1. Bekircan-Kurt CE, Yilmaz E, Arslan D, Yildiz FG, Dikmetas Ö, Ergul-Ulger Z, Kocabeyoglu S, Irkec M, Hekimsoy V, Tokgozoglu L, Tan E, Erdem-Ozdamar S. The functional and structural evaluation of small fibers in asymptomatic carriers of TTR p.Val50Met (Val30Met) mutation. Neuromuscul Disord. 2022 Jan;32(1):50-56. doi: 10.1016/j.nmd.2021.11.013. Epub 2021 Dec 2. PMID: 34980537.
2. Bekircan-Kurt CE, Inan B, Bulut O, Şengün İ, Karli N, Güneş N, Çokal BG, Güler SK, Yoldaş TK, Özcanyüz DG, Koç F, Ünlütürk Z, Erdoğan Ç, Uludağ B, Boz C, Tütüncü M, Akalin MA, Kamişli Ö, Özcan A, Koytak PK, Uluç K, Erdem-Özdamar S, Tan E. Neuropathic Pain Frequency in Neurology Outpatients: A Multicenter Study. Noro Psikiyatr Ars. 2021 Nov 15;58(4):257-260. doi: 10.29399/npa.27549. PMID: 34924783; PMCID: PMC8665285.
3. Sokmen O, Demirci M, Tan E. A case with Neurofascin-155 IgG antibody-associated combined central and peripheral demyelination: Successfully treated with anti-CD20 monoclonal antibody. Clin Neurol Neurosurg. 2021 Nov;210:106961. doi: 10.1016/j.clineuro.2021.106961. Epub 2021 Sep 28. PMID: 34624826.
4. Aksu-Menges E, Balci-Hayta B, Bekircan-Kurt CE, Aydinoglu AT, Erdem-Ozdamar S, Tan E. Two distinct skeletal muscle microRNA signatures revealing the complex mechanism of sporadic ALS. Acta Neurol Belg. 2021 Jul 9. doi: 10.1007/s13760-021-01743-w. Epub ahead of print. PMID: 34241798.
5. Gok-Dursun E, Gultekin-Zaim OB, Tan E, Unal-Cevik I. Cognitive impairment and affective disorder: A rare presentation of cerebellar stroke. Clin Neurol Neurosurg. 2021 Jul;206:106690. doi: 10.1016/j.clineuro.2021.106690. Epub 2021 May 17. PMID: 34022689.
6. Vural A, Şimşir G, Tekgül Ş, Koçoğlu C, Akçimen F, Kartal E, Şen NE, Lahut S, Ömür Ö, Saner N, Gül T, Bayraktar E, Palvadeau R, Tunca C, Pirkevi Çetinkaya C, Gündoğdu Eken A, Şahbaz I, Kovancılar Koç M, Öztop Çakmak Ö, Hanağası H, Bilgiçb B, Eraksoy M, Gündüz A, Apaydın H, Kızıltan G, Özekmekçi S, Siva A, Altıntaş A, Kaya Güleç ZE, Parman Y, Oflazer P, Deymeer F, Durmuş H, Şahin E, Çakar A, Tüfekçioğlu Z, Tektürk P, Çorbalı MO, Tireli H, Akdal G, Yiş U, Hız S, Şengün İ, Bora E, Serdaroğlu G, Erer Özbek S, Ağan K, İnce Günal D, Us Ö, Kurt SG, Aksoy D, Bora Tokçaer A, Elmas M, Gültekin M, Kumandaş S, Acer H, Kaya Özçora GD, Yayla V, Soysal A, Genç G, Güllüoğlu H, Kotan D, Özözen Ayas Z, Şahin HA, Tan E, Topçu M, Topçuoğlu ES, Akbostancı C, Koç F, Ertan S, Elibol B, Başak AN. The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice. Mov Disord. 2021 Jul;36(7):1676-1688. doi: 10.1002/mds.28518. Epub 2021 Feb 24. PMID: 33624863.
7. Diker S, Gelener P, Teralı K, Ergoren MC, Tunca C, Başak AN, Tan E. A combined clinical and computational approach to understand the SOD1^A4T-mediated pathogenesis of rapidly progressive familial amyotrophic lateral sclerosis. Acta Neurol Belg. 2021 Jan 9. doi: 10.1007/s13760-020-01588-9. Epub ahead of print. PMID: 33420941.
8. Pekgül F, Eroğlu-Ertuğrul NG, Bekircan-Kurt CE, Erdem-Ozdamar S, Çetinkaya A, Tan E, Konuşkan B, Karaağaoğlu E, Topçu M, Akarsu NA, Oguz KK, Anlar B, Özkara HA. Comprehensive clinical, biochemical, radiological and genetic analysis of 28 Turkish cases with suspected metachromatic leukodystrophy and their relatives. Mol Genet Metab Rep. 2020 Dec 11;25:100688. doi: 10.1016/j.ymgmr.2020.100688. PMID: 33335837; PMCID: PMC7734308.
