Post-COVID-19 longitudinally extensive transverse myelitis: is it a new entity?

por Arslan, Doruk, Acar-Ozen, Pinar, Gocmen, Rahsan, Elibol, Bulent, Karabudak, Rana, Tuncer, Asli
Publicado 2021

Sensorimotor integration training in Parkinson’s disease

por Fil-Balkan, Ayla, Salcı, Yeliz, Keklicek, Hilal, Armutlu, Kadriye, Aksoy, Songül, Kayıhan, Hülya, Elibol, Bülent
Publicado 2018

Cockayne syndrome type 3 with dystonia‐ataxia and clicking blinks

por Gültekin‐Zaim, Özge Berna, Yalçın‐Çakmaklı, Gül, Çolpak, Ayşe İlksen, Şimşek‐Kiper, Pelin Özlem, Utine, Gülen Eda, Elibol, Bülent
Publicado 2023

Intercountry comparisons of advanced Parkinson's disease symptoms and management: Analysis from the OBSERVE‐PD observational study

por Fasano, Alfonso, Fung, Victor S. C., Seppi, Klaus, Pirtosek, Zvezdan, Takáts, Annamária, Alobaidi, Ali, Onuk, Koray, Bergmann, Lars, Parra, Juan Carlos, Elibol, Bulent
Publicado 2022

Characterizing advanced Parkinson’s disease: OBSERVE-PD observational study results of 2615 patients

por Fasano, Alfonso, Fung, Victor S. C., Lopiano, Leonardo, Elibol, Bulent, Smolentseva, Irina G., Seppi, Klaus, Takáts, Annamária, Onuk, Koray, Parra, Juan Carlos, Bergmann, Lars, Sail, Kavita, Jalundhwala, Yash, Pirtosek, Zvezdan
Publicado 2019

Expert opinion on diagnosing, treating and managing patients with cerebrotendinous xanthomatosis (CTX): a modified Delphi study

por Stelten, Bianca M. L., Dotti, Maria Teresa, Verrips, Aad, Elibol, Bülent, Falik-Zaccai, Tzipora C., Hanman, Kate, Mignarri, Andrea, Sithole, Belina, Steiner, Robert D., Verma, Surabhi, Yahalom, Gilad, Zubarioglu, Tanyel, Mochel, Fanny, Federico, Antonio
Publicado 2021

Multicenter study of levodopa carbidopa intestinal gel in Parkinson’s disease: the Turkish experience

por GÜLTEKİN, Murat, ULUKAN, Çağrı, TEZCAN, Sabiha, DOĞU, Okan, HANAĞASI, Haşmet, BİLGİÇ, Başar, BORA TOKÇAER, Ayşe, ÇAKMUR, Raif, ELİBOL, Bülent, MİRZA, Meral, İNCE GÜNAL, Dilek, ERER ÖZBEK, Çiğdem Sevda, KENANGİL, Gülay, YILMAZ KÜSBECİ, Özge, AKBOSTANCI, Muhittin Cenk
Publicado 2020

DCTN1 mutations in Perry syndrome

por Farrer, Matthew J., Hulihan, Mary M., Kachergus, Jennifer M., Dächsel, Justus, Stoessl, A. Jon, Grantier, Linda L., Calne, Susan, Calne, Donald B., Lechevalier, Bernard, Chapon, Francoise, Tsuboi, Yoshio, Yamada, Tatsuo, Gutmann, Ludwig, Elibol, Bülent, Bhatia, Kailash P., Wider, Christian W., Vilariño-Güell, Carles, Ross, Owen A., Brown, Laura A., Castanedes-Casey, Monica, Dickson, Dennis W., Wszolek, Zbigniew K.
Publicado 2009