Neuroimaging, Biomarkers, and Management of Dementia with Lewy Bodies

Por Hanagasi, Hasmet A., Bilgiç, Başar, Emre, Murat
Publicado em 2013

Chorea-Ballismus Associated with Hyperglycemia

Por KOCASOY ORHAN, Elif, ATMACA, M. Mert, ATMACA, Melek, HANAĞASI, Haşmet A.
Publicado no Noro Psikiyatr Ars (2013)

Neuro-Behçet’s Disease with Chorea

Por GÜR ÖZMEN, Selen, HANAĞASI, Haşmet, GÜRVİT, Hakan, EMRE, Murat, AKMAN DEMİR, Gülşen
Publicado no Noro Psikiyatr Ars (2015)

Impact of Neuro-Behçet Disease Immunoglobulin G on Neuronal Apoptosis

Por GİRİŞ, Murat, BİRELLER, Sinem, KÜÇÜKALİ, Cem İsmail, HANAĞASI, Haşmet, DEĞİRMENCİOĞLU, Sevgin, TÜZÜN, Erdem
Publicado no Noro Psikiyatr Ars (2017)

Supranuclear Gaze Abnormality in Sporadic-Creutzfeldt Jacob Disease

Por GÜR ÖZMEN, Selen, GÜRVİT, Hakan, HANAĞASI, Haşmet A., ALPSAN GÖKMEN, Meltem Hale, EMRE, Murat
Publicado no Noro Psikiyatr Ars (2014)

Nasu Hakola Disease: A Rare Cause of Dementia and Cystic Bone Lesions, Report of a New Turkish Family

Por Köseoğlu, Emel, Tepgeç, Fatih, Yetkin, Mehmet Fatih, Uyguner, Oya, Ekinci, Ayten, Abdülrezzak, Ümmühan, Hanağasi, Haşmet
Publicado no Noro Psikiyatr Ars (2018)

Neuroinflammation Mediators are Reduced in Sera of Parkinson’s Disease Patients with Mild Cognitive Impairment

Por Kıçık, Ani, Tüzün, Erdem, Erdoğdu, Emel, Bılgıç, Başar, Tüfekçıoğlu, Zeynep, öztürk-Işik, Esin, Hanağasi, Haşmet, Gürvıt, Hakan
Publicado no Noro Psikiyatr Ars (2019)

A novel compound heterozygous mutation in TREM2 found in a Turkish frontotemporal dementia-like family()

Por Guerreiro, Rita, Bilgic, Basar, Guven, Gamze, Brás, José, Rohrer, Jonathan, Lohmann, Ebba, Hanagasi, Hasmet, Gurvit, Hakan, Emre, Murat
Publicado em 2013

The Relationship of White Matter Hyperintensities with Depressive Symptoms and Daily Living Activities in Early-Stage Alzheimer’s Disease Patients

Por BİLGİÇ, Başar, BAYRAM, Ali, HANAĞASI, Haşmet A., TÜMAÇ, Ayfer, UYSAL, Pınar, ŞENTÜRK, Gülben, ALPSAN, Hale, LOHMANN, Ebba, GÜRVİT, Hakan, EMRE, Murat
Publicado no Noro Psikiyatr Ars (2013)

Identification of PSEN1 and PSEN2 gene mutations and variants in Turkish dementia patients

Por Lohmann, Ebba, Guerreiro, Rita J., Erginel-Unaltuna, Nihan, Gurunlian, Nicole, Bilgic, Basar, Gurvit, Hakan, Hanagasi, Hasmet A., Luu, Nga, Emre, Murat, Singleton, Andrew
Publicado no Neurobiol Aging (2012)

PLA2G6 Mutations Related to Distinct Phenotypes: A New Case with Early-onset Parkinsonism

Por Giri, Anamika, Guven, Gamze, Hanagasi, Hasmet, Hauser, Ann-Kathrin, Erginul-Unaltuna, Nihan, Bilgic, Basar, Gurvit, Hakan, Heutink, Peter, Gasser, Thomas, Lohmann, Ebba, Simón-Sánchez, Javier
Publicado no Tremor Other Hyperkinet Mov (N Y) (2016)

Peripheral GRN mRNA and Serum Progranulin Levels as a Potential Indicator for Both the Presence of Splice Site Mutations and Individuals at Risk for Frontotemporal Dementia

