PROF.DR. SERAP TEBER    
Adı : SERAP
Soyadı : TEBER
E-posta :
Tel :
Ünvan : PROF.DR.
Birim : TIP FAKÜLTESİ
Bölüm :
Kişisel Akademik Bilgiler

Adı Soyadı: Serap Tıraş Teber

Doğum Tarihi: 11.1.1974

Öğrenim Durumu:

Derece

Bölüm/Program

Üniversite

Yıl

Y.Lisans

 Tıp Fakültesi

Ankara Üniversitesi

1991-1997

Tıpta Uzmanlık

 Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı

Ankara Üniversitesi

1997-2002

Yan Dal Uzmanlık

Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı, Çocuk Nörolojisi Bilim Dalı

Ankara Üniversitesi

2002-2005

Görevler:

Görev Unvanı

Görev Yeri

Yıl

Ar.Gör.

 Ankara  Üniversitesi, Tıp  Fakültesi

Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı

1997-2002

Yan Dal Asistanı

(Uzm.Dr)

 Ankara  Üniversitesi,Tıp  Fakültesi

 Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı/ Nöroloji Bilim Dalı

2002-2005

Uzm.Dr

Ankara  Üniversitesi,  Tıp  Fakültesi

Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı/Nöroloji Bilim Dalı

2005-2008

Yar.Doç.

 

 Ankara  Üniversitesi, Tıp  Fakültesi

Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı/ Nöroloji Bilim Dalı

2008-2010

Doç Dr

Atanma tarihi

 

04/01/2011

Doç Dr

 

Ankara  Hematoloji Onkoloji Hastanesi

Çocuk Sağlığı ve Hastalıkları Eğitim Araştırma Hastanesi

Çocuk Nörolojisi Birimi

2010-2013

Doç Dr

 

Ankara  Üniversitesi, Tıp  Fakültesi

Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı/ Nöroloji Bilim Dalı

5/2013-6/2016

Prof Dr

Ankara  Üniversitesi, Tıp  Fakültesi

Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı/ Nöroloji Bilim Dalı

6/2016-

Halen devam etmekte

 

 

 ESERLER
A. Uluslararası hakemli dergilerde yayımlanan makaleler :
A.1. Özçakar Z.B, Ekim M, Fitöz S, Teber S, Hizel S, Acar B, Yüksel S, Yalçınkaya F, ‘’Hypertension Induced Reversible Posterior Leukoencephalopathy Syndrome A Report Of Two Cases’’, Eur J Pediatr.163(12), 728-730 (2004).
A.2. Bilgiç A, Yılmaz S, Tıraş S, Deda G, Kılıç E.Z,  ‘’Depression And Anxiety Symptom Severity İn A Group Of Children With Epilepsy And Related Factors’’, Turkish Journal Of Psychiatry.17(3),1-8 (2006).
 
A.3. Ulu A, Günal D, Tıraş S,  Eğin Y, Deda G, Akar N.EPCR Gene A3 Haplotype And Elevated Soluble Endotelial Protein C Receptor(S EPCR) Levels İn Turkish Pediatric Stroke Patients, Thrombosis Research, 120(1), 47-52 (2007)
 
A.4. Akar N, Deda G, Tıraş Teber S, ‘’Pediatric Stroke, Homocysteine And MTHFR 677C-T And 1298 A-C’’, J Pediatr Hematol Oncol. 28(9), 632 (2006).
 
A.5. Ünal S, Teber S, Kendirli T, Deda G, Anlar B,  ‘’A Patient With Juvenile Form Of Myasthenia Gravis Presenting As Recurrent Pulmanary İnfection With Atelectasis’’, Pediatrics İnternational. 49(6), 1007-8 (2007).
 
A.6. Teber S, Sezer T, Kafalı M, Manzini C, Yüksel BK, Tekin M, Fitöz S, Walsh CA,  Deda G,’’ Severe muscle –eye-brain disease is associated with a homozygous mutation in the POMGnT1 gene’’, Eur J Pediatric Neurology. 12(2),133-6. (2008).
 
