Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 82

1.

The Effect of Viscosity-Modifying Admixture on the Extrudability of Limestone and Calcined Clay-Based Cementitious Material for Extrusion-Based 3D Concrete Printing.

Chen Y, Chaves Figueiredo S, Yalçinkaya Ç, Çopuroğlu O, Veer F, Schlangen E.

Materials (Basel). 2019 Apr 28;12(9). pii: E1374. doi: 10.3390/ma12091374.

2.

Oxidative stress among L-2-hydroxyglutaric aciduria disease patients: evaluation of dynamic thiol/disulfide homeostasis.

Cansever MS, Zubarioglu T, Oruc C, Kiykim E, Gezdirici A, Neselioglu S, Erel O, Yalcinkaya C, Aktuglu-Zeybek C.

Metab Brain Dis. 2019 Feb;34(1):283-288. doi: 10.1007/s11011-018-0354-8. Epub 2018 Nov 29.

PMID:
30499066
3.

Chromosome 14q11.2-q21.1 duplication: a rare cause of West syndrome.

Çetin ÖE, Yalçınkaya C, Karaman B, Demirbilek V, Tüysüz B.

Epileptic Disord. 2018 Jun 1;20(3):219-224. doi: 10.1684/epd.2018.0972.

4.

Megalencephalic leukoencephalopathy with subcortical cysts: Characterization of disease variants.

Hamilton EMC, Tekturk P, Cialdella F, van Rappard DF, Wolf NI, Yalcinkaya C, Çetinçelik Ü, Rajaee A, Kariminejad A, Paprocka J, Yapici Z, Bošnjak VM, van der Knaap MS; MLC Research Group.

Neurology. 2018 Apr 17;90(16):e1395-e1403. doi: 10.1212/WNL.0000000000005334. Epub 2018 Mar 21.

5.

Early diagnosed cerebrotendinous xanthomatosis patients: clinical, neuroradiological characteristics and therapy results of a single center from Turkey.

Zubarioglu T, Kiykim E, Yesil G, Demircioglu D, Cansever MS, Yalcinkaya C, Aktuglu-Zeybek C.

Acta Neurol Belg. 2019 Sep;119(3):343-350. doi: 10.1007/s13760-017-0851-2. Epub 2017 Oct 22.

PMID:
29058268
6.

Identification of 3 Novel Patients with CLCN2-Related Leukoencephalopathy due to CLCN2 Mutations.

Zeydan B, Uygunoglu U, Altintas A, Saip S, Siva A, Abbink TEM, van der Knaap MS, Yalcinkaya C.

Eur Neurol. 2017;78(3-4):125-127. doi: 10.1159/000478089. Epub 2017 Jul 26. No abstract available.

7.

Familial Adult-onset Alexander Disease: Clinical and Neuroradiological Findings of Three Cases.

Elmali AD, Çetinçelik Ü, Işlak C, Uzun Adatepe N, Karaali Savrun F, Yalçinkaya C.

Noro Psikiyatr Ars. 2016 Jun;53(2):169-172. doi: 10.5152/npa.2015.10193. Epub 2016 Jun 1. Erratum in: Noro Psikiyatr Ars. 2017 Sep;54(3):288.

8.

A rare lesion of the clitoris: atypical cellular blue naevus: case report.

Özdemir ED, Yalçınkaya C, Çoban G, Canpolat T, Okçu Heper A, Çelik H.

J Obstet Gynaecol. 2017 Jan;37(1):121-122. doi: 10.1080/01443615.2016.1225021. Epub 2016 Dec 7. No abstract available.

PMID:
27924655
9.

Beneficial Effects of Everolimus on Autism and Attention-Deficit/Hyperactivity Disorder Symptoms in a Group of Patients with Tuberous Sclerosis Complex.

Kilincaslan A, Kok BE, Tekturk P, Yalcinkaya C, Ozkara C, Yapici Z.

J Child Adolesc Psychopharmacol. 2017 May;27(4):383-388. doi: 10.1089/cap.2016.0100. Epub 2016 Oct 31.

PMID:
27797585
10.

A rare finding in epilepsy with myoclonic absences: focal seizure.

Çetin ÖE, Abanoz Y, Kıvrak E, Yalçınkaya C, Demirbilek V.

