Nusinersen in SMA 2 and 3: Risks vs benefits von Deymeer, Feza

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Muscle magnetic resonance imaging in spinal muscular atrophy type 3: Selective and progressive involvement von Durmus, Hacer, Yilmaz, Ravza, Gulsen‐Parman, Yesim, Oflazer‐Serdaroglu, Piraye, Cuttini, Marina, Dursun, Memduh, Deymeer, Feza

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Differential Cytokine Changes in Patients with Myasthenia Gravis with Antibodies against AChR and MuSK von Yilmaz, Vuslat, Oflazer, Piraye, Aysal, Fikret, Durmus, Hacer, Poulas, Kostas, Yentur, Sibel P, Gulsen-Parman, Yesim, Tzartos, Socrates, Marx, Alexander, Tuzun, Erdem, Deymeer, Feza, Saruhan-Direskeneli, Güher

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Genetic heterogeneity within the HLA region in three distinct clinical subgroups of myasthenia gravis von Saruhan-Direskeneli, Güher, Hughes, Travis, Yilmaz, Vuslat, Durmus, Hacer, Adler, Adam, Alahgholi-Hajibehzad, Mahdi, Aysal, Fikret, Yentür, Sibel P, Akalin, Mehmet Ali, Dogan, Oner, Marx, Alexander, Gülsen-Parman, Yesim, Oflazer, Piraye, Deymeer, Feza, Sawalha, Amr H

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Myasthenia gravis: MuSK MG, late-onset MG and ocular MG von Deymeer, Feza

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Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome von Plaster, Nikki M., Tawil, Rabi, Tristani-Firouzi, Martin, Canún, Sonia, Bendahhou, Saı̈d, Tsunoda, Akiko, Donaldson, Matthew R., Iannaccone, Susan T., Brunt, Ewout, Barohn, Richard, Clark, John, Deymeer, Feza, George, Alfred L., Fish, Frank A., Hahn, Angelika, Nitu, Alexandru, Ozdemir, Coskun, Serdaroglu, Piraye, Subramony, S.H., Wolfe, Gil, Fu, Ying-Hui, Ptáček, Louis J.

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History of Myasthenia Gravis Revisited von Deymeer, Feza

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Genotypic and phenotypic presentation of transthyretin-related familial amyloid polyneuropathy (TTR-FAP) in Turkey von Durmuş, Hacer, Matur, Zeliha, Atmaca, Murat Mert, Poda, Mehves, Çakar, Arman, Ulaş, Ümit Hıdır, Oflazer-Serdaroğlu, Piraye, Deymeer, Feza, Parman, Yesim G

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ATXN2 and its neighbouring gene SH2B3 are associated with increased ALS risk in the Turkish population von Lahut, Suna, Ömür, Özgür, Uyan, Özgün, Ağım, Zeynep Sena, Özoğuz, Aslihan, Parman, Yeşim, Deymeer, Feza, Oflazer, Piraye, Koç, Filiz, Özçelik, Hilmi, Auburger, Georg, Başak, A Nazlı

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Genome-wide copy number variation in sporadic amyotrophic lateral sclerosis in the Turkish population: deletion of EPHA3 is a possible protective factor von Uyan, Özgün, Ömür, Özgür, Ağım, Zeynep Sena, Özoğuz, Aslıhan, Li, Hong, Parman, Yeşim, Deymeer, Feza, Oflazer, Piraye, Koç, Filiz, Tan, Ersin, Özçelik, Hilmi, Başak, A Nazlı

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The association of PTPN22 R620W polymorphism is stronger with late-onset AChR-myasthenia gravis in Turkey von Kaya, Gizem A, Coşkun, Ayse N, Yılmaz, Vuslat, Oflazer, Piraye, Gülsen-Parman, Yeşim, Aysal, Fikret, Disci, Rian, Direskeneli, Haner, Marx, Alexander, Deymeer, Feza, Saruhan-Direskeneli, Güher

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Myasthenia Gravis after Botulinum Toxin Type A Injection von Durmuş Tekçe, Hacer, Deymeer, Feza, Oflazer Serdaroğlu, Piraye, Parman, Yeşim

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Transthyretin-Related Familial Amyloid Polyneuropathy: In the Light of New Developments von Çakar, Arman, Durmuş Tekçe, Hacer, Deymeer, Feza, Oflazer Serdaroğlu, Piraye, Parman, Yeşim G.

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Clinical course and outcome of an outpatient clinic population with myasthenia gravis and COVID‐19 von Gungor Tuncer, Ozlem, Deymeer, Feza

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Differential Diagnosis Approach to Bilateral Peripheral Facial Paralysis: A Case Report von Akçakaya, Nihan Hande, Alpsan Gökmen, Meltem Hale, Parman, Yeşim Gülşen, Deymeer, Feza, Oflazer, Piraye

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Nerve conduction studies in Charcot-Marie-Tooth disease in a cohort from Turkey von Deymeer, Feza, Matur, Zeliha, Poyraz, Muruvvet, Battaloglu, Esra, Oflazer-Serdaroglu, Piraye, Parman, Yesim

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Correction to: Clinical, electrophysiological, and genetic analysis of a family with two rare neuromuscular disorders: congenital myasthenic syndrome and hereditary polyneuropathy von Tezen, Didem, Khojakulov, Zakhiriddin, Gündüz, Ayşegül, Deymeer, Feza, Demirbilek, Veysi, Başak, Ayşe Nazlı

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Clinical and genetic characteristics of Emery-Dreifuss muscular dystrophy patients from Turkey: 30 years longitudinal follow-up study von Yunisova, Gulshan, Ceylaner, Serdar, Oflazer, Piraye, Deymeer, Feza, Parman, Yesim Gülşen, Durmus, Hacer

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Clinical, electrophysiological, and genetic analysis of a family with two rare neuromuscular disorders: congenital myasthenic syndrome and hereditary polyneuropathy von Tezen, Didem, Khojakulov, Zakhiriddin, Gündüz, Ayşegül, Deymeer, Feza, Demirbilek, Veysi, Başak, Ayşe Nazlı

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Studying Clinical and Genetic Characteristics of Emery-Dreifuss Muscular Dystrophy (4069) von Yunisova, Gulshan, Oflazer, Piraye, Deymeer, Feza, Çakar, Arman, Parman, Fatma Yesim, Durmus, Hacer

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