A.7. Teber S, Sezer T, Kafali M, Kendirli T, Siklar Z, Berberoglu M, Ocal G, Deda
G, ‘’Hypophosphatasia associated with pseudotumor cerebri and respiratory
İnsufficiency’’, Indian J Pediatr.75(2),186-8 (2008).
 
A.8. Yürürer D, Teber S, Deda G, Egin Y, Akar N, ‘’The Relation Between Cytokines,
Soluble Endothelial Protein C Receptor, and Factor VIII Levels in Turkish
Pediatric Stroke Patients’’, Clin Appl Thromb Hemost. 15(5):545-51 (2009)
A.9.  Cakmaklı G, Kurne A, Güven A, Serdaroğlu A, Topaloğlu H, Teber S, Anlar B,
‘’Childhood optic neuritis: The pediatric neurologist's perspective’’ , Eur J Paediatr
Neurol, 13(5):452-7 (2009).
 
A.10.  Oguz KK, Kurne A, Aksu AO, Karabulut E, Serdaroglu A, Teber S, Haspolat S,
Senbil N, Kurul S, Anlar B, ‘’ Assessment of citrullinated myelin by 1H-MR
spectroscopy in early-onset multiple sclerosis’’,  Am J Neuroradiol, 30(4),716-21 (2009) 
 
A.11. Unal O, Deda G, Teber S, Ertem M, Akar N, ‘’Thrombophilic risk factors in
epileptic children treated with valproic Acid’’ ,Pediatr Neurol, 40(2):102-6 (2009) 
 
A.12. Tıras ST, Gülhis Deda and Nejat Akar, ‘’ A note on homocysteine levels in children’’Thrombosis Research. 123(5), 799 (2009).

A.13. Teber S, Deda G, Akar N, Soylu K. Lipoprotein (a) Levels in Childhood Arterial Ischemic Stroke, Clin Appl Thromb Hemost.16(2):214-7 (2010)
A.14. Teber S, Comment on’’ Hypophosphatasia associated with pseudotumor cerebri and respiratory ınsufficiency’’, Indian J Pediatr.76,761 (2009).
A.15. Unal O, Deda G, Teber S, Ertem M, Akar N , Migraine, Valproic Acid, and Lipoprotein (a),Pedıatrıc Neurology,41(1),78-79 (2009)

