Search Results - "Hergüner, Özlem Mihriban"
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Albendazole-induced dystonic reaction: a case report
Published in Turkish journal of pediatrics (01-11-2011)“…Drug-induced dystonic reactions are a common presentation to the emergency department and typically occur with drugs like chlorpromazine, haloperidol and…”
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2
Hypokalemic periodic paralysis due to the SCN4A R672H mutation in a Turkish family
Published in Turkish journal of pediatrics (01-07-2010)“…Hypokalemic periodic paralysis (HypoPP) is an autosomal dominant disorder characterized by episodic attacks of muscle weakness associated with a decrease in…”
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3
Methylphenidate treatment outcomes and gender differences in attentional deficit and hyperactivity disorder with epilepsy: a follow-up study
Published in Anadolu psikiyatri dergisi (01-12-2019)“…[...]in the general group, all the differences between epileptic and non-epileptic males and ST-1/2, ST-1/3, SEC-1/2 and SEC-1/3 measurements in nonepileptic…”
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4
Tekrarlayan Fasiyal Paralizili bir olgu: Melkersson-Rosenthal Sendromu
Published in Cukurova Medical Journal (01-12-2014)“…Melkersson-Rosenthal sendromu (MRS), tekrarlayan fasiyal paralizi, orofasiyal ödem, dilde fissürle karakterize nadir bir nöromukokütanöz sendromdur…”
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5
L-2-Hidroksi Glutarik Asidüri: Üç Olgu Sunumu
Published in Cukurova Medical Journal (01-12-2014)“…L-2-hidroksiglutarik asidüri nadir rastlanan, otozomal resesif geçişli, metabolik bir hastalıktır. Hastalık zihinsel engellilik, ataksi, ekstrapiramidal…”
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6
Levetiracetam And Valproic Acid: Effects On The Liver Functions And Ammonia Level In Children
Published in Cukurova Medical Journal (01-01-2014)“…Purpose: There is evidence that levetiracetam and valproic acid causes a changes of serum ammonia level and liver function tests. The aim of this study was to…”
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7
Cranial Autonomic symptoms, neck pain: Challenges in pediatric migraine
Published in Annals of the Indian Academy of Neurology (01-07-2019)“…Objectives: More than just a headache, migraine attack is a severe, prolonged head pain preceded and/or followed by a constellation of symptoms. Getting a…”
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8
Pseudotumor cerebri in children: Etiology, clinical findings, prognosis
Published in Cukurova Medical Journal (01-02-2019)“…Purpose: Clinical and neuroimaging findings, aetiologies, treatment modalities and durations, response to treatment, and neurological sequelae of the patients…”
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9
Trisomy 9 Mosaicism Presenting With Epilepsy, And Facial Dysmorphism: A Case Report
Published in Cukurova Medical Journal (01-02-2014)“…Trisomy 9 syndrome is a rare genetic disorder. Trisomy 9 has two forms; 1) mosaic, 2) non-mosaic. The patients usually present similar clinical features,…”
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10
Epilepsy And McArdle Disease In A Child
Published in Cukurova Medical Journal (01-01-2015)“…McArdle's disease, defined by the lack of functional glycogen phosphorylase in striated muscle, is inherited as an autosomal recessive trait. Patients…”
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11
Coexistence Of Two Rare Genetic Disorders: Familial Mediterranean Fever And Neurofibromatosis Type 1 In A Child
Published in Cukurova Medical Journal (01-01-2015)“…Familial Mediterranean fever (FMF) is an autosomal recessive polysystemic disease characterized by attacks of relapsing and self-limiting fever, peritonitis,…”
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12
Idiopathic Childhood Occipital Lobe Epilepsies In Turkish Children
Published in Cukurova Medical Journal (01-03-2015)“…Purpose: Two forms of idiopathic occipital lobe epilepsy can be distinguished: an early onset or Panayiotopoulos type (PS), and a late onset or Gastaut type…”
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13
Nadir bir yürüme ve konuşma bozukluğu nedeni: Pontoserebellar hipoplazi tip 7
Published in Cukurova Medical Journal (2019)“…Pontoserebellar hipoplazi, nadir ve kötü prognozlu bir hastalıktır. Klinik olarak hastalar başlangıçta hipotoni ardından gelişen hipertoni, progresif…”
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14
Coexisting Duchenne Muscular Dystrophy And Gilbert’s Syndrome: A Case Report
Published in Cukurova Medical Journal (01-04-2013)“…Gilbert's syndrome is characterized by unconjugated hyperbilirubinemia. A 5-year-old boy presented to our hospital with mild hyperbilirubinemia. The patient…”
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15
L-2-Hidroksi Glutarik Asidüri: Üç Olgu Sunumu
Published in Cukurova Medical Journal (01-04-2014)“…L-2-hidroksiglutarik asidüri nadir rastlanan, otozomal resesif geçişli, metabolik bir hastalıktır.Hastalık zihinsel engellilik, ataksi, ekstrapiramidal…”
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16
Tekrarlayan Fasiyal Paralizili bir Olgu: Melkersson- Rosenthal Sendromu
Published in Cukurova Medical Journal (01-04-2014)“…Melkersson-Rosenthal sendromu (MRS), tekrarlayan fasiyal paralizi, orofasiyal ödem, dilde fissürle karakterize nadir bir nöromukokütanöz…”
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17
Nörolojik Hastalıklarda Kök Hücre Nakli
Published in Arşiv Kaynak Tarama Dergisi (01-01-2014)“…Nörolojik hastalıklar, sıklıkla nöronlarda kayıp veya progresif hasar nedeniyle oluşur. Son yıllarda kök hücre teknikleri ile gerek nöron, gerekse gliaların…”
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18
Risk factors affecting prognosis in infantile spasm
Published in International journal of neuroscience (02-11-2017)“…Aim: To assess risk factors that affect epilepsy prognosis and neurodevelopmental outcome and response to treatment in patients diagnosed with infantile spasm…”
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19
Çocuklarda vitamin B12 eksikliği ve epilepsi
Published in Trakya Üniversitesi Tip Fakültesi dergisi (2010)“…Amaç: Nöbet ile başvuran ve vit B12 eksikliği saptadığımız 7 olguyu dikkat çekici olması nedeniyle sunduk. Gereç ve Yöntemler: Hastanemize nöbet ile başvuran…”
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20
Methylphenidate treatment outcomes and gender differences in attentional deficit and hyperactivity disorder with epilepsy: a follow-up study/ Epilepsinin eslik ettigi dikkat eksikligi hiperaktivite bozuklugunda metilfenidat tedavi yaniti ve cinsiyet farkliliklari: Izleme calismasi
Published in Anadolu psikiyatri dergisi (01-12-2019)“…Objective: The aim of this study is to investigate the methylphenidate (MPH) treatment response in children and adolescents with Attention Deficit…”
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