9. Koc G, Odabasi Z, Tan E. Myasthenic Syndrome Caused by Hydroxychloroquine Used for COVID-19 Prophylaxis. J Clin Neuromuscul Dis. 2020 Sep;22(1):60-62. doi: 10.1097/CND.0000000000000316. PMID: 32833728.
10. Tunca C, Şeker T, Akçimen F, Coşkun C, Bayraktar E, Palvadeau R, Zor S, Koçoğlu C, Kartal E, Şen NE, Hamzeiy H, Özoğuz Erimiş A, Norman U, Karakahya O, Olgun G, Akgün T, Durmuş H, Şahin E, Çakar A, Başar Gürsoy E, Babacan Yıldız G, İşak B, Uluç K, Hanağası H, Bilgiç B, Turgut N, Aysal F, Ertaş M, Boz C, Kotan D, İdrisoğlu H, Soysal A, Uzun Adatepe N, Akalın MA, Koç F, Tan E, Oflazer P, Deymeer F, Taştan Ö, Çiçek AE, Kavak E, Parman Y, Başak AN. Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database. Hum Mutat. 2020 Aug;41(8):e7-e45. doi: 10.1002/humu.24055. Epub 2020 Jun 24. PMID: 32579787.
11. Kurt E, Bekircan-Kurt CE, Konuşkan B, Erkent İ, Tan E, Anlar B. Two sisters with anti-MuSK-positive myasthenia gravis. Clin Neurol Neurosurg. 2019 Jul;182:17-18. doi: 10.1016/j.clineuro.2019.04.011. Epub 2019 Apr 21. PMID: 31054424.
12. Balci-Hayta B, Bekircan-Kurt CE, Aksu E, Dayangac-Erden D, Tan E, Erdem- Ozdamar S. Establishment of primary myoblast cell cultures from cryopreserved skeletal muscle biopsies to serve as a tool in related research & development studies. J Neurol Sci. 2018 Oct 15;393:100-104. doi: 10.1016/j.jns.2018.08.018. Epub 2018 Aug 18. PMID: 30153568.
13. Güneş HN, Bekircan-Kurt CE, Tan E, Erdem-Özdamar S. The histopathological evaluation of small fiber neuropathy in patients with vitamin B12 deficiency. Acta Neurol Belg. 2018 Sep;118(3):405-410. doi: 10.1007/s13760-017-0847-y. Epub 2017 Oct 19. PMID: 29052170.
14. Kiliç AK, Kaymakamzade B, Saka E, Tan E. The Sole Initial Imaging Finding in Creutzfeldt-Jacob Disease: Focal FDG-PET Hypometabolism. Noro Psikiyatr Ars. 2018 Jul 4;56(3):226-228. doi: 10.5152/npa.2017.19471. PMID: 31523152; PMCID: PMC6732803.
15. Dericioglu N, Gocmen R, Tan E. Paraneoplastic striatal encephalitis and myelitis associated with anti-CV2/CRMP-5 antibodies in a patient with small cell lung cancer. Clin Neurol Neurosurg. 2018 Jul;170:117-119. doi: 10.1016/j.clineuro.2018.05.010. Epub 2018 May 16. PMID: 29777943.
16. Tunca C, Akçimen F, Coşkun C, Gündoğdu-Eken A, Kocoglu C, Çevik B, Bekircan-Kurt CE, Tan E, Başak AN. ERLIN1 mutations cause teenage-onset slowly progressive ALS in a large Turkish pedigree. Eur J Hum Genet. 2018 May;26(5):745-748. doi: 10.1038/s41431-018-0107-5. Epub 2018 Feb 16. PMID: 29453415; PMCID: PMC5945623.
17. 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 Disord. 2017 Nov;27(11):997-1008. doi: 10.1016/j.nmd.2017.06.004. Epub 2017 Jun 16. PMID: 28967462; PMCID: PMC5698850.
18. Bekircan-Kurt CE, Güneş HN, Yildiz FG, Saka E, Tan E, Erdem-Özdamar S. New mutations and genotype-phenotype correlation in late-onset Pompe patients. Acta Neurol Belg. 2017 Mar;117(1):269-275. doi: 10.1007/s13760-016-0738-7. Epub 2016 Dec 28. PMID: 28032299.
19. Yasrebi S, Yaman A, Tan E, Özçakar L. Multifocal Acquired Demyelinating Sensory and Motor Neuropathy: Unexpected Diagnosis After Ultrasound Imaging for a Humeral Fracture. Am J Phys Med Rehabil. 2016 Dec;95(12):e206. doi: 10.1097/PHM.0000000000000500. PMID: 27088473.
