Search Results - "Şakir ALTUNBAŞAK"

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  1. 1

    Neuronal loss is an early component of subacute sclerosing panencephalitis by Yüksel, Deniz, Diren, Barş, Ulubay, Hakan, Altunbaşak, Şakir, Anlar, Banu

    Published in Neurology (02-09-2014)
    “…OBJECTIVE:We performed diffusion tensor imaging (DTI) and magnetic resonance spectroscopy (MRS) studies in a group of patients with subacute sclerosing…”
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    Journal Article
  2. 2

    Congenital myasthenic syndrome in Turkey: clinical and genetic features in the long-term follow-up of patients by Gül Mert, Gülen, Özcan, Neslihan, Hergüner, Özlem, Altunbaşak, Şakir, Incecik, Faruk, Bişgin, Atıl, Ceylaner, Serdar

    Published in Acta neurologica Belgica (01-04-2021)
    “…Congenital Myasthenic Syndromes (CMS) are rare disorders that occur as a result of defects in the structure and in the function of neuromuscular junctions…”
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  3. 3

    Factors affecting epilepsy prognosis in patients with tuberous sclerosis by Gül Mert, Gülen, Altunbaşak, Şakir, Hergüner, Özlem, İncecik, Faruk, Övetti, Hilal Cansever, Özcan, Neslihan, Kuşçu, Duygu, Ünal, İlker

    Published in Child's nervous system (01-03-2019)
    “…Purpose We aimed to determine the characteristics of epileptic seizures that significantly affect the cognitive functions of 83 patients followed with tuberous…”
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  4. 4

    Neurofibromatosis type 1 and cardiac manifestations by Incecik, Faruk

    Published in Türk Kardiyoloji Derneği arşivi (01-12-2015)
    “…Cardiac manifestations of neurofibromatosis type 1 (NF1) may include hypertension, congenital heart disease, and hypertrophic cardiomyopathy. The aim of this…”
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  5. 5

    Telomerase activity in patients with neurofibromatosis Type-1 by Küpeli,Serhan, Altunbaşak,Şakir, İncecik,Faruk, Arkan,Ayçin

    Published in Cukurova Medical Journal (01-01-2018)
    “…Purpose: In various studies low telomerase activity have been shown to have a protective role in some types of cancer. Patients with neurofibromatosis type-1…”
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  6. 6

    Neurologic findings of nutritional vitamin B12 deficiency in children by Incecik, Faruk, Hergüner, M Ozlem, Altunbaşak, Sakir, Leblebisatan, Göksel

    Published in Turkish journal of pediatrics (01-01-2010)
    “…We report herein our interesting case series of 15 infants admitting with neurological symptoms who were found to have vitamin B12 deficiency. Infants who were…”
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  7. 7

    Evaluation of Critical Illness Polyneuropathy/Myopathy in Pediatric Intensive Care Unit by Arslan, Didar, Yıldızdaş, Rıza Dinçer, Horoz, Özden Özgür, Aslan, Nagehan, Çoban, Yasemin, Altunbaşak, Şakir, Balal, Mehmet, Haytoğlu, Zeliha

    Published in Çocuk acil ve yoğun bakım (18-12-2020)
    “…Introduction:The aim of this study was to determine the frequency of patients with critical illness polyneuropathy/myopathy followed by mechanical ventilator…”
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    Journal Article
  8. 8

    Acute disseminated encephalomyelitis: an evaluation of 15 cases in childhood by Incecik, Faruk, Hergüner, M Özlem, Altunbasak, Sakir

    Published in Turkish journal of pediatrics (01-05-2013)
    “…To describe our experience with acute disseminated encephalomyelitis (ADEM) and the relationships between the clinical course, magnetic resonance imaging (MRI)…”
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  9. 9

    Hypohidrosis and hyperthermia during topiramate treatment in children by Incecik, Faruk, Hergüner, M Ozlem, Altunbaşak, Sakir

    Published in Turkish journal of pediatrics (01-09-2012)
    “…Topiramate is one of the newer generation antiepileptic drugs with a beneficial clinical effect on various seizure types. In this study, we present the…”
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  10. 10

