Search Results - "KUMANDAS, SEFER"

Investigating the prevalence of febrile convulsion in Kayseri, Turkey: An assessment of the risk factors for recurrence of febrile convulsion and for development of epilepsy by Canpolat, Mehmet, Per, Huseyin, Gumus, Hakan, Elmali, Ferhan, Kumandas, Sefer

“…•The prevalence of febrile convulsion (FC) in Kayseri is 43/1000.•The risk of recurrence of FC increases 7.1-fold in individuals with a history of FC in first…”
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An analysis of 109 fetuses with prenatal diagnosis of complete agenesis of corpus callosum by Bayram, Ayşe Kaçar, Kütük, Mehmet Serdar, Doganay, Selim, Özgün, Mahmut Tuncay, Gümüş, Hakan, Başbuğ, Mustafa, Kumandaş, Sefer, Canpolat, Mehmet, Per, Hüseyin

“…Background Agenesis of the corpus callosum (ACC) is the most frequent commissural malformation of the brain. It continues to be an important cause of the…”
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Levels of Salivary Sialic Acid in Children with Autism Spectrum Disorder; Could It Be Related to Stereotypes and Hyperactivity? by Demirci, Esra, Guler, Yunus, Ozmen, Sevgi, Canpolat, Mehmet, Kumandas, Sefer

“…Sialic acid (Sia) is an essential nutrient for brain development, learning, memory and cognition and plays a role in neurodevelopment of infants. The aim of…”
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Clinical spectrum of the pseudotumor cerebri in children: Etiological, clinical features, treatment and prognosis by Per, Hüseyin, Canpolat, Mehmet, Gümüş, Hakan, Poyrazoğlu, Hatice Gamze, Yıkılmaz, Ali, Karaküçük, Sarper, Doğan, Hakkı, Kumandaş, Sefer

“…Abstract Objective: Pseudotumor cerebri (PTC) is a clinical condition characterized by signs and symptoms of increased intracranial pressure, such as headache…”
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PEX10-related autosomal recessive cerebellar ataxia with hearing loss by Kaya Özçora, Gül Demet, Miyatake, Satoko, Matsumoto, Naomichi, Canpolat, Mehmet, Erdoğan, Murat, Bayramov, Ruslan, Kumandaş, Sefer

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Evaluation of immunization status in patients with cerebral palsy: a multicenter CP-VACC study by Bozkaya-Yilmaz, Sema, Karadag-Oncel, Eda, Olgac-Dundar, Nihal, Gencpinar, Pinar, Sarioglu, Berrak, Arican, Pinar, Ersen, Atilla, Yilmaz-Ciftdoğan, Dilek, Yuksel, Merve Feyza, Bektas, Omer, Teber, Serap, Kilic, Betul, Calik, Mustafa, Karaca, Meryem, Canpolat, Mehmet, Kumandas, Sefer, Per, Huseyin, Gumus, Hakan, Ozturk, Selcan, Okuyaz, Cetin, Komur, Mustafa, Ipek, Rojan, Ozbudak, Pınar, Arhan, Ebru, Ince, Hulya, Gurbuz, Gurkan, Mert, Gulen Gul, Ozcan, Neslihan, Turker, Akgun Olmez, Gazeteci-Tekin, Hande, Kırık, Serkan, Günbey, Ceren, Çarman, Kürşat Bora, Yarar, Coşkun, Çavuşoğlu, Dilek

“…Children with chronic neurological diseases, including cerebral palsy (CP), are especially susceptible to vaccine-preventable infections and face an increased…”
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Reversible posterior leukoencephalopathy syndrome in childhood: report of nine cases and review of the literature by Gümüş, Hakan, Per, Hüseyin, Kumandaş, Sefer, Yıkılmaz, Ali

“…Reversible posterior leukoencephalopathy syndrome (RPLS) is recently described disorder with typical radiological findings in the posterior regions of the…”
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Treatment of pediatric refractory status epilepticus with topiramate by Akyildiz, Başak Nur, Kumandaş, Sefer

“…Objective We evaluated a topiramate (TPM) regimen for treating refractory status epilepticus in the largest pediatric series, reported to date. Methods…”
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Comparison of the Effectiveness of Rapamycin and Gabapentin Treatment in Rats with Induced Sciatic Nerve Injury by Canpolat, Mehmet, Halis Ali Çolpak, Dilek Günay Canpolat, Gözde, Özge Önder, Yetkin, Mehmet Fatih, Yay, Arzu Hanım, Gözde Ertürk Zararsız, Kumandaş, Sefer

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Detection of Novel NF1 Variants with Next-Generation DNA Sequencing Technology and Genotype-Phenotype Characteristics of Neurofibromatosis by Kiraz, Aslıhan, Gümüş, Hakan, Balta, Burhan, Erdoğan, Murat, Güven, Ahmet Sami, Savranlar, Ahmet, Çelik, Serkan Fazlı, Kumandaş, Sefer, Karaman, Zehra Filiz, Özdemi, Sevda Yeşim, Gümüş, Ümmü Gülsüm Özgül, Bayram, Nurettin, Per, Hüseyin

