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Best matches for Taşkıran E[au]:

HERC1 mutations in idiopathic intellectual disability. Utine GE et al. Eur J Med Genet. (2017)

Dermal fibroblast transcriptome indicates contribution of WNT signaling pathways in the pathogenesis of Apert syndrome. Çetinkaya A et al. Turk J Pediatr. (2017)

Genetic testing for DADA2: How can we avoid missing patients? Sönmez HE et al. Eur J Hum Genet. (2018)

Search results

Items: 1 to 50 of 64

1.

The investigation of therapeutic potential of oxytocin and liraglutide on vincristine-induced neuropathy in rats.

Erdoğan MA, Taşkıran E, Yiğittürk G, Erbaş O, Taşkıran D.

J Biochem Mol Toxicol. 2019 Nov 4:e22415. doi: 10.1002/jbt.22415. [Epub ahead of print]

PMID:
31682045
2.

ADA2 deficiency in a patient with Noonan syndrome-like disorder with loose anagen hair: The co-occurrence of two rare syndromes.

Akgun-Dogan O, Simsek-Kiper PO, Taskiran E, Lissewski C, Brinkmann J, Schanze D, Göçmen R, Cagdas D, Bilginer Y, Utine GE, Zenker M, Ozen S, Tezcan İ, Alikasifoglu M, Boduroğlu K.

Am J Med Genet A. 2019 Dec;179(12):2474-2480. doi: 10.1002/ajmg.a.61363. Epub 2019 Oct 4.

PMID:
31584751
3.

Intraoperative Neuromonitoring during Surgery for Cauda Equina and Conus Medullaris Tumors.

Taskiran E, Ulu MO, Akcil EF, Hanci M.

Turk Neurosurg. 2019 Jun 26. doi: 10.5137/1019-5149.JTN.26479-19.2. [Epub ahead of print]

4.

The Effect of Boron-Containing Nano-Hydroxyapatite on Bone Cells.

Gizer M, Köse S, Karaosmanoglu B, Taskiran EZ, Berkkan A, Timuçin M, Korkusuz F, Korkusuz P.

Biol Trace Elem Res. 2019 May 8. doi: 10.1007/s12011-019-01710-w. [Epub ahead of print]

PMID:
31069715
5.

Ophthalmo-acromelic syndrome in an infant.

Ürel-Demir G, Taşkıran EZ, Akgün-Doğan Ö, Şimşek-Kiper PÖ, Utine GE.

Eur J Med Genet. 2019 Jul;62(7):103664. doi: 10.1016/j.ejmg.2019.05.003. Epub 2019 May 5. Review.

PMID:
31067494
6.

Therapeutic Effects of Liraglutide, Oxytocin and Granulocyte Colony-Stimulating Factor in Doxorubicin-Induced Cardiomyopathy Model: An Experimental Animal Study.

Taşkıran E, Erdoğan MA, Yiğittürk G, Erbaş O.

Cardiovasc Toxicol. 2019 Dec;19(6):510-517. doi: 10.1007/s12012-019-09524-x.

PMID:
31054117
7.

A Monogenic Disease with a Variety of Phenotypes: Deficiency of Adenosine Deaminase 2.

Özen S, Batu ED, Taşkıran EZ, Özkara HA, Ünal Ş, Güleray N, Erden A, Karadağ Ö, Gümrük F, Çetin M, Sönmez HE, Bilginer Y, Ayvaz DÇ, Tezcan I.

J Rheumatol. 2019 May 1. pii: jrheum.181384. doi: 10.3899/jrheum.181384. [Epub ahead of print]

PMID:
31043544
8.

The Impact of Affective State on Quality of Life in Focal Epilepsy in Turkey.

Taskiran E, Matur Z, Gül G, Bebek N, Baykan B, Gökyigit A, Gürses C.

J Neurosci Rural Pract. 2019 Apr-Jun;10(2):267-272. doi: 10.4103/jnrp.jnrp_324_18.

9.

Further expanding the mutational spectrum and investigation of genotype-phenotype correlation in 3M syndrome.

Simsek-Kiper PO, Taskiran E, Kosukcu C, Arslan UE, Cormier-Daire V, Gonc N, Ozon A, Alikasifoglu A, Kandemir N, Utine GE, Alanay Y, Alikasifoglu M, Boduroglu K.

Am J Med Genet A. 2019 Jul;179(7):1157-1172. doi: 10.1002/ajmg.a.61154. Epub 2019 Apr 13.

