Clinical, biochemical, and molecular insights into Cerebrotendinous Xanthomatosis: A nationwide study of 100 Turkish individuals

Authors: Zubarioglu, Tanyel, Kıykım, Ertuğrul, Köse, Engin, Eminoğlu, Fatma Tuba, Teke Kısa, Pelin, Balcı, Mehmet Cihan, Özer, Işıl, İnci, Aslı, Çilesiz, Kübra, Canda, Ebru, Yazıcı, Havva, Öztürk-Hişmi, Burcu, Bulut, Fatma Derya, Dorum, Sevil, Akgun, Abdurrahman, Yalçın-Çakmaklı, Gül, Kılıç-Yıldırım, Gonca, Soyuçen, Erdoğan, Akçalı, Aylin, Güneş, Dilek, Durmuş, Aslı, Gündüz, Ayşegül, Kasapkara, Çiğdem Seher, Göksoy, Emine, Akar, Halil Tuna, Ersoy, Melike, Erdöl, Şahin, Yıldız, Yılmaz, Hanağası, Haşmet Ayhan, Arslan, Nur, Aktuğlu-Zeybek, Çiğdem

Source: In Molecular Genetics and Metabolism June 2024 142(2)

TREX1 p.A129fs and p.Y305C variants in a large multi-ethnic cohort of CADASIL-like unrelated patients

Authors: Foddis, Marco, Blumenau, Sonja, Holtgrewe, Manuel, Paquette, Kimberly, Westra, Kaitlyn, Alonso, Isabel, Macario, Maria do Carmo, Morgadinho, Ana Sofia, Velon, Ana Graça, Santo, Gustavo, Santana, Isabel, Mönkäre, Saana, Kuuluvainen, Liina, Schleutker, Johanna, Pöyhönen, Minna, Myllykangas, Liisa, Pavlovic, Aleksandra, Kostic, Vladimir, Dobricic, Valerija, Lohmann, Ebba, Hanagasi, Hasmet, Santos, Mariana, Guven, Gamze, Bilgic, Basar, Bras, Jose, Beule, Dieter, Dirnagl, Ulrich, Guerreiro, Rita, Sassi, Celeste

Source: In Neurobiology of Aging March 2023 123:208-215

Decreased levels of cytokines implicate altered immune response in plasma of moderate-stage Alzheimer’s disease patients

Authors: Koca, Sebile, Kiris, Irem, Sahin, Sevki, Cinar, Nilgun, Karsidag, Sibel, Hanagasi, Hasmet A., Yildiz, Gulsen B., Tarik Baykal, Ahmet

Source: In Neuroscience Letters 24 August 2022 786

Clinical and molecular genetic findings of hereditary Parkinson's patients from Turkey

Authors: Emekli, Inci, Tepgeç, Fatih, Samancı, Bedia, Toksoy, Güven, Hasanoğulları Kına, Gizem, Tüfekçioğlu, Zeynep, Başaran, Seher, Bilgiç, Başar, Gürvit, İ. Hakan, Emre, Murat, Uyguner, Zehra Oya, Hanagasi, Hasmet A.

Source: In Parkinsonism and Related Disorders December 2021 93:35-39

A new alpha-synuclein missense variant (Thr72Met) in two Turkish families with Parkinson's disease

Authors: Fevga, Christina, Park, Yangshin, Lohmann, Ebba, Kievit, Anneke J., Breedveld, Guido J., Ferraro, Federico, de Boer, Leon, van Minkelen, Rick, Hanagasi, Hasmet, Boon, Agnita, Wang, Wei, Petsko, Gregory A., Hoang, Quyen Q., Emre, Murat, Bonifati, Vincenzo

Source: In Parkinsonism and Related Disorders August 2021 89:63-72

Genetic and Epidemiological Insights into RAB32‐Linked Parkinson's Disease.

Authors: Radefeldt, Mandy, Lemke, Sabrina, Chaichoompu, Kridsadakorn, Paul, Jefri Jeya, Curado, Filipa, Valzania, Franco, Cavallieri, Francesco, Fioravanti, Valentina, Valente, Enza Maria, Avenali, Micol, Negrotti, Anna, Hanagasi, Hasmet A., Thonke, Sven, Matarazzo, Michele, Panzavolta, Andrea, Cerami, Chiara, Westenberger, Ana, Klein, Christine, Bauer, Peter, Beetz, Christian

Source: Movement Disorders; Jan2025, Vol. 40 Issue 1, p147-151, 5p

Event-related potential changes due to early-onset Parkinson’s disease in parkin (PARK2) gene mutation carriers and non-carriers

Authors: Uslu, Atilla, Ergen, Mehmet, Demirci, Hasan, Lohmann, Ebba, Hanagasi, Hasmet, Demiralp, Tamer

Source: In Clinical Neurophysiology July 2020 131(7):1444-1452

Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in Turkey

Authors: Kessler, Christoph, Atasu, Burcu, Hanagasi, Hasmet, Simón-Sánchez, Javier, Hauser, Ann-Kathrin, Pak, Meltem, Bilgic, Basar, Erginel-Unaltuna, Nihan, Gurvit, Hakan, Gasser, Thomas, Lohmann, Ebba

Source: In Parkinsonism and Related Disorders March 2018 48:34-39

The p.Thr11Met mutation in c19orf12 is frequent among adult Turkish patients with MPAN

Authors: Olgiati, Simone, Doğu, Okan, Tufekcioglu, Zeynep, Diler, Yunus, Saka, Esen, Gultekin, Murat, Kaleagasi, Hakan, Kuipers, Demy, Graafland, Josja, Breedveld, Guido J., Quadri, Marialuisa, Sürmeli, Reyhan, Sünter, Gülin, Doğan, Tuğrul, Yalçın, Ayşe Destina, Bilgiç, Başar, Elibol, Bülent, Emre, Murat, Hanagasi, Hasmet A., Bonifati, Vincenzo

Source: In Parkinsonism and Related Disorders June 2017 39:64-70

Quantitative Gait and Balance Outcomes for Ataxia Trials: Consensus Recommendations by the Ataxia Global Initiative Working Group on Digital-Motor Biomarkers.

