Natural History, Phenotypic Spectrum, and Discriminative Features of Multisystemic RFC1 Disease von Traschütz, Andreas, Cortese, Andrea, Reich, Selina, Dominik, Natalia, Faber, Jennifer, Jacobi, Heike, Hartmann, Annette M., Rujescu, Dan, Montaut, Solveig, Echaniz-Laguna, Andoni, Erer, Sevda, Schütz, Valerie Cornelia, Tarnutzer, Alexander A., Sturm, Marc, Haack, Tobias B., Vaucamps-Diedhiou, Nadège, Puccio, Helene, Schöls, Ludger, Klockgether, Thomas, van de Warrenburg, Bart P., Paucar, Martin, Timmann, Dagmar, Hilgers, Ralf-Dieter, Gazulla, Jose, Strupp, Michael, Moris, German, Filla, Alessandro, Houlden, Henry, Anheim, Mathieu, Infante, Jon, Basak, A. Nazli, Synofzik, Matthis

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

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Characterization of Recessive Parkinson Disease in a Large Multicenter Study von Lesage, Suzanne, Lunati, Ariane, Houot, Marion, Romdhan, Sawssan Ben, Clot, Fabienne, Tesson, Christelle, Mangone, Graziella, Toullec, Benjamin Le, Courtin, Thomas, Larcher, Kathy, Benmahdjoub, Mustapha, Arezki, Mohamed, Bouhouche, Ahmed, Anheim, Mathieu, Roze, Emmanuel, Viallet, François, Tison, François, Broussolle, Emmanuel, Emre, Murat, Hanagasi, Hasmet, Bilgic, Basar, Tazir, Meriem, Djebara, Mouna Ben, Gouider, Riadh, Tranchant, Christine, Vidailhet, Marie, Le Guern, Eric, Corti, Olga, Mhiri, Chokri, Lohmann, Ebba, Singleton, Andrew, Corvol, Jean‐Christophe, Brice, Alexis, Lesage, Suzanne, Lunati, Ariane, Houot, Marion, Ben Romdhan, Sawssan, Clot, Fabienne, Tesson, Christelle, Mangone, Graziella, Le Toullec, Benjamin, Courtin, Thomas, Larcher, Kathy, Benmahdjoub, Mustapha, Arezki, Mohammed, Bouhouche, Ahmed, Anheim, Mathieu, Roze, Emmanuel, Viallet, François, Tison, François, Broussolle, Emmanuel, Emre, Murat, Hanagasi, Hasmet, Bilgic, Basar, Ben Djebara, Mouna, Gouider, Riadh, Tazir, Meriem, Tranchant, Christine, Vidailhet, Marie, Le Guern, Eric, Corti, Olga, Mhiri, Chokri, Lohmann, Ebba, Singleton, Andy, Corvol, Jean‐Christophe, Brice, Alexis

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Vitamin D Receptor Gene Haplotype Is Associated with Late-Onset Alzheimer's Disease von Gezen-Ak, Duygu, Dursun, Erdinç, Bilgiç, Basar, Hanagasi, Hasmet, Ertan, Turan, Gürvit, Hakan, Emre, Murat, Eker, Engin, Ulutin, Turgut, Uysal, Ömer, Yilmazer, Selma

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A novel SACS p.Pro4154GlnfsTer20 mutation in a family with autosomal recessive spastic ataxia of Charlevoix-Saguenay von Samanci, Bedia, Gokalp, Ebru Erzurumluoglu, Bilgic, Basar, Gurvit, Hakan, Artan, Sevilhan, Hanagasi, Hasmet A.

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PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice von Messerschmidt, Clemens, Foddis, Marco, Blumenau, Sonja, Müller, Susanne, Bentele, Kajetan, Holtgrewe, Manuel, Kun-Rodrigues, Celia, Alonso, Isabel, do Carmo Macario, Maria, Morgadinho, Ana Sofia, Velon, Ana Graça, Santo, Gustavo, Santana, Isabel, Mönkäre, Saana, Kuuluvainen, Liina, Schleutker, Johanna, Pöyhönen, Minna, Myllykangas, Liisa, Senatore, Assunta, Berchtold, Daniel, Winek, Katarzyna, Meisel, Andreas, Pavlovic, Aleksandra, Kostic, Vladimir, Dobricic, Valerija, Lohmann, Ebba, Hanagasi, Hasmet, Guven, Gamze, Bilgic, Basar, Bras, Jose, Guerreiro, Rita, Beule, Dieter, Dirnagl, Ulrich, Sassi, Celeste

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Neurological features and outcomes of Wilson’s disease: a single-center experience von Samanci, Bedia, Sahin, Erdi, Bilgic, Basar, Tufekcioglu, Zeynep, Gurvit, Hakan, Emre, Murat, Demir, Kadir, Hanagasi, Hasmet A.

