Search Results - "Hergüner, Özlem Mihriban"

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  1. 1

    Albendazole-induced dystonic reaction: a case report by Incecik, Faruk, Hergüner, Mihriban Ozlem, Ozcan, Kenan, Altunbaşak, Sakir

    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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    Journal Article
  2. 2

    Hypokalemic periodic paralysis due to the SCN4A R672H mutation in a Turkish family by Incecik, Faruk, Hergüner, Mihriban Ozlem, Altunbaşak, Sakir, Lehman-Horn, Frank

    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. 3

    Methylphenidate treatment outcomes and gender differences in attentional deficit and hyperactivity disorder with epilepsy: a follow-up study by Ray, Perihan, Çelik, Gonca, Tahiroğlu, Ayşegül, Gamlı, İpek, Hergüner, Özlem

    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. 4

    Tekrarlayan Fasiyal Paralizili bir olgu: Melkersson-Rosenthal Sendromu by Bulut, Derya Fatma, Mert, Gülen Gül, İncecik, Faruk, Hergüner, Özlem Mihriban, Altunbaşak, Şakir

    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. 5

    L-2-Hidroksi Glutarik Asidüri: Üç Olgu Sunumu by İncecik, Faruk, Mungan, Neslihan, Hergüner, Özlem Mihriban, Kör, Deniz, Şeker, Berna, Altunbasak, Sakir

    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. 6

    Levetiracetam And Valproic Acid: Effects On The Liver Functions And Ammonia Level In Children by Hergüner,Mihriban Özlem, Altunbaşak,Şakir, İncecik,Faruk

    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. 7

    Cranial Autonomic symptoms, neck pain: Challenges in pediatric migraine by Haytoglu, Zeliha, Herguner, Mihriban

    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. 8

    Pseudotumor cerebri in children: Etiology, clinical findings, prognosis by Mert,Gülen Gül, Özcan,Neslihan, Beşen,Şeyda, Yar,Kemal, Hergüner,Mihriban Özlem, İncecik,Faruk, Altunbaşak,Şakir

    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. 9

    Trisomy 9 Mosaicism Presenting With Epilepsy, And Facial Dysmorphism: A Case Report by Hergüner,Mihriban Özlem, Altunbaşak,Şakir, İncecik,Faruk, Mert,Gülen

    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. 10

    Epilepsy And McArdle Disease In A Child by Altunbaşak,Şakir, İncecik,Faruk, Mert,Gülen, Hergüner,Mihriban Özlem, Beşen,Şeyda, Kor,Deniz, Yılmaz,Berna S

    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. 11

    Coexistence Of Two Rare Genetic Disorders: Familial Mediterranean Fever And Neurofibromatosis Type 1 In A Child by Yılmaz,Mustafa Volkan, Hergüner,Mihriban Özlem, Altunbaşak,Şakir, İncecik,Faruk, Beşen,Şeyda, Haytoğlu,Zeliha Uçar

    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. 12

    Idiopathic Childhood Occipital Lobe Epilepsies In Turkish Children by Altunbaşak,Şakir, Mert,Gülen, Hergüner,Mihriban Özlem, İncecik,Faruk

    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. 13

    Nadir bir yürüme ve konuşma bozukluğu nedeni: Pontoserebellar hipoplazi tip 7 by Bilge,Serap, Mert,Gülen Gül, Özcanyüz,Duygu, Özcan,Neslihan, Hergüner,Mihriban Özlem, İncecik,Faruk, Altunbaşak,Şakir

    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. 14

    Coexisting Duchenne Muscular Dystrophy And Gilbert’s Syndrome: A Case Report by Horoz,Özden Özgür, Hergüner,Mihriban Özlem, Altunbaşak,Şakir, İncecik,Faruk, Mert,Gülen

    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. 15

    L-2-Hidroksi Glutarik Asidüri: Üç Olgu Sunumu by Altunbaşak,Şakir, İncecik,Faruk, Hergüner,Mihriban Özlem, Kor,Deniz, Şeker,Berna

    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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    Journal Article
  16. 16

    Tekrarlayan Fasiyal Paralizili bir Olgu: Melkersson- Rosenthal Sendromu by Altunbaşak,Şakir, İncecik,Faruk, Bulut,Fatma Derya, Mert,Gülen Gül, Hergüner,Mihriban Özlem

    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. 17

    Nörolojik Hastalıklarda Kök Hücre Nakli by Hergüner,Mihriban Özlem

    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. 18

    Risk factors affecting prognosis in infantile spasm by Gul Mert, Gulen, Herguner, Mihriban Ozlem, Incecik, Faruk, Altunbasak, Sakir, Sahan, Duygu, Unal, Ilker

    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. 19

    Çocuklarda vitamin B12 eksikliği ve epilepsi by İNCECİK, Faruk, ALTUNBAŞAK, Şakir, HERGÜNER, Mihriban Özlem

    “…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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