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

Tekijä Yapici, Zuhal, Tuschl, Karin, Eraksoy, Mefkure
Julkaisussa Mov Disord Clin Pract (2019)

Validity and Reliability of the Turkish Version of the Monitoring My Multiple Sclerosis Scale

Tekijä POLAT, Cansu, TÜLEK, Zeliha, KÜRTÜNCÜ, Murat, ERAKSOY, Mefkure
Julkaisussa Noro Psikiyatr Ars (2017)

Validity and Reliability of the Turkish Version of the Multiple Sclerosis-Related Symptom Checklist

Tekijä TÜLEK, Zeliha, POLAT, Cansu, KÜRTÜNCÜ, Murat, ERAKSOY, Mefkure
Julkaisussa Noro Psikiyatr Ars (2017)

Inflammatory Demyelinating Diseases of Childhood: Case Report and Literature Review

Tekijä EKİZOĞLU, Esme, TEKTÜRK TOPALOĞLU, Pınar, YAPICI, Zuhal, ERAKSOY, Mefkûre
Julkaisussa Noro Psikiyatr Ars (2014)

Association of Demyelinating and Inflammatory Bowel Diseases: A Case Series and Overview of the Literature

Tekijä ATMACA, Murat Mert, ALTIOKKA UZUN, Güneş, SHUGAIV, Erkingül, KÜRTÜNCÜ, Murat, ERAKSOY, Mefküre
Julkaisussa Noro Psikiyatr Ars (2015)

Anti-neuronal antibodies associated with headache with neurological deficits and cerebrospinal fluid lymphocytosis

Tekijä Kürtüncü, Murat, Tüzün, Erdem, Kaya, Dilaver, İçöz, Sema, Barış Baslo, M., Ertaş, Mustafa, Akman-Demir, Gülşen, Eraksoy, Mefküre
Julkaistu 2008

Turkish families with juvenile motor neuron disease broaden the phenotypic spectrum of SPG11

Tekijä Iskender, Ceren, Kartal, Ece, Akcimen, Fulya, Kocoglu, Cemile, Ozoguz, Aslihan, Kotan, Dilcan, Eraksoy, Mefkure, Parman, Yesim G., Basak, Ayse Nazli
Julkaisussa Neurol Genet (2015)

High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus-Merzbacher disease

Tekijä Bilir, Birdal, Yapici, Zuhal, Yalcinkaya, Cengiz, Baris, Ibrahim, Carvalho, Claudia M. B., Bartnik, Magdalena, Ozes, Burcak, Eraksoy, Mefkure, Lupski, James R., Battaloglu, Esra
Julkaistu 2012