Tahir Turanli E - Search Results

1

Investigating the role of common and rare variants in multiplex multiple sclerosis families reveals an increased burden of common risk variation.

Everest E, Ahangari M, Uygunoglu U, Tutuncu M, Bulbul A, Saip S, Duman T, Sezerman U, Reich DS, Riley BP, Siva A, Tahir Turanli E. Everest E, et al. Among authors: tahir turanli e. Sci Rep. 2022 Oct 10;12(1):16984. doi: 10.1038/s41598-022-21484-x. Sci Rep. 2022. PMID: 36216875 Free PMC article.

2

CSF Proteomics Identifies Specific and Shared Pathways for Multiple Sclerosis Clinical Subtypes.

Avsar T, Durası İM, Uygunoğlu U, Tütüncü M, Demirci NO, Saip S, Sezerman OU, Siva A, Tahir Turanlı E. Avsar T, et al. Among authors: tahir turanli e. PLoS One. 2015 May 5;10(5):e0122045. doi: 10.1371/journal.pone.0122045. eCollection 2015. PLoS One. 2015. PMID: 25942430 Free PMC article.

3

Genome-wide analysis of schizophrenia and multiple sclerosis identifies shared genomic loci with mixed direction of effects.

Ahangari M, Everest E, Nguyen TH, Verrelli BC, Webb BT, Bacanu SA, Tahir Turanli E, Riley BP. Ahangari M, et al. Among authors: tahir turanli e. Brain Behav Immun. 2022 Aug;104:183-190. doi: 10.1016/j.bbi.2022.06.007. Epub 2022 Jun 14. Brain Behav Immun. 2022. PMID: 35714915

4

Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype.

Özkılınç Önen M, Onat UI, Uğurlu S, Timuçin AC, Öz Arslan D, Everest E, Özdoğan H, Tahir Turanlı E. Özkılınç Önen M, et al. Among authors: tahir turanli e. Rheumatology (Oxford). 2023 Sep 1;62(9):3188-3196. doi: 10.1093/rheumatology/kead044. Rheumatology (Oxford). 2023. PMID: 36692132

5

Other autoinflammatory disease genes in an FMF-prevalent population: a homozygous MVK mutation and a novel heterozygous TNFRSF1A mutation in two different Turkish families with clinical FMF.

Karacan İ, Uğurlu S, Tolun A, Tahir Turanlı E, Ozdogan H. Karacan İ, et al. Among authors: tahir turanli e. Clin Exp Rheumatol. 2017 Nov-Dec;35 Suppl 108(6):75-81. Epub 2017 Oct 27. Clin Exp Rheumatol. 2017. PMID: 29148404

6

A case with febrile attacks and vasculopathy associated with ADA2 and MEFV pathogenic variants.

Parlar K, Tahir Turanli E, Nuhoglu Kantarci E, Hacioglu A, Kirectepe Aydin A, Ayla AY, Voyvoda U, Ozdogan H, Ugurlu S. Parlar K, et al. Among authors: tahir turanli e. Mod Rheumatol Case Rep. 2023 Dec 29;8(1):121-124. doi: 10.1093/mrcr/rxad045. Mod Rheumatol Case Rep. 2023. PMID: 37542433

7

Increased expression of exon 2 deleted MEFV transcript in familial Mediterranean fever patients.

Kirectepe AK, Erdem GC, Senturk N, Arisoy N, Hatemi G, Ozdogan H, Kasapcopur O, Tahir Turanli E. Kirectepe AK, et al. Among authors: tahir turanli e. Int J Immunogenet. 2011 Aug;38(4):327-9. doi: 10.1111/j.1744-313X.2011.01015.x. Epub 2011 May 25. Int J Immunogenet. 2011. PMID: 21615705

8

A 9.5-year-old boy with recurrent neurological manifestations and severe hypertension, treated initially for polyarteritis nodosa, was subsequently diagnosed with adenosine deaminase type 2 deficiency (DADA2) which responded to anti-TNF-α.

Sahin S, Adrovic A, Barut K, Baran S, Tahir Turanli E, Canpolat N, Kizilkilic O, Ozkaya O, Kasapcopur O. Sahin S, et al. Among authors: tahir turanli e. Paediatr Int Child Health. 2020 Feb;40(1):65-68. doi: 10.1080/20469047.2018.1559495. Epub 2019 Jan 15. Paediatr Int Child Health. 2020. PMID: 30642227

9

Investigation of neuro-inflammatory parameters in a cuprizone induced mouse model of multiple sclerosis.

Avşar T, Çelikyapi Erdem G, Terzioğlu G, Tahir Turanli E. Avşar T, et al. Among authors: tahir turanli e. Turk J Biol. 2021 Oct 18;45(5):644-655. doi: 10.3906/biy-2104-88. eCollection 2021. Turk J Biol. 2021. PMID: 34803461 Free PMC article.

10

Peripheral blood mononuclear cell proteome profile in Behçet's syndrome.

Kirectepe Aydin A, Özgüler Y, Uçar D, Kasap M, Akpınar G, Seyahi E, Tahir Turanli E. Kirectepe Aydin A, et al. Among authors: tahir turanli e. Rheumatol Int. 2020 Jan;40(1):65-74. doi: 10.1007/s00296-019-04417-2. Epub 2019 Aug 14. Rheumatol Int. 2020. PMID: 31414226

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