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Eating Difficulties and Relationship With Nutritional Status Among Patients With Dementia von CILIZ, Ozlem, TULEK, Zeliha, HANAGASI, Hasmet, BILGIC, Basar, GURVIT, I. Hakan

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Peripheral TREM2 mRNA levels in early and late-onset Alzheimer disease’s patients von Guven, Gamze, Bilgic, Basar, Samanci, Bedia, Gurvit, Hakan, Hanagasi, Hasmet, Donmez, Cagla, Aslan, Rukiye, Lohmann, Ebba, Erginel-Unaltuna, Nihan

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Corticobasal Syndrome as Alzheimer’s Disease Subtype: A Case Report von Doğan, Faruk Uğur, Samancı, Bedia, Bilgiç, Basar, Hanağası, Haşmet Ayhan, Gürvit, Hakan

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

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Genotype-Phenotype correlations of SCARB2 associated clinical presentation: a case report and in-depth literature review von Atasu, Burcu, Acarlı, Ayse Nur Ozdag, Bilgic, Basar, Baykan, Betül, Demir, Erol, Ozluk, Yasemin, Turkmen, Aydin, Hauser, Ann-Kathrin, Guven, Gamze, Hanagasi, Hasmet, Gurvit, Hakan, Emre, Murat, Gasser, Thomas, Lohmann, Ebba

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Caregiver support and burden drive intention to engage in a peer-to-peer exchange of services among caregivers of dementia patients von Aksin, O Zeynep, Bilgic, Basar, Guner, Perihan, Gunes, Evrim D, Kuscu, Kemal, Ormeci, E Lerzan, Sayin, Serpil, Eser, Hale Yapici

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Autoimmune Encephalitis with Antibodies Against A-Amino-3hydroxy-5-Methyl-4-Isoxazolepropionic Acid Receptor and [gamma]-Aminobutyric Acid-Beta Receptor: Case Report von Dogan, Faruk Ugur, Samanci, Bedia, Yilmaz, Vuslat, Hanagasi, Hasmet Ayhan, Gurvjt, Ibrahim Hakan, Tuzun, Erdem, Bilgic, Basar

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A novel PSEN2 p.Ser175Phe variant in a family with Alzheimer’s disease von Guven, Gamze, Samanci, Bedia, Gulec, Cagri, Hanagasi, Hasmet, Gurvit, Hakan, Gokalp, Ebru Erzurumluoglu, Tepgec, Fatih, Guler, Suleyman, Uyguner, Oya, Bilgic, Basar

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The effects of progressive muscle relaxation exercise on dementia caregivers von BAYKAL, Dilek, BILGIC, Basar

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A comprehensive analysis of copy number variation in a Turkish dementia cohort von Dehghani, Nadia, Guven, Gamze, Kun-Rodrigues, Celia, Gouveia, Catarina, Foster, Kalina, Hanagasi, Hasmet, Lohmann, Ebba, Samanci, Bedia, Gurvit, Hakan, Bilgic, Basar, Bras, Jose, Guerreiro, Rita

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Do Alzheimer’s Disease Patients Appear Younger than Their Real Age? von Tufekcioglu, Zeynep, Bilgic, Başar, Zeylan, Abdullah Emir, Salah, Albert Ali, Dibeklioglu, Hamdi, Emre, Murat

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Morphometric analysis of medial temporal lobe subregions in Alzheimer's disease using high-resolution MRI von Hari, Emre, Kurt, Elif, Ulasoglu-Yildiz, Cigdem, Bayram, Ali, Bilgic, Başar, Demiralp, Tamer, Gurvit, Hakan

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The association of serum clusterin levels and Clusterin rs11136000 polymorphisms with Alzheimer disease in a Turkish cohort von Guven, Gamze, Ozer, Ebru, Bilgic, Basar, Hanagasi, Hasmet, Gurvit, Hakan, Lohmann, Ebba, Erginel-Unaltuna, Nihan

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