The Turkish Journal of Pediatrics 2019 , Vol 61 , Num 6
The lung microbiome in neonates.

A comparison of bone mineral density in adolescent swimmers, pentathletes and figure skaters.

Mental health of Syrian refugee adolescents: how far have we come?.

Long term follow-up of children with chronic hepatitis B: a single center experience.

Systemic onset juvenile idiopathic arthritis: a single center experience.

Maternal adipose tissue, antenatal steroids, and Respiratory Distress syndrome: complex relations.

Extracorporeal membrane oxygenation for the support of pediatric patients with acute fulminant myocarditis.

The role of cardiac troponin T in detection of cardiac damage and long term mortality in children with chronic renal disease.

Clinical experiences in Turkish paediatric patients with chronic recurrent multifocal osteomyelitis.

Thymic output changes in children with clinical findings signaling a probable primary immunodeficiency.

Is antibiotic lock therapy effective for the implantable longterm catheter-related bloodstream infections in children?.

Childhood sclerosing cholangitis associations in a Tunisian tertiary care hospital: a many-faceted disease.

Congenital heart disease and thyroid dysfunction in Down syndrome reported at Children`s Hospital, Lahore, Pakistan.

Systolic dysfunction of systemic ventricle in patients who underwent a Fontan operation.

Bi-allelic mutations in PRUNE lead to neurodegeneration with spinal motor neuron involvement and hyperCKaemia.

Vedolizumab treatment in a patient with X-linked agammaglobulinemia, is it safe and efficient?.

A case of craniopagus parasiticus: an antenatal diagnosis by ultrasound screening at 16 weeks of gestation and a literature review of recently reported cases.

A novel mutation in SLC2A1 gene causing GLUT-1 deficiency syndrome in a young adult patient.

Rapid onset of altered mental status with progressive autonomic instability and hypoventilation in a 2-year-old male.

Pathological findings of central nervous system, two GM1 gangliosidosis autopsy cases.

Fibrodysplasia ossificans progressiva – can we diagnose it right at the outset?.

A pediatric case of Ortner`s syndrome caused by heritable pulmonary arterial hypertension and review of the literature.

Schwartz Jampel syndrome responding positively to carbamazepine therapy: a case report and a novel mutation.

A neonate with tracheobronchial cobblestone mucosa presenting with acute severe hypercapnia.

Multifocal mesenchymal hamartoma of the chest wall in a newborn.

Spontaneously resolved uterine prolapse in a neonate with spina bifida.

Response to: Arthropathy-like findings and a carpal tunnel syndrome as the presenting features of Scheie syndrome: Three cases from the same family.

Pediatric primary anaplastic ganglioglioma with malignant neuronal component.

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