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Dergi Makaleleri

 

  1. Yunisova G, Ceylaner S, Oflazer P, Deymeer F, Parman YG, Durmus H. Clinical and genetic characteristics of Emery-Dreifuss muscular dystrophy patients from Turkey: 30 years longitudinal follow-up Neuromuscul Disord. 2022 Sep;32(9):718-727. doi: 10.1016/j.nmd.2022.07.397
  2. Gungor Tuncer O, Deymeer F. Clinical course and outcome of an outpatient clinic population with myasthenia gravis and COVID-19. Muscle Nerve. 2022;65(4):447-452. doi:10.1002/mus.27497
  3. Durmus H, Sticht H, Ceylaner S, Hashemolhosseini S, Deymeer F. Rare slow channel congenital myasthenic syndromes without repetitive compound muscle action potential and dramatic response to low dose fluoxetine. Acta Neurol Belg. 2021 Dec;121(6):1755-1760. doi: 10.1007/s13760-020- 01505-0

 

  1. Vural A, Şimşir G, Tekgül Ş, et al. The complex genetic landscape of hereditary ataxias in Turkey and implications in clinical Mov Disord. 2021;36(7):1676-1688. doi:10.1002/mds.28518

 

  1. Çakar A, Atmaca MM, Kotan D, Durmuş H, Deymeer F, Oflazer P, Parman Y. Lumbar spinal stenosis: A rare presentation of hereditary transthyretin amyloidosis. Noro Psikiyatr Ars. 2020 Oct 11;59(1):77-79. doi: 29399/npa.26124

 

  1. Deymeer F. Myasthenia gravis: MuSK MG, late-onset MG and ocular MG. Acta Myol. 2020;39(4):345-352. Published 2020 Dec doi:10.36185/2532-1900-038

 

  1. Deymeer F. History of myasthenia gravis revisited. Noro Psikiyatr Ars. 2020;58(2):154-162. Published 2020 Nov 7. doi:10.29399/npa.27315

 

  1. Yilmaz V, Tuzun E, Durmus H, Oflazer P, Aysal F, Parman Y, Gungor-Tuncer O, Deymeer F, Saruhan-Direskeneli G. The treatment effect on peripheral B cell markers in antibody positive myasthenia gravis patients. J Neuroimmunol. 2020 Dec 15;349:577402. doi: 1016/j.jneuroim.2020.577402

 

  1. Deymeer F. Nusinersen in SMA 2 and 3: Risks vs benefits [published correction appears in 2020 Nov 24;95(21):987]. Neurology. 2020;95(4):151-152. doi:10.1212/WNL.0000000000009919

 

  1. Tunca C, Şeker T, Akçimen F, et al. Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database. Hum 2020;41(8):e7-e45. doi:10.1002/humu.24055

 

  1. Yildiz Celik S, Durmus H, Yilmaz V, Saruhan Direskeneli G, Gulsen Parman Y, Serdaroglu Oflazer P, Deymeer Late-onset generalized myasthenia gravis: clinical features, treatment, and outcome. Acta Neurol Belg. 2020 Feb;120(1):133-140. doi: 10.1007/s13760-019-01252-x

 

  1. Toksoy G, Durmus H, Aghayev A, et al. Mutation spectrum of 260 dystrophinopathy patients from Turkey and important highlights for genetic counseling. Neuromuscul Disord. 2019;29(8):601-613. doi:10.1016/j.nmd.2019.03.012

  1. Çebi M, Durmuş H, Yılmaz V, Yentür SP, Aysal F, Oflazer P, Parman Y, Deymeer F, Saruhan- Direskeneli G. Relation of HLA-DRB1 to IgG4 autoantibody and cytokine production in muscle- specific tyrosine kinase myasthenia gravis (MuSK-MG). Clin Exp Immunol. 2019 Aug;197(2):214- doi: 10.1111/cei.13302

 

  1. Hocaoğlu M, Durmuş H, Özkan B, Yentür SP, Doğan Ö, Parman Y, Deymeer F, Saruhan- Direskeneli G. Increased costimulatory molecule expression of thymic and peripheral B cells and a sensitivity to IL-21 in myasthenia gravis. J Neuroimmunol. 2018 Oct 15;323:36-42. doi: 1016/j.jneuroim.2018.07.006

 

  1. Durmus H, Shen XM, Serdaroglu-Oflazer P, Kara B, Parman-Gulsen Y, Ozdemir C, Brengman J, Deymeer F, Engel AG. Congenital myasthenic syndromes in Turkey: Clinical clues and prognosis with long term follow-up. Neuromuscul Disord. 2018 Apr;28(4):315-322. doi: 1016/j.nmd.2017.11.013

 

  1. Shen XM, Brengman JM, Shen S, Durmus H, Preethish-Kumar V, Yuceyar N, Vengalil S, Nalini A, Deymeer F, Sine SM, Engel AG. Mutations causing congenital myasthenia reveal principal coupling pathway in the acetylcholine receptor ε-subunit. JCI Insight. 2018 Jan 25;3(2):e97826. doi: 1172/jci.insight.97826

 

