Exome sequencing identifies titin mutations causing hereditary myopathy with early respiratory failure (HMERF) in families of diverse ethnic origins

por Toro, Camilo, Olivé, Montse, Dalakas, Marinos C, Sivakumar, Kumaraswami, Bilbao, Juan M, Tyndel, Felix, Vidal, Noemí, Farrero, Eva, Sambuughin, Nyamkhishig, Goldfarb, Lev G
Publicado 2013

Differentiating between visual hallucination-free dementia with Lewy bodies and corticobasal syndrome on the basis of neuropsychology and perfusion single-photon emission computed...

por Misch, Michael R, Mitchell, Sara, Francis, Philip L, Sherborn, Kayla, Meradje, Katayoun, McNeely, Alicia A, Honjo, Kie, Zhao, Jiali, Scott, Christopher JM, Caldwell, Curtis B, Ehrlich, Lisa, Shammi, Prathiba, MacIntosh, Bradley J, Bilbao, Juan M, Lang, Anthony E, Black, Sandra E, Masellis, Mario
Publicado 2014