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Best matches for Kasapçopur Ö[au]:

Juvenile Idiopathic Arthritis. Barut K et al. Balkan Med J. (2017)

Pediatric vasculitis. Barut K et al. Curr Opin Rheumatol. (2016)

Juvenile Spondyloarthropathies. Adrovic A et al. Curr Rheumatol Rep. (2016)

Search results

Items: 1 to 50 of 182

1.

Polyarteritis nodosa: lessons from 25 years of experience.

Sönmez HE, Armağan B, Ayan G, Barut K, Batu ED, Erden A, Uğurlu S, Bilginer Y, Kasapçopur Ö, Karadağ Ö, Bilgen SA, Özdoğan H, Ozen S.

Clin Exp Rheumatol. 2018 Oct 30. [Epub ahead of print]

PMID:
30418125
2.

The frequency of juvenile spondyloarthropathies in childhood familial Mediterranean fever.

Ozer E, Seker D, Taner E, Adrovic A, Sahin S, Barut K, Kasapcopur O.

Clin Exp Rheumatol. 2018 Nov 5. [Epub ahead of print]

PMID:
30418123
3.

Childhood-onset Takayasu arteritis: A 15-year experience from a tertiary referral center.

Sahin S, Hopurcuoglu D, Bektas S, Belhan E, Adrovic A, Barut K, Canpolat N, Caliskan S, Sever L, Kasapcopur O.

Int J Rheum Dis. 2018 Nov 5. doi: 10.1111/1756-185X.13425. [Epub ahead of print]

PMID:
30397997
4.

Evaluation of six-minute walk test in juvenile systemic sclerosis.

Koker O, Adrovic A, Sahin S, Yildiz M, Barut K, Omeroglu RE, Kasapcopur O.

Rheumatol Int. 2018 Oct 26. doi: 10.1007/s00296-018-4185-z. [Epub ahead of print]

PMID:
30367202
5.

Canakinumab in patients with systemic juvenile idiopathic arthritis and active systemic features: results from the 5-year long-term extension of the phase III pivotal trials.

Ruperto N, Brunner HI, Quartier P, Constantin T, Wulffraat NM, Horneff G, Kasapcopur O, Schneider R, Anton J, Barash J, Berner R, Corona F, Cuttica R, Fouillet-Desjonqueres M, Fischbach M, Foster HE, Foell D, Radominski SC, Ramanan AV, Trauzeddel R, Unsal E, Levy J, Vritzali E, Martini A, Lovell DJ; Paediatric Rheumatology International Trials Organisation (PRINTO) and the Pediatric Rheumatology Collaborative Study Group (PRCSG).

Ann Rheum Dis. 2018 Dec;77(12):1710-1719. doi: 10.1136/annrheumdis-2018-213150. Epub 2018 Sep 29.

6.

The Assessment of Serum Endocan Levels in Children With Juvenile Idiopathic Arthritis.

Yilmaz Y, Berru Durmuş R, Saraçoğlu B, Şahin S, Adrovic A, Barut K, Özel Yildiz S, Kasapçopur Ö, Eker Ömeroğlu R.

Arch Rheumatol. 2017 Oct 16;33(2):168-173. doi: 10.5606/ArchRheumatol.2018.6528. eCollection 2018 Jun.

7.

Comparison of familial Mediterranean fever and juvenile idiopathic arthritis patients according to family origin.

Barut K, Pamuk G, Adrovic A, Şahin S, Kaplan A, Güler M, Kasapçopur Ö.

Turk Pediatri Ars. 2018 Mar 1;53(1):31-36. doi: 10.5152/TurkPediatriArs.2018.5818. eCollection 2018 Mar.

8.

SEROLOGICAL SCREENING FOR CELIAC DISEASE IN CHILDREN WITH COLCHICINE-RESISTANT FAMILIAL MEDITERRANEAN FEVER.

Şahin Y, Barut K, Kutlu T, Cokugras FC, Adrovic A, Sahin S, Erkan T, Kasapcopur O.

Arq Gastroenterol. 2018 Apr-Jun;55(2):175-178. doi: 10.1590/S0004-2803.201800000-31.

9.

Effects of Video Games-Based Task-Oriented Activity Training (Xbox 360 KinectTM) on Activity Performance and Participation in Patients with Juvenile Idiopathic Arthritis: A Randomized Clinical Trial.

Arman N, Tarakci E, Tarakci D, Kasapcopur O.

Am J Phys Med Rehabil. 2018 Jul 16. doi: 10.1097/PHM.0000000000001001. [Epub ahead of print]

PMID:
30020092
10.

