• İstanbul Üniversitesi Tıp Fakültesi Çocuk Nöroloji Anabilim Dalı Kat 3 ve 5 PK 34293 Çapa-İstanbul
Soru Sor

Makaleler

  • Makaleler
6890 Okunma
  1.  Yalçın AD, M. Özgüzel, Z. Yapici, S. Öztürk ve H. Forta, “Kortikosteroidtherapie beim Landau – Kleffner Syndrom”, Monatsschr Kinderheilkd, 143, 39-42 (1995).
  2. Yalcin AD, Z. Yapici ve H. Forta, “Pedincular hallucinosis: three cases with thalamic involvement”, European Journal of Neurology, 3 (5), 438-440 (1996).
  3. Yapici Z, M. Eraksoy, “Bilateral Demyelinating Tumefactive Lesions in Three Children Presented with Hemiparesis”, Journal of Child Neurology, 17, 655-660 (2002).
  4. Eraksoy M, Kurtuncu M, Akman-Demir G, Kılınç M, Gedizoglu M, Mirza M, Anlar B, Kutlu C, Demirkıran M, İdrisoğlu H, Compston A, Sawer S, Study Group (TMSGSG). A whole genome screen for linkage in Turkish multiple sclerosis. J Neuroimmunology 143; 17-24 (2003).
  5. Yapici Z., “A difficult case (not just a child with simple learning disability, beware the opercular  syndrome),”  Practical Neurology, 4, 56-57 (2004).
  6. Yapici Z, M. Eraksoy, “Non-progressive congenital ataxia with cerebellar hypoplasia in three families”, Acta Paediatrica, 94 (2), 248-253 (2005).
  7. Yapici Z, A. Dinçer ve M. Eraksoy, “Proton spectroscopic findings in children with epilepsy owing to tuberous sclerosis”,  Journal of Child Neurology, 20, 517-522 (2005).
  8. İmer M, B. Özeren, S. Karadereler, Z. Yapıcı, B. Omay, H. Hanağası, M. Eraksoy “Destructive Stereotactic Surgery for Treatment of Dystonia”, Surgical Neurology, 64 (S2), S2:89-S295 (2005).
  9. Saruhan-Direskeneli G, C. Gürses, V. Demirbilek, S. Yentür, G. Yılmaz, A.E. Önal, Z. Yapici C. Yalçınkaya, Ö. Çokar, G. Akman-Demir, A. Gökyiğit “Elevated interleukin-12 and CXCL10 in subacute sclerosing panencephalitis”, Cytokine, 32, 104-110 (2005).
  10. Yentür S, C. Gürses, V. Demirbilek, G. Yılmaz, A.E. Önal, Z. Yapici, C. Yalçınkaya, Ö. Çokar, A. Gökyiğit, G. Saruhan-Direskeneli “Alterations in cell-mediated immune response in subacute sclerosing panencephalitis”,  Journal of Neuroimmunology, 170, 179-185 (2005).
  11. Onal AE, C. Gurses, G. Saruhan-Direskeneli, G. Yılmaz, V. Demirbilek, SP. Yentur, S. Ozel, Z. Yapici, Y. Tumerdem, A. Gokyigit “Subacute sclerosing panencephalitis surveillance study in İstanbul”, Brain and Development, 28, 183-189 (2006).
  12. Yapici Z, “Subacute Sclerosing Panencephalitis Presenting with Balint Syndrome”, Brain and Development, 28, 398-400 (2006).  
  13. Baş F, F. Darendeliler, Z. Yapici, S. Gökalp, R. Budak, N. Saka, H. Günöz “Worster-Drought Syndrome (Congenital Bilateral Perisylvian Syndrome) with Empty Sella and Panhypopituitarism:A case report”, Journal of Pediatric Endocrinology & Metabolism, 19, 535-540 (2006).
