Your search returned 8 results.

Results
	1.	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. [electronic resource] by Karacan, İlker Uğurlu, Serdal Tolun, Aslıhan Tahir Turanlı, Eda Ozdogan, Huri Producer: 20180213 In: Clinical and experimental rheumatology vol. 35 Suppl 108 Availability: No items available. Save to lists Add to cart (remove)
	2.	Peripheral blood mononuclear cell proteome profile in Behçet's syndrome. [electronic resource] by Kirectepe Aydin, Asli Özgüler, Yeşim Uçar, Didar Kasap, Murat Akpınar, Gürler Seyahi, Emire Tahir Turanli, Eda Producer: 20210212 In: Rheumatology international vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Analysis of MEFV exon methylation and expression patterns in familial Mediterranean fever. [electronic resource] by Kirectepe, Asli K Kasapcopur, Ozgur Arisoy, Nil Celikyapi Erdem, Gokce Hatemi, Gulen Ozdogan, Huri Tahir Turanli, Eda Producer: 20111104 In: BMC medical genetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A twin study in Behçet's syndrome. [electronic resource] by Masatlioglu, Seval Seyahi, Emire Tahir Turanli, Eda Fresko, Izzet Gogus, Feride Senates, Ebubekir Oguz Savran, Fatma Yazici, Hasan Producer: 20110120 In: Clinical and experimental rheumatology vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	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. [electronic resource] by Sahin, Sezgin Adrovic, Amra Barut, Kenan Baran, Selen Tahir Turanli, Eda Canpolat, Nur Kizilkilic, Osman Ozkaya, Ozan Kasapcopur, Ozgur Producer: 20210222 In: Paediatrics and international child health vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	The prevalence of Behçet's syndrome, familial Mediterranean fever, HLA-B51 and MEFV gene mutations among ethnic Armenians living in Istanbul, Turkey. [electronic resource] by Seyahi, Emire Tahir Turanli, Eda Mangan, Mehmet Serhat Celikyapi, Gokce Oktay, Veysel Cevirgen, Dilsen Kuzuoglu, Duygu Ozoglu, Susan Yazici, Hasan Producer: 20110120 In: Clinical and experimental rheumatology vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	7.	Atypical phenotype of an old disease or typical phenotype of a new disease: deficiency of adenosine deaminase 2. [electronic resource] by Çakan, Mustafa Aktay-Ayaz, Nuray Karadağ, Şerife Gül Tahir-Turanlı, Eda Stafstrom, Kelsey Bainter, Wayne Geha, Raif S Chou, Janet Producer: 20200713 In: The Turkish journal of pediatrics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	CSF Proteomics Identifies Specific and Shared Pathways for Multiple Sclerosis Clinical Subtypes. [electronic resource] by Avsar, Timucin Durası, İlknur Melis Uygunoğlu, Uğur Tütüncü, Melih Demirci, Nuri Onat Saip, Sabahattin Sezerman, O Uğur Siva, Aksel Tahir Turanlı, Eda Producer: 20160425 In: PloS one vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)