Volume 42 Issue 3 (2000)

Published: September 28, 2000

Original Articles

Polymorphisms of surfactant protein A genes and the risk of bronchopulmonary dysplasia in preterm infants
B Weber, A Borkhardt, S Stoll-Becker, I Reiss, L Gortner
Pages: 181-185
Abstract
Dual-probe pH monitoring for the assessment of gastroesophageal reflux in the course of chronic hoarseness in children
N Kalach, L Gumpert, P Contencin, C Dupont
Pages: 186-191
Abstract
Allogeneic bone marrow transplantation for children with myelodysplastic syndrome
D Uçkan, M Cetin, G Hiçsönmez, I Tezcan, A M Tuncer
Pages: 192-197
Abstract
Fludarabine, cytarabine, G-CSF and idarubicin (FLAG-IDA) for the treatment of relapsed or poor risk childhood acute leukemia
N Yalman, N Sarper, O Devecioğlu, S Anak, E Eryilmaz, M Can, H Yenilmez, L Ağaoğlu, G Gedikoğlu
Pages: 198-204
Abstract
Hemophilic arthropathy: evaluation of clinical and radiological characteristics and disability
M Dalyan, S Tuncer, S Kemahli
Pages: 205-209
Abstract
Clinical features of 21 patients with lissencephaly type I (agyria-pachygyria)
M Ozmen, Y Yilmaz, M Calişkan, O Minareci, N Aydinli
Pages: 210-214
Abstract
Microdeletion of 22q11 (CATCH 22) in children with conotruncal heart defect and extracardiac malformations
M Alikaşifoğlu, N Malkoç, N Ceviz, S Ozme, S Uludoğan, E Tunçbilek
Pages: 215-218
Abstract
Serratia marcescens: an emerging microorganism in the neonatal intensive care unit
C Aygün, S Yiğit, D Gür, G Erdem, O Oran, G Tekinalp, M Yurdakök
Pages: 219-222
Abstract
Ventricular diastolic filling indices in pulmonary stenosis
F A Paç, S Ozkutlu, M Saraçlar, N O Kutlu
Pages: 223-226
Abstract
Unguarded tricuspid orifice diagnosed by echocardiography: a clinical study
A Kiliç, S Ozkutlu, N Günal
Pages: 227-229
Abstract

Case Reports

Hereditary angioedema: case report of a family
M Yilmaz, S G Kendirli, D Altintaş, G Bingöl
Pages: 230-233
Abstract
Ivemark syndrome: asplenia with kidney collecting duct cysts and polysplenia with cerebellar cyst
V Krźelj, I Kragić, M Glavina-Durdov, R Jakl, M Bucat, I Kuzmić-Prusac
Pages: 234-238
Abstract
A case of isotretinoin embryopathy with bilateral anotia and Taussig-Bing malformation
N Ceviz, B Ozkan, S Eren, R Ors, R Olguntürk
Pages: 239-241
Abstract
Teratoid Wilms' tumor: a case report
I Karaca, A Sencan, R Ortaç, A Bostanci-Sencan, E Mir
Pages: 242-245
Abstract
Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome) in a Turkish child
H Tekgül, S Tütüncüoğlu
Pages: 246-249
Abstract
Body stalk anomaly in monozygotic twinning: a case report
F Aksoy, F A Karayel, R Ramazanoğlu
Pages: 250-252
Abstract
Thoracic ectopic kidney in a child: a case report
H I Aydin, S U Sarici, F Alpay, E Gökçay
Pages: 253-255
Abstract
Acute lymphoblastic leukemia in a child with Wilson disease
A Yüce, N Koçak, S Yetgin, H Ozen, F Gürakan, I Yenicesu
Pages: 256-257
Abstract
Biphasic pulmonary blastoma in a child
B Uçar, N Akgün, O Bör, S Işiksoy, M Kuşku, S Dernek, O Paşaoğlu
Pages: 258-263
Abstract
Juvenile hyaline fibromatosis in one Turkish child
S Uğraş, N Akpolat, A Metin
Pages: 264-266
Abstract

Letters to the Editor

Leukocytoclastic vasculitis associated with methotrexate therapy
A Düzova, A Soysal, S Ozen, C Akyüz, A Gököz, S Yetgin
Pages: 267-268
Abstract
Concurrent presence of HBsAg and anti-HBs in children
H Ozen, N Koçak, A Yüce, I Gürakan
Pages: 269
Abstract