  1. Orhan EK, Kiraç LB, DİKmen PY, Matur Z, Ertaş M, Öge AE, Deymeer F, Yazici J, Baslo Electromyography in pediatric population. Noro Psikiyatr Ars. 2018 Mar 19;55(1):36-39. doi: 10.5152/npa.17023

 

  1. Sirin NG, Kocasoy Orhan E, Durmus H, Deymeer F, Baslo MB. Repetitive nerve stimulation and jitter measurement with disposable concentric needle electrode in newly diagnosed myasthenia gravis Neurophysiol Clin. 2018 Oct;48(5):261-267. doi: 10.1016/j.neucli.2018.01.003

 

  1. Gokyigit MC, Ekmekci H, Durmus H, Karlı N, Koseoglu E, Aysal F, Kotan D, Ali A, Koytak PK, Karasoy H, Yaman A, Sengun İS, Sayin R, Tiftikcioglu BI, Soysal A, Tutkavul K, Bayrak AO, Kısabay A, Elci MA, Yayla V, Yılmaz İA, Ozdamar SE, Erdogan C, Tasdemir N, Serdaroglu Oflazer P; Turkish Study Group for Late Onset Pompe Disease. A database for screening and registering late onset Pompe disease in Turkey. Neuromuscul Disord. 2018 Mar;28(3):262-267. doi: 1016/j.nmd.2017.12.008

 

  1. Gungor-Tuncer O, Yilmaz V, Toker A, Saruhan-Direskeneli G, Gulsen-Parman Y, Oflazer- Serdaroglu P, Deymeer F. Prompt response to prednisone predicts benign course in MuSK-MG. Eur 2017;78(3-4):137-142. doi: 10.1159/000479228

 

  1. Durmus H, Yilmaz R, Gulsen-Parman Y, Oflazer-Serdaroglu P, Cuttini M, Dursun M, Deymeer Muscle magnetic resonance imaging in spinal muscular atrophy type 3: Selective and progressive involvement. Muscle Nerve. 2017 May;55(5):651-656. doi: 10.1002/mus.25385

 

  1. Alahgholi-Hajibehzad M, Durmuş H, Aysal F, Gülşen-Parman Y, Oflazer P, Deymeer F, Saruhan- Direskeneli G. The effect of interleukin (IL)-21 and CD4+ CD25++ T cells on cytokine production of CD4+ responder T cells in patients with myasthenia gravis. Clin Exp Immunol. 2017 Nov;190(2):201-207. doi: 1111/cei.13006

 

  1. Inal-Gültekin G, Toptaş-Hekimoğlu B, Görmez Z, Gelişin Ö, Durmuş H, Ergüner B, Demirci H, Sağıroğlu MŞ, Parman Y, Deymeer F, Yılmaz-Aydoğan H, Pençe S, Bekircan-Kurt CE, Tan E, Erdem-Özdamar S, Üstek D, Giger U, Öztürk O, Serdaroğlu-Oflazer P. Myophosphorylase (PYGM) mutations determined by next generation sequencing in a cohort from Turkey with McArdle disease. Neuromuscul 2017 Nov;27(11):997-1008. doi: 10.1016/j.nmd.2017.06.004

  1. İnal HS, Tarakçı E, Tarakçı D, Aksoy G, Mergen Kılıç S, Beşer H, Beşer Ç, Özdinçler AR, Durmuş Tekçe H, Parman FY, Deymeer F, Oflazer ZP. Turkish version of the Motor Function Measure Scale (MFM-32) for neuromuscular diseases: a cross-cultural adaptation, reliability, and validity Turk J Med Sci. 2017 Dec 19;47(6):1826-1833. doi: 10.3906/sag-1603-91

 

  1. Durmuş H, Ayhan Ö, Çırak S, Deymeer F, Parman Y, Franke A, Eiber N, Chevessier F, Schlötzer- Schrehardt U, Clemen CS, Hashemolhosseini S, Schröder R, Hemmrich-Stanisak G, Tolun A, Serdaroğlu-Oflazer P. Neuromuscular endplate pathology in recessive desminopathies: Lessons from man and Neurology. 2016 Aug 23;87(8):799-805. doi: 10.1212/WNL.0000000000003004

 

  1. Durmuş-Tekçe H, Matur Z, Mert Atmaca M, Poda M, Çakar A, Hıdır Ulaş Ü, Oflazer-Serdaroğlu P, Deymeer F, Parman YG. Genotypic and phenotypic presentation of transthyretin-related familial amyloid polyneuropathy (TTR-FAP) in Turkey. Neuromuscul Disord. 2016 Jul;26(7):441-6. doi: 1016/j.nmd.2016.04.013

 

  1. Saruhan-Direskeneli G, Hughes T, Yilmaz V, Durmus H, Adler A, Alahgholi-Hajibehzad M, Aysal F, Yentür SP, Akalin MA, Dogan O, Marx A, Gülsen-Parman Y, Oflazer P, Deymeer F, Sawalha Genetic heterogeneity within the HLA region in three distinct clinical subgroups of myasthenia gravis. Clin Immunol. 2016 May;166-167:81-8. doi: 10.1016/j.clim.2016.05.003

