Volume 49 Issue 3 (2007)

Published: September 28, 2007

Review Articles

Probiotics and prebiotics in pediatrics: where are we now?
Genetic factors in neonatal hyperbilirubinemia and kernicterus

Original Articles

Evaluation of clinical characteristics, diagnosis and management in childhood immune thrombocytopenic purpura: a single center's experience
Demographic and clinical features of child abuse and neglect cases
Neurological soft signs in comorbid learning and attention deficit hyperactivity disorders
Association between mannose binding lectin polymorphisms and predisposition to bacterial meningitis
Doxycycline in autoimmune central nervous system disorders in children: an in vitro study
Demographic status and prevalence of intestinal parasitic infections in schoolchildren in Izmir, Turkey
Nutritional status and risk factors of chronic malnutrition in children under five years of age in Aydin, a western city of Turkey
Evaluation of risk factors in developmental dysplasia of the hip: results of infantile hip ultrasonography

Case Reports

Atypical presentations of SSPE: a clinical study in four cases
Hypocalcemic seizure due to congenital rickets in the first day of life
Severe graft versus host disease in a patient with globoid cell leukodystrophy following umbilical cord blood transplantation: resemblance to the twitcher mouse model
Successful treatment of retroperitoneal giant cell-type malignant fibrous histiocytoma in a 5-year-old boy
Septated pericarditis associated with Kawasaki disease: a brief case report
Splenic abscesses in therapy-resistant acute myeloblastic leukemia presenting as recurrent febrile neutropenia and unresolved splenomegaly
Lipofibromatosis in a two-year-old girl: a case report
Maternal origin and clinical findings in a case with trisomy 22
A rare cause of neonatal seizure: incontinentia pigmenti
Co-infection with Mycoplasma pneumoniae and cytomegalovirus resulting in an acute demyelinating polyneuropathy in a pediatric patient

Short Communication

Mutational analysis of the human MBX gene in four Korean families demonstrating microphthalmia with congenital cataract

Letter to the Editor

Identification of 7th hexosaminidase A mutation of Tay-Sachs disease in the Turkish population