PMID:
30980518
10.

Transcriptome analysis reveals differentially expressed genes between human primary bone marrow mesenchymal stem cells and human primary dermal fibroblasts.

Taşkiran EZ, Karaosmanoğlu B.

Turk J Biol. 2019 Feb 7;43(1):21-27. doi: 10.3906/biy-1808-81. eCollection 2019.

11.

A Novel Missense LIG4 Mutation in a Patient With a Phenotype Mimicking Behçet's Disease.

Taskiran EZ, Sonmez HE, Kosukcu C, Tavukcuoglu E, Yazici G, Esendagli G, Batu ED, Kiper POS, Bilginer Y, Alikasifoglu M, Ozen S.

J Clin Immunol. 2019 Jan;39(1):99-105. doi: 10.1007/s10875-018-0587-7. Epub 2019 Jan 8.

PMID:
30617623
12.

Hyperphosphatasia with mental retardation syndrome type 4 In two siblings-expanding the phenotypic and mutational spectrum.

Akgün Doğan Ö, Demir GÜ, Kosukcu C, Taskiran EZ, Simsek-Kiper PÖ, Utine GE, Alikaşifoğlu M, Boduroğlu K.

Eur J Med Genet. 2019 Jun;62(6):103535. doi: 10.1016/j.ejmg.2018.09.002. Epub 2018 Sep 11.

PMID:
30217754
13.

Genetic testing for DADA2: How can we avoid missing patients?

Sönmez HE, Batu ED, Taşkıran EZ, Alikaşifoğlu M, Bilginer Y, Özen S.

Eur J Hum Genet. 2018 Nov;26(11):1563-1565. doi: 10.1038/s41431-018-0240-1. Epub 2018 Sep 11. No abstract available.

14.

Clinical and molecular evaluation of 16 patients with Rett syndrome.

Zengin-Akkuş P, Taşkıran EZ, Kabaçam S, Şimşek-Kiper PÖ, Haliloğlu G, Boduroğlu K, Utine GE.

Turk J Pediatr. 2018;60(1):1-9. doi: 10.24953/turkjped.2018.01.001.

15.

Further delineation of spondyloepimetaphyseal dysplasia Faden-Alkuraya type: A RSPRY1-associated spondylo-epi-metaphyseal dysplasia with cono-brachydactyly and craniosynostosis.

Simsek-Kiper PO, Taskiran EZ, Kosukcu C, Urel-Demir G, Akgun-Dogan O, Yilmaz G, Utine GE, Nishimura G, Boduroglu K, Alikasifoglu M.

Am J Med Genet A. 2018 Sep;176(9):2009-2016. doi: 10.1002/ajmg.a.40427. Epub 2018 Jul 31.

PMID:
30063090
16.

Can Neutrophil-to-Lymphocyte Ratio, Monocyte-to-Lymphocyte Ratio, and Platelet-to-Lymphocyte Ratio at Day +100 be used as a prognostic marker in Multiple Myeloma patients with autologous transplantation?

Solmaz Medeni S, Acar C, Olgun A, Acar A, Seyhanlı A, Taskıran E, Sevindik OG, Alacacıoglu I, Piskin O, Ozcan MA, Demirkan F, Undar B, Ozsan GH.

Clin Transplant. 2018 Sep;32(9):e13359. doi: 10.1111/ctr.13359. Epub 2018 Aug 26.

PMID:
30053318
17.

Whole Exome Sequencing in Early-onset Systemic Lupus Erythematosus.

Batu ED, Koşukcu C, Taşkıran E, Sahin S, Akman S, Sözeri B, Ünsal E, Bilginer Y, Kasapcopur O, Alikaşifoğlu M, Ozen S.

J Rheumatol. 2018 Dec;45(12):1671-1679. doi: 10.3899/jrheum.171358. Epub 2018 Jul 15.

PMID:
30008451
18.

Highly selective SGLT2 inhibitor dapagliflozin reduces seizure activity in pentylenetetrazol-induced murine model of epilepsy.

Erdogan MA, Yusuf D, Christy J, Solmaz V, Erdogan A, Taskiran E, Erbas O.

BMC Neurol. 2018 Jun 7;18(1):81. doi: 10.1186/s12883-018-1086-4.

19.

Epigenotype and phenotype correlations in patients with Beckwith-Wiedemann syndrome.

Bilgin B, Kabaçam S, Taşkıran E, Şimşek-Kiper PÖ, Alanay Y, Boduroğlu K, Utine GE.

