Browsing by Author "Icagasioglu, D"
Now showing items 1-8 of 8
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An adrenal cyst in a newborn
Icagasioglu, D; Caksen, H; Yildiz, E; Kocyigit, C; Cevit, O (SPRINGER-VERLAG, 2003)Adrenal cysts (AC) are rare, particularly in the newborn period. Almost all ACs in newborns were diagnosed on exploratory laparotomy or at autopsy. We report a newborn with an AC that was diagnosed after an exploratory ... -
Blood glucose levels and hypoglycaemia in full term neonates during the first 48 hours of life
Tanzer, F; Yazar, N; Yazar, H; Icagasioglu, D (OXFORD UNIV PRESS, 1997)Thirty-five fun term infants (35-41 weeks' gestation) were included in the study, Infants of mothers with complications of pregnancy, such as toxaemia, anaemia, diabetes, or hypertension were Plot included, All infants ... -
Childhood achalasia
Icagasioglu, D; Tanzer, F; Gultekin, A; Bayram, G; Sekreter, E (TURKISH J PEDIATRICS, 1996)Achalasia is a motility disorder of the esophagus characterized by absence of normal peristalsis and failure of relaxation of the lower esophageal sphincter. Among the most common clinical findings are vomiting and weight ... -
Combined genetic defects in a child with ischemic stroke: Case report
Deda, G; Icagasioglu, D; Caksen, H; Akar, N (SAGE PUBLICATIONS INC, 2002)A 10-year-old Turkish boy was admitted with mild right spastic hemiplegia. First, he experienced sudden numbness and weakness in the right extremities at the age of 2 years and was diagnosed with right hemiparesis. His ... -
High-dose intravenous immune globulin in the management of severe Guillain-Barre syndrome
Baskin, E; Turkay, S; Icagasioglu, D; Tanzer, F; Cevit, O (TURKISH J PEDIATRICS, 1996)Guillain-Barre syndrome (GBS) is the most common muse of acute generalized paralysis. Although the muse and pathogenesis of GBS remain unknown, there is increasing evidence to suggest that this syndrome has an immunological ... -
Magnetic resonance spectroscopy and diffusion-weighted imaging findings in a child with Leigh's disease
Atalar, MH; Egilmez, H; Bulut, S; Icagasioglu, D (BLACKWELL PUBLISHING, 2005)… -
Psychotic disorder in a case with Hallervorden-Spatz disease
Oner, O; Oner, P; Deda, G; Icagasioglu, D (BLACKWELL MUNKSGAARD, 2003)Objective: Hallervorden - Spatz disease is a rare autosomal recessive condition, with early onset of predominantly extrapyramidal dysfunction. The symptoms of the disease are dystonia, rigidity, choreoathetosis, pyramidal ... -
Serum lipids, vitamin B12 and folic acid levels in children receiving long-term valproate therapy
Geda, G; Caksen, H; Icagasioglu, D (ACTA MEDICA BELGICA, 2002)In this study, serum triglyceride, total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (HDL-C), very low-density lipoprotein cholesterol (VLDL-C), vitamin B12 and folic ...