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Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic features Dori, Amir; Arad, Michael; Wasserstrum, Yishay; Pollak, Arthur; Nikitin, Vera; Ben-David, Merav; Shamash, Jana; Nahum, Ayelet Hashachar; Shavit-Stein, Efrat; Domachevsky, Liran; Kuperstein, Rafael; Dominissini, Dan; Shelestovich, Natalia; Sadeh, Menachem; Pras, Elon; Greenbaum, Lior 分享 收藏
Early diagnosis of ATTR amyloidosis through targeted follow-up of identified carriers of TTR gene mutations* Conceicao, Isabel; Damy, Thibaud; Romero, Manuel; Galan, Lucia; Attarian, Shahram; Luigetti, Marco; Sadeh, Menachem; Sarafov, Stayko; Tournev, Ivailo; Ueda, Mitsuharu 分享 收藏
Kyphoscoliosis peptidase (KY) mutation causes a novel congenital myopathy with core targetoid defects Straussberg, Rachel; Schottmann, Gudrun; Sadeh, Menachem; Gill, Esther; Seifert, Franziska; Halevy, Ayelet; Qassem, Kaiyal; Rendu, John; van der Ven, Peter F. M.; Stenzel, Werner; Schuelke, Markus 分享 收藏
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Novel mutation in VCP gene causes atypical amyotrophic lateral sclerosis Gonzalez-Perez, Paloma; Cirulli, Elizabeth T.; Drory, Vivian E.; Dabby, Ron; Nisipeanu, Puiu; Carasso, Ralph L.; Sadeh, Menachem; Fox, Andrew; Festoff, Barry W.; Sapp, Peter C.; McKenna-Yasek, Diane; Goldstein, David B.; Brown, Robert H., Jr.; Blumen, Sergiu C. 分享 收藏
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Low-level laser therapy applied transcranially to rats after induction of stroke significantly reduces long-term neurological deficits Oron, Amir; Oron, Uri; Chen, Jieli; Eilam, Anda; Zhang, Chunling; Sadeh, Menachem; Lampl, Yair; Streeter, Jackson; DeTaboada, Luis; Chopp, Michael 分享 收藏
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