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HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulinMUKHERJEE, Odity; PASTOR, Pau; LEVITCH, Denise et al.Annals of neurology. 2006, Vol 60, Num 3, pp 314-322, issn 0364-5134, 9 p.Article

TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusionsCAIRNS, Nigel J; NEUMANN, Manuela; CARTER, Deborah et al.The American journal of pathology. 2007, Vol 171, Num 1, pp 227-240, issn 0002-9440, 14 p.Article

Neuropathologic heterogeneity in HDDD1 : A familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and Progranulin mutationBEHRENS, Maria I; MUKHERJEE, Odity; CHAKRAVERTY, Sumi et al.Alzheimer disease and associated disorders. 2007, Vol 21, Num 1, pp 1-7, issn 0893-0341, 7 p.Article

Potentiation of insulin-stimulated glucose transport by the AMP-activated protein kinaseJU, Jeong-Sun; GITCHO, Michael A; CASMAER, Carter A et al.American journal of physiology. Cell physiology. 2007, Vol 61, Num 1, issn 0363-6143, C564-C572Article

Pathogenic cysteine mutations affect progranulin function and production of mature granulinsJUN WANG; VAN DAMME, Philip; CRUCHAGA, Carlos et al.Journal of neurochemistry. 2010, Vol 112, Num 5, pp 1305-1315, issn 0022-3042, 11 p.Article

TDP-43 A315T Mutation in Familial Motor Neuron DiseaseGITCHO, Michael A; BALOH, Robert H; BAKER, Matt et al.Annals of neurology. 2008, Vol 63, Num 4, pp 535-538, issn 0364-5134, 4 p.Article

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