Familial Mediterranean fever and periodic fever, aphthous stomatitis, pharyngitis, and adenitis (PFAPA) syndrome: shared features and main differences.

Adrovic A, Sahin S, Barut K, Kasapcopur O.

Rheumatol Int. 2018 Jul 17. doi: 10.1007/s00296-018-4105-2. [Epub ahead of print] Review.

PMID:
30019226
11.

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 Jul 15. pii: jrheum.171358. doi: 10.3899/jrheum.171358. [Epub ahead of print]

PMID:
30008451
12.

Canakinumab for the Treatment of Autoinflammatory Recurrent Fever Syndromes.

De Benedetti F, Gattorno M, Anton J, Ben-Chetrit E, Frenkel J, Hoffman HM, Koné-Paut I, Lachmann HJ, Ozen S, Simon A, Zeft A, Calvo Penades I, Moutschen M, Quartier P, Kasapcopur O, Shcherbina A, Hofer M, Hashkes PJ, Van der Hilst J, Hara R, Bujan-Rivas S, Constantin T, Gul A, Livneh A, Brogan P, Cattalini M, Obici L, Lheritier K, Speziale A, Junge G.

N Engl J Med. 2018 May 17;378(20):1908-1919. doi: 10.1056/NEJMoa1706314.

PMID:
29768139
13.

LACC1 Gene Defects in Familial Form of Juvenile Arthritis.

Karacan I, Uğurlu S, Şahin S, Everest E, Kasapçopur Ö, Tolun A, Özdoğan H, Turanli ET.

J Rheumatol. 2018 May;45(5):726-728. doi: 10.3899/jrheum.170834. No abstract available.

PMID:
29717096
14.

Juvenile Scleroderma-What has Changed in the Meantime?

Adrovic A, Sahin S, Barut K, Kasapcopur O.

Curr Rheumatol Rev. 2018;14(3):219-225. doi: 10.2174/1573397114666180423105056.

PMID:
29692255
15.

The Turkish version of the Juvenile Arthritis Multidimensional Assessment Report (JAMAR).

Demirkaya E, Ozen S, Sozeri B, Ayaz NA, Kasapcopur O, Unsal E, Makay BB, Barut K, Fidanci BE, Simsek D, Cakan M, Consolaro A, Bovis F, Ruperto N; Paediatric Rheumatology International Trials Organisation (PRINTO).

Rheumatol Int. 2018 Apr;38(Suppl 1):395-402. doi: 10.1007/s00296-018-3982-8. Epub 2018 Apr 7.

16.

The safety of live-attenuated vaccines in patients using IL-1 or IL-6 blockade: an international survey.

Jeyaratnam J, Ter Haar NM, Lachmann HJ, Kasapcopur O, Ombrello AK, Rigante D, Dedeoglu F, Baris EH, Vastert SJ, Wulffraat NM, Frenkel J.

Pediatr Rheumatol Online J. 2018 Mar 21;16(1):19. doi: 10.1186/s12969-018-0235-z.

17.

Genotype-phenotype investigation of 35 patients from 11 unrelated families with camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome.

Yilmaz S, Uludağ Alkaya D, Kasapçopur Ö, Barut K, Akdemir ES, Celen C, Youngblood MW, Yasuno K, Bilguvar K, Günel M, Tüysüz B.

Mol Genet Genomic Med. 2018 Mar;6(2):230-248. doi: 10.1002/mgg3.364. Epub 2018 Feb 4.

18.

TNF-alpha 863C > A promoter and TNFRII 196T > G exonic variationsmay be risk factors for juvenile idiopathic arthritis

Batar B, Özman S, Barut K, Kasapçopur Ö, Güven M.

Turk J Med Sci. 2017 Dec 19;47(6):1819-1825. doi: 10.3906/sag-1612-23.

PMID:
29306244
19.

Juvenile systemic lupus erythematosus in Turkey: demographic, clinical and laboratory features with disease activity and outcome.

Sahin S, Adrovic A, Barut K, Canpolat N, Ozluk Y, Kilicaslan I, Caliskan S, Sever L, Kasapcopur O.

Lupus. 2018 Mar;27(3):514-519. doi: 10.1177/0961203317747717. Epub 2017 Dec 12.

PMID:
29233038
20.

Mucolipidosis type III gamma: Three novel mutation and genotype-phenotype study in eleven patients.

Tüysüz B, Kasapçopur Ö, Alkaya DU, Şahin S, Sözeri B, Yeşil G.

Gene. 2018 Feb 5;642:398-407. doi: 10.1016/j.gene.2017.11.052. Epub 2017 Nov 21.

