Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Meral Ozmen"'
Publikováno v:
Tuberculin Skin Test in Children. 13:89-94
Autor:
Atakan Aydin, Zeynep Hosbay Yildirim, Ahmet Bicer, Feride Bilir, Gonul Acar, Safiye Ozkan, Meral Ozmen, Metin Erer
Publikováno v:
Hand and Microsurgery, Vol 1, Iss 3, Pp 89-94 (2012)
Objectives: Obstetric palsy is the term used for the clinical conditions caused by the traction injury of the brachial plexus during delivery. During nerve regeneration process, cocontraction may occur around shoulder and elbow muscles and cause cont
Autor:
Yakup, Ergul, Baris, Ekici, Kemal, Nisli, Burak, Tatli, Fatih, Binboga, Gonul, Acar, Meral, Ozmen, Rukiye Eker, Omeroglu
Publikováno v:
Journal of paediatrics and child health. 48(7)
We evaluated ambulatory patients with Duchenne muscular dystrophy from the cardiovascular standpoint and studied the correlation between the results of electrocardiographic (ECG) findings, left ventricular ejection fraction (LVEF), troponin T and N-t
Publikováno v:
Acta neurologica Belgica. 111(4)
A 10-year-old male presented with vision loss and behavioral changes. He had midpoint pupils with no reaction to light and normal funduscopic examination. Cranial magnetic resonance imaging revealed bilateral cortical lesions at parieto-occipital lob
Autor:
Burak, Tatlı, Nur, Aydınlı, Mine, Calışkan, Meral, Ozmen, Bülent, Kara, Ahmet, Yaramış, Cengiz, Dilber, Kutluhan, Yılmaz, Yasemin, Küçükuğurluoğlu, Barış, Ekici
Publikováno v:
Journal of paediatrics and child health. 47(10)
To define clinical features of patients with alternating hemiplegia of childhood.We retrospectively reviewed the clinical presentation and course of the disease in patients diagnosed between January 2003 and December 2008 at the Pediatric Neurology D
Publikováno v:
The Turkish journal of pediatrics. 51(1)
Varicella is largely a childhood disease, with more than 90% of cases occurring in children younger than 10 years. The primary infection is characterized by generalized vesicular dermal exanthemas, which are extremely contagious. Secondary bacterial
Autor:
Bülent, Kara, Abdullah, Uzümcü, Oya, Uyguner, Rasim Ozgür, Rosti, Ayça, Koçbaş, Meral, Ozmen, Hülya, Kayserili
Publikováno v:
The Turkish journal of pediatrics. 50(5)
Ataxia with vitamin E deficiency (AVED) is a rare autosomal recessive disorder, usually with a phenotype resembling Friedreich ataxia, caused by selective impairment of gastrointestinal vitamin E absorption. Vitamin E supplementation improves symptom
Autor:
Bülent, Kara, Birsen, Karaman, Meral, Ozmen, Rasim Ozgür, Rosti, Mine, Calişkan, Hülya, Kayserili, Seher, Başaran
Publikováno v:
The Turkish journal of pediatrics. 50(2)
The diagnosis of Angelman syndrome (AS) is based on the clinical features, behavior, EEG findings, and genetic abnormalities. The physical, clinical and behavioral aspects appear to attributable to localized central nervous system (CNS) dysfunction o
Publikováno v:
The Turkish journal of pediatrics. 47(4)
Topiramate (TPM) has peculiar side effects such as speech difficulties, weight loss, oligohidrosis and hyperthermia. We present the frequency and severity of hypohidrosis in our patients under TPM treatment. One hundred and two patients treated with
Autor:
Ayhan, Söğüt, Meral, Ozmen, Serra, Sencer, Mine, Calişkan, Nur, Aydinli, Türkan, Ertuğrul, Gönül, Peksayar
Publikováno v:
The Turkish journal of pediatrics. 44(2)
Tuberous sclerosis (TS) is an autosomal dominant, multisystemic and neurocutaneous disease with high spontaneous mutation rate, and it mostly involves the skin, brain, kidneys, heart and the eyes. This study included 35 patients diagnosed with tubero