 

  1. Stergiou C, Lazaridis K, Zouvelou V, Tzartos J, Mantegazza R, Antozzi C, Andreetta F, Evoli A, Deymeer F, Saruhan-Direskeneli G, Durmus H, Brenner T, Vaknin A, Berrih-Aknin S, Behin A, Sharshar T, De Baets M, Losen M, Martinez-Martinez P, Kleopa KA, Zamba-Papanicolaou E, Kyriakides T, Kostera-Pruszczyk A, Szczudlik P, Szyluk B, Lavrnic D, Basta I, Peric S, Tallaksen C, Maniaol A, Gilhus NE, Casasnovas Pons C, Pitha J, Jakubíkova M, Hanisch F, Bogomolovas J, Labeit D, Labeit S, Tzartos SJ. Titin antibodies in “seronegative” myasthenia gravis–A new role for an old J Neuroimmunol. 2016 Mar 15;292:108-15. doi: 10.1016/j.jneuroim.2016.01.018

 

  1. Tsonis AI, Zisimopoulou P, Lazaridis K, Tzartos J, Matsigkou E, Zouvelou V, Mantegazza R, Antozzi C, Andreetta F, Evoli A, Deymeer F, Saruhan-Direskeneli G, Durmus H, Brenner T, Vaknin A, Berrih-Aknin S, Behin A, Sharshar T, De Baets M, Losen M, Martinez-Martinez P, Kleopa KA, Zamba-Papanicolaou E, Kyriakides T, Kostera-Pruszczyk A, Szczudlik P, Szyluk B, Lavrnic D, Basta I, Peric S, Tallaksen C, Maniaol A, Casasnovas Pons C, Pitha J, Jakubíkova M, Hanisch F, Tzartos SJ. MuSK autoantibodies in myasthenia gravis detected by cell based assay–A multinational J Neuroimmunol. 2015 Jul 15;284:10-7. doi: 10.1016/j.jneuroim.2015.04.015

 

  1. Yilmaz V, Oflazer P, Aysal F, Durmus H, Poulas K, Yentur SP, Gulsen-Parman Y, Tzartos S, Marx A, Tuzun E, Deymeer F, Saruhan-Direskeneli G. Differential cytokine changes in patients with myasthenia gravis with antibodies against AChR and MuSK. PLoS One. 2015 Apr 20;10(4):e0123546. doi: 1371/journal.pone.0123546

 

  1. Alahgholi-Hajibehzad M, Oflazer P, Aysal F, Durmuş H, Gülşen-Parman Y, Marx A, Deymeer F, Saruhan-Direskeneli G. Regulatory function of CD4+CD25++ T cells in patients with myasthenia gravis is associated with phenotypic changes and STAT5 signaling: 1,25-Dihydroxyvitamin D3 modulates the suppressor activity. J Neuroimmunol. 2015 Apr 15;281:51-60. doi: 1016/j.jneuroim.2015.03.008

 

  1. Yilmaz V, Oflazer P, Aysal F, Parman YG, Direskeneli H, Deymeer F, Saruhan-Direskeneli G. B cells produce less IL-10, IL-6 and TNF-α in myasthenia gravis. Autoimmunity. 2015 Jun;48(4):201- doi: 10.3109/08916934.2014.992517

 

  1. Özoğuz A, Uyan Ö, Birdal G, Iskender C, Kartal E, Lahut S, Ömür Ö, Agim ZS, Eken AG, Sen NE, Kavak P, Saygı C, Sapp PC, Keagle P, Parman Y, Tan E, Koç F, Deymeer F, Oflazer P, Hanağası H, Gürvit H, Bilgiç B, Durmuş H, Ertaş M, Kotan D, Akalın MA, Güllüoğlu H, Zarifoğlu M, Aysal F, Döşoğlu N, Bilguvar K, Günel M, Keskin Ö, Akgün T, Özçelik H, Landers JE, Brown RH,

Başak AN. The distinct genetic pattern of ALS in Turkey and novel mutations. Neurobiol Aging. 2015 Apr;36(4):1764.e9-1764.e18. doi: 10.1016/j.neurobiolaging.2014.12.032

 

  1. Kaya GA, Coşkun AN, Yılmaz V, Oflazer P, Gülsen-Parman Y, Aysal F, Disci R, Direskeneli H, Marx A, Deymeer F, Saruhan-Direskeneli G. The association of PTPN22 R620W polymorphism is stronger with late-onset AChR-myasthenia gravis in Turkey. PLoS One. 2014 Aug 13;9(8):e104760. doi: 1371/journal.pone.0104760

 

  1. Zisimopoulou P, Evangelakou P, Tzartos J, Lazaridis K, Zouvelou V, Mantegazza R, Antozzi C, Andreetta F, Evoli A, Deymeer F, Saruhan-Direskeneli G, Durmus H, Brenner T, Vaknin A, Berrih- Aknin S, Frenkian Cuvelier M, Stojkovic T, DeBaets M, Losen M, Martinez-Martinez P, Kleopa KA, Zamba-Papanicolaou E, Kyriakides T, Kostera-Pruszczyk A, Szczudlik P, Szyluk B, Lavrnic D, Basta I, Peric S, Tallaksen C, Maniaol A, Tzartos SJ. A comprehensive analysis of the epidemiology and clinical characteristics of anti-LRP4 in myasthenia gravis. J Autoimmun. 2014 Aug;52:139-45. doi: 1016/j.jaut.2013.12.004