20. Vural A, Göçmen R, Kurne AT, Oğuz KK, Temuçin ÇM, Tan E, Karabudak R, Meinl E, Erdem Özdamar S. Fulminant Central Plus Peripheral Nervous System Demyelination without Antibodies to Neurofascin. Can J Neurol Sci. 2016 Jan;43(1):149-56. doi: 10.1017/cjn.2015.238. Epub 2015 Aug 14. PMID: 26271726.
21. Bekircan-Kurt CE, Tan E, Erdem Özdamar S. The Activation of RAGE and NF-KB in Nerve Biopsies of Patients with Axonal and Vasculitic Neuropathy. Noro Psikiyatr Ars. 2015 Sep;52(3):279-282. doi: 10.5152/npa.2015.8801. Epub 2015 Jul 7. PMID: 28360724; PMCID: PMC5353062.
22. Bekircan-Kurt CE, Güneş N, Yılmaz A, Erdem-Özdamar S, Tan E. Three Turkish families with different transthyretin mutations. Neuromuscul Disord. 2015 Sep;25(9):686-92. doi: 10.1016/j.nmd.2015.05.010. Epub 2015 May 27. PMID: 26115788.
23. Kilinç M, Yildirim SA, Tan E. The effects of electrical stimulation and exercise therapy in patients with limb girdle muscular dystrophy. A controlled clinical trial. Neurosciences (Riyadh). 2015 Jul;20(3):259-66. doi: 10.17712/nsj.2015.3.201501097. PMID: 26166595; PMCID: PMC4710330.
24. Kilic AK, Kurne AT, Saatci I, Tan E. A rare cause of radiculomyelitis: dural arteriovenous fistula. JAMA Neurol. 2015 Feb;72(2):217-8. doi: 10.1001/jamaneurol.2014.2077. PMID: 25436872.
25. Kara M, Özçakar L, Tan E, Akıncı A. Ultrasonographic imaging of the sciatic nerve in a patient with knife injury. Muscle Nerve. 2015 Feb;51(2):303-4. doi: 10.1002/mus.24514. Epub 2014 Dec 23. PMID: 25388275.
26. 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 Jan 10. pii: S0197-4580(14)00849-5. doi: 10.1016/j.neurobiolaging.2014.12.032
27. Bekircan-Kurt CE, Tuncer Kurne A, Erdem-Ozdamar S, Kalyoncu U, Karabudak R, Tan E. The course of myasthenia gravis with systemic lupus erythematosus. Eur Neurol. 2014;72(5-6):326-9. doi: 10.1159/000365568. Epub 2014 Oct 14.
28. Kılınç M, Livanelioglu A, Yıldırım SA, Tan E. Effects of transcutaneous electrical nerve stimulation in patients with peripheral and central neuropathic pain. J Rehabil Med. 2014 Feb 18. doi: 10.2340/16501977-1271
29. 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: 10.1371/journal.pone.0072381
30. Cetin N, Balci-Hayta B, Gundesli H, Korkusuz P, Purali N, Talim B, Tan E, Selcen D, Erdem- Ozdamar S, Dincer P. A novel desmin mutation leading to autosomal recessive limb-girdle muscular dystrophy: distinct histopathological outcomes compared with desminopathies. J Med Genet. 2013 Jul;50(7):437-43.
31. Kaymakamzade B, Kansu T, Tan E, Dericioğlu N. LGI1 related limbic encephalitis and response to immunosuppressive therapy. J Neurol. 2011 Nov;258(11):2075-7.
32. Erbas T, Ertas M, Yucel A, Keskinaslan A, Senocak M; TURNEP Study Group.Prevalence of peripheral neuropathy and painful peripheral neuropathy in Turkish diabetic patients. J Clin Neurophysiol. 2011 Feb;28(1):51-5.
33. Bedlack RS, Genge A, Amato AA, Shaibani A, Jackson CE, Kissel JT, Wall C, King WM, Cupler E, Lou JS, Ensrud E, Tan E, Goldstein JM, Katz J, Dimachkie MM, Barohn RJ, Mozaffar T. Correspondence regarding: TDP-43 proteinopathy and motor neuron disease in chronic traumatic encephalopathy. J.Neuropathol Exp Neurol 2010:69;918-29. J Neuropathol Exp Neurol. 2011 Jan;70(1):96-7
34. Sommer CL, Brandner S, Dyck PJ, Harati Y, LaCroix C, Lammens M, Magy L, Mellgren SI, Morbin M, Navarro C, Powell HC, Schenone AE, Tan E, Urtizberea A, Weis J; Peripheral Nerve Society Guideline on processing and evaluation of nerve biopsies. Peripheral Nerve Society. J Peripher Nerv Syst. 2010 Sep;15(3):164-75.