Childs Nerv Syst. 2016 Nov;32(11):2053-2055. Epub 2016 Sep 5. No abstract available.

PMID:
27596001
11.

Prenatal unilateral cerebellar hypoplasia diagnosed as PHACE syndrome.

Erturk O, Uygunoglu U, Celkan T, Yalcinkaya C.

Childs Nerv Syst. 2016 Apr;32(4):587-8. doi: 10.1007/s00381-016-3027-0. Epub 2016 Jan 29. No abstract available.

PMID:
26825811
12.

Clinical and neuroradiological approach to fucosidosis in a child with atypical presentation.

Zubarioglu T, Kiykim E, Zeybek CA, Cansever MS, Benbir G, Aydin A, Yalcinkaya C.

Ann Indian Acad Neurol. 2015 Oct-Dec;18(4):471-4. doi: 10.4103/0972-2327.160090.

13.

Neonatal nonketotic hyperglycinemia: diffusion-weighted magnetic resonance imaging and diagnostic clues.

Zubarioglu T, Kiykim E, Cansever MS, Aktuglu Zeybek C, Yalcinkaya C.

Acta Neurol Belg. 2016 Dec;116(4):671-673. Epub 2015 Dec 24. No abstract available.

PMID:
26702626
14.

Epilepsy Surgery in Children with Lesional Partial Epilepsies.

Erturk O, Ozkara C, Yalcinkaya C, Dervent A, Yeni SN, Demirbilek V, Unver O, Uysal S, Ozyurt E, Uzan M.

Turk Neurosurg. 2015;25(6):900-4. doi: 10.5137/1019-5149.JTN.11342-14.1.

15.

Phenotypic Expansion of Congenital Disorder of Glycosylation Due to SRD5A3 Null Mutation.

Tuysuz B, Pehlivan D, Özkök A, Jhangiani S, Yalcinkaya C, Zeybek ÇA, Muzny DM, Lupski JR, Gibbs R, Jaeken J.

JIMD Rep. 2016;26:7-12. doi: 10.1007/8904_2015_478. Epub 2015 Jul 29.

16.

Inherited metabolic disorders in Turkish patients with autism spectrum disorders.

Kiykim E, Zeybek CA, Zubarioglu T, Cansever S, Yalcinkaya C, Soyucen E, Aydin A.

Autism Res. 2016 Feb;9(2):217-23. doi: 10.1002/aur.1507. Epub 2015 Jun 7.

PMID:
26055667
17.

A different technique for the closure of trocar sites.

Yalcinkaya C, Coban G, Parlakgumus A, Caglar P, Cologlu H, Ozdemir H.

Clin Exp Obstet Gynecol. 2015;42(2):139-40.

PMID:
26054105
18.

The impact of sweeping the membranes on cervical length and labor: a randomized clinical trial.

Parlakgumus HA, Yalcinkaya C, Haydardedeoglu B, Tarim E.

Ginekol Pol. 2014 Sep;85(9):682-7.

PMID:
25322540
19.

Unilateral cerebellar and brain stem hypoplasia in a child with a postnatal diagnosis of dissecting aneurysm in basilar artery.

Akkas-Yazici S, Benbir G, Kocer N, Yalcinkaya C.

Neuropediatrics. 2014 Dec;45(6):392-5. doi: 10.1055/s-0034-1387168. Epub 2014 Aug 6.

PMID:
25098833
20.

Cerebrotendinous xanthomatosis: the effectiveness of high-dose piracetam for the treatment of cerebellar and sensorial ataxia.

Uygunoglu U, Gunduz A, Menku SF, Yilmaz B, Hatipoglu E, Yalcinkaya C, Saip S, Apaydin H.

Cerebellum. 2014 Dec;13(6):787-90. doi: 10.1007/s12311-014-0587-y. No abstract available.

PMID:
25084753
21.

Does bleeding affect fetal Doppler parameters during genetic amniocentesis?

Iskender C, Tarım E, Cok T, Kalaycı H, Parlakgümüş A, Yalçınkaya C.

J Turk Ger Gynecol Assoc. 2014 Jun 1;15(2):100-3. doi: 10.5152/jtgga.2014.0031. eCollection 2014.

22.

Salvage surgery of the limb with severe pseudoamniotic band syndrome: case report and literature review.