  14. Yapici Z,  N. Dörtcan, B. Baykan, F. Okan, A. Dinçer, C. Baykal, M. Eraksoy, “Neurological Aspects of Tuberous Sclerosis in Relation to MRI/MR-Spectroscopy Findings in Children”, Neurol Res, 29: 449-54 (2007).
  15. Okan F,  A. Coban , Z. Ince, Z. Yapici, G. Can, “Analgesia in preterm newborns: the comparative effects of sucrose and glucose”, Eur J Pediatr, 166: 1017-24 (2007).
  16. Yapici Z, E. Tüzün, V. Altunayoğlu, A. Erdoğan, M. Eraksoy, “High interleukin-10 production is associated with anti-acetylcholine receptor antibody production and treatment response in juvenile myasthenia gravis”, Int J Neurol Sci, 117: 1505-12 (2007).
  17. Yilmaz V, Demirbilek V, Gürses C, Yentür SP, Uysal S, Yapici Z, Yilmaz G, Muncey A, Cokar O, Onal E, Gökyiğit A, Saruhan-Direskeneli G, “Interleukin (IL)-12, IL-2, interferon-gamma gene polymorphisms in subacute sclerosing panencephalitis patients”, J Neurovirol, 13: 410-5 (2007).
  18. Okan F, Z. Yapici, A. Bulbul “Incontinentia pigmenti mimicking a herpes simplex virus infection in the newborn”, Childs Nerv Syst, 24: 149-151 (2008).
  19. Senbil N, Z. Yapici, Y Gurer  “Paroxysmal nonkinesigenic and hypnogenic dyskinesia associated with streptococcal infection”, Paediatr Int, 50, 255-6 (2008).
  20. Steenweg ME, GS Salomons, Z. Yapici, G Uziel, E. Scalais, DI Zafeiriou, ML Ruiz-Falco, V Mejaski-Bosnjak, P Augoustides-Savvopoulou, M Wajner, J Walter, NM Verhoeven-Duif, EA Struys, C Jakobs, MS van der Knaap “L-2-Hydroxyglutaric aciduria: pattern of MR imaging abnormalities in 56 patients”, Radiology,  251: 856-65 (2009).
  21. Yapici Z, G. Benbir, S. Saltik, L. He, GK Brown, RW Taylor, A Dincer, S Naidu, C Yalcinkaya, “Two cases with progressive cystic leukoencephalopathy”, Neuropediatrics, 40: 47-51 (2009).
  22. Dibbens LM, Mullen S, Helbig I, Mefford HC, Bayly MA, Bellows S, Leu C, Trucks H, Obermeier T, Wittig M, Franke A, Caglayan H, Yapici Z; EPICURE Consortium, Sander T, Eichler EE, Scheffer IE, Mulley JC, Berkovic SF, “Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance”, Hum Mol Genet, 18 (19): 3626-31 (2009).
  23. Steenweg ME, Jakobs C, Errami A, van Dooren SJ, Adeva Bartolomé MT, Aerssens P, Augoustides-Savvapoulou P, Baric I, Baumann M, Bonafé L, Chabrol B, Clarke JT, Clayton P, Coker M, Cooper S, Falik-Zaccai T, Gorman M, Hahn A, Hasanoglu A, King MD, de Klerk HB, Korman SH, Lee C, Meldgaard Lund A, Mejaški-Bošnjak V, Pascual-Castroviejo I, Raadhyaksha A, Rootwelt T, Roubertie A, Ruiz-Falco ML, Scalais E, Schimmel U, Seijo-Martinez M, Suri M, Sykut-Cegielska J, Trefz FK, Uziel G, Valayannopoulos V, Vianey-Saban C, Vlaho S, Vodopiutz J, Wajner M, Walter J, Walter-Derbort C, Yapici Z, Zafeiriou DI, Spreeuwenberg MD, Celli J, den Dunnen JT, van der Knaap MS, Salomons GS “An overview of L-2-hydroxyglutarate dehydrogenase gene (L2HGDH) variants: a genotype-phenotype study”, Hum Mutat, 31 (4): 380-90 (2010).
