Search Results - "Deda, Gülhis"

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    Effects of levetiracetam and valproic acid treatment on liver function tests, plasma free carnitine and lipid peroxidation in childhood epilepsies by Haznedar, Pınar, Doğan, Özlem, Albayrak, Pelin, Öz Tunçer, Gökçen, Teber, Serap, Deda, Gülhis, Eminoglu, F. Tuba

    Published in Epilepsy research (01-07-2019)
    “…[Display omitted] The relationship between anti-epileptic usage and oxidative damage has not yet been clearly understood. In our study, we investigated…”
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    Hashimoto’s encephalopathy presenting as pseudobulbar palsy by Oz Tuncer, Gokcen, Teber, Serap, Kutluk, Muhammed Gültekin, Albayrak, Pelin, Deda, Gülhis

    Published in Child's nervous system (01-06-2018)
    “…Introduction Hashimoto’s encephalopathy (HE) is an autoimmune condition with varied neurological and psychiatric features. HE is very unusual as a cause of…”
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    Anti-N-methyl-D-aspartate receptor encephalitis that developed after herpes encephalitis: a case report and literature review by Bektaş, Ömer, Tanyel, Tutku, Kocabaş, Bilge Aldemir, Fitöz, Suat, Ince, Erdal, Deda, Gülhis

    Published in Neuropediatrics (01-12-2014)
    “…Herpes encephalitis (HE) is among the most common forms of viral encephalitis. Earlier publications indicate the development of acyclovir-refractory…”
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    A celiac case mimicking mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) by Aksoy, Erhan, Tıraş-Teber, Serap, Deda, Gülhis

    Published in Turkish journal of pediatrics (01-11-2016)
    “…Celiac disease (CD) is a chronic disease involving a number of systems in addition to gastrointestinal tract. Although not clear, it has been supposed that the…”
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    Neurological findings spectrum in Celiac disease by Aksoy, Erhan, Tıraş-Teber, Serap, Kansu, Aydan, Deda, Gülhis, Kartal, Ayşe

    Published in Turkish journal of pediatrics (2016)
    “…We aimed to provide early diagnosis by determining possible Celiac disease related subclinical or symptomatic neurological abnormalities in children in order…”
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    Complete paralytic botulism mimicking a deep coma in a child by Azapağası, Ebru, Kendirli, Tanıl, Öz-Tuncer, Gökçen, Albayrak, Pelin, Teber, Serap, Deda, Gülhis

    Published in Turkish journal of pediatrics (2017)
    “…Botulism is a rare cause of neuroparalysis. Delay in diagnosis and treatment exerts adverse impact on mortality and morbidity. We report a child with complete…”
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    Electroencephalogram Variations in Pediatric Migraines and Tension-Type Headaches by Ozkan, Mehpare, MD, Teber, Serap T., MD, Deda, Gülhis, MD

    Published in Pediatric neurology (01-03-2012)
    “…Abstract This study evaluates specific electroencephalogram abnormalities in pediatric migraine and tension-type headaches, and demonstrates the clinical value…”
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    Cerebral sinovenous thrombosis in children and neonates: clinical experience, laboratory, treatment, and outcome by Bektaş, Ömer, Teber, Serap, Akar, Nejat, Uysal, Leyla Zümrüt, Arsan, Saadet, Atasay, Begüm, Deda, Gülhis

    Published in Clinical and applied thrombosis/hemostasis (01-11-2015)
    “…Our aim is to present the etiology and risk factors for cerebral sinovenous thrombosis (CSVT) and the radiological findings, anticoagulant therapy used, and…”
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    A case of Dravet Syndrome with a newly defined mutation in the SCN1A gene by Tunçer, Gökçen Öz, Teber, Serap, Albayrak, Pelin, Kutluk, Muhammet Gültekin, Deda, Gülhis

    Published in Turk Pediatri Arsivi (01-12-2018)
    “…Dravet syndrome is a catastrophic progressive epileptic syndrome. De novo loss of function mutations on the SCN1A gene coding voltage-gated sodium channels are…”
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    Endothelial protein C receptor and pediatric arterial stroke by Akar, Nejat, Karabıyık, Afife, Deda, Gülhis

    Published in Turkish journal of haematology (01-03-2013)
    “…The aim of this study was to investigate the endothelial protein C receptor (EPCR) gene A3 haplotype and plasma soluble EPCR (sEPCR) levels in Turkish…”
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  13. 13

    A novel protein C inhibitor gene mutation in pediatric stroke patients after bone marrow transplantation by Torun, Didem, Deda, Gülhis, Ertem, Mehmet, Uysal, Zümrüt, Yılmaz, Erkan, Akar, Nejat

    Published in Molecular biology reports (01-09-2013)
    “…Protein C inhibitor is a heparin dependent serine protease inhibitor found in human plasma, urine and other body fluids. It was originally identified as an…”
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    Lipoprotein (a) levels in childhood arterial ischemic stroke by Teber, Serap, Deda, Gülhis, Akar, Nejat, Soylu, Kazim

    Published in Clinical and applied thrombosis/hemostasis (01-04-2010)
    “…Lipoprotein (a) is a cholesterol-rich plasma lipoprotein with a lipid composition similar to that of low-density lipoproteins (LDL). Many prospective and…”
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    EPCR gene A3 haplotype and elevated soluble endothelial protein C receptor (sEPCR) levels in Turkish pediatric stroke patients by Ulu, Arzu, Gunal, Denizay, Tiras, Serap, Egin, Yonca, Deda, Gülhis, Akar, Nejat

    Published in Thrombosis research (01-01-2007)
    “…Abstract Introduction High plasma levels of sEPCR lead to dysfunction of the EPCR-mediated coagulation. We have evaluated the role of EPCR A3 haplotype with…”
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    TNF-α −308G/A and IL-6 −174 G/C polymorphisms in the Turkish pediatric stroke patients by Karahan, Zeynep Ceren, Deda, Gülhis, Sipahi, Tansu, Elhan, Atilla H., Akar, Nejat

    Published in Thrombosis research (2005)
    “…Introduction: Stroke is an important cause of mortality and morbidity in the pediatric age group. There is increasing evidence on the role of proinflammatory…”
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    Fetal and neonatal cardiac rhabdomyomas: clinical presentation, outcome and association with tuberous sclerosis complex by Atalay, Semra, Aypar, Ebru, Uçar, Tayfun, Altuğ, Nahide, Deda, Gülhis, Teber, Serap, Tutar, Ercan

    Published in Turkish journal of pediatrics (01-09-2010)
    “…Rhabdomyoma is the most common pediatric heart tumor. Cardiac rhabdomyomas (CRs) have a natural history of spontaneous regression and are closely associated…”
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    FXIII Gene Val34Leu Polymorphism in Turkish Children with Cerebral Infarct by Akar, Nejat, Dönmez, Buket, Deda, Gülhis

    Published in Journal of child neurology (01-02-2007)
    “…A common polymorphism of the FXIIIA gene, which is characterized by a Val → Leu exchange at amino acid position 34 (FXIII Val34Leu), was studied in this…”
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    The relation between cytokines, soluble endothelial protein C receptor, and factor VIII levels in Turkish pediatric stroke patients by Yürürer, Denizay, Teber, Serap, Deda, Gülhis, Egin, Yonca, Akar, Nejat

    Published in Clinical and applied thrombosis/hemostasis (01-10-2009)
    “…The aim of the authors is to examine the relationship between the cytokine levels that are thought to be involved in stroke etiopathogenesis (tumor necrosis…”
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