35. Firat F, Ozen G, Yildiz G, Sağlam A, Onder S, Tan E, Ozdemir E. Late relapse of acute myeloblastic leukemia as myeloid sarcoma causing radiculopathy. Leuk Res. 2010 Dec;34(12):e348-50
36. Unal-Cevik I, Onal MZ, Odabasi Z, Tan E. IVIG- responsive multiple cranial neuropathy: a pharyngo-facial variant of Guillain-Barre syndrome. Acta Neurol BeIg. 2009 Dec;109(4):317-21.
37. Vargel I, Demirci M, Erdem S, Firat P, Sürücü HS, Tan E, Keçik A. A comparison of various_vascularization-perfusion venous nerve grafts with conventional nerve grafts in rats.
38. Unal-Cevik I, Onal MZ, Odabasi Z,Tan E. IVIG-Responsive multiple cranial neuropathy: a pharyngo-facial variant of Guillaine-Barre syndrome. Acta Neurol Belg. 2009;109:317-21.
39. Vargel I, Demirci M, Erdem S, Fırat P, Sürücü HS, Tan E, Keçik A.  A comparison of various vascularization-perfusion venous nerve grafts with conventional nerve grafts in rats. J Reconstr Microsurg 2009;25:425-437.
40. Aksu S, Tan E, Meriç A, Atay S, Kilinç M. Effects of electrical stimülatiom om muscle strength and functional activities on patients with limb girdle muscular dystrophy:A pilot study. Neurorehabilitation & Neural Repair 2008;22:587.
41. Uluc K, Temucin CM, Ozdamar SE, Demirci M, Tan E. Near-nerve needle sensory and medial plantar nerve conduction studies in patients with small-fiber sensory neuropathy. Eur J Neurol 2008;15:928-932. 
42. Sommer C, Brandner S, Dyck PJ, Magy L, Mellgren SI, Morbin M, Schenone A, Tan E, Weis J. 147th ENMC International Workshop: Guideline on processing and evaluation of sural nerve biopsies, 15-17 December 2006, The Netherlands. Neuromuscular Disorder. 2008 ; 18:90-96.
43. Sommer C, Geis C, Haanpaa M, Serra J, Tan E, Cruccu G. Questionnaire on neuropathic pain: a European neurologist survey. Neurol Sci 2007;28:136-141. 
44. Atay S, Kılınc M, Aksu-Yıldırım S, Erdem-Özdamar S, Tan E. Falls in muscle disorders. Neuromuscular Disorders 2006;16:S175-S176.
45. Kocaefe YÇ, Erdem-Ozdamar Si Sivri HS, Cuşkun T, Tan E, Ozguc M. Comprehensive analysis reveals distinct mtDMA features in mitochondrial neurogastrointestinal encephalomyopathy syndrome (MNGIE). Neuromuscular Disorders 2006:16:S57-58.
46. Balcı B, Aurino S, Haliloğlu G, Talim B, Erdem S, Akçoren Z, Tan E, Caglar M, Richard I, Nigro V, Topaloğlu H, Dincer P. Calpain-3 mutations in Turkey. Eur J Pediatr 2006;13:1-6
47. Kursun O,  Arsava EM, Oğuz KK, Tan E, Kansu T. SUNCT associated with Devic’s syndrome. Cephalalgia 2005;26:221-224.
48. Demir E, Bomont P, Erdem S, Cavalier L, Demirci M, Kose G, Muftuoglu S, Cakar AN, Tan E, Aysun S, Topcu M, Guicheney P, Koenig M, Topaloglu H. Giant axonal neuropathy: clinical and genetic study in six cases.  J Neurol Neurosurg Psychiatry. 2005;76:825-32.
49. Gurer G, Erdem S, Kocaefe C, Ozguc M, Tan E. Expression of matrix metalloproteinases in vasculitic neuropathy. Rheumatol Int. 2004;24:255-9.
50. Uluc K, Arsava EM, Ozkan B, Cila A, Zorlu F, Tan E. Primary leptomeningeal sarcomatosis; a pathology proven case with challenging MRI and clinical findings. J Neurooncol 2004;66:307-12.
51. Aksu S, Karakaya İ, Karakaya NG, Kılınç M, Tan E.  Combined physiotherapy program results on musculoskeletal pain in neuromuscular diseases. Pain Clinic 2003;15:287-291.
52. Erdem S, Ammar N, Nelis E, Demirci M, Demir E, Ceuterick C, Timmermann V, deJonghe P, Topaloğlu H, Tan E. Clinical and pathological features of genetically defined autosomal recessive hereditary sensory motor neuropathy in Turkish families. Neurology 2003; (suppl 1) 60.
53. Demir E, Irobi J, Erdem S, Demirci M, Tan E, Timmermann V, De Jonghe P, Topaloğlu H. Andermann syndrome in a Turkish patient. J Child Neurol 2003;18:76-79. 