  24. Okan F, A. Ozdil, A. Bulbul, Z. Yapici, A. Nuhoglu. Analgesic effects of skin-to-skin contact and breastfeeding in procedural pain in healthy term neonates. Ann Trop Paediatr, 30 (2): 119-28 (2010).
  25. Alp R, Alp SI, Palanci Y, Sur H, Boru UT, Ozge A, Yapici Z. Use of the International Classification of Headache Disorders, Second Edition, criteria in the diagnosis of primary headache in schoolchildren: epidemiology study from eastern Turkey. Cephalalgia, 30 (7): 868-77 (2010).
  26. Akman-Demir G, Tüzün E, Waters P, Içöz S, Kürtüncü M, Jarius S, Yapıcı Z, Mutlu M, Yeşilot N, Vincent A, Eraksoy M. Prognostic implications of aquaporin-4 antibody status in neuromyelitis optica patients. J Neurol, 258 (3): 464-70, 2011.
  27. Yalçin O, Baykan B, Ağan K, Yapici Z, Yalçin D, Dizdarer G, Türkdoğan D, Ozkara C, Unalp A, Uludüz D, Gül G, Kuşcu D, Ayta S, Tutkavul K, Comu S, Tatli B, Meral C, Bebek N, Cağlayan SH. An association analysis at 2q36 reveals a new candidate susceptibility gene for juvenile absence epilepsy and/or absence seizures associated with generalized tonic-clonic seizures. Epilepsia, 52: 975-83 (2011).
  28. Uluduz D, Kürtüncü M, Yapici Z, Seyahi E, Kasapçopur O, Ozdogan H, Saip S, Akman-Demir G, Siva A. Clinical characteristics of pediatric-onset neuro-Behcet disease. Neurology, 77 (21): 1900-5 (2011).
  29. Erturk O, Karslıgil B, Cokar O, Yapici Z, Demirbilek V, Gurses C, Yalcinkaya C, Gokyigit A, Direskeneli GS, Yentur S, Onal E, Yilmaz G, Dervent A. Challenges in diagnosing SSPE. Child Nerv Syst, 27 (12): 2041-4 (2011).
  30. Elmi H, Kilinçaslan A, Oztürk M, Yapici Z. A case with hyperkinetic frontal lobe epilepsy presenting as a psychiatric disturbance. Turk J Pediatr, 53: 574-8 (2011).
  31. Bilir B, Yapici Z, Yalcinkaya C, Baris I, Carvalho CM, Bartnik M, Ozes B, Eraksoy M, Lupski JR, Battaloglu E. High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus-Merzbacher disease. Clin Genet. 83(1): 66-72 (2013).
  32. Consortium E, Consortium E, Steffens M, Leu C, Ruppert AK, Zara F, Striano P, Robbiano A, Capovilla G, Tinuper P, Gambardella A, Bianchi A, La Neve A, Crichiutti G, de Kovel CG, Kasteleijn-Nolst Trenité D, de Haan GJ, Lindhout D, Gaus V, Schmitz B, Janz D, Weber YG, Becker F, Lerche H, Steinhoff BJ, Kleefuß-Lie AA, Kunz WS, Surges R, Elger CE, Muhle H, von Spiczak S, Ostertag P, Helbig I, Stephani U, Møller RS, Hjalgrim H, Dibbens LM, Bellows S, Oliver K, Mullen S, Scheffer IE, Berkovic SF, Everett KV, Gardiner MR, Marini C, Guerrini R, Lehesjoki AE, Siren A, Guipponi M, Malafosse A, Thomas P, Nabbout R, Baulac S, Leguern E, Guerrero R, Serratosa JM, Reif PS, Rosenow F, Mörzinger M, Feucht M, Zimprich F, Kapser C, Schankin CJ, Suls A, Smets K, De Jonghe P, Jordanova A, Caglayan H, Yapici Z, Yalcin DA, Baykan B, Bebek N, Ozbek U, Gieger C, Wichmann HE, Balschun T, Ellinghaus D, Franke A, Meesters C, Becker T, Wienker TF, Hempelmann A, Schulz H, Rüschendorf F, Leber M, Pauck SM, Trucks H, Toliat MR, Nürnberg P, Avanzini G, Koeleman BP, Sander T. Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.  Hum Mol Genet. 21 (24): 5359-72 (2012).
