P88 Using whole exome sequencing to identify the mutation causing oculopharyngodistal myopathy
Wagner, M, Laval, S, Mueller, J, Durmus, H, Serdaroglu-Oflazer, P, Lochmüller, H
Published in Neuromuscular disorders : NMD (01.03.2012)
Published in Neuromuscular disorders : NMD (01.03.2012)
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Journal Article
Mutation spectrum of 260 dystrophinopathy patients from Turkey and important highlights for genetic counseling
Toksoy, G, Durmus, H, Aghayev, A, Bagirova, G, Sevinc Rustemoglu, B, Basaran, S, Avci, S, Karaman, B, Parman, Y, Altunoglu, U, Yapici, Z, Tekturk, P, Deymeer, F, Topaloglu, H, Kayserili, H, Oflazer-Serdaroglu, P, Uyguner, ZO
Published in Neuromuscular disorders : NMD (01.08.2019)
Published in Neuromuscular disorders : NMD (01.08.2019)
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Journal Article
Oculopharyngodistal myopathy is a distinct entity: clinical and genetic features of 47 patients
Durmus, H, Laval, S H, Deymeer, F, Parman, Y, Kiyan, E, Gokyigiti, M, Ertekin, C, Ercan, I, Solakoglu, S, Karcagi, V, Straub, V, Bushby, K, Lochmüller, H, Serdaroglu-Oflazer, P
Published in Neurology (18.01.2011)
Published in Neurology (18.01.2011)
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Journal Article
G.P.8
Ozcan, O, Durmus, H, Tarhan, O, Polat, Z, Deymeer, F, Parman, Y, Oflazer-Serdaroglu, P
Published in Neuromuscular disorders : NMD (01.10.2014)
Published in Neuromuscular disorders : NMD (01.10.2014)
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Journal Article
G.P.138
Yildiz-Celik, S, Durmus, H, Hajibehzad, M, Yilmaz, V, Oflazer-Serdaroglu, P, Parman, Y, Saruhan-Direskeneli, G, Deyemeer, F
Published in Neuromuscular disorders : NMD (01.10.2014)
Published in Neuromuscular disorders : NMD (01.10.2014)
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Journal Article
Late-onset non-thymomatous generalized myasthenia gravis
Durmus, H, Yilmaz, V, Serdaroglu-Oflazer, P, Gulsen-Parman, Y, Saruhan-Direskeneli, G, Deymeer, F
Published in Journal of the neurological sciences (15.10.2013)
Published in Journal of the neurological sciences (15.10.2013)
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Journal Article
G.P.58 Muscle MRI in a filaminopathy family: Involvement of paraspinals is earlier and more severe than of thigh muscles
Ozturk Yavuz, A, Goldfarb, L, Tuncer, O, Dursun, M, Olive, M, Deymeer, F, Parman, Y, Tuncay, R, Serdaroglu-Oflazer, P
Published in Neuromuscular disorders : NMD (01.10.2012)
Published in Neuromuscular disorders : NMD (01.10.2012)
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Journal Article
135. Electrophysiological decrement and transient weakness in myotonic syndromes
Matur, Z, Ciftci, F.D, Kara, B, Serdaroglu-Oflazer, P, Parman, Y, Basak, N, Jurkat-Rott, K, Lehmann-Horn, F, Deymeer, F
Published in Clinical neurophysiology (01.06.2012)
Published in Clinical neurophysiology (01.06.2012)
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Journal Article
G.P.10.08 Myophosphorylase deficiency and calpainopathy in the same patient
Pulur, N, Parman, Y, Deymeer, F, Serdaroglu-Oflazer, P
Published in Neuromuscular disorders : NMD (01.09.2009)
Published in Neuromuscular disorders : NMD (01.09.2009)
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Journal Article
P5.56 Myofibrillar myopathy associated with filamin C mutations: Refining the phenotype and new insights in pathogenesis
Vorgerd, M, Kley, R.A, Serdaroglu-Oflazer, P, Odgerel, Z, Olive, M, Lee, H.S, Hahn, Y, van der Ven, P.F.M, Höhfeld, J, Kirschner, J, Bilbao, J.M, Goldfarb, L.G, Fürst, D.O
Published in Neuromuscular disorders : NMD (01.10.2011)
Published in Neuromuscular disorders : NMD (01.10.2011)
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Journal Article
M.P.1.10 Anti-MuSK antibodies are not associated with prolonged pure ocular symptoms
Sirin, G, Yilmaz, V, Parman, Y, Serdaroglu-Oflazer, P, Saruhan-Direskeneli, G, Deymeer, F
Published in Neuromuscular disorders : NMD (01.10.2008)
Published in Neuromuscular disorders : NMD (01.10.2008)
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Journal Article
G.P.11.09 Congenital end - plate acetylcholinesterase deficiency and the effect of ephedrine on clinical findings, lung functions and nocturnal parameters
Kiyan, E, Kara, B, Serdaroglu Oflazer, P, Parman, Y, Tasdemir, N, Deymeer, F, Engel, A.G
Published in Neuromuscular disorders : NMD (01.09.2009)
Published in Neuromuscular disorders : NMD (01.09.2009)
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Journal Article
Evaluation of maximum oxygen utilization in McArdle patients before and after exercise training
Gelisin, O, Durmus, H, Yakal, S, Kasikcioglu, E, Parman, Y, Deymeer, F, Oflazer-Serdaroğlu, P
Published in Neuromuscular disorders : NMD (01.10.2015)
Published in Neuromuscular disorders : NMD (01.10.2015)
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Journal Article
P.253GNE myopathy in Turkey: clinical features and novel mutations
Durmus, H., Ceylaner, S., Deymeer, F., Parman, Y., Oflazer-Serdaroglu, P.
Published in Neuromuscular disorders : NMD (01.10.2019)
Published in Neuromuscular disorders : NMD (01.10.2019)
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Journal Article
Myophosphorylase (PYGM) mutations in Turkish patients with McArdle disease: A next generation sequencing study
Inal Gültekin, G, Toptaş Hekimoğlu, B, Görmez, Z, Durmuş, H, Demirci, H, Sağıroğlu, M, Parman, Y, Deymeer, F, Yılmaz, H, Pençe, S, Kurt, C, Tan, E, Özdamar, S, Giger, U, Öztürk, O, Serdaroğlu-Oflazer, P
Published in Neuromuscular disorders : NMD (01.10.2015)
Published in Neuromuscular disorders : NMD (01.10.2015)
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Journal Article
G.P.8: Dramatic improvement after injection augmentation in oculopharyngodistal myopathy
Ozcan, O., Durmus, H., Tarhan, O., Polat, Z., Deymeer, F., Parman, Y., Oflazer-Serdaroglu, P.
Published in Neuromuscular disorders : NMD (01.10.2014)
Published in Neuromuscular disorders : NMD (01.10.2014)
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Journal Article
G.P.138: Late-onset non-thymomatous generalized myasthenia gravis
Yildiz-Celik, S., Durmus, H., Hajibehzad, M., Yilmaz, V., Oflazer-Serdaroglu, P., Parman, Y., Saruhan-Direskeneli, G., Deyemeer, F.
Published in Neuromuscular disorders : NMD (01.10.2014)
Published in Neuromuscular disorders : NMD (01.10.2014)
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Journal Article