A.16.Travaglini L, Brancati F, Attie-Bitach T, Audollent S, Bertini E, Kaplan J, Perrault I, Iannicelli M, Mancuso B, Rigoli L, Rozet JM, Swistun D, Tolentino J, Dallapiccola B, Gleeson JG, Valente EM; International JSRD Study Group, Zankl A, Leventer R, Grattan-Smith P, Janecke A, D'Hooghe M, Sznajer Y, Van Coster R, Demerleir L, Dias K, Moco C, Moreira A, Kim CA, Maegawa G, Petkovic D, Abdel-Salam GM, Abdel-Aleem A, Zaki MS, Marti I, Quijano-Roy S, Sigaudy S, de Lonlay P, Romano S, Touraine R, Koenig M, Lagier-Tourenne C, Messer J, Collignon P, Wolf N, Philippi H, Kitsiou Tzeli S, Halldorsson S, Johannsdottir J, Ludvigsson P, Phadke SR, Udani V, Stuart B, Magee A, Lev D, Michelson M, Ben-Zeev B, Fischetto R, Benedicenti F, Stanzial F, Borgatti R, Accorsi P, Battaglia S, Fazzi E, Giordano L, Pinelli L, Boccone L, Bigoni S, Ferlini A, Donati MA, Caridi G, Divizia MT, Faravelli F, Ghiggeri G, Pessagno A, Briguglio M, Briuglia S, Salpietro CD, Tortorella G, Adami A, Castorina P, Lalatta F, Marra G, Riva D, Scelsa B, Spaccini L, Uziel G, Del Giudice E, Laverda AM, Ludwig K, Permunian A, Suppiej A, Signorini S, Uggetti C, Battini R, Di Giacomo M, Cilio MR, Di Sabato ML, Leuzzi V, Parisi P, Pollazzon M, Silengo M, De Vescovi R, Greco D, Romano C, Cazzagon M, Simonati A, Al-Tawari AA, Bastaki L, Mégarbané A, Sabolic Avramovska V, de Jong MM, Stromme P, Koul R, Rajab A, Azam M, Barbot C, Martorell Sampol L, Rodriguez B, Pascual-Castroviejo I, Teber S, Anlar B, Comu S, Karaca E, Kayserili H, Yüksel A, Akcakus M, Al Gazali L, Sztriha L, Nicholl D, Woods CG, Bennett C, Hurst J, Sheridan E, Barnicoat A, Hennekam R, Lees M, Blair E, Bernes S, Sanchez H, Clark AE, DeMarco E, Donahue C, Sherr E, Hahn J, Sanger TD, Gallager TE, Dobyns WB, Daugherty C, Krishnamoorthy KS, Sarco D, Walsh CA, McKanna T, Milisa J, Chung WK, De Vivo DC, Raynes H, Schubert R, Seward A, Brooks DG, Goldstein A, Caldwell J, Finsecke E, Maria BL, Holden K, Cruse RP, Swoboda KJ, Viskochil D. ‘’Expanding CEP290 mutational spectrum in ciliopathies’’,  Am J Med Genet A. 149 (10), 2173-80 (2009) .
A.17. Atalay S, Aypar E, Uçar T, Altuğ N, Deda G, Teber S, Tutar E, ‘’Fetal ve neonatal cardiac rhabdomyomas.clinical presentaion, outcome and association with tuberous sclerosis complex’’, The Turkish Journal Of Pediatrics, 52 (5):481-7 (2010).
A.18. Yilmaz E, Akar R, Teber ST, Deda G, Adiguzel Y, Akar N. ‘’Relationship between functional promoter polymorphism in the XBP1 gene (-116C/G) and atherosclerosis, ischemic stroke and hyperhomocysteinemia’’, Mol Biol Rep.37(1): 269-72 (2010) 
 