Çöloğlu H, Özkan B, Çöloğlu Ö, Yalçınkaya C, Uysal AÇ, Borman H.

Handchir Mikrochir Plast Chir. 2014 Apr;46(2):121-4. doi: 10.1055/s-0033-1358452. Epub 2014 Apr 28. Review.

PMID:
24777463
23.

CLP1 founder mutation links tRNA splicing and maturation to cerebellar development and neurodegeneration.

Schaffer AE, Eggens VR, Caglayan AO, Reuter MS, Scott E, Coufal NG, Silhavy JL, Xue Y, Kayserili H, Yasuno K, Rosti RO, Abdellateef M, Caglar C, Kasher PR, Cazemier JL, Weterman MA, Cantagrel V, Cai N, Zweier C, Altunoglu U, Satkin NB, Aktar F, Tuysuz B, Yalcinkaya C, Caksen H, Bilguvar K, Fu XD, Trotta CR, Gabriel S, Reis A, Gunel M, Baas F, Gleeson JG.

Cell. 2014 Apr 24;157(3):651-63. doi: 10.1016/j.cell.2014.03.049.

24.

Autosomal recessive spastic tetraplegia caused by AP4M1 and AP4B1 gene mutation: expansion of the facial and neuroimaging features.

Tüysüz B, Bilguvar K, Koçer N, Yalçınkaya C, Çağlayan O, Gül E, Sahin S, Çomu S, Günel M.

Am J Med Genet A. 2014 Jul;164A(7):1677-85. doi: 10.1002/ajmg.a.36514. Epub 2014 Apr 3.

PMID:
24700674
25.

A close look at EEG in subacute sclerosing panencephalitis.

Demir N, Cokar O, Bolukbasi F, Demirbilek V, Yapici Z, Yalcinkaya C, Direskeneli GS, Yentur S, Onal E, Yilmaz G, Dervent A.

J Clin Neurophysiol. 2013 Aug;30(4):348-56. doi: 10.1097/WNP.0b013e31829ddcb6.

PMID:
23912572
26.

Obstetrical complications associated with first-trimester screening markers in twin pregnancies.

Iskender C, Tarım E, Çok T, Yalcınkaya C, Kalaycı H, Yanık FB.

J Obstet Gynaecol Res. 2013 Nov;39(11):1495-9. doi: 10.1111/jog.12091. Epub 2013 Jul 15.

PMID:
23855638
27.

Brain white matter oedema due to ClC-2 chloride channel deficiency: an observational analytical study.

Depienne C, Bugiani M, Dupuits C, Galanaud D, Touitou V, Postma N, van Berkel C, Polder E, Tollard E, Darios F, Brice A, de Die-Smulders CE, Vles JS, Vanderver A, Uziel G, Yalcinkaya C, Frints SG, Kalscheuer VM, Klooster J, Kamermans M, Abbink TE, Wolf NI, Sedel F, van der Knaap MS.

Lancet Neurol. 2013 Jul;12(7):659-68. doi: 10.1016/S1474-4422(13)70053-X. Epub 2013 May 22.

28.

Recessive loss of function of the neuronal ubiquitin hydrolase UCHL1 leads to early-onset progressive neurodegeneration.

Bilguvar K, Tyagi NK, Ozkara C, Tuysuz B, Bakircioglu M, Choi M, Delil S, Caglayan AO, Baranoski JF, Erturk O, Yalcinkaya C, Karacorlu M, Dincer A, Johnson MH, Mane S, Chandra SS, Louvi A, Boggon TJ, Lifton RP, Horwich AL, Gunel M.

Proc Natl Acad Sci U S A. 2013 Feb 26;110(9):3489-94. doi: 10.1073/pnas.1222732110. Epub 2013 Jan 28.

29.

Operative hysteroscopy preserving virginity: a new technique.

Yalcinkaya C, Kalayci H, Simsek E, Iskender CT, Parlakgumus HA.

Clin Exp Obstet Gynecol. 2013;40(4):572-3.

PMID:
24597259
30.

Fetal axillary cystic hygroma: a novel association with triple X syndrome.

Iskender C, Tarım E, Cok T, Yalcinkaya C, Kalaycı H, Sahin F.