Authors: Ilg, Winfried, Milne, Sarah, Schmitz-Hübsch, Tanja, Alcock, Lisa, Beichert, Lukas, Bertini, Enrico, Mohamed Ibrahim, Norlinah, Dawes, Helen, Gomez, Christopher M., Hanagasi, Hasmet, Kinnunen, Kirsi M., Minnerop, Martina, Németh, Andrea H., Newman, Jane, Ng, Yi Shiau, Rentz, Clara, Samanci, Bedia, Shah, Vrutangkumar V., Summa, Susanna, Vasco, Gessica

Source: Cerebellum; Aug2024, Vol. 23 Issue 4, p1566-1592, 27p

Subject Terms: ATAXIA, CEREBELLAR ataxia, BIOMARKERS, DIGITAL health, SPINOCEREBELLAR ataxia

Dementia in Parkinson's disease

Authors: Hanagasi, Hasmet A., Tufekcioglu, Zeynep, Emre, Murat

Source: In Journal of the Neurological Sciences 15 March 2017 374:26-31

Clinical and genetic features of PKAN patients in a tertiary centre in Turkey

Authors: Akcakaya, Nihan Hande, Iseri, Sibel Ugur, Bilir, Birdal, Battaloglu, Esra, Tekturk, Pinar, Gultekin, Murat, Akar, Gokcen, Yigiter, Remzi, Hanagasi, Hasmet, Alp, Recep, Cagirici, Sultan, Eraksoy, Mefkure, Ozbek, Ugur, Yapici, Zuhal

Source: In Clinical Neurology and Neurosurgery March 2017 154:34-42

Frequency of frontotemporal dementia-related gene variants in Turkey

Authors: Artan, Sevilhan, Erzurumluoglu Gokalp, Ebru, Samanci, Bedia, Ozbabalik Adapinar, Demet, Bas, Hasan, Tepgec, Fatih, Qomi Ekenel, Emilia, Cilingir, Oguz, Bilgic, Basar, Gurvit, Hakan, Hanagasi, Hasmet Ayhan, Kocagil, Sinem, Durak Aras, Beyhan, Uyguner, Oya, Emre, Murat

Source: In Neurobiology of Aging October 2021 106:332-332

Analysis of the tremor in juvenile myoclonic epilepsy

Authors: Aydin-Özemir, Zeynep, Matur, Zeliha, Baykan, Betul, Bilgic, Başar, Tekturk, Pınar, Bebek, Nerses, Gurses, Candan, Hanagasi, Hasmet, Oge, Ali Emre

Source: In Epilepsy Research December 2016 128:140-148

Expression changes of genes associated with apoptosis and survival processes in Parkinson’s disease

Authors: Yalçınkaya, Nazli, Haytural, Hazal, Bilgiç, Başar, Özdemir, Özkan, Hanağası, Haşmet, Küçükali, Cem İsmail, Özbek, Zeynep, Akcan, Uğur, İdrisoğlu, Halil Atilla, Gürvit, Hakan, Tüzün, Erdem

Source: In Neuroscience Letters 26 February 2016 615:72-77

Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insights.

Authors: Atasu, Burcu, Simón-Sánchez, Javier, Hanagasi, Hasmet, Bilgic, Basar, Hauser, Ann-Kathrin, Guven, Gamze, Heutink, Peter, Gasser, Thomas, Lohmann, Ebba

Source: Journal of Medical Genetics; May2024, Vol. 61 Issue 5, p443-451, 9p

The interleukin 1 alpha, interleukin 1 beta, interleukin 6 and alpha-2-macroglobulin serum levels in patients with early or late onset Alzheimer's disease, mild cognitive impairment or Parkinson's disease

Authors: Dursun, Erdinç, Gezen-Ak, Duygu, Hanağası, Haşmet, Bilgiç, Başar, Lohmann, Ebba, Ertan, Sibel, Atasoy, İrem L., Alaylıoğlu, Merve, Araz, Ömür Selin, Önal, Burak, Gündüz, Ayşegül, Apaydın, Hülya, Kızıltan, Güneş, Ulutin, Turgut, Gürvit, Hakan, Yılmazer, Selma

Source: In Journal of Neuroimmunology 15 June 2015 283:50-57

A patient with early-onset Alzheimer's disease with a novel PSEN1 p.Leu424Pro mutation

Authors: Guven, Gamze, Erginel-Unaltuna, Nihan, Samanci, Bedia, Gulec, Cagri, Hanagasi, Hasmet, Bilgic, Basar

Source: In Neurobiology of Aging December 2019 84:238-238

Differentiating symptomatic Parkin mutations carriers from patients with idiopathic Parkinson’s disease: Contribution of automated segmentation neuroimaging method

Authors: Bilgic, Basar, Bayram, Ali, Arslan, Ali Bilgin, Hanagasi, Hasmet, Dursun, Burcu, Gurvit, Hakan, Emre, Murat, Lohmann, Ebba

Source: In Parkinsonism and Related Disorders June 2012 18(5):562-566

A homozygous frameshift mutation of sepiapterin reductase gene causing parkinsonism with onset in childhood

Authors: Lohmann, Ebba, Köroğlu, Çiğdem, Hanagasi, Hasmet A., Dursun, Burcu, Taşan, Erşan, Tolun, Aslıhan

Source: In Parkinsonism and Related Disorders February 2012 18(2):191-193