Search Results - Eraksoy, Mefkure

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  1. 1
    Hypermanganesemia with Dystonia 1: A Novel Mutation and Response to Iron Supplementation

    Hypermanganesemia with Dystonia 1: A Novel Mutation and Response to Iron Supplementation by Yapici, Zuhal, Tuschl, Karin, Eraksoy, Mefkure

    Published 2019
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  2. 2
    Validity and Reliability of the Turkish Version of the Monitoring My Multiple Sclerosis Scale

    Validity and Reliability of the Turkish Version of the Monitoring My Multiple Sclerosis Scale by POLAT, Cansu, TÜLEK, Zeliha, KÜRTÜNCÜ, Murat, ERAKSOY, Mefkure

    Published 2017
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  3. 3
    Validity and Reliability of the Turkish Version of the Multiple Sclerosis-Related Symptom Checklist

    Validity and Reliability of the Turkish Version of the Multiple Sclerosis-Related Symptom Checklist by TÜLEK, Zeliha, POLAT, Cansu, KÜRTÜNCÜ, Murat, ERAKSOY, Mefkure

    Published 2017
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  4. 4
    Inflammatory Demyelinating Diseases of Childhood: Case Report and Literature Review

    Inflammatory Demyelinating Diseases of Childhood: Case Report and Literature Review by EKİZOĞLU, Esme, TEKTÜRK TOPALOĞLU, Pınar, YAPICI, Zuhal, ERAKSOY, Mefkûre

    Published 2014
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  5. 5
    Association of Demyelinating and Inflammatory Bowel Diseases: A Case Series and Overview of the Literature

    Association of Demyelinating and Inflammatory Bowel Diseases: A Case Series and Overview of the Literature by ATMACA, Murat Mert, ALTIOKKA UZUN, Güneş, SHUGAIV, Erkingül, KÜRTÜNCÜ, Murat, ERAKSOY, Mefküre

    Published 2015
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  6. 6
    Detailed Evaluation of Macular Ganglion Cell Complex in Patients with Multiple Sclerosis

    Detailed Evaluation of Macular Ganglion Cell Complex in Patients with Multiple Sclerosis by ÖZBİLEN, Kemal Turgay, GÜNDÜZ, Tuncay, KARTAL, Selva Nur ÇUKUROVA, CEYLAN, Nihan AKSU, ERAKSOY, Mefküre, KÜRTÜNCÜ, Murat

    Published 2021
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  7. 7
    Anti-neuronal antibodies associated with headache with neurological deficits and cerebrospinal fluid lymphocytosis

    Anti-neuronal antibodies associated with headache with neurological deficits and cerebrospinal fluid lymphocytosis by Kürtüncü, Murat, Tüzün, Erdem, Kaya, Dilaver, İçöz, Sema, Barış Baslo, M., Ertaş, Mustafa, Akman-Demir, Gülşen, Eraksoy, Mefküre

    Published 2008
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  8. 8
    Turkish families with juvenile motor neuron disease broaden the phenotypic spectrum of SPG11

    Turkish families with juvenile motor neuron disease broaden the phenotypic spectrum of SPG11 by Iskender, Ceren, Kartal, Ece, Akcimen, Fulya, Kocoglu, Cemile, Ozoguz, Aslihan, Kotan, Dilcan, Eraksoy, Mefkure, Parman, Yesim G., Basak, Ayse Nazli

    Published 2015
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  9. 9
    High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus-Merzbacher disease

    High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus-Merzbacher disease by Bilir, Birdal, Yapici, Zuhal, Yalcinkaya, Cengiz, Baris, Ibrahim, Carvalho, Claudia M. B., Bartnik, Magdalena, Ozes, Burcak, Eraksoy, Mefkure, Lupski, James R., Battaloglu, Esra

    Published 2012
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