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

Por Yapici, Zuhal, Tuschl, Karin, Eraksoy, Mefkure
Publicado no Mov Disord Clin Pract (2019)

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

Por POLAT, Cansu, TÜLEK, Zeliha, KÜRTÜNCÜ, Murat, ERAKSOY, Mefkure
Publicado no Noro Psikiyatr Ars (2017)

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

Por TÜLEK, Zeliha, POLAT, Cansu, KÜRTÜNCÜ, Murat, ERAKSOY, Mefkure
Publicado no Noro Psikiyatr Ars (2017)

Inflammatory Demyelinating Diseases of Childhood: Case Report and Literature Review

Por EKİZOĞLU, Esme, TEKTÜRK TOPALOĞLU, Pınar, YAPICI, Zuhal, ERAKSOY, Mefkûre
Publicado no Noro Psikiyatr Ars (2014)

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

Por ATMACA, Murat Mert, ALTIOKKA UZUN, Güneş, SHUGAIV, Erkingül, KÜRTÜNCÜ, Murat, ERAKSOY, Mefküre
Publicado no Noro Psikiyatr Ars (2015)

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

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

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

Por Iskender, Ceren, Kartal, Ece, Akcimen, Fulya, Kocoglu, Cemile, Ozoguz, Aslihan, Kotan, Dilcan, Eraksoy, Mefkure, Parman, Yesim G., Basak, Ayse Nazli
Publicado no Neurol Genet (2015)

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

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