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Results: 1-8 |
Results: 8

Authors: Hughes, CA Byrne, PC Webb, S McMonagle, P Patterson, V Hutchinson, M Parfrey, NA
Citation: Ca. Hughes et al., SPG15, a new locus for autosomal recessive complicated HSP on chromosome 14q, NEUROLOGY, 56(9), 2001, pp. 1230-1233

Authors: Curry, MP Golden-Mason, L Nolan, N Parfrey, NA Hegarty, JE O'Farrelly, C
Citation: Mp. Curry et al., Expansion of peripheral blood CD5(+) B cells is associated with mild disease in chronic hepatitis C virus infection, J HEPATOL, 32(1), 2000, pp. 121-125

Authors: McMonagle, P Byrne, PC Fitzgerald, B Webb, S Parfrey, NA Hutchinson, M
Citation: P. Mcmonagle et al., Phenotype of AD-HSP due to mutations in the SPAST gene - Comparison with AD-HSP without mutations, NEUROLOGY, 55(12), 2000, pp. 1794-1800

Authors: Byrne, PC McMonagle, P Webb, S Fitzgerald, B Parfrey, NA Hutchinson, M
Citation: Pc. Byrne et al., Age-related cognitive decline in hereditary spastic paraparesis linked to chromosome 2p, NEUROLOGY, 54(7), 2000, pp. 1510-1517

Authors: Hand, CK Harmon, DL Kennedy, SM FitzSimon, JS Collum, LMT Parfrey, NA
Citation: Ck. Hand et al., Localization of the gene for autosomal recessive congenital hereditary endothelial dystrophy (CHED2) to chromosome 20 by homozygosity mapping, GENOMICS, 61(1), 1999, pp. 1-4

Authors: Leahy, DT Mulcahy, HE O'Donoghue, DP Parfrey, NA
Citation: Dt. Leahy et al., bcl-2 protein expression is associated with better prognosis in colorectalcancer, HISTOPATHOL, 35(4), 1999, pp. 360-367

Authors: Parfrey, NA El-Sheikh, A Monckton, EA Cockfield, SM Halloran, PF Linetsky, E
Citation: Na. Parfrey et al., Interferon-gamma gene expression during acute graft-versus-host disease: Relationship to MHC induction and tissue injury, J PATHOLOGY, 189(1), 1999, pp. 99-104

Authors: Callaghan, M Hand, CK Kennedy, SM FitzSimon, JS Collum, LMT Parfrey, NA
Citation: M. Callaghan et al., Homozygosity mapping and linkage analysis demonstrate that autosomal recessive congenital hereditary endothelial dystrophy (CHED) and autosomal dominant CHED are genetically distinct, BR J OPHTH, 83(1), 1999, pp. 115-119
Risultati: 1-8 |