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Page 1
Leflunomide treatment in juvenile idiopathic arthritis.
Ayaz NA, Karadağ ŞG, Çakmak F, Çakan M, Tanatar A, Sönmez HE. Ayaz NA, et al. Among authors: cakan m. Rheumatol Int. 2019 Sep;39(9):1615-1619. doi: 10.1007/s00296-019-04385-7. Epub 2019 Jul 20. Rheumatol Int. 2019. PMID: 31327053
Two cases of periodic fever syndrome with coexistent mevalonate kinase and Mediterranean fever gene mutations.
Çakan M, Aktay-Ayaz N, Keskindemirci G, Karadağ ŞG. Çakan M, et al. Turk J Pediatr. 2017;59(4):467-470. doi: 10.24953/turkjped.2017.04.015. Turk J Pediatr. 2017. PMID: 29624229 Free article.
Cakan M, Aktay-Ayaz N, Keskindemirci G, Karadag SG. Two cases of periodic fever syndrome with coexistent mevalonate kinase and Mediterranean fever gene mutations. ...
Cakan M, Aktay-Ayaz N, Keskindemirci G, Karadag SG. Two cases of periodic fever syndrome with coexistent mevalonate kinase and
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). Demirkaya E, et al. Among authors: cakan m. Rheumatol Int. 2018 Apr;38(Suppl 1):395-402. doi: 10.1007/s00296-018-3982-8. Epub 2018 Apr 7. Rheumatol Int. 2018. PMID: 29637329 Free PMC article.
Diagnostic utility of a targeted next-generation sequencing gene panel in the clinical suspicion of systemic autoinflammatory diseases: a multi-center study.
Karacan İ, Balamir A, Uğurlu S, Aydın AK, Everest E, Zor S, Önen MÖ, Daşdemir S, Özkaya O, Sözeri B, Tufan A, Yıldırım DG, Yüksel S, Ayaz NA, Ömeroğlu RE, Öztürk K, Çakan M, Söylemezoğlu O, Şahin S, Barut K, Adroviç A, Seyahi E, Özdoğan H, Kasapçopur Ö, Turanlı ET. Karacan İ, et al. Among authors: cakan m. Rheumatol Int. 2019 May;39(5):911-919. doi: 10.1007/s00296-019-04252-5. Epub 2019 Feb 19. Rheumatol Int. 2019. PMID: 30783801
Correction to: Diagnostic utility of a targeted next-generation sequencing gene panel in the clinical suspicion of systemic autoinflammatory diseases: a multi-center study.
Karacan İ, Balamir A, Uğurlu S, Aydın AK, Everest E, Zor S, Önen MÖ, Daşdemir S, Özkaya O, Sözeri B, Tufan A, Yıldırım DG, Yüksel S, Ayaz NA, Ömeroğlu RE, Öztürk K, Çakan M, Söylemezoğlu O, Şahin S, Barut K, Adroviç A, Seyahi E, Özdoğan H, Kasapçopur Ö, Turanlı ET. Karacan İ, et al. Among authors: cakan m. Rheumatol Int. 2019 May;39(5):921. doi: 10.1007/s00296-019-04280-1. Rheumatol Int. 2019. PMID: 30887163
An extreme entity in differential diagnosis of musculoskeletal involvement-fibrodysplasia ossificans progressiva: a case based review.
Çakan M, Aktay-Ayaz N, Karadağ ŞG, Keskindemirci G. Çakan M, et al. Turk J Pediatr. 2018;60(5):593-597. doi: 10.24953/turkjped.2018.05.021. Turk J Pediatr. 2018. PMID: 30968644 Free article.
Cakan M, Aktay-Ayaz N, Karadag SG, Keskindemirci G. An extreme entity in differential diagnosis of musculoskeletal involvement-fibrodysplasia ossificans progressiva: a case based review. ...
Cakan M, Aktay-Ayaz N, Karadag SG, Keskindemirci G. An extreme entity in differential diagnosis of musculoskeletal involvement
133 results