Tahir Turanli E - Search Results

1

Analysis of MEFV exon methylation and expression patterns in familial Mediterranean fever.

Kirectepe AK, Kasapcopur O, Arisoy N, Celikyapi Erdem G, Hatemi G, Ozdogan H, Tahir Turanli E. Kirectepe AK, et al. Among authors: tahir turanli e. BMC Med Genet. 2011 Aug 7;12:105. doi: 10.1186/1471-2350-12-105. BMC Med Genet. 2011. PMID: 21819621 Free PMC article.

2

The prevalence of Behçet's syndrome, familial Mediterranean fever, HLA-B51 and MEFV gene mutations among ethnic Armenians living in Istanbul, Turkey.

Seyahi E, Tahir Turanli E, Mangan MS, Celikyapi G, Oktay V, Cevirgen D, Kuzuoglu D, Ozoglu S, Yazici H. Seyahi E, et al. Among authors: tahir turanli e. Clin Exp Rheumatol. 2010 Jul-Aug;28(4 Suppl 60):S67-75. Epub 2010 Sep 24. Clin Exp Rheumatol. 2010. PMID: 20868574

3

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

4

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

5

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

6

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.

7

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

8

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

9

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

10

A twin study in Behçet's syndrome.

Masatlioglu S, Seyahi E, Tahir Turanli E, Fresko I, Gogus F, Senates E, Oguz Savran F, Yazici H. Masatlioglu S, et al. Among authors: tahir turanli e. Clin Exp Rheumatol. 2010 Jul-Aug;28(4 Suppl 60):S62-6. Epub 2010 Sep 24. Clin Exp Rheumatol. 2010. PMID: 20868573

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