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Results: 1-8 |
Results: 8
Iron and iron management proteins in neurobiology
Authors: Connor, JR Menzies, SL Burdo, JR Boyer, PJ
Citation: Jr. Connor et al., Iron and iron management proteins in neurobiology, PED NEUROL, 25(2), 2001, pp. 118-129
Genetic and cellular defects contributing to benign tumor formation in neurofibromatosis type 1
Authors: Rutkowski, JL Wu, KS Gutmann, DH Boyer, PJ Legius, E
Citation: Jl. Rutkowski et al., Genetic and cellular defects contributing to benign tumor formation in neurofibromatosis type 1, HUM MOL GEN, 9(7), 2000, pp. 1059-1066
Solitary sciatic nerve lymphoma as an initial manifestation of diffuse neurolymphomatosis - Case report and review of the literature
Authors: Quinones-Hinojosa, A Friedlander, RM Boyer, PJ Batchelor, TT Chiocca, EA
Citation: A. Quinones-hinojosa et al., Solitary sciatic nerve lymphoma as an initial manifestation of diffuse neurolymphomatosis - Case report and review of the literature, J NEUROSURG, 92(1), 2000, pp. 165-169
Signals for proinflammatory cytokine secretion by human Schwann cells
Authors: Rutkowski, JL Tuite, GF Lincoln, PM Boyer, PJ Tennekoon, GI Kunkel, SL
Citation: Jl. Rutkowski et al., Signals for proinflammatory cytokine secretion by human Schwann cells, J NEUROIMM, 101(1), 1999, pp. 47-60
Decreased CD8 cell-mediated viral suppression and other immunologic characteristics of women who transmit human immunodeficiency virus to their infants
Authors: Plaeger, S Bermudez, S Mikyas, Y Harawa, N Dickover, R Mark, D Dillon, M Bryson, YJ Boyer, PJ Sinsheimer, JS
Citation: S. Plaeger et al., Decreased CD8 cell-mediated viral suppression and other immunologic characteristics of women who transmit human immunodeficiency virus to their infants, J INFEC DIS, 179(6), 1999, pp. 1388-1394
A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tan gene (P301L) (vol 122, pg 741, 1999)
Authors: Bird, TD Nochlin, D Poorkaj, P Cherrier, M Payami, H Peskind, E Lampe, TH Nemens, E Boyer, PJ Schellenberg, GD
Citation: Td. Bird et al., A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tan gene (P301L) (vol 122, pg 741, 1999), BRAIN, 122, 1999, pp. 1398-1398
A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L)
Authors: Bird, TD Nochlin, D Poorkaj, P Cherrier, M Kaye, J Payami, H Peskind, E Lampe, TH Nemens, E Boyer, PJ Schellenberg, GD
Citation: Td. Bird et al., A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L), BRAIN, 122, 1999, pp. 741-756
A 13-year-old girl with a relapsing-remitting neurologic disorder - Syndrome of mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
Authors: Dashe, JF Gonzalez, RG Boyer, PJ
Citation: Jf. Dashe et al., A 13-year-old girl with a relapsing-remitting neurologic disorder - Syndrome of mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)., N ENG J MED, 339(26), 1998, pp. 1914-1923
Risultati: 1-8 |