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Neuromuscular Disorders : NMD|February 3, 1998
Segmental distribution of muscle weakness in SMA III: implications for deterioration in muscle strength with timeF Deymeer, P Serdaroğlu, M Poda, et al.
Human Molecular Genetics|July 1, 1994
Proof of a non-functional muscle chloride channel in recessive myotonia congenita (Becker) by detection of a 4 base pair deletionR Heine, A L George, U Pika, et al.
Clinical Genetics|January 5, 2001
Mutational analysis and genotype/phenotype correlation in Turkish Charcot-Marie-Tooth Type 1 and HNPP patientsN Bissar-Tadmouri, Y Parman, L Boutrand, et al.
Muscle & Nerve|September 15, 1998
Transient weakness and compound muscle action potential decrement in myotonia congenitaF Deymeer, S Cakirkaya, P Serdaroğlu, et al.
Muscle & Nerve|January 12, 1999
Electrical myotonia in heterozygous carriers of recessive myotonia congenitaF Deymeer, F Lehmann-Horn, P Serdaroğlu, et al.
Human Genetics|August 1, 1992
DNA analysis in Turkish Duchenne/Becker muscular dystrophy familiesE Battaloğlu, M Telatar, F Deymeer, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 7, 2007
Cortical excitability in Duchenne muscular dystrophyV Yayla, A E Oge, F Deymeer, et al.
The Turkish Journal of Pediatrics|April 1, 1992
Carrier detection by DNA analysis in Duchenne muscular dystrophy familiesE Battaloğlu, M Telatar, F Deymeer, et al.
Clinical and Experimental Immunology|July 4, 2017
The effect of interleukin (IL)-21 and CD4<sup>+</sup> CD25<sup>++</sup> T cells on cytokine production of CD4<sup>+</sup> responder T cells in patients with myasthenia gravisM Alahgholi-Hajibehzad, H Durmuş, F Aysal, et al.
Annals of Human Genetics|June 5, 2001
Deletion pattern in the dystrophin gene in Turks and a comparison with Europeans and IndiansS Onengüt, G N Kavaslar, E Battaloğlu, et al.
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