PMID:
29170090
21.

Role of genetics in pediatric rheumatology.

Turanlı ET, Everest E, Balamir A, Aydın AK, Kasapçopur Ö.

Turk Pediatri Ars. 2017 Sep 1;52(3):113-121. doi: 10.5152/TurkPediatriArs.2017.4953. eCollection 2017 Sep. Review.

22.

PFAPA Syndrome in a Population with Endemic Familial Mediterranean Fever.

Pehlivan E, Adrovic A, Sahin S, Barut K, Kul Cınar O, Kasapcopur O.

J Pediatr. 2018 Jan;192:253-255. doi: 10.1016/j.jpeds.2017.08.078. Epub 2017 Oct 12.

PMID:
29031862
23.

The performance of classification criteria for juvenile spondyloarthropathies.

Adrovic A, Sezen M, Barut K, Sahin S, Acikel C, Demirkaya E, Kasapcopur O.

Rheumatol Int. 2017 Dec;37(12):2013-2018. doi: 10.1007/s00296-017-3837-8. Epub 2017 Oct 10.

PMID:
29018906
24.

New Insights into Cardiac Involvement in Juvenile Scleroderma: A Three-Dimensional Echocardiographic Assessment Unveils Subclinical Ventricle Dysfunction.

Dedeoglu R, Adroviç A, Oztunç F, Sahin S, Barut K, Kasapcopur O.

Pediatr Cardiol. 2017 Dec;38(8):1686-1695. doi: 10.1007/s00246-017-1714-6. Epub 2017 Sep 14.

PMID:
28913656
25.

Familial Mediterranean fever in childhood: a single-center experience.

Barut K, Sahin S, Adrovic A, Sinoplu AB, Yucel G, Pamuk G, Aydın AK, Dasdemir S, Turanlı ET, Buyru N, Kasapcopur O.

Rheumatol Int. 2018 Jan;38(1):67-74. doi: 10.1007/s00296-017-3796-0. Epub 2017 Aug 21.

PMID:
28828621
26.

Development and Initial Validation of the Macrophage Activation Syndrome/Primary Hemophagocytic Lymphohistiocytosis Score, a Diagnostic Tool that Differentiates Primary Hemophagocytic Lymphohistiocytosis from Macrophage Activation Syndrome.

Minoia F, Bovis F, Davì S, Insalaco A, Lehmberg K, Shenoi S, Weitzman S, Espada G, Gao YJ, Anton J, Kitoh T, Kasapcopur O, Sanner H, Merino R, Astigarraga I, Alessio M, Jeng M, Chasnyk V, Nichols KE, Huasong Z, Li C, Micalizzi C, Ruperto N, Martini A, Cron RQ, Ravelli A, Horne A; Pediatric Rheumatology International Trials Organization, the Childhood Arthritis and Rheumatology Research Alliance, the Pediatric Rheumatology Collaborative Study Group, and the Histiocyte Society.

J Pediatr. 2017 Oct;189:72-78.e3. doi: 10.1016/j.jpeds.2017.06.005. Epub 2017 Aug 12.

PMID:
28807357
27.

Evaluation of pulmonary artery pressure in patients with juvenile systemic lupus erythematosus (jSLE).

Adrovic A, Dedeoglu R, Sahin S, Barut K, Koka A, Cengiz D, Oztunc F, Kasapcopur O.

Bosn J Basic Med Sci. 2018 Feb 20;18(1):66-71. doi: 10.17305/bjbms.2017.2178.

28.

REST Final-Exon-Truncating Mutations Cause Hereditary Gingival Fibromatosis.

Bayram Y, White JJ, Elcioglu N, Cho MT, Zadeh N, Gedikbasi A, Palanduz S, Ozturk S, Cefle K, Kasapcopur O, Coban Akdemir Z, Pehlivan D, Begtrup A, Carvalho CMB, Paine IS, Mentes A, Bektas-Kayhan K, Karaca E, Jhangiani SN, Muzny DM; Baylor-Hopkins Center for Mendelian Genomics, Gibbs RA, Lupski JR.

Am J Hum Genet. 2017 Jul 6;101(1):149-156. doi: 10.1016/j.ajhg.2017.06.006.

29.

Erratum to: Evaluation of cardiac functions in juvenile systemic lupus erythematosus with two-dimensional speckle tracking echocardiography.

Dedeoglu R, Şahin S, Koka A, Öztunç F, Adroviç A, Barut K, Cengiz D, Kasapçopur Ö.

