Yazar "Canaz, Hüseyin" için Tıp Fakültesi Makale Koleksiyonu listeleme
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Investigation of dose-dependent neuroprotective effect of human recombinant erythropoietin in acute spinal cord injury induced rats
Özdemir, Bülent; Batçık, Ersegun; Ayçiçek, Ezgi; Canaz, Gökhan; Akdemir, Osman; Alataş, İbrahim; Canaz, Hüseyin (e-Century Publishing, 2016)The aim of this study was to investigate the dose dependent neuroprotective effect of recombinant human erythropoietin (r-Hu-EPO) in acute spinal cord injury induced rats. The rats were allocated into 4 groups of 8 rats ... -
Morphometric and ultrastructural analysis of the effect of bromocriptine and cyclosporine on the vasospastic femoral artery of rats.
Tokmak, Mehmet; Başocak, Kahan; Canaz, Hüseyin; Canaz, Gökhan; İplikçioğlu, Celal (e-Century Publishing, 2015)Vasospasm is the main causes of mortality and morbidity in patiens with subarachnoid hemorrhage (SAH). The arterial narrowing mechanism that develops after SAH is not yet fully understood but many studies showed that ... -
The role of urodynamic studies in the diagnosis and treatment of patients with spina bifida
Alatas, İbrahim; Demirci, H; Canaz, Hüseyin; Akdemir, O; Baydın, S; Özel, Kerem (Medknow Publications, 2015)Aim: Spina bifida (SB) is a congenital deformity that is frequently seen in infancy. Surgical treatment and clinical follow-up of patients with the diagnosis of SB are important to provide education to the patients and ... -
Statistical analysis of associated vertebra and costal anomalies in spina bifida patients
Alataş, İbrahim; Canaz, Hüseyin; Saraçoğlu, Ayten; Kafalı, Haluk; Canaz, Gökhan; Tokmak, Mehmet (De Gruyter Open / Romanian Society of Neurosurgery, 2016)Objective: Spina bifida is one of the most severe birth defects and can happen as a result of disrupted primary neurulation. Congenital vertebra and costa anomalies are more frequently seen with spina bifida, and associated ... -
Three level spinal dysraphism: multiple composite Type 1 and Type 2 split cord malformation
Alataş, İbrahim; Gündağ, Meliha; Canaz, Hüseyin; Emel, E (De Gruyter Open / Romanian Society of Neurosurgery, 2014)It has reported an uncommon case a 3 year-old girl a composite split cord malformation (SCM) with two different levels of SCM type1 and one level SCM type2, tight filum and sacral dermal sinus. The patient was admitted ...