A.19. Öztürk A, Eğin Y, Deda G, Teber S, Akar N. ‘’Protein Z G79A polimorphism in Turkish pediatric cerebral infarct patients’’, Turkish Journal of Hematology, 25(3): 133-135. (2008)
A.20 Teber S, Sezer T, Aypar E, Kendirli T, Atalay S, Deda G. ‘’Congenital myotonic dystrophy associated with Moebius syndrome and double-outlet right ventricle’’.Pediatr Int, 52(3):501-2 (2010)
A.21. Iannicelli M, Brancati F, Mougou-Zerelli S, Mazzotta A, Thomas S, Elkhartoufi N, Travaglini L, Gomes C, Ardissino GL, Bertini E, Boltshauser E, Castorina P, D'Arrigo S, Fischetto R, Leroy B, Loget P, Bonnière M, Starck L, Tantau J, Gentilin B, Majore S, Swistun D, Flori E, Lalatta F, Pantaleoni C, Penzien J, Grammatico P; International JSRD Study Group: Ali Pacha L, Tazir M, Zankl A, Leventer R, Grattan-Smith P, Janecke A, D'Hooghe M, Sznajer Y, Van Coster R, Demerleir L, Dias K, Moco C, Moreira A, Ae Kim C, Maegawa G, Loncarevic D, Mejaski-Bosnjak V, Petkovic D, Abdel-Salam GM, Abdel-Aleem A, Zaki MS, Marti I, Quijano-Roy S, Sigaudy S, de Lonlay P, Romano S, Verloes A, Touraine R, Koenig M, Lagier-Tourenne C, Messer J, Collignon P, Wolf N, Philippi H, Lemke J, Dacou-Voutetakis C, Kitsiou Tzeli S, Pons R, Sztriha L, Halldorsson S, Johannsdottir J, Ludvigsson P, Phadke SR, Udani V, Stuart B, Magee A, Lev D, Michelson M, Ben-Zeev B, Di Giacomo M, Gentile M, Guanti G, D'Addato O, Papadia F, Spano M, Bernardi F, Seri M, Benedicenti F, Stanzial F, Borgatti R, Accorsi P, Battaglia S, Fazzi E, Giordano L, Izzi C, Pinelli L, Boccone L, Guanciali P, Romoli R, Bigoni S, Ferlini A, Andreucci E, Donati MA, Genuardi M, Caridi G, Divizia MT, Faravelli F, Ghiggeri G, Pessagno, Amorini M, Briguglio M, Briuglia S, Rigoli L, Salpietro C, Tortorella G, Adami A, Marra G, Riva D, Scelsa B, Spaccini L, Uziel G, Coppola G, Del Giudice E, Vitiello G, Laverda AM, Ludwig K, Permunian A, Suppiej A, Macaluso C, Signorini S, Uggetti C, Battini R, Di Giacomo M, Priolo M, Cilio MR, D'Amico A, Di Sabato ML, Emma F, Leuzzi V, Parisi P, Stringini G, Zanni G, Pollazzon M, Renieri A, Vascotto M, Silengo M, De Vescovi R, Greco D, Romano C, Cazzagon M, Simonati A, Al-Tawari AA, Bastaki L, Mégarbané A, Matuleviciene A, Sabolic Avramovska V, Said E, de Jong MM, Prescott T, Stromme P, von der Lippe C, Koul R, Rajab A, Azam M, Barbot C, Jocic-Jakubi B, Gener Querol B, Martorell Sampol L, Rodriguez B, Pascual-Castroviejo I, Strozzi S, Fluss J, Teber S, Topcu M, Anlar B, Comu S, Karaca E, Kayserili H, Yüksel A, Akgul M, Akcakus M, Al Gazali L, Nicholl D, Woods CG, Bennett C, Hurst J, Sheridan E, Barnicoat A, Carr L, Hennekam R, Lees M, McKay F, Yates L, Blair E, Bernes S, Sanchez H, Clark AE, DeMarco E, Donahue C, Sherr E, Hahn J, Sanger TD, Gallager TE, Dobyns WB, Daugherty C, Krishnamoorthy KS, Sarco D, Walsh CA, McKanna T, Milisa J, Cjung WK, De Vivo DC, Raynes H, Schubert R, Seward A, Brooks DG, Goldstein A, Caldwell J, Finsecke E, Maria BL, Holden K, Cruse RP, Swoboda KJ, Viskochil D., Dallapiccola B, Gleeson JG, Attie-Bitach T, Valente EM.’’Novel TMEM67 mutations and genotype-phenotype correlates in meckelin-related ciliopathies’’.Hum Muta, 31(5):E1319-31(2010)
A.22. Karagol BS, Erdeve O, Arsan S, Atasay B, Ekim M, Teber S, Deda G.’’Status epilepticus and capillary leak syndrome in a neonate related to perinatal hypoxic-ischemic encephalopathy’’.Indian J Pediatr, 77(4):439-41 (2010).
A.23. Tunc T, Mungan IA, Okulu E, Tiras ST, Tekin M, Atasay B, Arsan S, Turmen T.‘'Hyperekplexia in a neonate: a novel finding in Fukuyama type congenital muscular dystrophy’’.Genet Couns, 20(3):275-9(2009)
A24. Dönmez b. N, Teber S, Deda G, Akar N. ‘’T102 polymorphism of the serotonin (5- HT) 2A receptor gene in Turkish children with cerebral infarct’’, Turkish J Hematology, 24,14-17 (2007).
A.25. Teber S, Bektas Ö, Yılmaz A, Aksoy E, Akar N,  Deda G, ‘’Lipoprotein a levels in pediatric migraine’’ ,Pediatr Neurol, 45(4):225-8 (2011)
 