Turk J Pediatr. 2018;60(5):506-513. doi: 10.24953/turkjped.2018.05.006.

20.

Hypomorphic RAG1 defect in a child presented with pulmonary hemorrhage and digital necrosis.

Taşkıran EZ, Sönmez HE, Ayvaz DÇ, Koşukcu C, Batu ED, Esenboğa S, Topaloğlu R, Orhan D, Bilginer Y, Alikaşifoğlu M, Özen S, Tezcan İ.

Clin Immunol. 2018 Feb;187:92-94. doi: 10.1016/j.clim.2017.10.010. Epub 2017 Nov 7. No abstract available.

PMID:
29107076
21.

Human bone marrow mesenchymal stem cells secrete endocannabinoids that stimulate in vitro hematopoietic stem cell migration effectively comparable to beta-adrenergic stimulation.

Köse S, Aerts-Kaya F, Köprü ÇZ, Nemutlu E, Kuşkonmaz B, Karaosmanoğlu B, Taşkıran EZ, Altun B, Uçkan Çetinkaya D, Korkusuz P.

Exp Hematol. 2018 Jan;57:30-41.e1. doi: 10.1016/j.exphem.2017.09.009. Epub 2017 Oct 10.

PMID:
29030083
22.

Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome.

Taskiran EZ, Karaosmanoglu B, Koşukcu C, Doğan ÖA, Taylan-Şekeroğlu H, Şimşek-Kiper PÖ, Utine EG, Boduroğlu K, Alikaşifoğlu M.

Am J Med Genet A. 2017 Dec;173(12):3143-3152. doi: 10.1002/ajmg.a.38495. Epub 2017 Oct 8.

PMID:
28988429
23.

Neonatal-Onset Recurrent Guillain-Barré Syndrome-Like Disease: Clues for Inherited CD59 Deficiency.

Ardicli D, Taskiran EZ, Kosukcu C, Temucin C, Oguz KK, Haliloglu G, Alikasifoglu M, Topaloglu H.

Neuropediatrics. 2017 Dec;48(6):477-481. doi: 10.1055/s-0037-1604483. Epub 2017 Aug 11. No abstract available.

PMID:
28800659
24.

The effects of temperament and character traits on perceived social support and quality of life in patients with epilepsy.

Demirci K, Demirci S, Taşkıran E, Kutluhan S.

Epilepsy Behav. 2017 Sep;74:22-26. doi: 10.1016/j.yebeh.2017.05.039. Epub 2017 Jun 29.

PMID:
28668603
25.

Multimodal Intraoperative Neurophysiological Monitoring in Neurosurgical Oncology.

Brandmeier S, Taskiran E, Bolukbasi FH, Sari R, Elmaci I.

Turk Neurosurg. 2018;28(2):204-210. doi: 10.5137/1019-5149.JTN.19177-16.1.

26.

HERC1 mutations in idiopathic intellectual disability.

Utine GE, Taşkıran EZ, Koşukcu C, Karaosmanoğlu B, Güleray N, Doğan ÖA, Kiper PÖ, Boduroğlu K, Alikaşifoğlu M.

Eur J Med Genet. 2017 May;60(5):279-283. doi: 10.1016/j.ejmg.2017.03.007. Epub 2017 Mar 18.

PMID:
28323226
27.

Dermal fibroblast transcriptome indicates contribution of WNT signaling pathways in the pathogenesis of Apert syndrome.

Çetinkaya A, Taşkıran E, Soyer T, Şimşek-Kiper PÖ, Utine GE, Tunçbilek G, Boduroğlu K, Alikaşifoğlu M.

Turk J Pediatr. 2017;59(6):619-624. doi: 10.24953/turkjped.2017.06.001.

28.

Ictal kissing: Electroclinical features of an unusual ictal phenomenon.

Özkara Ç, Taşkıran E, Çarpraz İY, Bilir E, Demir AB, Bora İ, Aydoğdu İ, Delil Ş, Chassoux F.

Seizure. 2016 Nov;42:44-48. doi: 10.1016/j.seizure.2016.09.013. Epub 2016 Oct 1.

29.

Multimodal Intraoperative Neurophysiological Monitoring in Spinal Cord Surgery.

Taskiran E, Brandmeier S, Ozek E, Sari R, Bolukbasi F, Elmaci I.

Turk Neurosurg. 2017;27(3):436-440. doi: 10.5137/1019-5149.JTN.16414-15.1.