  33. EPICURE Consortium, Leu C, de Kovel CG, Zara F, Striano P, Pezzella M, Robbiano A, Bianchi A, Bisulli F, Coppola A, Giallonardo AT, Beccaria F, Trenité DK, Lindhout D, Gaus V, Schmitz B, Janz D, Weber YG, Becker F, Lerche H, Kleefuss-Lie AA, Hallman K, Kunz WS, Elger CE, Muhle H, Stephani U, Møller RS, Hjalgrim H, Mullen S, Scheffer IE, Berkovic SF, Everett KV, Gardiner MR, Marini C, Guerrini R, Lehesjoki AE, Siren A, Nabbout R, Baulac S, Leguern E, Serratosa JM, Rosenow F, Feucht M, Unterberger I, Covanis A, Suls A, Weckhuysen S, Kaneva R, Caglayan H, Turkdogan D, Baykan B, Bebek N, Ozbek U, Hempelmann A, Schulz H, Rüschendorf F, Trucks H, Nürnberg P, Avanzini G, Koeleman BP, Sander T. Collaborators (122) Zimprich F, Mçrzinger M, Feucht M, Suls A, Weckhuysen S, Claes L, Deprez L, Smets K, Van Dyck T, Deconinck T, De Jonghe P, Velizarova R, Dimova P, Radionova M, Tournev I, Kancheva D, Kaneva R, Jordanova A, Møller RS, Hjalgrim H, Møller RS, Lehesjoki AE, Siren A, Baulac M, Baulac S, Gourfinkel-An I, Helbig I, Muhle H, von Spiczak S, Ostertag P, Stephani U, Leber M, Leu C, Sander T, Toliat MR, Trucks H, Nürnberg P, Hempelmann A, Rüschendorf F, Sander T, Elger CE, Hallmann K, Kleefuss-Lie AA, Kunz WS, Gaus V, Janz D, Sander T, Schmitz B, Klein KM, Reif PS, Oertel WH, Hamer HM, Rosenow F, Becker F, Weber Y, Lerche H, Marini C, Guerrini R, Mei D, Norci V, Zara F, Striano P, Robbiano A, Pezzella M, Bianchi A, Gambardella A, Tinuper P, La Neve A, Capovilla G, Vigliano P, Crichiutti G, Vanadia F, Vignoli A, Coppola A, Striano S, Egeo G, Giallonardo AT, Franceschetti S, Belcastro V, Benna P, Coppola G, De Palo A, Ferlazzo E, Vecchi M, Martinelli V, Bisulli F, Beccaria F, Del Giudice E, Mancardi M, Stranci G, Scabar A, Gobbi G, Giordano I, Guerero R, Giraldez BG, Serratosa JM, Koeleman BP, de Kovel C, Lindhout D, de Haan GJ, Ozbek U, Bebek N, Baykan B, Ozdemir O, Ugur S, Kocasoy-Orhan E, Yücesan E, Cine N, Gokyigit A, Gurses C, Gul G, Ayta S, Yapici Z, Ozkara C, Caglayan H, Yalcin O, Yalcin D, Turkdogan D, Arslan K, Bozdemir H, Dizdarer G, Uluduz D. Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies. Epilepsia. 2012 Feb;53(2):308-18. doi: 10.1111/j.1528-1167.2011.03379.x.