Por Guven, Gamze, Bilgic, Başar, Tufekcioglu, Zeynep, Erginel Unaltuna, Nihan, Hanagasi, Hasmet, Gurvit, Hakan, Singleton, Andrew, Hardy, John, Emre, Murat, Gulec, Cagri, Bras, Jose, Guerreiro, Rita, Lohmann, Ebba
Publicado no J Alzheimers Dis (2019)

Evaluation of Incidence and Clinical Features of Antibody-Associated Autoimmune Encephalitis Mimicking Dementia

Por Çoban, Arzu, İsmail Küçükali, Cem, Bilgiç, Başar, Yalçınkaya, Nazlı, Haytural, Hazal, Ulusoy, Canan, Turan, Selin, Çakır, Sibel, Üçok, Alp, Ünübol, Hüseyin, Hanagasi, Hasmet A., Gürvit, Hakan, Tüzün, Erdem
Publicado em 2014

Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia–like Syndrome Without Bone Involvement

Por Guerreiro, Rita João, Lohmann, Ebba, Brás, José Miguel, Gibbs, Jesse Raphael, Rohrer, Jonathan D., Gurunlian, Nicole, Dursun, Burcu, Bilgic, Basar, Hanagasi, Hasmet, Gurvit, Hakan, Emre, Murat, Singleton, Andrew, Hardy, John
Publicado em 2013

Mutations in TYROBP are not a common cause of dementia in a Turkish cohort

Por Darwent, Lee, Carmona, Susana, Lohmann, Ebba, Guven, Gamze, Kun-Rodrigues, Celia, Bilgic, Basar, Hanagasi, Hasmet, Gurvit, Hakan, Erginel-Unaltuna, Nihan, Pak, Meltem, Hardy, John, Singleton, Andrew, Brás, Jose, Guerreiro, Rita
Publicado no Neurobiol Aging (2017)

Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease

Por Guerreiro, Rita Joao, Lohmann, Ebba, Kinsella, Emma, Bras, Jose Miguel, Luu, Nga, Gurulian, Nicole, Dursun, Burcu, Bilgi, Basar, Santana, Isabel, Hanagasi, Hasmet, Gurvit, Hakan, Gibbs, Raphael, Oliveira, Catarina, Emre, Murat, Singleton, Andrew
Publicado em 2011

Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients

Por Guven, Gamze, Lohmann, Ebba, Bras, Jose, Gibbs, J. Raphael, Gurvit, Hakan, Bilgic, Basar, Hanagasi, Hasmet, Rizzu, Patrizia, Heutink, Peter, Emre, Murat, Erginel-Unaltuna, Nihan, Just, Walter, Hardy, John, Singleton, Andrew, Guerreiro, Rita
Publicado no PLoS One (2016)

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 no Turk J Med Sci (2020)

Early-Onset L-dopa-Responsive Parkinsonism with Pyramidal Signs Due to ATP13A2, PLA2G6, FBXO7 and Spatacsin Mutations

Por Paisán-Ruiz, Coro, Guevara, Rocio, Federoff, Monica, Hanagasi, Hasmet, Sina, Fardaz, Elahi, Elahe, Schneider, Susanne A., Schwingenschuh, Petra, Bajaj, Nin, Emre, Murat, Singleton, Andrew B., Hardy, John, Bhatia, Kailash P., Brandner, Sebastian, Lees, Andrew J., Houlden, Henry
Publicado no Mov Disord (2010)

Turkish Standardization of Movement Disorders Society Unified Parkinson's Disease Rating Scale and Unified Dyskinesia Rating Scale

Por Akbostanci, Muhittin C., Bayram, Ece, Yilmaz, Volkan, Rzayev, Sefer, Özkan, Serhat, Tokcaer, Ayse Bora, Saka, Esen, Durmaz Celik, Fatma N., Barut, Banu Özen, Tüfekcioglu, Zeynep, Acarer, Ahmet, Balaban, Hatice, Erer, Sevda, Dogu, Okan, Kibaroglu, Seda, Aydin, Nursel, Hanagasi, Hasmet, Elibol, Bülent, Emre, Murat, Stebbins, Glenn T., Goetz, Christopher G.
Publicado no Mov Disord Clin Pract (2017)