日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Myasthenia-Like Presentations Following PD-1 Inhibitors: CD8+ Myositis, Myasthenia, or Both?

PD-1抑制剂治疗后出现类似重症肌无力的症状:CD8+肌炎、重症肌无力,还是两者兼有?

Ucem, Selen; Yunisova, Gulshan; Bulus, Eser; Lacin, Sahin; Oflazer, Piraye

Recurrent de-novo gain-of-function mutation in SPTLC2 confirms dysregulated sphingolipid production to cause juvenile amyotrophic lateral sclerosis

SPTLC2基因中反复出现的新生功能获得性突变证实鞘脂生成失调是导致青少年肌萎缩侧索硬化症的原因。

Dohrn, Maike F; Beijer, Danique; Lone, Museer A; Bayraktar, Elif; Oflazer, Piraye; Orbach, Rotem; Donkervoort, Sandra; Foley, A Reghan; Rose, Aubrey; Lyons, Michael; Louie, Raymond J; Gable, Kenneth; Dunn, Teresa; Chen, Sitong; Danzi, Matt C; Synofzik, Matthis; Bönnemann, Carsten G; Nazlı Başak, A; Hornemann, Thorsten; Zuchner, Stephan

Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelines

面肩肱型肌营养不良症基因诊断最佳实践指南:2012 年指南更新

Giardina, Emiliano; Camaño, Pilar; Burton-Jones, Sarah; Ravenscroft, Gina; Henning, Franclo; Magdinier, Frederique; van der Stoep, Nienke; van der Vliet, Patrick J; Bernard, Rafaëlle; Tomaselli, Pedro J; Davis, Mark R; Nishino, Ichizo; Oflazer, Piraye; Race, Valerie; Vishnu, Venugopalan Y; Williams, Victoria; Sobreira, Cláudia F R; van der Maarel, Silvere M; Moore, Steve A; Voermans, Nicol C; Lemmers, Richard J L F

Lumbar Spinal Stenosis: A Rare Presentation of Hereditary Transthyretin Amyloidosis

腰椎管狭窄:遗传性转甲状腺素蛋白淀粉样变性的一种罕见表现

Çakar, Arman; Atmaca, Murat Mert; Kotan, Dilcan; Durmuş, Hacer; Deymeer, Feza; Oflazer, Piraye; Parman, Yeşim

Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry)

建立和实施欧洲McArdle病及其他肌肉糖原贮积症患者登记系统(EUROMAC登记系统)

Pinós, Tomàs; Andreu, Antoni L; Bruno, Claudio; Hadjigeorgiou, Georgios M; Haller, Ronald G; Laforêt, Pascal; Lucía, Alejandro; Martín, Miguel A; Martinuzzi, Andrea; Navarro, Carmen; Oflazer, Piraye; Pouget, Jean; Quinlivan, Ros; Sacconi, Sabrina; Scalco, Renata S; Toscano, Antonio; Vissing, John; Vorgerd, Matthias; Wakelin, Andrew; Martí, Ramon

Giant cell myositis and myocarditis revisited

巨细胞肌炎和心肌炎再探

Oflazer, Piraye

Relation of HLA-DRB1 to IgG4 autoantibody and cytokine production in muscle-specific tyrosine kinase myasthenia gravis (MuSK-MG)

HLA-DRB1 与 IgG4 自身抗体以及肌肉特异性酪氨酸激酶重症肌无力 (MuSK-MG) 中细胞因子产生的关系

M Çebi, H Durmuş, V Yılmaz, S P Yentür, F Aysal, P Oflazer, Y Parman, F Deymeer, G Saruhan-Direskeneli

Congenital myasthenic syndromes in Turkey: Clinical clues and prognosis with long term follow-up

土耳其先天性重症肌无力综合征:临床线索和长期随访预后

Durmus, Hacer; Shen, Xin-Ming; Serdaroglu-Oflazer, Piraye; Kara, Bulent; Parman-Gulsen, Yesim; Ozdemir, Coskun; Brengman, Joan; Deymeer, Feza; Engel, Andrew G

The effect of interleukin (IL)-21 and CD4(+) CD25(++) T cells on cytokine production of CD4(+) responder T cells in patients with myasthenia gravis

白细胞介素 (IL)-21 和 CD4(+)CD25(++) T 细胞对重症肌无力患者 CD4(+) 应答 T 细胞细胞因子产生的影响

Alahgholi-Hajibehzad, M; Durmuş, H; Aysal, F; Gülşen-Parman, Y; Oflazer, P; Deymeer, F; Saruhan-Direskeneli, G

The distinct genetic pattern of ALS in Turkey and novel mutations

土耳其ALS独特的遗传模式和新的突变

Özoğuz, Aslıhan; Uyan, Özgün; Birdal, Güneş; Iskender, Ceren; Kartal, Ece; Lahut, Suna; Ömür, Özgür; Agim, Zeynep Sena; Eken, Aslı Gündoğdu; Sen, Nesli Ece; Kavak, Pınar; Saygı, Ceren; Sapp, Peter C; Keagle, Pamela; Parman, Yeşim; Tan, Ersin; Koç, Filiz; Deymeer, Feza; Oflazer, Piraye; Hanağası, Haşmet; Gürvit, Hakan; Bilgiç, Başar; Durmuş, Hacer; Ertaş, Mustafa; Kotan, Dilcan; Akalın, Mehmet Ali; Güllüoğlu, Halil; Zarifoğlu, Mehmet; Aysal, Fikret; Döşoğlu, Nilgün; Bilguvar, Kaya; Günel, Murat; Keskin, Özlem; Akgün, Tahsin; Özçelik, Hilmi; Landers, John E; Brown, Robert H; Başak, A Nazlı