 

  1. Gungor-Tuncer O, Orhan EK, Yilmaz V, Parman Y, Oflazer P, Saruhan-Direskeneli G, Deymeer F. Prepubertal anti-Musk positive myasthenia gravis with long remission. Neuromuscul Disord. 2014 Jan;24(1):36-9. doi: 1016/j.nmd.2013.07.01

 

  1. Alahgholi-Hajibehzad M, Yilmaz V, Gülsen-Parman Y, Aysal F, Oflazer P, Deymeer F, Saruhan- Direskeneli G. Association of HLA-DRB1∗14, -DRB1∗16 and -DQB1∗05 with MuSK-myasthenia gravis in patients from Turkey. Hum Immunol. 2013 Dec;74(12):1633-5. doi: 1016/j.humimm.2013.08.271

 

  1. Uyan Ö, Ömür Ö, Ağım ZS, Özoğuz A, Li H, Parman Y, Deymeer F, Oflazer P, Koç F, Tan E, Özçelik H, Başak AN. Genome-wide copy number variation in sporadic amyotrophic lateral sclerosis in the Turkish population: deletion of EPHA3 is a possible protective factor. PLoS One. 2013 Aug 26;8(8):e72381. doi: 1371/journal.pone.0072381

 

  1. Selcen D, Shen XM, Milone M, Brengman J, Ohno K, Deymeer F, Finkel R, Rowin J, Engel AG. GFPT1-myasthenia: clinical, structural, and electrophysiologic heterogeneity. Neurology. 2013 Jul 23;81(4):370-8. doi: 1212/WNL.0b013e31829c5e9c

 

  1. Orhan EK, Deymeer F, Oflazer P, Parman Y, Baslo Jitter analysis with concentric needle electrode in the masseter muscle for the diagnosis of generalised myasthenia gravis. Clin Neurophysiol. 2013 Nov;124(11):2277-82. doi: 10.1016/j.clinph.2013.04.344

 

  1. Lahut S, Ömür Ö, Uyan Ö, Ağım ZS, Özoğuz A, Parman Y, Deymeer F, Oflazer P, Koç F, Özçelik H, Auburger G, Başak AN. ATXN2 and its neighbouring gene SH2B3 are associated with increased ALS risk in the Turkish PLoS One. 2012;7(8):e42956. doi: 10.1371/journal.pone.0042956

 

  1. Ekizoğlu E, Yılmaz V, Içöz S, Birişik Ö, Tüzün E, Akman-Demir G, Saruhan-Direskeneli G, Deymeer F. Aquaporin-4 antibody seropositivity in myasthenia gravis patients with thymoma. Muscle 2013 Feb;47(2):306-7

 

  1. Shugaiv E, Kiyat-Atamer A, Tüzün E, Deymeer F, Oflazer P, Parman Y, Akman-Demir G. Coexistence of Guillain-Barré syndrome and Behçet’s disease. Clin Exp Rheumatol 2013;31(3 Suppl 77):88-9

 

  1. Oflazer PS, Deymeer F, Parman Y. Sporadic-inclusion body myositis (s-IBM) is not so prevalent in Istanbul/Turkey: a muscle based survey. Acta Myol 2011;30(1):34-6

  1. Tüzün E, Yılmaz V, Parman Y, Oflazer P, Deymeer F, Saruhan-Direskeneli G. Increased complement consumption in MuSK-antibody-positive myasthenia gravis patients. Med Princ Pract. 2011;20(6):581-3. doi: 1159/000330031

 

  1. Deymeer F, Matur Z, Poyraz M, Battaloglu E, Oflazer-Serdaroglu P, Parman Y. Nerve conduction studies in Charcot-Marie-Tooth disease in a cohort from Turkey. Muscle Nerve. 2011 May;43(5):657-64. doi: 1002/mus.21932

 

  1. Durmus H, Laval SH, 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. Oculopharyngodistal myopathy is a distinct entity: clinical and genetic features of 47 patients. Neurology. 2011 Jan 18;76(3):227-35. doi: 1212/WNL.0b013e318207b043

 

  1. Kiyan E, Okumus G, Cuhadaroglu C, Deymeer F. Sleep apnea in adult myotonic dystrophy patients who have no excessive daytime sleepiness. Sleep Breath. 2010 Feb;14(1):19-24. doi: 1007/s11325-009-0270-6

 

  1. Toker A, Tanju S, Ziyade S, Ozkan B, Sungur Z, Parman Y, Serdaroglu P, Deymeer F. Early outcomes of video-assisted thoracoscopic resection of thymus in 181 patients with myasthenia gravis: who are the candidates for the next morning discharge? Interact Cardiovasc Thorac Surg. 2009 Dec;9(6):995-8. doi: 1510/icvts.2009.214635