  34. Alp R, Alp SI, Planci Y, Yapici Z, Boru UT. The Prevalence of Multiple Sclerosis in the Caucasus Region of Turkey: Door-To-Door Epidemiological Field Study. Archives of Neuropsychiatry, 49 (4): 272-275 (2012).
  35. Møller RS, Weber YG, Klitten LL, Trucks H, Muhle H, Kunz WS, Mefford HC, Franke A, Kautza M, Wolf P, Dennig D, Schreiber S, Rückert IM, Wichmann HE, Ernst JP, Schurmann C, Grabe HJ, Tommerup N, Stephani U, Lerche H, Hjalgrim H, Helbig I, Sander T; EPICURE Consortium. Zimprich F, Mörzinger M, Feucht M, Suls A, Weckhuysen S, Claes L, Deprez L, Smets K, Van Dyck T, Deconinck T, De Jonghe P, Velizarova R, Dimova P, Radionova M, Tournev I, Kancheva D, Kaneva R, Jordanova A, Kolonivej D, Møller RS, Kjelgaard DB, Hjalgrim H, Helsinki B, Lehesjoki AE, Siren A, Baulac S, Leguern E, Campus K, Helbig I, Muhle H, von Spiczak S, Ostertag P, Stephani U, Leber M, Leu C, Sander T, Toliat MR, Trucks H, Nürnberg P, Hempelmann A, Rüschendorf F, Sander T, Elger CE, Kleefuß-Lie AA, Kunz W, Surges R, Gaus V, Janz D, Sander T, Schmitz B, Klein KM, Reif PS, Oertel WH, Hamer HM, Rosenow F, Becker F, Weber Y, Lerche H, Marini C, Guerrini R, Mei D, Norci V, Zara F, Striano P, Robbiano A, Pezzella M, Bianchi A, Gambardella A, Tinuper P, La Neve A, Capovilla G, Vigliano P, Crichiutti G, Vanadia F, Vignoli A, Coppola A, Striano S, Giallonardo EM, Franceschetti S, Belcastro V, Benna P, Coppola G, De Palo A, Ferlazzo E, Vecchi M, Martinelli V, Bisulli F, Beccaria F, Del Giudice E, Mancardi M, Stranci G, Scabar A, Gobbi G, Giordano I, Koeleman BP, de Kovel C, Lindhout D, de Haan GJ, Ozbeck U, Bebek N, Baykan B, Ozdemir O, Ugur S, Kocasoy-Orhan E, Yücesan E, Cine N, Gokyigit A, Gurses C, Gul G, Yapici Z, Ozkara C, Caglayan H, Yalcin O, Yapici Z, Yalcin D, Turkdogan D, Ozkara C, Dizdarer G.Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy. Epilepsia. Feb;54(2):256-64 (2013).
  36. Molero-Luis M, Serrano M, Ormazábal A, Pérez-Dueñas B, García-Cazorla A, Pons R, Artuch R. Amartino H, Arrabal L, Campistol J, Casado M, Castro de Castro P, Cormand B, Dinopoulos A, Domingo R, Durarte ST, Fernández-Álvarez E, Desviat LR, Hegde A, López-Laso E, Montero R, Ortez C, Pérez B, Pineda M, Sierra C, Szlago M, Schenone AB, Ruiz Á, Sequeira S, Tondo M, Yapici Z, Iniesta R. Neurotransmitter Working Group. Homovanillic acid in cerebrospinal fluid of 1388 children with neurological disorders. Dev Med Child Neurol. Jun;55(6):559-66 (2013).
  37. Durmus H, Kurtuncu M, Tuzun E, Pehlivan M, Akman-Demir G, Yapıcı Z, Eraksoy M. Comparative clinical characteristics of early- and adult-onset multiplesclerosis patients with seizures. Acta Neurol Belg., 113 (4):421-6 (2013).
  38. Demir N, Cokar O, Bolukbasi F, Demirbilek V, Yapici Z, Yalcinkaya C, Direskeneli GS, Yentur S, Onal E, Yilmaz G, Dervent A. A close look at EEG in subacute sclerosing panencephalitis. J Clin Neurophysiol. 30(4): 348-56 (2013).