54. Oguz B, Oguz KK, Cila A, Tan E. Diffuse spinal and intercostal nerve involvement in chronic inflammatory demyelinating polyradiculo-neuropathy: MRI findings.  Eur Radiol. 2003 Dec;13 Suppl 4:L230-4
55. Kurne A, Bakar B, Arsava EM, Tan E. Pregnancy associated quadriparesis in a patient with Von-Hippel Lindau disease. J Neurol. 2003;250:234-5.
56. Kocaefe Ç, Erdem S, Özgüç M, Tan E.   Four Novel Thymıdıne Phosphorylase Gene Mutatıons In Mıtochondrıal Neurogastroıntestınal Encephalomyopathy Syndrome (Mngıe) Patıents. Eur J Human Genet  2003;11:102-104.
57. Senderek J, Bergmann C, Stendel C, Kirfel J, Verpoorten N, De Jonghe P, Timmerman V, Chrast R, H G Verheijen M, Lemke G, Battaloğlu E, Parman Y, Erdem S, Tan E, Topaloğlu H, Hahn A, Müller-Felber W, Rizzuto N, Fabrizi GM, Stuhrmann M, Rudnik-Schoneborn S, Zuchner S, Michael Schroder J, Buchheim E, Straub V, Klepper J, Huehne K, Rautenstrauss B, Buttner R, Nelis E, Zerres K. Mutations in a gene encoding a novel SH3/TPR domain protein cause autosomal recessive Charcot-Marie-Tooth type 4C neuropathy. Am J Hum Genet 2003:73;1106-1119.
58. Aksu S, Kilinç M, Tan E. The effectiveness of home exercise program in myopathic patients. J Neurol 2002;249(Suppl 1) 89
59. E. Nelis, S. Erdem, P.Y.K. Van den Bergh, M.-C. Belpaire-Dethiou,  C. Ceuterick, V. Van Gerwen, A. Cuesta, L. Pedrola, F. Palau, A.A.W.M. Gabreels-Festen, C. Verellen, E. Tan, M. Demirci, C. Van Broeckhoven,  P. De Jonghe, H. Topaloglu,  and V. Timmerman Mutations in GDAP1: Autosomal recessive CMT with demyelination and axonopathy . Neurology 2002; 59: 1865-1872.
60. Anlar B, Deda G, Erdem S,  Tan E, Korkusuz P. Chronic acquired polyneuropathy in infancy . J Neurol 2002; 249: 1469-1471. 
61. Nelis E, Erdem S, Tan E, Löfgren A, Ceuterick C, De Jonghe P, Van Broeckhoven C, Timmerman V and Topaloglu H.  A novel homozygous missense mutation in the myotubularin-related protein 2 gene associated with recessive Charcot-Marie-Tooth disease with irregularly folded myelin sheaths, Neuromusc Disord 2002; 12: 869-873. 
62. Uluç K, Arsava M, Erdem S, Tan E. Proximal myopathy with diffuse white matter involvement in myotonic dystrophy type I. J Neurol 2002; 249: 629-630. 
63. Tanyel FC, Erdem S, Büyükpamukçu N, Tan E. Smooth muscle within incomplete obliterations of processus vaginalis lacks apoptotic nuclei. Urologia Internationalis 2002;69:42-5.
64. Arslan S, Erdem S, Sivri A, Hascelik Z, Tan E. Exercise-induced apoptosis of rat skeletal muscle and the effect of meloxicam. Rheumatol Int. 2002;21:133-6.
65. Soykan I, Cetinkaya H, Erdem S, Tan E, Aydin F, Bahar K, Ozden A. Mitochondrial neurogastrointestinal encephalomyopathy: diagnostic features of two patients.  J Clin Gastroenterol. 2002;34:446-8. 
66. Serdaroglu A, Gucuyener K, Erdem S, Kose G, Tan E, Okuyaz C. Role of apoptosis in Duchenne's muscular dystrophy.  J Child Neurol. 2002;17:66-8.  
67. Üner AH, Abalı H, Engin H, Akyol A, ruacan Ş, Tan E, Güllü I, Altundağ K, Güler N. Myasthenia Gravis and Lymphoblastic Lymphoma involving the thymus: A rare association. Leukemia and Lymphoma 2001;42:527-531.
68. Gürer G, Şahin G, Cekirge S, Tan E, Sarıbas O:  Acute bilateral cerebellar infarction in the territory of the medial branches of posterior inferior cerebellar arteries.  Clin Neurol Neurosurg. 2001 ;103:194-6.
69. Erdem S,  Demirci M, Tan E. Focal myopathy mimicking posterior interosseous nerve syndrome. Muscle Nerve  2001; 24 :969-972.
70. Tanyel FC, Erdem S, Büyükpamukçu N, Tan E. Cremaster muscle is not sexually dimorphic, but those from boys with undescended testis reflects alterations related to the autonomic innervation. J Ped Surg. 2001;36:877-880.