 

  1. Deymeer F, Serdaroglu P, Parman Y, Poda M. Natural history of SMA IIIb: muscle strength decreases in a predictable sequence and magnitude. Neurology. 2008 Aug 26;71(9):644-9. doi: 1212/01.wnl.0000324623.89105.c4

 

  1. Li J, Qi H, Tüzün E, Allman W, Yilmaz V, Saini SS, Deymeer F, Saruhan-Direskeneli G, Christadoss P. Mannose-binding lectin pathway is not involved in myasthenia gravis pathogenesis. J 2009 Mar 31;208(1-2):40-5. doi: 10.1016/j.jneuroim.2008.12.013

 

  1. Toker A, Tanju S, Sungur Z, Parman Y, Senturk M, Serdaroglu P, Dilege S, Deymeer F. Videothoracoscopic thymectomy for nonthymomatous myasthenia gravis: results of 90 patients. Surg Endosc. 2008 Apr;22(4):912-6. doi: 1007/s00464-007-9507-2

 

  1. Yayla V, Oge AE, Deymeer F, Gurvit H, Akca-Kalem S, Parman Y, Oflazer Cortical excitability in Duchenne muscular dystrophy. Clin Neurophysiol. 2008 Feb;119(2):459-65. doi: 10.1016/j.clinph.2007.09.125

 

  1. Parman Y, Ciftci F, Poyraz M, Halefoglu AM, Oge AE, Eraksoy M, Saruhan-Direskeneli G, Deymeer F, Battaloglu E. X-linked Charcot-Marie-Tooth disease and multiple sclerosis. J Neurol. 2007 Jul;254(7):953-5. doi: 1007/s00415-006-0324-7

 

  1. Yilmaz V, Tütüncü Y, Bariş Hasbal N, Parman Y, Serdaroglu P, Deymeer F, Saruhan-Direskeneli
  2. Polymorphisms of interferon-gamma, interleukin-10, and interleukin-12 genes in myasthenia gravis. Hum Immunol. 2007 Jun;68(6):544-9. doi: 10.1016/j.humimm.2007.02.003

 

  1. Deymeer F, Gungor-Tuncer O, Yilmaz V, Parman Y, Serdaroglu P, Ozdemir C, Vincent A, Saruhan-Direskeneli G. Clinical comparison of anti-MuSK- vs anti-AChR-positive and seronegative myasthenia Neurology. 2007 Feb 20;68(8):609-11. doi: 10.1212/01.wnl.0000254620.45529.97

 

  1. Baslo MB, Deymeer F, Serdaroglu P, Parman Y, Ozdemir C, Cuttini M. Decrement pattern in Lambert-Eaton myasthenic syndrome is different from myasthenia gravis. Neuromuscul Disord. 2006 Jul;16(7):454-8. doi: 1016/j.nmd.2006.05.009

  1. Shen XM, Deymeer F, Sine SM, Engel AG. Slow-channel mutation in acetylcholine receptor alphaM4 domain and its efficient knockdown. Ann Neurol. 2006 Jul;60(1):128-36. doi: 1002/ana.20861

 

  1. Saruhan-Direskeneli G, Kiliç A, Parman Y, Serdaroğlu P, Deymeer F. HLA-DQ polymorphism in Turkish patients with myasthenia gravis. Hum Immunol. 2006 Apr-May;67(4-5):352-8. doi: 1016/j.humimm.2006.02.039

 

  1. Deymeer F, Akca S, Kocaman G, Parman Y, Serdaroglu P, Oktem-Tanor O, Coban O, Vincent A. Fasciculations, autonomic symptoms and limbic encephalitis: a thymoma-associated Morvan’s-like Eur Neurol. 2005;54(4):235-7. doi: 10.1159/000090719

 

  1. Parman Y, Battaloglu E, Baris I, Bilir B, Poyraz M, Bissar-Tadmouri N, Williams A, Ammar N, Nelis E, Timmerman V, De Jonghe P, Najafov A, Deymeer F, Serdaroglu P, Brophy PJ, Said Clinicopathological and genetic study of early-onset demyelinating neuropathy. Brain. 2004 Nov;127(Pt 11):2540-50. doi: 10.1093/brain/awh275

 

  1. Bissar-Tadmouri N, Nelis E, Züchner S, Parman Y, Deymeer F, Serdaroglu P, De Jonghe P, Van Gerwen V, Timmerman V, Schröder JM, Battaloglu E. Absence of KIF1B mutation in a large Turkish CMT2A family suggests involvement of a second gene. Neurology. 2004 May 11;62(9):1522-5. doi:10.1212/01.wnl.0000123253.57555.3a

 

  1. Öztürk A, Deymeer F, Serdaroğlu P, Parman Y, Özdemir C. Distribution of extremity muscle weakness in myasthenia gravis: sparing of tibialis anterior Acta Myol 2003;22(2):58-60

 

  1. Akbas F, Serdaroglu P, Deymeer F, Aysal F, Erginel-Unaltuna N. Molecular and clinical study of two myotonic dystrophy homozygotes. J Med Genet. 2001 Nov;38(11):E40. doi: 1136/jmg.38.11.e40

