Browsing by Author "Tanzer, Fatos"
Now showing items 1-5 of 5
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Analysis of a 1-year-old cystinuric patient with recurrent renal stones
Tanzer, Fatos; Ozgur, Arzu; Bardakci, Fevzi; Cankorkmaz, Levent; Ayan, Semih (BLACKWELL PUBLISHING, 2006)Cystinuria is a hereditary disorder of cystine and dibasic amino acids (lysine, arginine, ornithine) transport across the luminal membrane of renal tubules and intestine, resulting in recurrent nephrolithiasis. Cystine ... -
Helicobacter pylori infection in mother and infant pairs in Anatolia
Hizel, Selda; Ozden, Ali; Tanzer, Fatos; Kisa, Ucler; Misirlioglu, Emine Dibek; Buyukkayhan, Derya; Kisa, Ozgul (AVES, 2010)Background/aims: The aim of this prospective study was to determine the seroprevalence rates of Helicobacter pylori in mother and infant pairs and to discuss the possible fecal-oral transmission route of Helicobacter pylori ... -
Investigation of wound healing in rat lung tissues in the postpartum period
Karadayi, Sule; Sahin, Ekber; Nadir, Aydin; Tuncer, Ersin; Silig, Yavuz; Korkmaz, Ilhan; Tanzer, Fatos; Sezer, Hafize; Kaptanoglu, Melih (SPANDIDOS PUBL LTD, 2012)To assess the wound healing capabilities of damaged lung tissue in the postpartum period, we investigated the parameters related to wound healing in a rat model of lung damage. Rats were divided into six groups: IA, I B, ... -
Transmission of Helicobacter pylori infection in mother-infant pairs
Selda, Hizel Bulbul; Ozden, Ali; Tanzer, Fatos; Kisa, Ucler; Buyukkayhan, Derya; Misirrlioglou, Emine Dibek; Kisa, Ozgul (AMER ACAD PEDIATRICS, 2008)… -
Type I cystinuria and its genetic basis in a population of Turkish school children
Tanzer, Fatos; Ozgur, Arzu; Bardakci, Fevzi (BLACKWELL PUBLISHING, 2007)Objectives: Cystinuria is a common inherited disorder characterized by an abnormal urinary excretion of cystine and dibasic amino acids resulting in nephrolithiasis. The SLC3A1 gene, which encodes a dibasic amino acid ...