“…Objective: Neurofibromatosis type 1 (NF1, #162200) is a common neurological disorder with de novo or inherited germline mutations of the Neurofibromin (NF1,…”
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Childhood Stroke: Results of 130 Children From a Reference Center in Central Anatolia, Turkey by Per, Huseyin, MD, Unal, Ekrem, MD, Poyrazoglu, Hatice Gamze, MD, Ozdemir, Mehmet Akif, MD, Donmez, Halil, MD, Gumus, Hakan, MD, Uzum, Kazım, MD, Canpolat, Mehmet, MD, Akyildiz, Basak Nur, MD, Coskun, Abdulhakim, MD, Kurtsoy, Ali, MD, Kumandas, Sefer, MD

“…Abstract Background Although stroke among children is rare, it can cause significant morbidity and mortality. We aim to share our experience of children with…”
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The Effects of Ketogenic Diet on Seizures, Cognitive Functions, and Other Neurological Disorders in Classical Phenotype of Glucose Transporter 1 Deficiency Syndrome by Gumus, Hakan, Bayram, Ayşe Kaçar, Kardas, Fatih, Canpolat, Mehmet, Çağlayan, Ahmet Okay, Kumandas, Sefer, Kendirci, Mustafa, Per, Huseyin

“…The purpose of this study was to characterize patients who were diagnosed with glucose transporter protein 1 deficiency syndrome (Glut1D), and also to assess…”
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Misdiagnosis of gastroesophageal reflux disease as epileptic seizures in children by Bayram, Ayşe Kaçar, Canpolat, Mehmet, Karacabey, Neslihan, Gumus, Hakan, Kumandas, Sefer, Doğanay, Selim, Arslan, Duran, Per, Hüseyin

“…Abstract Background Gastroesophageal reflux disease (GERD) can mimic epileptic seizure, and may be misdiagnosed as epilepsy. On the other hand, GERD can be…”
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Pepper spray inhalation-induced acute polyneuropathy mimicking Guillain-Barre syndrome by Özçora, Gül Demet Kaya, Çıraklı, Sevgi, Canpolat, Mehmet, Doğanay, Selim, Kumandaş, Sefer

“…Peripheral neuropathy is the most common reaction to toxic chemical substances in the nervous system. Toxic neuropathies are often misdiagnosed because there…”
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Long-Term Follow-Up of Patients with a Diagnosis of Posterior Reversible Encephalopathy Syndrome by Canpolat, Mehmet, Kaya Özçora, Gül Demet, Poyrazoğlu, Hakan, Per, Huseyin, Çoşkun, Abdulhakim, Gümüş, Hakan, Arslan, Duran, Ünal, Ekrem, Karakükçü, Musa, Patıroğlu, Türkan, Kumandaş, Sefer

“…The essential characteristics of posterior reversible encephalopathy syndrome (PRES) are the presence of acute onset neurologic symptoms, focal vasogenic edema…”
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Maternal uniparental isodisomy is responsible for serious molybdenum cofactor deficiency by GÜMÜŞ, HAKAN, GHESQUIERE, STIJN, PER, HÜSEYIN, KONDOLOT, MEDA, ICHIDA, KIMIYOSHI, POYRAZOĞLU, GAMZE, KUMANDAŞ, SEFER, ENGELEN, JOHN, DUNDAR, MUNIS, ÇAĞLAYAN, AHMET OKAY

“…Molybdenum cofactor (MoCo) deficiency is a rare autosomal recessive inherited metabolic disorder resulting in the combined deficiency of aldehyde oxidase,…”
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Hereditary spastic paraplegia with recessive trait caused by mutation in KLC4 gene by Bayrakli, Fatih, Poyrazoglu, Hatice Gamze, Yuksel, Sirin, Yakicier, Cengiz, Erguner, Bekir, Sagiroglu, Mahmut Samil, Yuceturk, Betul, Ozer, Bugra, Doganay, Selim, Tanrikulu, Bahattin, Seker, Askin, Akbulut, Fatih, Ozen, Ali, Per, Huseyin, Kumandas, Sefer, Altuner Torun, Yasemin, Bayri, Yasar, Sakar, Mustafa, Dagcinar, Adnan, Ziyal, Ibrahim

“…We report an association between a new causative gene and spastic paraplegia, which is a genetically heterogeneous disorder. Clinical phenotyping of one…”
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The relation between antiepileptic drug type and cognitive functions in childhood epilepsy: A prospective observational study by Canpolat, Mehmet, Per, Huseyin, Gumus, Hakan, Kumandas, Sefer, Hanci, Fatma

“…Aim: This study investigated the effect of antiepileptic drug monotherapy on cognitive functions in pediatric epilepsy patients. Methods: 98 recently diagnosed…”
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Primary soliter and multiple intracranial cyst hydatid disease: Report of five cases by Per, Hüseyin, Kumandaş, Sefer, Gümüş, Hakan, Kurtsoy, Ali

“…Abstract Echinococcosis is a parasitic disease caused by infestation of various body tissues by the encysted larvae of Echinococcosis granulosa , the tapeworm…”
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Intracranial hemorrhages and late hemorrhagic disease associated cholestatic liver disease by Per, Hüseyin, Arslan, Duran, Gümüş, Hakan, Çoskun, Abdulhakim, Kumandaş, Sefer

“…Deficiency of vitamin K predisposes to early, classic or late hemorrhagic disease of the newborn (HDN); of which late HDN may be associated with serious and…”
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