Birth Defects Res A Clin Mol Teratol. 2012 Nov;94(11):955-7. doi: 10.1002/bdra.23083. Epub 2012 Oct 26.

PMID:
23109196
31.

Multiple small hyperintense lesions in the subcortical white matter on cranial MR images in two Turkish brothers with cold-induced sweating syndrome caused by a novel missense mutation in the CRLF1 gene.

Tüysüz B, Kasapçopur O, Yalçınkaya C, Işık Haşıloğlu Z, Knappskog PM, Boman H.

Brain Dev. 2013 Jun;35(6):596-601. doi: 10.1016/j.braindev.2012.08.011. Epub 2012 Sep 29.

PMID:
23026229
32.

A novel GJC2 mutation associated with hypomyelination and Müllerian agenesis syndrome: coincidence or a new entity?

Yalcinkaya C, Erturk O, Tuysuz B, Yesil G, Verbeke JI, Keyser B, Stuhrmann M, Steinemann D, Sistermans EA, van der Knaap MS.

Neuropediatrics. 2012 Jun;43(3):159-61. doi: 10.1055/s-0032-1313912. Epub 2012 May 19.

PMID:
22610664
33.

Novel NDE1 homozygous mutation resulting in microhydranencephaly and not microlyssencephaly.

Guven A, Gunduz A, Bozoglu TM, Yalcinkaya C, Tolun A.

Neurogenetics. 2012 Aug;13(3):189-94. doi: 10.1007/s10048-012-0326-9. Epub 2012 Apr 15.

PMID:
22526350
34.

Prenatal diagnosis of right diaphragmatic eventration associated with fetal hydrops.

Iskender C, Tarım E, Yalcınkaya C.

J Obstet Gynaecol Res. 2012 May;38(5):858-62. doi: 10.1111/j.1447-0756.2011.01831.x.

PMID:
22519886
35.

High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus-Merzbacher disease.

Bilir B, Yapici Z, Yalcinkaya C, Baris I, Carvalho CM, Bartnik M, Ozes B, Eraksoy M, Lupski JR, Battaloglu E.

Clin Genet. 2013 Jan;83(1):66-72. doi: 10.1111/j.1399-0004.2012.01846.x. Epub 2012 Feb 20.

36.

Stump appendicitis and chorioamnionitis due to incomplete appendectomy: a case report.

Bellı S, Yalçinkaya C, Ezer A, Bolat F, Çolakoğlu T, Şımşek E.

Turk J Gastroenterol. 2011 Oct;22(5):540-3.

37.

Challenges in diagnosing SSPE.

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.

Childs Nerv Syst. 2011 Dec;27(12):2041-4. doi: 10.1007/s00381-011-1603-x. Epub 2011 Oct 15.

PMID:
22002104
38.

Hypomyelination and congenital cataract: broadening the clinical phenotype.

Biancheri R, Zara F, Rossi A, Mathot M, Nassogne MC, Yalcinkaya C, Erturk O, Tuysuz B, Di Rocco M, Gazzerro E, Bugiani M, van Spaendonk R, Sistermans EA, Minetti C, van der Knaap MS, Wolf NI.

Arch Neurol. 2011 Sep;68(9):1191-4. doi: 10.1001/archneurol.2011.201. Review.

PMID:
21911699
39.

Recessive LAMC3 mutations cause malformations of occipital cortical development.

Barak T, Kwan KY, Louvi A, Demirbilek V, Saygı S, Tüysüz B, Choi M, Boyacı H, Doerschner K, Zhu Y, Kaymakçalan H, Yılmaz S, Bakırcıoğlu M, Cağlayan AO, Oztürk AK, Yasuno K, Brunken WJ, Atalar E, Yalçınkaya C, Dinçer A, Bronen RA, Mane S, Ozçelik T, Lifton RP, Sestan N, Bilgüvar K, Günel M.

Nat Genet. 2011 Jun;43(6):590-4. doi: 10.1038/ng.836. Epub 2011 May 15.

40.

Are pregnancy complications increased in poor responders?

Parlakgümüş HA, Haydardedeoğlu B, Simşek E, Cok T, Yalçınkaya C, Iskender C, Kılıçdağ EB.

J Turk Ger Gynecol Assoc. 2011 Mar 1;12(1):1-3. doi: 10.5152/jtgga.2011.01. eCollection 2011.