30.

Loss-of-Function Mutations in ELMO2 Cause Intraosseous Vascular Malformation by Impeding RAC1 Signaling.

Cetinkaya A, Xiong JR, Vargel İ, Kösemehmetoğlu K, Canter Hİ, Gerdan ÖF, Longo N, Alzahrani A, Camps MP, Taskiran EZ, Laupheimer S, Botto LD, Paramalingam E, Gormez Z, Uz E, Yuksel B, Ruacan Ş, Sağıroğlu MŞ, Takahashi T, Reversade B, Akarsu NA.

Am J Hum Genet. 2016 Aug 4;99(2):299-317. doi: 10.1016/j.ajhg.2016.06.008. Epub 2016 Jul 28.

31.

Exogenously administered adenosine attenuates renal damage in streptozotocin-induced diabetic rats.

Taşkıran E, Erbaş O, Yiğittürk G, Meral A, Akar H, Taşkıran D.

Ren Fail. 2016 Sep;38(8):1276-82. doi: 10.1080/0886022X.2016.1207054. Epub 2016 Jul 14.

PMID:
27418253
32.

Central defect type partial ACL injury model on goat knees: the effect of infrapatellar fat pad excision.

Karakilic B, Taskiran E, Doganavsargil B, Uzun B, Celik S, Kaya Bicer E.

J Orthop Surg Res. 2015 Sep 4;10:137. doi: 10.1186/s13018-015-0281-x.

33.

A Case Series of Adenosine Deaminase 2-deficient Patients Emphasizing Treatment and Genotype-phenotype Correlations.

Batu ED, Karadag O, Taskiran EZ, Kalyoncu U, Aksentijevich I, Alikasifoglu M, Özen S.

J Rheumatol. 2015 Aug;42(8):1532-4. doi: 10.3899/jrheum.150024. No abstract available.

PMID:
26233953
34.

Unilateral suppression of probable antipsychotic drug-induced parkinsonism.

Demirci S, Demirci K, Taskiran E, Koyuncuoglu HR.

Acta Neurol Belg. 2015 Dec;115(4):827-8. doi: 10.1007/s13760-015-0449-5. Epub 2015 Mar 19. No abstract available.

PMID:
25786356
35.

The value of magnetic resonance arthrography in the evaluation of repaired menisci.

Kececi B, Bicer EK, Arkun R, Argin M, Taskiran E.

Eur J Orthop Surg Traumatol. 2015 Jan;25(1):173-9. doi: 10.1007/s00590-014-1450-z. Epub 2014 Apr 10.

PMID:
24719084
36.

Mutations in ANKS6 cause a nephronophthisis-like phenotype with ESRD.

Taskiran EZ, Korkmaz E, Gucer S, Kosukcu C, Kaymaz F, Koyunlar C, Bryda EC, Chaki M, Lu D, Vadnagara K, Candan C, Topaloglu R, Schaefer F, Attanasio M, Bergmann C, Ozaltin F.

J Am Soc Nephrol. 2014 Aug;25(8):1653-61. doi: 10.1681/ASN.2013060646. Epub 2014 Mar 7.

37.

TMCO1 deficiency causes autosomal recessive cerebrofaciothoracic dysplasia.

Alanay Y, Ergüner B, Utine E, Haçariz O, Kiper PO, Taşkıran EZ, Perçin F, Uz E, Sağiroğlu MŞ, Yuksel B, Boduroglu K, Akarsu NA.

Am J Med Genet A. 2014 Feb;164A(2):291-304. doi: 10.1002/ajmg.a.36248. Epub 2013 Nov 5. Review.

PMID:
24194475
38.

Ictal kissing behavior: neurological and psychodynamic overview.

Taşkıran E, Özmen M, Kılıc Ö, Sentürk A, Özkara C.

Epilepsy Behav. 2013 Nov;29(2):326-9. doi: 10.1016/j.yebeh.2013.07.032. Epub 2013 Sep 9.

PMID:
24029004
39.

Frequency of mutations in PROP-1 gene in Turkish children with combined pituitary hormone deficiency.

Kandemir N, Vurallı D, Taşkıran E, Gönç N, Özön A, Alikaşifoğlu A, Yılmaz E.

Turk J Pediatr. 2012 Nov-Dec;54(6):570-5.

PMID:
23692781
40.

DGKE variants cause a glomerular microangiopathy that mimics membranoproliferative GN.