  39. Siegl C, Hamminger P, Jank H, Ahting U, Bader B, Danek A, Gregory A, Hartig M, Hayflick S, Hermann A, Prokisch H, Sammler EM, Yapici Z, Prohaska R, Salzer U. Alterations of red cell membrane properties in nneuroacanthocytosis. PLoS One. 8(10): e76715 (2013).
  40. Ekizoğlu E, Tektürk Topaloğlu P, Yapici Z, Eraksoy M. Inflammatory Demyelinating Diseases of Childhood: Case Report and Literature Review. Noro Psikiyatr Ars. Mar;51(1):74-78 (2014).
  41. van Berge L, Hamilton EM, Linnankivi T, Uziel G, Steenweg ME, Isohanni P, Wolf NI, Krägeloh-Mann I, Brautaset NJ, Andrews PI, de Jong BA, al Ghamdi M, van Wieringen WN, Tannous BA, Hulleman E, Würdinger T, van Berkel CG, Polder E, Abbink TE, Struys EA, Scheper GC, van der Knaap MS; LBSL Research Group. Alehan F, Appleton RE, Boltshauser E, Brockmann K, Calado E, Carius A, de Coo IF, van Coster R, El-Zind S, Erturk O, Fadeeva L, Feigenbaum A, Gökben S, Gorman M, Gulati S, Hnevsova P, Joost K, Köhler W, Kolk A, Kristoferitsch W, Lemos Silveira E, Lin J, Lutz S, Mendonça C, Nuttin C, Opladen T, Savoiardo M, Schiffmann R, Seitz A, Serkov S, Sharma S, Stockler S, Temple IK, Uluc K, Vojta S, Wilms G, Wong B, Yapici Z. Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation: clinical and genetic characterization and target for therapy. Brain.137(Pt 4):1019-29 (2014). 
  42. Yentur SP, Aydin HN, Gurses C, Demirbilek V, Kuru U, Uysal S, Yapici Z, Baris S, Yilmaz G, Cokar O, Onal E, Gokyigit A, Saruhan-Direskeneli G. Granzyme B Gene Polymorphism Associated with Subacute Sclerosing Panencephalitis. Neuropediatrics. 45 (5): 309-13 (2014).
  43. Melchionda L, Haack TB, Hardy S, Abbink TE, Fernandez-Vizarra E, Lamantea E, Marchet S, Morandi L, Moggio M, Carrozzo R, Torraco A, Diodato D, Strom TM, Meitinger T, Tekturk P, Yapici Z, Al-Murshedi F, Stevens R, Rodenburg RJ, Lamperti C, Ardissone A, Moroni I, Uziel G, Prokisch H, Taylor RW, Bertini E, van der Knaap MS, Ghezzi D, Zeviani M. Mutations in APOPT1, Encoding a Mitochondrial Protein, Cause Cavitating Leukoencephalopathy with Cytochrome c Oxidase Deficiency. Am J Hum Genet. 95(3):315-25 (2014).
  44. Burns R, Majczenko K, Xu J, Peng W, Yapici Z, Dowling JJ, Li JZ, Burmeister M. Homozygous splice mutation in CWF19L1 in a Turkish family with recessive ataxia syndrome. Neurology. 83 (23):2175-82 (2014).
  45. Yentur SP, Gurses C, Demirbilek V, Adin-Cinar S, Kuru U, Uysal S, Yapici Z, Yilmaz G, Cokar O, Onal E, Gökyigit A, Saruhan-Direskeneli G. A Decrease of Regulatory T Cells and Altered Expression of NK Receptors Are Observed in Subacute Sclerosing Panencephalitis. Viral Immunol. 27(10):506-11 (2014).