71. Arslan Ş, Erdem S,  Kılınç K, Sivri A, Tan E. Free radical changes in rat muscle tissue after  exercise. Rheumatology Int. 2001;20:109-112.
72. Tanyel FC, Erdem S,  Altunay H, Ergün L, Özcan Z, Alanay B, Buyukpamukcu N, Tan E. Distribution and morphometry of fiber types in cremaster muscles of with inguinal hernia or undescended testis. Pathol Res Pract 2000; 196:613-617.
73. Tanyel FC, Erdem S,  Tan E, Buyukpamukcu N. Among cremaster muscles those obtained from boys with undescended testis reveal significant neurologic alterations. BJU Int 2000;85:116-119. 
74. Dincer P, Akcoren Z, Demir E, Richard I, Sancak O, Kale G, Ozme E,  Karaduman  A, Tan E, Urtizberea JA, Beckmann JS, Topaloglu H.   A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families.  J Med Genet. 2000; 37:361-7.
75. Arslan Ş, Erdem S, Kılınç K, Sivri A, Tan E. Exercise induced changes in hypoxantine levels in rat muscle tissue. Neuromuscular Disorders 2000;10:372-373.
76. Arslan Ş, Erdem S, Sivri A, Tan E. The role of meloxicam on exercise induced apoptosis. Neuromuscular Disorders 2000;10:372.
77. Demir E, Erdem S, demirci M, Tan E, Topaloğlu H. Autosomal dominant hereditary motor neuropathy presenting with arthrogyroposis multiplex in the neonate. Neuromuscular Disorders 2000;10:364.
78. Ohno K, Engel AG, Brengman JM, Xin-Ming Shen, Heidenrich FR, Vincent A, Milone M, Tan E, Anlar B, Walsh P, Nakano S, Akiguchi I: The spectrum of mutations causing endplate acetylcholinesterase deficiency. Ann Neurol 2000;47:162-170.
79. Tanyel FC, Erdem S, Büyükpamukçu N, Tan E:  Among cremaster     muscles those obtained from boys with undescended testis reveal significant neurologic alterations. Br J Urol  2000;85:116-119.
80. Topaloğlu H, Dinçer P, Urtizberea JA, Akçaören Z, Richard I, Kale G, Özme Ş, Karaduman A, Demir E, Tan E, Kaplan JC, Beckmann JS. Autosomal recessive limb girdle dystrophies in Turkey: experience from 58 families. Neuromuscular Disorders 1999;9;497. 
81. Arslan S, Erdem S, Kılınc K, Sivri A, Tan E: Free radical changes in rat muscle tissue after exercise. Neuromuscular Disorders 1999;9; 495.
82. Arslan S, Erdem S, Kılınç K, Sivri A, Tan E. Exercise induced changes in hypoxanthine levels in rat muscle tissue. Neuromuscular Disorders 2000;10:372.
83. Cengiz B, Sucak G, Kuruoğlu R, Tan E. Hypereosinophilic syndrome: progression of peripheral neuropathy despite controlled eosinophil levels. Acta  Neurol Belg 1999;99:133-137.
84. Demir E, Demirci M, erdem S, Tan E, Goebel HH, Topaloğlu H.  Neuroaxonal dystrophy or giant axonal neuropathy:experience in a sibship of 4. Neuromuscular Disorders 1999;9;493.
85. Gurer G, Sahin G, Erdem S, Tan E: Inclusion body myositis with granulomatous myopathy. Neuromuscular Disorders 1999;9;480. 
86. Tan E: Peripheral Neuropathy in Behcet’s disease. Neuromuscular Disorders 1999;9;483.
87. Erdem S, Tan E. Giant Cell Myositis: A Case with myasthenia gravis, Thymoma, autoimmune thyroiditis and autoimmune diabetes mellitus. Neuromuscular Disorders 1999;9;481-482.
88. Aksu S, Karaduman A, Tan E. The effects of exercise in ALS. Neuromuscular Disorders 1999;9;495.
89. Tan E, Erdem S, Topaloğlu H, Kuruoğlu R. Cramp-Myalgia-Fasciculation Syndrome: Evidence of demyelination of the peripheral nerve.  Neuromuscular Disorders 1999;9; 491.
90. Serdaroglu A, Erdem S, Gucuyener K, Kose G, Tan E: Role of apoptosis in Duchenne muscular dystrophy. Neuromuscular Disorders 1999;9; 488. Kuruoglu R, Erdem S, Tan E: Chronic progressive monomelic sensory neuropathy of the right lower extremity. Neuromuscular Disorders 1999;9; 491.
91. Ünal I, Erdem S, Elibol B, Tan E. Rigid spine syndrome with fiber type disproportion. Muscle Nerve 1999;47;542-543.