A.26. Teber S, Akar N, Deda G. ‘’Childhood migraine and hypercoagulopathy’’ .Br J Haematol, 155(4):527-8 (2011)
A.27. Aydoğdu O, Burgu B, Teber S, Altugan S, Gökçe I, Deda G, Soygür T.’’A challenging review of          zchildhood incontinence: rare complications of dysfunctional elimination syndrome in an epileptic boy’’, Turk J Pediatr, 53(1):100-3 (2011)
A.28. Ozkan M, Teber ST, Deda. Electroencephalogram variations in pediatric migraines and tension-type headaches. , Pediatr Neurol, 46(3):154-7 (2012)
A.29. Bektas O, Arıca B, Teber S, Yılmaz A, Zeybek H, Kaymak S, Deda G. Chloral hydrate and/or hydroxyzine for sedation in pediatric EEG recording.
Brain Dev. 2014 Feb;36(2):130-6.
 
A.30. Değerliyurt A, Teber S, Karakaya G, Güven A, Şeker ED, Arhan EP, Şayli TR.
Pseudotumor cerebri/idiopathic intracranial hypertension in children: an experience of a tertiary care hospital.Brain Dev. 2014 Sep;36(8):690-9. 
 
A.31. Bektas O, Teber S, Akar N, Uysal LZ, Arsan S, Atasay B, Deda G.
Cerebral Sinovenous Thrombosis in Children and Neonates: Clinical Experience, Laboratory, Treatment, and Outcome. Clin Appl Thromb Hemost. 2015 Nov;21(8):777-82
 
A.32. Yazal Erdem A, Azık F, Tavil B, Teber S, Tunç B, Uçkan D.
Busulfan triggers epileptic seizures under levetiracetam and valproic acid therapy.
Pediatr Transplant. 2014 Jun;18(4):412-3.
 
A.33. Değerliyurt A, Teber S, Bektaş O, Senkon G. Panayiotopoulos syndrome: a case series from Turkey. Epilepsy Behav. 2014 Jul;36:24-32
 