41.

Prenatal diagnosis of McKusick-Kaufman/Bardet-Biedl syndrome.

Parlakgumus A, Yalcinkaya C, Kilicdag E.

BMJ Case Rep. 2011 Mar 24;2011. pii: bcr0220113808. doi: 10.1136/bcr.02.2011.3808.

42.

Unilateral cerebellar hypoplasia with different clinical features.

Benbir G, Kara S, Yalcinkaya BC, Karhkaya G, Tuysuz B, Kocer N, Yalcinkaya C.

Cerebellum. 2011 Mar;10(1):49-60. doi: 10.1007/s12311-010-0225-2.

PMID:
20967575
43.

Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations.

Bilgüvar K, Oztürk AK, Louvi A, Kwan KY, Choi M, Tatli B, Yalnizoğlu D, Tüysüz B, Cağlayan AO, Gökben S, Kaymakçalan H, Barak T, Bakircioğlu M, Yasuno K, Ho W, Sanders S, Zhu Y, Yilmaz S, Dinçer A, Johnson MH, Bronen RA, Koçer N, Per H, Mane S, Pamir MN, Yalçinkaya C, Kumandaş S, Topçu M, Ozmen M, Sestan N, Lifton RP, State MW, Günel M.

Nature. 2010 Sep 9;467(7312):207-10. doi: 10.1038/nature09327. Epub 2010 Aug 22.

44.

Dysembryoplastic neuroepithelial tumors and gangliogliomas: clinical results of 52 patients.

Ozlen F, Gunduz A, Asan Z, Tanriverdi T, Ozkara C, Yeni N, Yalcinkaya C, Ozyurt E, Uzan M.

Acta Neurochir (Wien). 2010 Oct;152(10):1661-71. doi: 10.1007/s00701-010-0696-4. Epub 2010 Jun 5.

PMID:
20526635
45.

Familial microhydranencephaly, a family that does not map to 16p13.13-p12.2: relationship with hereditary fetal brain degeneration and fetal brain disruption sequence.

Behunova J, Zavadilikova E, Bozoglu TM, Gunduz A, Tolun A, Yalcinkaya C.

Clin Dysmorphol. 2010 Jul;19(3):107-18. doi: 10.1097/MCD.0b013e32833946e9.

PMID:
20375726
46.

A patient with Duchenne muscular dystrophy and autism demonstrates a hemizygous deletion affecting Dystrophin.

Erturk O, Bilguvar K, Korkmaz B, Bayri Y, Bayrakli F, Arlier Z, Ozturk AK, Yalcinkaya C, Tuysuz B, State MW, Gunel M.

Am J Med Genet A. 2010 Apr;152A(4):1039-42. doi: 10.1002/ajmg.a.33312. No abstract available.

PMID:
20358624
47.

Four novel SCN1A mutations in Turkish patients with severe myoclonic epilepsy of infancy (SMEI).

Arlier Z, Bayri Y, Kolb LE, Erturk O, Ozturk AK, Bayrakli F, Bilguvar K, Moliterno JA, Dervent A, Demirbilek V, Yalcinkaya C, Korkmaz B, Tuysuz B, Gunel M.

J Child Neurol. 2010 Oct;25(10):1265-8. doi: 10.1177/0883073809357241. Epub 2010 Jan 28.

PMID:
20110217
48.

Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophy.

Kolb LE, Arlier Z, Yalcinkaya C, Ozturk AK, Moliterno JA, Erturk O, Bayrakli F, Korkmaz B, DiLuna ML, Yasuno K, Bilguvar K, Ozcelik T, Tuysuz B, State MW, Gunel M.

Neurogenetics. 2010 Jul;11(3):319-25. doi: 10.1007/s10048-009-0232-y. Epub 2010 Jan 15.

PMID:
20082205
49.

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
50.

Two cases with progressive cystic leukoencephalopathy.

Yapici Z, Benbir G, Saltik S, He L, Brown GK, Taylor RW, Dincer A, Naidu S, Yalcinkaya C.

Neuropediatrics. 2009 Feb;40(1):47-51. doi: 10.1055/s-0029-1225626. Epub 2009 Jul 28.

PMID:
19639529

Supplemental Content

Loading ...
Support Center