92. Sipahi T, Okumuş N, Şahin F, Kuyucu N, Tan E, Gürer Y. Congenital insensitivity to pain with anhidrosis: report of a 68-day-old case. Eur J Pediatr 1999;158:268-269.
93. Bora AT, Cengiz B, Kuruoğlu R, Tan E: Nerve conduction studies with demyelinating features in peripheral neuropathy caused by solvent exposure. Electroenceph Clin Neurophysiol 1998;106:83. 
94. Tan J, Haydari D, Erdem S, Tan E. In vivo effects of sera from rheumatoid arthritis patients: Histological study on rat nerves. Muscle Nerve  1998; (suppl 7):S158.
95. Erdem S, Sarıbaş O, Tan E. Experimental peripheral neuropathy induced in adult rats by intraneurally injected neuro-Behçet serum. Neurology 1998;50:A145-146.
96. Dincer P, Leturcq F, Richard I, Piccolo F, Yalnızoglu D, Toma C, Akçören Z, Broux O, Deburgrave N, Brenguier L, Roudaut C, Urtizberea A, Jung D, Tan E, Jeanpierre M, Campbell KP, Kaplan JC, Beckmann JS, Topaloglu H. A Biochemical, Genetic, and Clinical Survey of Autosomal Recessive Limb Girdle Muscular Dystrophies in Turkey. Ann Neurol 1997,42:222-229.
97. Tan E, Topaloğlu H, Sewry C, Zorlu Y, Naom I, Erdem S, Mariella D’Alessandro, Muntoni F, Dubowitz V: Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency. Neuromuscular Disorders 1997;7:85-89.
98. Seyrantepe V, Saygı S, Tan E, Özgüç M, Topaloğlu H: A patient with MELAS and the mitochondrial tRNA 3243 mutation. Develop Med  1995;37(suppl    72):114. 
99. Topaloğlu H, Tan E,  Dinçer  P,  Erdem  S,  Akçören  Z.  Good clinical  observation  is  essential  before  molecular  studies. Lancet 1995;346:1490.
100. Tan E, Lynn J, Amato AA, Kissel  J,  Rammohan  K,  Sahenk  Z, Warmolts JR, Jackson CE, Barohn RJ, Mendell  JR. Immuno-suppressive treatment of motor neuron syndromes  (in  reply  to  Pestronk) (letter)  Arch Neurol 1995;52: 230-231.
101. Erdem E, Kıratlı H, Erbaş T, Varlı K, Eldem B, Akalın S,  Tan E, Topaloğlu H, Gedikoğlu G. Cerebellar  ataxia  associated  with hypogonadotropic hypogonadism  and  chorioretinopathy:  a  poorly recognized association. Clin Neurol Neurosurg 1994;96:86-91.
102. Tan E, Lynn J, Amato AA, Kissel  J,  Rammohan  K,  Sahenk  Z, Warmolts JR, Jackson CE, Barohn RJ, Mendell JR. Immuno-suppressive treatment of motor neuron syndromes: Attempts  to  distinguish  a treatable disorder. Arch Neurol 1994;51:194-200.
103. Demirci M, Tan E, Elibol B, Gedikoğlu G, Sarıbaş  O.  Hepatic myelopathy Neurology 1993;43:629.
104. Tan J, Akın S, Beyazova M, Sepici V, Tan E. Sympathetic  skin response and R-R interval variation in rheumatoid arthritis:  Two simple tests for the assessment of autonomic function. Am  J  Phys Med Rehab 1993;72:196-203.
105. Tan E, Lynn J, Amato AA, Kissel  J,  Rammohan  K,  Sahenk  Z, Warmolts JR, Jackson CE, Barohn RJ, Mendell   JR. Immuno-suppressive treatment of motor neuron syndromes: Attempts  to  distinguish  a treatable disorder. Neurology 1993;43:416-417.
106. Sahenk Z, Tan E, Kissel JT, Lynn J, Barohn  RJ,  Mendell JR.Immuno-suppressive treatment  in  motor  neuron  syndromes:  Sural nerve biopsy findings. Neurology 1993;43:258.
107. Erdem E, Namer IJ, Sarıbaş O, Aras T, Tan E, Bekdik C, Zileli T.  Cerebral  fat  embolism   studied   with   MRI   and   SPECT. Neuroradiology 1993;35:199-201.
108. Tan E,  Hajinazarian  MO,  Bay  W,  Mendell  J.  Acute  renal failure  resulting from intravenous  immunoglobulin therapy . Arch Neurol 1993;50:137-139.
109. Demirci M, Tan E, Elibol B, Gedikoğlu G, Saribaş  O.  Spastic paraparesis associated with portal-systemic venous  shunting  due to congenital hepatic fibrosis. Neurology 1992;42:983-985.