    Mutation analysis of 6 spinocerebellar ataxia (SCA) types in patients from southern Turkey by Pazarci, Perçin, Kasap, Halil, Koç, Ayşe Filiz, Altunbaşak, Sakir, Erkoç, Mehmet Ali

    “…Spinocerebellar ataxias (SCAs) are complex clinical and genetically heterogeneous, mostly autosomal dominant neurodegenerative diseases. At present, more than…”
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  11. 11

    Ring chromosome 14 syndrome presenting with intractable epilepsy: a case report by Incecik, Faruk, Hergüner, M Ozlem, Mert, Gülen, Erdem, Sevcan, Altunbaşak, Sakir

    Published in Turkish journal of pediatrics (01-09-2013)
    “…Ring chromosome 14 syndrome is a rare genetic disorder. Typically, children with this syndrome have distinct facial features, development delay, microcephaly,…”
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  12. 12

    Evaluation of sixteen children with pseudotumor cerebri by Incecik, Faruk, Hergüner, M Ozlem, Altunbaşak, Sakir

    Published in Turkish journal of pediatrics (01-01-2011)
    “…Pseudotumor cerebri (PTC) is a clinical condition characterized by signs and symptoms of increased intracranial pressure, such as headache and papilledema. A…”
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  13. 13

    Pyridoxine-dependent epilepsy in two Turkish patients in Turkey and review of the literature by Gül-Mert, Gülen, İncecik, Faruk, Hergüner, M Özlem, Ceylaner, Serdar, Altunbaşak, Şakir

    Published in Turkish journal of pediatrics (01-07-2015)
    “…Pyridoxine-dependent epilepsy (PDE) is a rare autosomal recessive enzyme defect in the vitamin B6 metabolism characterized by intractable seizures which are…”
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  14. 14

    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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  15. 15

    Pseudotumor Cerebri in a Child With Familial Mediterranean Fever by Incecik, Faruk, Herguner, Ozlem M, Yilmaz, Mustafa, Altunbasak, Sakir

    Published in Archives of rheumatology (01-09-2015)
    “…Familial Mediterranean fever is an autosomal recessive polysystemic disease characterized by attacks of relapsing and self-limiting fever, peritonitis,…”
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  16. 16

    Cyclosporin Treatment in Three Children With Chronic Inflammatory Demyelinating Neuropathy by OZLEM HERGÜNER, M, INCECIK, Faruk, ALTUNBASAK, Sakir

    Published in Pediatric neurology (01-09-2009)
    “…Chronic inflammatory demyelinating neuropathy is an uncommon acquired polyneuropathy in children. Oral prednisolone, intravenous methyl prednisolone, and…”
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  17. 17

    Joubert syndrome: report of 11 cases by İncecik, Faruk, Hergüner, M Özlem, Altunbaşak, Şakir, Gleeson, Joseph G

    Published in Turkish journal of pediatrics (01-11-2012)
    “…Joubert syndrome (JS) is an autosomal recessive condition characterized by hypotonia, ataxia, psychomotor delay, and variable occurrence of oculomotor apraxia…”
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  18. 18

    Oncologic manifestations in children with neurofibromatosis type 1 in Turkey by İncecik, Faruk, Altunbaşak, Şakir, Hergüner, M Özlem, Bayram, İbrahim, Küpeli, Serhan, Demirbilek, Hüseyin

    Published in Turkish journal of pediatrics (01-05-2013)
    “…Children with neurofibromatosis type 1 (NF1) are predisposed to malignancies such as brain tumors, leukemia, and pheochromocytomas. The aim of this study was…”
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  19. 19

    Clinical Characteristics of 10 Patients With Continuous Spikes and Waves During Slow Sleep Syndrome by HERGIINER, M. Ozlem, INCECIK, Faruk, ALTUNBASAK, Sakir, KIRIS, Nurcihan

    Published in Pediatric neurology (01-06-2008)
    “…Continuous spikes and waves during slow sleep syndrome is characterized by the presence of spike-and-wave discharges in at least 85% of non–rapid eye movement…”
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  20. 20

    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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