Transcript levels of plastin 3 and neuritin 1 modifier genes in spinal muscular atrophy siblings von Yener, İnci Hande, Topaloglu, Haluk, Erdem‐Özdamar, Sevim, Dayangac‐Erden, Didem

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Identifying A Cut-Off Point for Timed Up and Go Test in Neuromuscular Diseases von Savcun Demirci, Cevher, Sütçü, Gülşah, Ayvat, Fatma, Onursal Kılınç, Özge, Doğan, Mert, Ayvat, Ender, Bekircan-Kurt, Can Ebru, Erdem-Özdamar, Sevim, Yıldırım, Sibel Aksu, Kılınç, Muhammed, Tan, Ersin

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Remission with fingolimod in a case of demyelinating polyneuropathy von Erdener, Şefik E, Nurlu, Gülay, Göçmen, Rahşan, Erdem-Özdamar, Sevim, Kurne, Aslı

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Fulminant Central Plus Peripheral Nervous System Demyelination without Antibodies to Neurofascin von Vural, Atay, Göçmen, Rahşan, Kurne, Aslı Tuncer, Oğuz, Kader Karlı, Temuçin, Çağrı Mesut, Tan, Ersin, Karabudak, Rana, Meinl, Edgar, Erdem Özdamar, Sevim

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The Neurophysiologic Frequency of Hereditary Neuropathy with Liability to Pressure Palsy in Entrapment Neuropathies von Yıldız, F. Gökçem, Nurlu, Gülay, Erdem Özdamar, Sevim, Temuçin, Çağrı Mesut

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Overexpression of amyloid beta precursor protein enhances expression and secretion of ST6Gal1 in C2C12 myogenic cell line von Balci-Hayta, Burcu, Erdem-Özdamar, Sevim, Dinçer, Pervin

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Proinflammatory effect of AbetaPP induced ST6GAL1 secretion from C2C12 myogenic cell line / [C2C12 miyojenik hücre hattında AbetaPP tarafından indüklenen ST6GAL1 salgılanmasının pr... von Hayta, Burcu Balcı, Özdamar, Sevim Erdem, Dinçer, Pervin

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Toscana virus associated with Guillain–Barré syndrome: a case–control study von Okar, Serhat Vahip, Bekircan-Kurt, Can Ebru, Hacıoğlu, Sabri, Erdem-Özdamar, Sevim, Özkul, Aykut, Ergünay, Koray

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The histopathological evaluation of small fiber neuropathy in patients with vitamin B12 deficiency von Güneş, Hafize Nalan, Bekircan-Kurt, Can Ebru, Tan, Ersin, Erdem-Özdamar, Sevim

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Comprehensive evaluation of velopharyngeal function in myasthenia gravis patients von Dumbak, Aydan Baştuğ, Kayıkcı, Maviş Emel Kulak, Şahin, Mehmet İlhan, Kuşçu, Oğuz, Bekircan-Kurt, Can Ebru, Özdamar, Sevim Erdem

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Expert opinion on the diagnostic odyssey and management of late-onset Pompe disease: a neurologist's perspective von Erdem Ozdamar, Sevim, Koc, Ayse Filiz, Durmus Tekce, Hacer, Kotan, Dilcan, Ekmekci, Ahmet Hakan, Sengun, Ihsan Sukru, Yuceyar, Ayse Nur, Uluc, Kayihan

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Autologous Stem Cell Transplantation in a Patient with Refractory anti-MuSK-Positive Myasthenia Gravis and Familial Mediterranean Fever von Inan, Berin, Bekircan-Kurt, Can Ebru, Demiroğlu, Haluk, Göker, Hakan, Erdem-Özdamar, Sevim, Tan, Ersin

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A Novel Amplification-Refractory Mutation System-PCR Strategy to Screen MT-TL1 Pathogenic Variants in Patient Repositories von Bulduk, Bengisu Kevser, Kiliç, Hasan Basri, Bekircan-Kurt, Can Ebru, Haliloğlu, Göknur, Erdem Özdamar, Sevim, Topaloğlu, Haluk, Kocaefe, Y Çetin

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Reliability and Validity of Turkish Myasthenia Gravis-Activities of Daily Living Scale von Karanfil, Ecem, Salcı, Yeliz, Fil-Balkan, Ayla, Bekircan-Kurt, Can Ebru, Erdem Özdamar, Sevim, Armutlu, Kadriye

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Three Turkish families with different transthyretin mutations von Bekircan-Kurt, Can Ebru, Güneş, Nalan, Yılmaz, Arda, Erdem-Özdamar, Sevim, Tan, Ersin

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Spinal muscular atrophy type III: Molecular genetic characterization of Turkish patients von Bora-Tatar, Gamze, Yesbek-Kaymaz, Ayse, Bekircan-Kurt, Can Ebru, Erdem-Özdamar, Sevim, Erdem-Yurter, Hayat

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New mutations and genotype–phenotype correlation in late-onset Pompe patients von Bekircan-Kurt, Can Ebru, Güneş, Hafize Nalan, Yildiz, F. Gokcem, Saka, Esen, Tan, Ersin, Erdem-Özdamar, Sevim

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Recent therapeutic developments in spinal muscular atrophy von Bora, Gamze, Ayşe, Yeşbek-Kaymaz, Can Ebru, Bekircan Kurt, Vildan Göknur, Haliloğlu, Haluk Aydın, Topaloğlu, Hayat, Erdem Yurter, Sevim, Erdem Özdamar

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Giant cell myositis associated with myasthenia gravis and thymoma von Inan, Berin, Bekircan Kurt, Can Ebru, Yildiz, Fatma Gokcem, Erdem Ozdamar, Sevim, Temucin, Cagri Mesut, Tan, Ersin

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S39 Familial amyloid polyneuropathy (FAP): All aspects of the disease from diagnosis to treatment: Disease description: What is FAP? von Özdamar, Sevim Erdem

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