sabiha Güngör1, Sezin Akansoy1, Ümit Sakallı2, Diclehan Orhan3, Melda Çağlar3
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Septated pericarditis associated with Kawasaki disease: a brief case report
Arzu Sonçağı1, İlker Devrim1, Tevfik Karagöz1, Embiya Dilber2, Alpay Çeliker1, Seza Özen1, Gülten Seçmeer1
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Splenic abscesses in therapy-resistant acute myeloblastic leukemia presenting as recurrent febrile neutropenia and unresolved splenomegaly
Lale Olcay1, Gürbüz Dingil2, Emin Yıldırım3, Gülay Dilek4, Ece Dirim5
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Lipofibromatosis in a two-year-old girl: a case report
Ayşegül Sarı1, Mine Tunakan1, Betül Bolat1, Handan Çakmakçı2, Erdener Özer3
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Maternal origin and clinical findings in a case with trisomy 22
Ercan Mıhçı1, Şükran Taçoy1, Sezin Yakut2, Hakan Ongun3, İbrahim Keser2, Bahar Kılıçarslan4, Gülseren Bağcı2, Güven Lüleci2
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A rare cause of neonatal seizure: incontinentia pigmenti
Münevver Türkmen1, Kayı Eliaçık1, Kübra Temoçin2, Ekin Şavk3, Ayşe Tosun1, Emel Dikicioğlu4
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Co-infection with Mycoplasma pneumoniae and cytomegalovirus resulting in an acute demyelinating polyneuropathy in a pediatric patient
Filippo Greco, Vincenzo Salvo, Anna Sorge, Silvia Perrini, Rosaria Garozzo, Giovanni Sorge
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Mutational analysis of the human MBX gene in four Korean families demonstrating microphthalmia with congenital cataract
Toshinobu Miyamoto1, Young S. Yu2, Hisashi Sato1, Hiroaki Hayashi1, Naoko Sakugawa1, Mutsuo Ishikawa1, Kazuo Sengoku1
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Identification of 7th hexosaminidase A mutation of Tay-Sachs disease in the Turkish population
İncilay Sinici1, Evren Önder1, Meral Topçu2, H. Asuman Özkara1
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