Ozaltin F, Li B, Rauhauser A, An SW, Soylemezoglu O, Gonul II, Taskiran EZ, Ibsirlioglu T, Korkmaz E, Bilginer Y, Duzova A, Ozen S, Topaloglu R, Besbas N, Ashraf S, Du Y, Liang C, Chen P, Lu D, Vadnagara K, Arbuckle S, Lewis D, Wakeland B, Quigg RJ, Ransom RF, Wakeland EK, Topham MK, Bazan NG, Mohan C, Hildebrandt F, Bakkaloglu A, Huang CL, Attanasio M.

J Am Soc Nephrol. 2013 Feb;24(3):377-84. doi: 10.1681/ASN.2012090903. Epub 2012 Dec 28.

41.

The effect of colchicine on pyrin and pyrin interacting proteins.

Taskiran EZ, Cetinkaya A, Balci-Peynircioglu B, Akkaya YZ, Yilmaz E.

J Cell Biochem. 2012 Nov;113(11):3536-46. doi: 10.1002/jcb.24231.

PMID:
22730186
42.

C1q deficiency: identification of a novel missense mutation and treatment with fresh frozen plasma.

Topaloglu R, Taskiran EZ, Tan C, Erman B, Ozaltin F, Sanal O.

Clin Rheumatol. 2012 Jul;31(7):1123-6. doi: 10.1007/s10067-012-1978-4. Epub 2012 May 11.

PMID:
22576477
43.

Disruption of PTPRO causes childhood-onset nephrotic syndrome.

Ozaltin F, Ibsirlioglu T, Taskiran EZ, Baydar DE, Kaymaz F, Buyukcelik M, Kilic BD, Balat A, Iatropoulos P, Asan E, Akarsu NA, Schaefer F, Yilmaz E, Bakkaloglu A; PodoNet Consortium.

Am J Hum Genet. 2011 Jul 15;89(1):139-47. doi: 10.1016/j.ajhg.2011.05.026. Epub 2011 Jun 30.

44.

Posterior tibial slope as a risk factor for anterior cruciate ligament rupture in soccer players.

Senişik S, Ozgürbüz C, Ergün M, Yüksel O, Taskiran E, Işlegen C, Ertat A.

J Sports Sci Med. 2011 Dec 1;10(4):763-7. eCollection 2011.

45.

Tibial bone density in athletes with medial tibial stress syndrome: a controlled study.

Ozgürbüz C, Yüksel O, Ergün M, Işlegen C, Taskiran E, Denerel N, Karamizrak O.

J Sports Sci Med. 2011 Dec 1;10(4):743-7. eCollection 2011.

46.

Inversion/Eversion strength dysbalance in patients with medial tibial stress syndrome.

Yüksel O, Ozgürbüz C, Ergün M, Işlegen C, Taskiran E, Denerel N, Ertat A.

J Sports Sci Med. 2011 Dec 1;10(4):737-42. eCollection 2011.

47.

Functional deficiencies of sulfite oxidase: Differential diagnoses in neonates presenting with intractable seizures and cystic encephalomalacia.

Sass JO, Gunduz A, Araujo Rodrigues Funayama C, Korkmaz B, Dantas Pinto KG, Tuysuz B, Yanasse Dos Santos L, Taskiran E, de Fátima Turcato M, Lam CW, Reiss J, Walter M, Yalcinkaya C, Camelo Junior JS.

Brain Dev. 2010 Aug;32(7):544-9. doi: 10.1016/j.braindev.2009.09.005. Epub 2009 Sep 29.

PMID:
19793632
48.

Herpes zoster oticus associated with varicella zoster virus encephalitis.

Eskiizmir G, Uz U, Taşkiran E, Unlü H.

Laryngoscope. 2009 Apr;119(4):628-30. doi: 10.1002/lary.20111.

PMID:
19213041
49.

MEFV mutations in systemic onset juvenile idiopathic arthritis.

Ayaz NA, Ozen S, Bilginer Y, Ergüven M, Taşkiran E, Yilmaz E, Beşbaş N, Topaloğlu R, Bakkaloğlu A.

Rheumatology (Oxford). 2009 Jan;48(1):23-5. doi: 10.1093/rheumatology/ken409. Epub 2008 Nov 4.

PMID:
18984609
50.

[Autologous osteochondral transplantation].

Taşkiran E, Ozçelik C.

Acta Orthop Traumatol Turc. 2007;41 Suppl 2:70-8. Review. Turkish.

PMID:
18180587

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