Clin Rheumatol. 2017 Nov;36(11):2631. doi: 10.1007/s10067-017-3739-x. No abstract available.

PMID:
28685376
30.

Significance of pentraxin-3 in patients with juvenile scleroderma.

Adrovic A, Sahin S, Barut K, Durmus S, Uzun H, Kasapcopur O.

Clin Exp Rheumatol. 2017 Sep-Oct;35 Suppl 106(4):221-222. Epub 2017 Jun 20. No abstract available.

PMID:
28664833
31.

Brief Report: Deficiency of Complement 1r Subcomponent in Early-Onset Systemic Lupus Erythematosus: The Role of Disease-Modifying Alleles in a Monogenic Disease.

Demirkaya E, Zhou Q, Smith CK, Ombrello MJ, Deuitch N, Tsai WL, Hoffmann P, Remmers EF, Takeuchi M, Park YH, Chae J, Barut K, Simsek D, Adrovic A, Sahin S, Caliskan S, Chandrasekharappa SC, Hasni SA, Ombrello AK, Gadina M, Kastner DL, Kaplan MJ, Kasapcopur O, Aksentijevich I.

Arthritis Rheumatol. 2017 Sep;69(9):1832-1839. doi: 10.1002/art.40158. Epub 2017 Jul 10.

32.

Evaluation of myocardial deformation in patients with Kawasaki disease using speckle-tracking echocardiography during mid-term follow-up - CORRIGENDUM.

Dedeoglu R, Barut K, Oztunc F, Atik S, Adrovic A, Sahin S, Cengiz D, Kasapcopur O.

Cardiol Young. 2017 Sep;27(7):1386. doi: 10.1017/S1047951117001044. Epub 2017 May 23. No abstract available.

PMID:
28532518
33.

Clinical, imaging and genotypical features of three deceased and five surviving cases with ADA2 deficiency.

Sahin S, Adrovic A, Barut K, Ugurlu S, Turanli ET, Ozdogan H, Kasapcopur O.

Rheumatol Int. 2018 Jan;38(1):129-136. doi: 10.1007/s00296-017-3740-3. Epub 2017 May 17.

PMID:
28516235
34.

The impact of peer victimization and psychological symptoms on quality of life in children and adolescents with systemic lupus erythematosus.

Uzuner S, Sahin S, Durcan G, Adrovic A, Barut K, Kilicoglu AG, Bilgic A, Bahali K, Kasapcopur O.

Clin Rheumatol. 2017 Jun;36(6):1297-1304. doi: 10.1007/s10067-017-3650-5. Epub 2017 Apr 27.

PMID:
28451871
35.

Pentraxin-3 levels are associated with vasculitis and disease activity in childhood-onset systemic lupus erythematosus.

Sahin S, Adrovic A, Barut K, Durmus S, Gelisgen R, Uzun H, Kasapcopur O.

Lupus. 2017 Sep;26(10):1089-1094. doi: 10.1177/0961203317699286. Epub 2017 Mar 14.

PMID:
28420068
36.

Juvenile Idiopathic Arthritis.

Barut K, Adrovic A, Şahin S, Kasapçopur Ö.

Balkan Med J. 2017 Apr 5;34(2):90-101. doi: 10.4274/balkanmedj.2017.0111.

37.

Evaluation of myocardial deformation in patients with Kawasaki disease using speckle-tracking echocardiography during mid-term follow-up.

Dedeoglu R, Barut K, Oztunc F, Atik S, Adrovic A, Sahin S, Cengiz D, Kasapcopur O.

Cardiol Young. 2017 Sep;27(7):1377-1385. doi: 10.1017/S1047951117000580. Epub 2017 Apr 5. Erratum in: Cardiol Young. 2017 Sep;27(7):1386.

PMID:
28376935
38.

Emotional and behavioral influence of headache in Pediatric rheumatic diseases.

Dogangun B, Tavsanli ME, Sen E, Guntel M, Kasapcopur O, Sohtaoglu M, Stat EY, Saip S, Uluduz D.

J Clin Neurosci. 2017 Aug;42:134-138. doi: 10.1016/j.jocn.2017.03.025. Epub 2017 Mar 22. No abstract available.

PMID:
28342706
39.

Comparison of Disease Characteristics, Organ Damage, and Survival in Patients with Juvenile-onset and Adult-onset Systemic Lupus Erythematosus in a Combined Cohort from 2 Tertiary Centers in Turkey.

Artim-Esen B, Şahin S, Çene E, Şahinkaya Y, Barut K, Adrovic A, Özlük Y, Kılıçaslan I, Omma A, Gül A, Öcal L, Kasapçopur Ö, İnanç M.