 

  1. Planté-Bordeneuve V, Parman Y, Guiochon-Mantel A, Alj Y, Deymeer F, Serdaroglu P, Eraksoy M, Said G. The range of chronic demyelinating neuropathy of infancy: a clinico-pathological and genetic study of 15 unrelated cases. J Neurol. 2001 Sep;248(9):795-803. doi: 1007/s004150170096

 

  1. Christodoulou K, Deymeer F, Serdaroğlu P, Ozdemir C, Poda M, Georgiou DM, Ioannou P, Tsingis M, Zamba E, Middleton LT. Mapping of the second Friedreich’s ataxia (FRDA2) locus to chromosome 9p23-p11: evidence for further locus heterogeneity. Neurogenetics. 2001 Jul;3(3):127- doi: 10.1007/s100480100112

 

  1. Onengüt S, Kavaslar GN, Battaloğlu E, Serdaroğlu P, Deymeer F, Ozdemir C, Calafell F, Tolun A. Deletion pattern in the dystrophin gene in Turks and a comparison with Europeans and Indians. Ann Hum 2000 Jan;64(Pt 1):33-40. doi: 10.1017/S0003480000007934

 

  1. Plaster NM, Tawil R, Tristani-Firouzi M, Canún S, Bendahhou S, Tsunoda A, Donaldson MR, Iannaccone ST, Brunt E, Barohn R, Clark J, Deymeer F, George AL Jr, Fish FA, Hahn A, Nitu A, Ozdemir C, Serdaroglu P, Subramony SH, Wolfe G, Fu YH, Ptácek LJ. Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen’s syndrome. Cell. 2001 May 18;105(4):511-9. doi: 1016/s0092-8674(01)00342-7

 

  1. Bissar-Tadmouri N, Parman Y, Boutrand L, Deymeer F, Serdaroglu P, Vandenberghe A, Battaloglu
  2. Mutational analysis and genotype/phenotype correlation in Turkish Charcot-Marie-Tooth Type 1 and HNPP patients. Clin Genet. 2000 Nov;58(5):396-402. doi: 10.1034/j.1399-0004.2000.580511.x

 

  1. Bissar-Tadmouri N, Gulsen-Parman Y, Latour P, Deymeer F, Serdaroglu P, Vandenberghe A, Battaloglu Two novel mutations in the MPZ gene coding region in Charcot-Marie-Tooth type 1

patients of Turkish origin: S54P, [I30del; GVYI29ins]. Hum Mutat. 1999 Nov;14(5):449. doi: 10.1002/(SICI)1098-1004(199911)14:5<449::AID-HUMU17>3.0.CO;2-H

 

  1. Middleton L, Ohno K, Christodoulou K, Brengman J, Milone M, Neocleous V, Serdaroğlu P, Deymeer F, Ozdemir C, Mubaidin A, Horany K, Al-Shehab A, Mavromatis I, Mylonas I, Tsingis M, Zamba E, Pantzaris M, Kyriallis K, Engel AG. Chromosome 17p-linked myasthenias stem from defects in the acetylcholine receptor epsilon-subunit gene. Neurology. 1999 Sep 22;53(5):1076-82. doi: 1212/wnl.53.5.1076

 

  1. Deymeer F, Serdaroğlu P, Ozdemir Familial infantile myasthenia: confusion in terminology. Neuromuscul Disord. 1999 May;9(3):129-30. doi: 10.1016/s0960-8966(99)00004-8

 

  1. Deymeer F, Lehmann-Horn F, Serdaroğlu P, Cakirkaya S, Benz S, Rüdel R, Ozdemir C. Electrical myotonia in heterozygous carriers of recessive myotonia congenita. Muscle Nerve. 1999 Jan;22(1):123-5. doi: 1002/(sici)1097-4598(199901)22:1<123::aid-mus20>3.0.co;2-y

 

  1. Deymeer F, Cakirkaya S, Serdaroğlu P, Schleithoff L, Lehmann-Horn F, Rüdel R, Ozdemir C. Transient weakness and compound muscle action potential decrement in myotonia congenita. Muscle Nerve. 1998 Oct;21(10):1334-7. doi: 10.1002/(sici)1097-4598(199810)21:10<1334::aid- mus16>3.0.co;2-1

 

  1. Fleischhauer R, Mitrovic N, Deymeer F, Lehmann-Horn F, Lerche H. Effects of temperature and mexiletine on the F1473S Na+ channel mutation causing paramyotonia congenita. Pflugers Arch. 1998 Oct;436(5):757-65. doi: 1007/s004240050699

 

  1. Wagner S, Deymeer F, Kürz LL, Benz S, Schleithoff L, Lehmann-Horn F, Serdaroğlu P, Ozdemir C, Rüdel R. The dominant chloride channel mutant G200R causing fluctuating myotonia: clinical findings, electrophysiology, and channel pathology. Muscle Nerve. 1998 Sep;21(9):1122-8. doi: 1002/(sici)1097-4598(199809)21:9<1122::aid-mus2>3.0.co;2-9

