J. R. Gorospe

<i>GFAP</i> mutations, age at onset, and clinical subtypes in Alexander disease

Morgan J. Prust, Jiaxian Wang, Hiroki Morizono et al. · Neurology · 2011 · 249 citations · Full text

Molecular findings in symptomatic and pre-symptomatic Alexander disease patients

J. R. Gorospe, S. Naidu, Vandana Puri et al. · Neurology · 2002 · 100 citations

Decreased platelet expression of myosin regulatory light chain polypeptide (MYL9) and other genes with platelet dysfunction and CBFA2/RUNX1 mutation: insights from platelet expression profiling

Liyun Sun, J. R. Gorospe, Eric P. Hoffman et al. · Journal of Thrombosis and Haemostasis · 2006 · 86 citations · Full text

Molecular Regulation, Genetics, Cbfa2/runx1 Mutation +16

Discrepancy between neuroimaging findings and clinical phenotype in Alexander disease.

Argirios Dinopoulos, J. R. Gorospe, John C. Egelhoff et al. · PubMed · 2007 · 21 citations · Full text

Neurological Disorder, Clinical Neurology, Pathology +18