A.34. Travaglini L1, Brancati F, Silhavy J, Iannicelli M, Nickerson E, Elkhartoufi N, Scott E, Spencer E, Gabriel S, Thomas S, Ben-Zeev B,Bertini E, Boltshauser E, Chaouch M, Cilio MR, de Jong MM, Kayserili H, Ogur G, Poretti A, Signorini S, Uziel G, Zaki MS;International JSRD Study Group, Johnson C, Attié-Bitach T, Gleeson JG, Valente EM.
Collaborators :(227)
Ali Pacha L, Zankl A, Leventer R, Grattan-Smith P, Janecke A, Koch J, Freilinger M, D'Hooghe M, Sznajer Y, Vilain C,Van Coster R, Demerleir L, Dias K, Moco C, Moreira A, Ae Kim C, Maegawa G, Dakovic I, Loncarevic D, Mejaski-Bosnjak V, Petkovic D, Abdel-Salam GM, Abdel-Aleem A, Marti I, Pinard JM, Quijano-Roy S, Sigaudy S, de Lonlay P, Romano S,Verloes A, Touraine R, Koenig M, Dollfus H, Flori E, Fradin M, Lagier-Tourenne C, Messer J, Collignon P, Penzien JM,Bussmann C, Merkenschlager A, Philippi H, Kurlemann G, Grundmann K, Dacou-Voutetakis C, Kitsiou Tzeli S, Pons R,Jerney J, Halldorsson S, Johannsdottir J, Ludvigsson P, Phadke SR, Girisha KM, Doshi H, Udani V, Kaul M, Stuart B,Magee A, Spiegel R, Shalev S, Mandel H, Lev D, Michelson M, Idit M, Ben-Zeev B, Gershoni-Baruch R, Ficcadenti A,Fischetto R, Gentile M, Della Monica M, Pezzani M, Graziano C, Seri M, Benedicenti F, Stanzial F, Borgatti R,Romaniello R, Accorsi P, Battaglia S, Fazzi E, Giordano L, Pinelli L, Boccone L, Barone R, Sorge G, Briatore E, Bigoni S, Ferlini A, Donati MA, Biancheri R, Caridi G, Divizia MT, Faravelli F, Ghiggeri G, Mirabelli M, Pessagno A, Rossi A,Uliana V, Amorini M, Briguglio M, Briuglia S, Salpietro CD, Tortorella G, Adami A, Bonati MT, Castorina P, D'Arrigo S,Lalatta F, Marra G, Moroni I, Pantaleoni C, Riva D, Scelsa B, Spaccini L, Del Giudice E, Ludwig K, Permunian A, Suppiej A, Macaluso C, Pichiecchio A, Battini R, Di Giacomo M, Priolo M, Timpani P, Pagani G, Di Sabato ML, Emma F, Leuzzi V, Mancini F, Majore S, Micalizzi A, Parisi P, Romani M, Stringini G, Zanni G, Ulgheri L, Pollazzon M, Renieri A, Belligni E, Grosso E, Pieri I, Silengo M, Devescovi R, Greco D, Romano C, Cazzagon M, Simonati A, Al-Tawari AA, Bastaki L,Mégarbané A, Sabolic Avramovska V, Said E, Stromme P, Koul R, Rajab A, Azam M, Barbot C, Salih MA, Tabarki B,Jocic-Jakubi B, Martorell Sampol L, Rodriguez B, Pascual-Castroviejo I, Gener B, Puschmann A, Starck L, Capone A,Lemke J, Fluss J, Niedrist D, Hennekam RC, Wolf N, Gouider-Khouja N, Kraoua I, Ceylaner S, Teber S, Akgul M, Anlar B,Comu S, Kayserili H, Yüksel A, Akcakus M, Caglayan AO, Aldemir O, Al Gazali L, Sztriha L, Nicholl D, Woods CG,Bennett C, Hurst J, Sheridan E, Barnicoat A, Hemingway C, Lees M, Wakeling E, Blair E, Bernes S, Sanchez H, Clark AE, DeMarco E, Donahue C, Sherr E, Hahn J, Sanger TD, Gallager TE, Daugherty C, Krishnamoorthy KS, Sarco D,Walsh CA, McKanna T, Milisa J, Chung WK, De Vivo DC, Raynes H, Schubert R, Seward A, Brooks DG, Goldstein A,Caldwell J, Finsecke E, Maria BL, Holden K, Cruse RP, Karaca E, Swoboda KJ, Viskochil D, Dobyns WB
Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders. Eur J Hum Genet. 2013 Oct;21(10):1074-8.
 
A.35. Kurt-Şükür ED, Özçakar ZB, Fitöz S, Yilmaz S, Teber S, Ünal İnce E, Ekim M, Yalçinkaya F.Two children with steroid-responsive nephrotic syndrome complicated by cerebral venous sinus thrombosis.Nefrologia. 2015;35(5):497-500
 
A.36. Micalizzi A, Poretti A, Romani M, Ginevrino M, Mazza T, Aiello C, Zanni G, Baumgartner B, Borgatti R, Brockmann K, Camacho A, Cantalupo G, Haeusler M, Hikel C, Klein A, Mandrile G, Mercuri E, Rating D, Romaniello R, Santorelli FM, Schimmel M, Spaccini L, Teber S, von Moers A, Wente S, Ziegler A, Zonta A, Bertini E, Boltshauser E, Valente EM. Clinical, neuroradiological and molecular characterization of cerebellar dysplasia with cysts (Poretti-Boltshauser syndrome).
Eur J Hum Genet. 2016 Mar 2. doi: 10.1038/ejhg.2016.19. [Epub ahead of print]
 
