| Evidence of nuclear DNA fragmentation following hypoxia‐ischemia in the infant rat brain, and transient forebrain ischemia in the adult gerbil I Ferrer, A Tortosa, A Macaya, A Sierra, D Moreno, F Munell, R Blanco, ... Brain pathology 4 (2), 115-122, 1994 | 169 | 1994 |
| Altered lipid composition in cortical lipid rafts occurs at early stages of sporadic Alzheimer's disease and facilitates APP/BACE1 interactions N Fabelo, V Martín, R Marín, D Moreno, I Ferrer, M Díaz Neurobiology of aging 35 (8), 1801-1812, 2014 | 162 | 2014 |
| TAR DNA-Binding protein 43 accumulation in protein aggregate myopathies M Olivé, A Janué, D Moreno, J Gámez, B Torrejón-Escribano, I Ferrer Journal of Neuropathology & Experimental Neurology 68 (3), 262-273, 2009 | 108 | 2009 |
| Proteasomal expression, induction of immunoproteasome subunits, and local MHC class I presentation in myofibrillar myopathy and inclusion body myositis I Ferrer, B Martín, JG Castaño, JJ Lucas, D Moreno, M Olivé Journal of neuropathology and experimental neurology 63 (5), 484-498, 2004 | 102 | 2004 |
| Desmin-related myopathy: clinical, electrophysiological, radiological, neuropathological and genetic studies M Olivé, L Goldfarb, D Moreno, E Laforet, A Dagvadorj, N Sambuughin, ... Journal of the neurological sciences 219 (1-2), 125-137, 2004 | 96 | 2004 |
| Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patient M Olivé, A Shatunov, L Gonzalez, O Carmona, D Moreno, LG Quereda, ... Neuromuscular Disorders 18 (12), 929-933, 2008 | 65 | 2008 |
| New cardiac and skeletal protein aggregate myopathy associated with combined MuRF1 and MuRF3 mutations M Olivé, S Abdul-Hussein, A Oldfors, J González-Costello, ... Human molecular genetics 24 (13), 3638-3650, 2015 | 61 | 2015 |
| Expression of mutant ubiquitin (UBB+1) and p62 in myotilinopathies and desminopathies M Olivé, FW Van Leeuwen, A Janué, D Moreno, B Torrejón‐Escribano, ... Neuropathology and applied neurobiology 34 (1), 76-87, 2008 | 61 | 2008 |
| Involvement of clusterin and the aggresome in abnormal protein deposits in myofibrillar myopathies and inclusion body myositis I Ferrer, M Carmona, R Blanco, D Moreno, B Torrejón‐Escribano, M Olive Brain pathology 15 (2), 101-108, 2005 | 49 | 2005 |
| Target genes of neuron-restrictive silencer factor are abnormally up-regulated in human myotilinopathy M Barrachina, J Moreno, S Juvés, D Moreno, M Olivé, I Ferrer The American journal of pathology 171 (4), 1312-1323, 2007 | 31 | 2007 |
| A novel mutation in the caveolin-3 gene causing familial isolated hyperCKaemia L Alias, P Gallano, D Moreno, R Pujol, JA Martı́nez-Matos, M Baiget, ... Neuromuscular Disorders 14 (5), 321-324, 2004 | 29 | 2004 |
| Nemaline myopathy type 6: clinical and myopathological features M Olivé, LG Goldfarb, HS Lee, Z Odgerel, A Blokhin, L Gonzalez‐Mera, ... Muscle & nerve 42 (6), 901-907, 2010 | 24 | 2010 |
| Overexpression of semicarbazide‐sensitive amine oxidase in human myopathies M Olivé, M Unzeta, D Moreno, I Ferrer Muscle & Nerve: Official Journal of the American Association of …, 2004 | 15 | 2004 |
| PO-1210: Local treatment on the outcome of immunecheckpoint inhibitors in metastatic urothelial carcinoma J Maldonado, RM Barrera, N Vidal, N Feltes, M Domenech, J Puente, ... Radiotherapy and Oncology 152, S637-S638, 2020 | | 2020 |
| Nemaline myopathy type 6: clinical and myopathological features M Olivé i Plana, LG Goldfarb, HS Lee, Z Odgerel, A Blokhin, ... Muscle & Nerve, 2010, vol. 42, num. 6, p. 901-907, 2010 | | 2010 |
| Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patient M Olivé i Plana, A Shatunov, L González Mera, O Carmona, D Moreno, ... Neuromuscular Disorders, 2008, vol. 18, num. 12, p. 929-933, 2008 | | 2008 |