110. Sahenk Z, Barohn RJ, Kissel J, Tan E,  Mendell  J.  Inclusion body  "myositis":  Evidence  against   a   primary   inflammatory myopathy and a possible  pathogenic  role  for  an  amyloidogenic protein. Neurology 1992;42(suppl 3):337 .
111. Tan E, Hajinazarian MO, Bay W, Mendell JR: Acute renal failure: Serious complication of intravenous immunoglobulin G (IVIG) treatment. Neurology 1992;42:335
112. Tan  E,  Rammohan  KW,  Kissel  JT,  Sahenk  Z,  Mendell  JR. Antiganglioside   antibodies:Control    population    establishes specificity for recognition of motor neuron variants. Ann  Neurol 1991;30:260-261.
113. Sahenk Z, Mendell JR, Lee D, Tan E, Boesel CP.  Evidence  for impaired   axonal   stimulus   in   congenital   hypomyelinating/ amyelinating neuropathies. Neurology 1991;41(Suppl 1):340.
114. Tan E, Namer IJ, Ciğer A, Zileli T, Küçükali T. The prognosis of subacute sclerosing panencephalitis in  adults:  Report  of  8 cases  and  review  of  the  literature.  Clin  Neurol  Neurosurg 1991;93:205-209.
115. Tan E, Kansu T, Kırkalı P, Zileli T. Lid lag and the Guillain-­Barré syndrome. J Clin Neuroophthalmol 1990;10:121-123.
116. Tan E, Kansu T, Zileli T. Severe  ptosis   without  ophthalmoplegia  due  to  porphyric  neuropathy.   Clin  Neurol  Neurosurg 1990;92:287-288. 
117.  Tan  E,  Kansu  T.  Bilateral   horizontal  gaze   palsy   in multiple sclerosis.    J Clin Neuroophthalmol 1990;10:124-127.
118. Dalkara T, Tan E, Erdemli G, Onur R, Zileli T: NMDA Receptor antagonist MK-801 reduces ischemic neuronal dysfunction in rats hippocampus; An Electrophysiological study. Eur J Pharmacol 1990;183:949.
119. Erdemli G, Dalkara T, Tan E, Onur  R.  Glycine,  alanine  and serine potentiate glutamate neurotoxicity  in  cerebral  ischemia via NMDA receptors. Eur J Pharmacol 1990;183:476.
120. Barış YI, Tan E, Kalyoncu F, Artvinli M,  Şahin  AA.  Digital clubbing in hashish addicts. Chest 1990;98:1545-1546.
121. Saygı S, Tan E, Kansu T, Önol B, Sungur A, Erbengi A,  Zileli T. Bilateral internuclear ophthalmoplegia as an initial  sign  of metastatic breast carcinoma. Neuro-ophthalmol 1990;10:181-185. 
122. Tan E, Kansu T, Saygı S, Zileli T. Apraxia of eyelid  closure and phonation. A case with SPECT findings. Neuro-ophthalmol 1990;10:205-207.
123. Tan E,  Kansu  T,  Saygı  S,  Zileli  T.  Alternating  Horner Syndrome: A case report  and  review  of  the  literature.  Neuro-ophthalmol 1990;10:19-22. 
124. Tan E, Namer IJ, Ciğer A, Zileli T. Playing  on  an  imaginary giant   backgammon board:   A    peculiar    ictal    behavior.    Clin Electroencephalog 1990;21:126-128.
125.  TanE, Ciğer A, Zileli T. Whistling Epilepsy:  A case  report. Clin Electroencephalog  1990;21:110-111. 
126. Tan E, Can U, Kansu T, Barış YI, Zileli T. Parinaud   syndrome due to solitary pineal metastasis. Eur Neurol 1990;30:200-202. 
127. Namer  IJ,  Tan  E,  Akalın  E,   Selekler   K,   Zileli   T. Un cas d’hémiballisme au cours d’une méningite a cryptocoque.  Rev Neurol 1990;146:153-154.
128. Dalkara T, Tan E,  Erdemli  G,  Onur  R,  Zileli  T.  Electrophysiological evidence for activation of NMDA receptors  and  its antagonism  by   MK-801   in   cerebral   ischemia.   Brain   Res 1990:532;101-106.
129. Demirci M, Tan E, Durguner M, Zileli T,  Eryılmaz  M.   Spinal brucellosis.  A  case  with  "Cauliflower"  appearence   in   CT. Neuroradiol 1989;31:282-283.
130. Tan E, Kürkçüoğlu N, Atalağ M, Gököz A, Zileli T.  Progressive hemifacial  atrophy  with  localized  scleroderma.   Eur   Neurol 1989;29:15-17. 
131. Namer IJ,  Tan E,  Ciğer  A,  Zileli  T.  Crises  épileptiques partielles   complexes  premier  symptome   d'une   panencéphalite subaigue sclérosante. Rev Neurol 1986;142:921-925.