A.37. Oz Tuncer G, Teber S, Kutluk MG, Albayrak P, Deda G.
Andersen-Tawil Syndrome with Early Onset Myopathy: 2 Cases.
J Neuromuscul Dis. 2017;4(1):93-95. doi: 10.3233/JND-160188
 
A.38. Yılmaz Ü, Anlar B, Gücüyener K; Turkish Pediatric Multiple Sclerosis Study Group: Yaramış A4Cansu A5Ünalp A6Aksoy A7Bayram AK8Kartal A9Tosun A10Serdaroğlu A3Konuşkan B2Sarıoğlu B11Yüzbaşı BK10Kılıç B12Taşkın BD13Bulut C14Yılmaz C13Yarar C15Okuyaz Ç16Gençsel Ç7Yüksel D7Arslan EA5Gürkaş E13Faruk Incecik17Serdaroğlu G18Deda G19Gürbüz G6Gümüş H8Acer H8Tekgül H18Çaksen H14Per H8Erol İ20Çarman KB15Canpolat M8Özkan M21Direk MÇ16Kutluk MG19Arslan M22Sönmez FM23Dündar NO24Koçak O15Aydın ÖF25Toptaş Ö7Duman Ö26Hergüner Ö17Bozkurt Ö26Arıcan P24Yılmaz S18Gökben S18Işıkay S27Kumandaş S8Edizer S6Kurul SH28Saygı S20Teber S19Güngör S12Altunbaşak Ş17Haspolat Ş26Sezer T29Yılmaz TS30Yiş U28Öztoprak Ü7Aydoğmuş Ü13Topçu Y21Öztürk Z3Karalök ZS1. Characteristics of pediatric multiple sclerosis: The Turkish pediatric multiple sclerosis database.Eur J Paediatr Neurol. 2017 Nov;21(6):864-872.
 
A.39. Somer D, Yilmaz A, Tiras Teber S, Cinar FG.
Late Presentation of Ataxia, Areflexia, and Electrophysiological Abnormalities as Part of Miller Fisher Syndrome: Case Report.Neuroophthalmology. 2016 Jun 8;40(4):197-200
 
A.40. Aksoy E, Tıraş-Teber S, Deda G.A celiac case mimicking mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).Turk J Pediatr. 2016;58(6):662-665.
 
A.41. Aksoy E, Tıraş-Teber S, Kansu A, Deda G, Kartal A.
Neurological findings spectrum in Celiac disease.Turk J Pediatr. 2016;58(3):233-240
 
 
A.42. Oz Tuncer G, Teber S, Kutluk MG, Albayrak P, Deda G.Hashimoto'sencephalopathy presenting as pseudobulbar palsy.Childs Nerv Syst. 2018 Jun;34(6):1251-1254
 
A.43. Azapağası E, Kendirli T, Öz-Tuncer G, Albayrak P, Teber S, Deda G. Complete paralytic botulism mimicking a deep coma in a child. Turk J Pediatr. 2017;59(5):581-585.
 
A.44. Oz Tuncer G, Teber S, Kutluk MG, Albayrak P, Deda G.
Andersen-Tawil Syndrome with Early Onset Myopathy: 2 Cases.
J Neuromuscul Dis. 2017;4(1):93-95
 
A.45. Yılmaz Ü, Anlar B, Gücüyener K; Turkish Pediatric Multiple Sclerosis Study Group.
Characteristics of pediatric multiple sclerosis: The Turkish pediatric multiple sclerosis database. Eur J Paediatr Neurol. 2017 Nov;21(6):864-872
 
A.46. Tunçer GÖ, Teber S, Albayrak P, Kutluk MG, Deda G A case of Dravet Syndrome with a newly defined mutation in the SCN1A gene. Turk Pediatri Ars. 2018 Dec 1;53(4):259-262. doi: 10.5152/TurkPediatriArs.2018
 
A.47. Haznedar P, Doğan Ö, Albayrak P, Öz Tunçer G, Teber S, Deda G, Eminoglu FT.
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