J Rheumatol. 2017 May;44(5):619-625. doi: 10.3899/jrheum.160340. Epub 2017 Mar 15.

PMID:
28298568
40.

Idiopathic Pulmonary Hemosiderosis in a Child with Recurrent Macrophage Activation Syndrome Secondary to Systemic Juvenile Idiopathic Arthritis.

Barut K, Sahin S, Adrovic A, Sen V, Kasapcopur O.

Case Rep Pediatr. 2017;2017:5693501. doi: 10.1155/2017/5693501. Epub 2017 Jan 30.

41.

The frequency of the celiac disease among children with familial Mediterranean fever.

Sahin Y, Adrovic A, Barut K, Kutlu T, Cullu-Cokugras F, Sahin S, Kasapcopur O, Erkan T.

Mod Rheumatol. 2017 Nov;27(6):1036-1039. doi: 10.1080/14397595.2016.1270497. Epub 2017 Feb 21.

PMID:
28151032
42.

Juvenile dermatomyositis: a tertiary center experience.

Barut K, Aydin PO, Adrovic A, Sahin S, Kasapcopur O.

Clin Rheumatol. 2017 Feb;36(2):361-366. doi: 10.1007/s10067-016-3530-4. Epub 2017 Jan 5.

PMID:
28058540
43.

Serum vitamin D levels during activation and remission periods of patients with juvenile idiopathic arthritis and familial Mediterranean fever.

Dağdeviren-Çakır A, Arvas A, Barut K, Gür E, Kasapçopur Ö.

Turk J Pediatr. 2016;58(2):125-131.

44.

Vitamin D levels in children with familial Mediterranean fever.

Onur H, Kasapcopur O.

Clin Exp Rheumatol. 2017 May-Jun;35 Suppl 104(2):8. Epub 2016 Nov 10. No abstract available.

45.

A novel assessment tool for clinical care of patients with autoinflammatory disease: juvenile autoinflammatory disease multidimensional assessment report.

Konukbay D, Gattorno M, Yildiz D, Frenkel J, Acikel C, Sozeri B, Makay B, Aktay Ayaz N, Barut K, Kisaarslan A, Bilginer Y, Karaman D, Peru H, Simsek D, Aydog O, Unsal E, Gunduz Z, Fidanci BE, Kone-Paut I, Kasapcopur O, Ravelli A, Ozen S, Demirkaya E; and the FMF Arthritis Vasculitis and Orphan disease Research in Paediatric Rheumatology.

Clin Exp Rheumatol. 2016 Sep-Oct;34(6 Suppl 102):129-135. Epub 2016 Oct 25.

PMID:
27791950
46.

Inceased frequency of psoriasis in the families of the children with familial Mediterranean fever.

Barut K, Guler M, Sezen M, Kasapçopur O.

Clin Exp Rheumatol. 2016 Sep-Oct;34(6 Suppl 102):S137. Epub 2016 May 24. No abstract available.

PMID:
27243382
47.

Genetic and clinical features of cryopyrin-associated periodic syndromes in Turkish children.

Eroglu FK, Kasapcopur O, Beşbaş N, Ozaltin F, Bilginer Y, Barut K, Mensa-Vilaro A, Nakagawa K, Heike T, Nishikomori R, Arostegui J, Ozen S.

Clin Exp Rheumatol. 2016 Sep-Oct;34(6 Suppl 102):S115-S120. Epub 2016 May 10.

PMID:
27191192
48.

Systemic-onset juvenile idiopathic arthritis or incomplete Kawasaki disease: a diagnostic challenge.

Sahin S, Adrovic A, Barut K, Kasapcopur O.

Clin Exp Rheumatol. 2017 May-Jun;35 Suppl 104(2):10. Epub 2016 Oct 26. No abstract available.

49.

Sjögren's syndrome associated with systemic lupus erythematosus.

Taşdemir M, Hasan C, Ağbaş A, Kasapçopur Ö, Canpolat N, Sever L, Çalışkan S.

Turk Pediatri Ars. 2016 Sep 1;51(3):166-168. eCollection 2016 Sep.

50.

Potential of Serum and Urinary Matrix Metalloproteinase-9 Levels for the Early Detection of Renal Involvement in Children With Henoch-Schönlein Purpura.

Erol M, Yigit O, Tasdemir M, Bostan Gayret O, Buke O, Gunes A, Hamilcikan S, Kasapcopur O.

Iran J Pediatr. 2016 Jun 5;26(4):e6129. eCollection 2016 Aug.

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