 

  1. Deymeer F, Oge AE, Serdaroğlu P, Yazici J, Ozdemir C, Baslo The use of botulinum toxin in localizing neuromyotonia to the terminal branches of the peripheral nerve. Muscle Nerve. 1998 May;21(5):643-6. doi: 10.1002/(sici)1097-4598(199805)21:5<643::aid-mus12>3.0.co;2-w

 

  1. Deymeer F, Serdaroğlu P, Poda M, Gülşen-Parman Y, Ozçelik T, Ozdemir C. Segmental distribution of muscle weakness in SMA III: implications for deterioration in muscle strength with Neuromuscul Disord. 1997 Dec;7(8):521-8. doi: 10.1016/s0960-8966(97)00113-2

 

  1. Mailänder V, Heine R, Deymeer F, Lehmann-Horn F. Novel muscle chloride mutations and their effects on heterozygous carriers. Amer J Hum Genet 1996;58:317-324

 

  1. Kavaslar GN, Telatar M, Serdaroglu P, Deymeer F, Ozdemir C, Tolun A. Identification of a one- basepair deletion in exon 6 of the dystrophin gene. Hum Mutat. 1995;6(1):85-6. doi: 1002/humu.1380060116

 

  1. Deymeer F, Jones HR Jr. Pediatric median mononeuropathies: a clinical and electromyographic Muscle Nerve. 1994 Jul;17(7):755-62. doi: 10.1002/mus.880170709

 

  1. Heine R, George AL Jr, Pika U, Deymeer F, Rüdel R, Lehmann-Horn F. Proof of a non-functional muscle chloride channel in recessive myotonia congenita (Becker) by detection of a 4 base pair Hum Mol Genet. 1994 Jul;3(7):1123-8. doi: 10.1093/hmg/3.7.1123

 

  1. Yates JR, Warner JP, Smith JA, Deymeer F, Azulay JP, Hausmanowa-Petrusewicz I, Zaremba J, Borkowska J, Affara NA, Ferguson-Smith MA. Emery-Dreifuss muscular dystrophy: linkage to markers in distal J Med Genet. 1993 Feb;30(2):108-11. doi: 10.1136/jmg.30.2.108

  1. Deymeer F, Oge AE, Bayindir C, Kaymaz C, Nişanci Y, Adalet K, Yates JR, Ozdemir C. Emery- Dreifuss muscular dystrophy with unusual features. Muscle Nerve. 1993 Dec;16(12):1359-65. doi: 1002/mus.880161214

 

  1. Battaloglu E, Telatar M, Deymeer F, Serdaroğlu P, Özdemir C, Kuseyri F, Yüksel-Apak M, Apak S, Tolun A. Carrier detection by DNA analysis in Turkish Duchenne muscular dystrophy families. The Turkish J Pediatrics 1992;34:79-92

 

  1. Battaloğlu E, Telatar M, Deymeer F, Serdaroğlu P, Kuseyri F, Ozdemir C, Apak M, Tolun A. DNA analysis in Turkish Duchenne/Becker muscular dystrophy families. Hum Genet. 1992 Aug;89(6):635-9. doi: 1007/BF00221954

 

  1. Deymeer F, Smith TW, DeGirolami U, Drachman DA. Thalamic dementia and motor neuron Neurology. 1989 Jan;39(1):58-61. doi: 10.1212/wnl.39.1.58

 

  1. Deymeer F, Leviton A. Posttraumatic seizures: an assessment of the epidemiologic literature. Cent Nerv Syst 1985 Spring;2(1):33-43. doi: 10.1089/cns

 

  1. Deymeer F, Leviton A. Perinatal factors and seizure disorders: an epidemiologic review. Epilepsia. 1985 Jul-Aug;26(4):287-98. doi: 1111/j.1528-1157.1985.tb05652.x

 

  1. Kulla L, Deymeer F, Smith TW, Weiner M, Mullins TF 3rd. Intracranial dissecting and saccular aneurysms in polycystic kidney Arch Neurol. 1982 Dec;39(12):776-8. doi: 10.1001/archneu

 

 

Kitap Bölümleri ve Editörlük

 

Durmuş H, Serdaroglu-Oflazer P, Deymeer F: Emery-Dreifuss Muscular Dystrophy. Nuclear Envelopathies. In HR Jones, BT Darras, DC De Vivo (eds): Neuromuscular Diseases of Infancy, Childhood, and Adolescence: A Clinician’s Approach. Academic Press, 2015:667-678.

 

Deymeer F: Congenital Myasthenic Syndromes. In HR Jones, TM Burns, MJ Aminoff, Pomeroy SL (eds): The Netter Collection of Medical Illustrations. Nervous System. Part II Spinal Cord and Peripheral Motor and Sensory Systems. Elsevier,2013:253.

 

Deymeer F: Emery-Dreifuss Muscular Dystrophy. In HR Jones, BT Darras, DC De Vivo (eds): Neuromuscular Diseases of Infancy, Childhood, and Adolescence: A Clinician’s Approach.

Butterworth-Heinemann,2002:753-763.

