Mitochondrial Neurogastrointestinal Encephalopathy Due to Mutations in RRM2B

Por Shaibani, Aziz, Shchelochkov, Oleg A., Zhang, Shulin, Katsonis, Panagiotis, Lichtarge, Olivier, Wong, Lee-Jun, Shinawi, Marwan
Publicado em 2009

Double-blind, placebo-controlled study of HGF gene therapy in diabetic neuropathy

Por Kessler, John A, Smith, A Gordon, Cha, Bong-Soo, Choi, Sung Hee, Wymer, James, Shaibani, Aziz, Ajroud-Driss, Senda, Vinik, Aaron
Publicado no Ann Clin Transl Neurol (2015)

The effects of an intronic polymorphism in TOMM40 and APOE genotypes in sporadic inclusion body myositis

Por Gang, Qiang, Bettencourt, Conceicao, Machado, Pedro M., Fox, Zoe, Brady, Stefen, Healy, Estelle, Parton, Matt, Holton, Janice L., Hilton-Jones, David, Shieh, Perry B., Zanoteli, Edmar, De Paepe, Boel, De Bleecker, Jan, Shaibani, Aziz, Ripolone, Michela, Violano, Raffaella, Moggio, Maurizio, Barohn, Richard J., Dimachkie, Mazen M., Mora, Marina, Mantegazza, Renato, Zanotti, Simona, Hanna, Michael G., Houlden, Henry
Publicado no Neurobiol Aging (2015)

Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis

Por Gang, Qiang, Bettencourt, Conceição, Machado, Pedro M., Brady, Stefen, Holton, Janice L., Pittman, Alan M., Hughes, Deborah, Healy, Estelle, Parton, Matthew, Hilton-Jones, David, Shieh, Perry B., Needham, Merrilee, Liang, Christina, Zanoteli, Edmar, de Camargo, Leonardo Valente, De Paepe, Boel, De Bleecker, Jan, Shaibani, Aziz, Ripolone, Michela, Violano, Raffaella, Moggio, Maurizio, Barohn, Richard J., Dimachkie, Mazen M., Mora, Marina, Mantegazza, Renato, Zanotti, Simona, Singleton, Andrew B., Hanna, Michael G., Houlden, Henry
Publicado no Neurobiol Aging (2016)