  46. Ortez C, Duarte ST, Ormazábal A, Serrano M, Pérez A, Pons R, Pineda M, Yapici Z, Fernández-Álvarez E, Domingo-Jiménez R, De Castro P, Artuch R, García-Cazorla A. Cerebrospinal fluid synaptic proteins as useful biomarkers in tyrosine hydroxylase deficiency. Mol Genet Metab. 114 (1): 34-40 (2015).
  47. Cluitmans JC, Tomelleri C, Yapici Z, Dinkla S, Bovee-Geurts P, Chokkalingam V, De Franceschi L, Brock R, Bosman GJ. Abnormal red cell structure and function in neuroacanthocytosis. PLoS One. 10 (5) e0125580 (2015).
  48. Halac G, Sezer GM, Saglam NO, Tekturk P, Demir AD, Demir S, Akcay F, Uslu A, Yapıcı Z, Asil T. The relationship between Willis-Ekbom disease and serum ferritin levels among children in Northwestern Turkey. Neurosciences (Riyadh). 20(4): 336-40 (2015).
  49. Kim M, Sandford E, Gatica D, Qiu Y, Liu X, Zheng Y, Schulman BA, Xu J, Semple I, Ro SH, Kim B, Mavioglu RN, Tolun A, Jipa A, Takats S, Karpati M, Li JZ, Yapici Z, Juhasz G, Lee JH, Klionsky DJ, Burmeister M. Mutation in ATG5 reduces autophagy and leads to ataxia with developmental delay. Elife. 5. pii: e12245. doi: 10.7554/eLife.12245 (2016).
  50. Tekturk P, Erdogan ET, Kurt A, Kocagoncu E, Kucuk Z, Kinay D,Yapici Z, Aksu S, Baykan B, Karamursel S. Transcranial direct current stimulation improves seizure control in patients with Rasmussen encephalitis. Epileptic Disord.18(1):58-66 (2016).
  51. Akcakaya NH, Tekturk P, Cagatay A, Tur EK, Yapici Z. Atypical enterovirus encephalitis causing behavioral changes and autism-like clinical manifestations: case report. Acta Neurol Belg. 116 (4): 679-681 (2016).
  52. Burmeister M, Lee JH, Schulman BA, Yapici Z, Tolun A, Juhasz G, Li JZ, Klionsky DJ. A role of autophagy in spinocerebellar ataxia-Rare exception or general principle? Autophagy.12(7):1208-9 (2016).
  53. Yapici Z, Akcakaya NH, Tekturk P, Iseri SU, Ozbek U. A Novel Gene Mutation in PANK2 in a Patient with Severe Jaw-Opening Dystonia. Brain Dev. 38(8): 755-8 (2016).
  54. Samanci B, Tektürk P, Tüzün E, Erdağ E, Kınay D, Yapıcı Z, Baykan B. Neuronal autoantibodies in patients with Rasmussen's encephalitis. Epileptic Disord. 18(2): 204-10 (2016).
  55. Erer Özbek S, Yapıcı Z, Tüzün E, Giriş M, Duran S, Taşkapılıoğlu Ö, Okan M. A case of hyperkinetic movement disorder associated with LGI1 antibodies. Turk J Pediatr. 57(5):514-7 (2015).
  56. Tekturk P, Erdogan ET, Kurt A, Vanli-Yavuz EN, Ekizoglu E, Kocagoncu E, Kucuk Z, Aksu S, Bebek N, Yapici Z, Gurses C, Gokyigit A, Baykan B, Karamursel S. The effect of transcranial direct current stimulation on seizure frequency of patients with mesial temporal lobe epilepsy with hippocampal sclerosis. Clin Neurol Neurosurg.149:27-32 (2016).
  57. Baykal C, Tekturk P, Polat Ekinci A, Buyukbabani N, Baykan B, Yapici Z. Fibromatous lesion of the scalp: is it an underestimated sign of tuberous sclerosis? J Eur Acad Dermatol Venereol. 31(2):e110-e112, (2017).
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