 

Deymeer F, Serdaroğlu P, Özdemir C: Juvenile and late-onset myasthenia gravis. In F Deymeer (ed): Neuromuscular Diseases: From Basic Mechanisms to Clinical Management. Basel, Karger,2000:113- 127.

 

Deymeer F (ed). Neuromuscular Diseases: From Basic Mechanisms to Clinical Management. Basel, Karger,2000.

ULUSAL YAYINLAR

 

Dergi makaleleri

 

Gencer M, Deymeer F. Kronik inflamatuar demiyelinizan poliradikülonöropati; tipik olgularda klinik bulgular. Türkiye Klinikleri ; 2022 (baskıda).

 

Güngör Tunçer Ö, Deymeer F. Nöromusküler hastalıklar. Çelik Gökyiğit M, editör. COVID19 ve Nöroloji. 1. Baskı. Ankara: Türkiye Klinikleri; 2021. p.67-72.

 

Durmuş Tekçe H, Deymeer F. Distrofik ve non-distrofik miyotoniler. Taşdemir N, editör. Kas Hastalıkları. 1. Baskı. Ankara: Türkiye Klinikleri; 2020. p.60-6.

 

Durmuş Tekçe H, Deymeer F. Konjenital miyastenik sendromlar. Tanrıdağ T, editör. Nöromusküler Kavşak Hastalıkları. 1. Baskı. Ankara: Türkiye Klinikleri; 2019. p.55-64.

 

Kocasoy-Orhan E, Baysal-Kıraç L, Yalınay-Dikmen P, Matur Z, Ertaş M, Öge AE, Deymeer F, Yazıcı J, Baslo MB. Pediatrik populasyonda elektromiyografi: İstanbul Tıp Fakültesi deneyimleri. Nöropsikiyatri Arşivi 2018;55: 36-39.

 

Gür S, Deymeer F, Oflazer P, Gülşen Parman Y. Poems sendromu ve multisentrik Castleman hastalığında ağrılı polinöropati: Olgu sunumu. Nöropsikiyatri Arşivi 2011; 48: 211-214.

 

Deymeer F. Konjenital miyastenik sendromlar. Türkiye Klinikleri 2011;4(2):110-6. Deymeer F. Myasthenia gravis’te tanı ve tedavi. Türkiye Klinikleri 2010;3(2):37-44. Deymeer F. Nöromüsküler hastalıklarda elektromiyografi. Doktor 2006;33:48-50.

Deymeer F. Myasthenia gravis’te kriz. Türkiye Klinikleri J Int Med Sci 2006;2(22):92-96.

 

Deymeer F. Myasthenia gravis’te tedavi. Türkiye Klinikleri 2005;(1)22:38-43.

 

Deymeer F. Miyotonik sendromlar. Klinik Gelişim 1995;8:3733-3737.

 

Aysal F, Deymeer F, Serdaroğlu P, Öge AE, Çakır N, Tütüncü A, Özdemir C. Botulizm: Dört olgu nedeniyle klinik ve elektrofizyolojisi. Klinik Gelişim 1995;8:3761-3765.

 

Deymeer F, Özdemir C, Serdaroğlu P, Erseven G, Onursal E, Barlas C. Myasthenia Gravis’te timektomi sonuçları (94 olguluk inceleme). Nöro-Psikiatri Arşivi 1988;25(3-4):81-90.

 

 

Kitap Bölümleri

 

Serdaroğlu, P, Durmuş-Tekçe H, Deymeer F. Kas ve Nöromüsküler Kavşak Hastalıkları. A. Emre Öge,

  1. Baykan, B. Bilgiç (eds): Nöroloji (4. Baskı). Nobel Tıp Kitapevleri, 2022:1011-1067.

 

Durmuş-Tekçe H, Deymeer F. Spinal Müsküler Atrofi. A. Emre Öge, B. Baykan, B. Bilgiç (eds): Nöroloji (4. Baskı). Nobel Tıp Kitapevleri, 2022: 705-707.

 

Durmuş-Tekçe H, Deymeer F. Miyastenia Gravis. Koray Dural, Berker Özkan, Berkant Özpolat (eds): Timus Hastalıkları ve Tedavisi. Nobel Tıp Kitapevleri, 2019: 75-81.

Saruhan-Direskeneli G, Deymeer F. Otoimmun Nöromüsküler Kavşak Hastalıkları. Rana Karabudak (ed): Temel ve Klinik Nöroimmunoloji. Ada Basın Yayın, 2013: 545-568.

 

Deymeer F. Nöromüsküler Kavşak Hastalıkları. Murat Emre (ed): Nöroloji Temel Kitabı. Güneş Tıp Kitabevleri, 2013: 426-439.

 

Deymeer F. İskelet Kası İyon Kanallarının Herediter Hastalıkları. Murat Emre (ed): Nöroloji Temel Kitabı. Güneş Tıp Kitabevleri, 2013: 423-426.

 

Deymeer F: Oküler Myasthenia Gravis. P Aydın, T Kansu, N Torun (eds): Nöro-Oftalmoloji El Kitabı. Güneş Tıp Kitabevi,2007:193-204.