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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Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindred von Gulsuner, Suleyman, Tekinay, Ayse Begum, Doerschner, Katja, Boyaci, Huseyin, Bilguvar, Kaya, Unal, Hilal, Ors, Aslihan, Onat, O Emre, Atalar, Ergin, Basak, A Nazli, Topaloglu, Haluk, Kansu, Tulay, Tan, Meliha, Tan, Uner, Gunel, Murat, Ozcelik, Tayfun

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Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humans von Ozcelik, Tayfun, Akarsu, Nurten, Uz, Elif, Caglayan, Safak, Gulsuner, Suleyman, Onat, Onur Emre, Tan, Meliha, Tan, Uner

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Facial Asymmetry in Right- and Left-Handed Men and Women von KelesL, Papatya, Díyarbakirli, Semíh, Tan, Melíha, Tan, Üner

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A Rare Complication Developing After Hematopoietic Stem Cell Transplantation: Wernicke's Encephalopathy von Solmaz, Soner, Gereklioğlu, Çiğdem, Tan, Meliha, Demir, Şenay, Yeral, Mahmut, Korur, Aslı, Boğa, Can, Özdoğu, Hakan

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Spinal MRI findings of guillain-barré syndrome von Alkan, Ozlem, Yildirim, Tulin, Tokmak, Naime, Tan, Meliha

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Reply to Herz et al. and Humphrey et al.: Genetic heterogeneity of cerebellar hypoplasia with quadrupedal locomotion von Ozcelik, Tayfun, Akarsu, Nurten, Uz, Elif, Caglayan, Safak, Gulsuner, Suleyman, Onat, Onur Emre, Tan, Meliha, Tan, Uner

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Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion von Onat, Onur Emre, Gulsuner, Suleyman, Bilguvar, Kaya, Nazli Basak, Ayse, Topaloglu, Haluk, Tan, Meliha, Tan, Uner, Gunel, Murat, Ozcelik, Tayfun

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Diagnostic value of T2-weighted gradient-echo MRI for segmental evaluation in cerebral venous sinus thrombosis von Altinkaya, Naime, Demir, Senay, Alkan, Ozlem, Tan, Meliha

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Sex Difference in Susceptibility to Epileptic Seizures in Rats: Importance of Estrous Cycle von Tan, Meliha, Tanb, Uner

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Topiramate for the Treatment of Hypnic Headache: A Case Report, Including Polysomnography von Meliha Tan, Sibel Karaca, Başak Karakurum Göksel, Mehmet Ali Habeşoğlu

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Isolated Hand Palsy Due to Small Cortical Infarcts: A Report of Two Cases von Meliha Tan, Sibel Karaca, Başak Karakurum Göksel, Özlem Alkan

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A new case of Uner Tan syndrome-With late childhood quadrupedalism von Tan, Meliha, Karaca, Sibel, Tan, Uner

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Unertan Syndrome: A New Variant of Unertan Syndrome: Running on All Fours in Two Upright-Walking Children von Tan, Uner, Tan, Meliha

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Incidences of asymmetries for the palmar grasp reflex in neonates and hand preference in adults von Tan, Uner, Tan, and Meliha

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Woman with Sickle Cell Disease with Current Sigmoid Sinus Thrombosis and History of Inadequate Warfarin Use during a Past Thrombotic Event von Çelikbilek, Asuman, Çelikbilek, Mehmet, Bozkurt, Alper, Karakurum Göksel, Başak, Tan, Meliha, Özdoğu, Hakan

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Curvelinear Correlations Between Total Testosterone Levels and Fluid Intelligence in Men and Women von Tan, Üner, Tan, Meliha

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Human quadrupedalism is not an epiphenomenon caused by neurodevelopmental malformation and ataxia von Karaca, Sibel, Tan, Meliha, Tan, Uner

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Magnetic resonance imaging brain size/IQ relations in Turkish University students von Tan, Üner, Tan, Meli̇ha, Polat, Pinar, Ceylan, Yaşar, Suma, Selami̇, Okur, Adnan

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Evaluation of brain perfusion in Alzheimer disease with perfusion computed tomography and comparison to elderly patient without dementia von Yildirim, Tülin, Karakurum Göksel, Başak, Demir, Şenay, Tokmak, Naime, Tan, Meliha

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