Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("WHARTON, Stephen B")

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 20 of 20

  • Page / 1
Export

Selection :

  • and

Foreign body reaction with delayed extrusion of ganciclovir implant in a patient with immune recovery vitritis syndromeTAGURI, Abdel Hakim; DHILLON, Baljean; WHARTON, Stephen B et al.American journal of ophthalmology. 2002, Vol 133, Num 1, pp 147-149, issn 0002-9394Article

Microarray analysis of the astrocyte transcriptome in the aging brain: relationship to Alzheimer's pathology and APOE genotypeSIMPSON, Julie E; INCE, Paul G; BRAYNE, Carol et al.Neurobiology of aging. 2011, Vol 32, Num 10, pp 1795-1807, issn 0197-4580, 13 p.Article

The cellular and molecular pathology of the motor system in hereditary spastic paraparesis dur to mutation of the spastin geneWHARTON, Stephen B; MCDERMOTT, Christopher J; GRIERSON, Andrew J et al.Journal of neuropathology and experimental neurology. 2003, Vol 62, Num 11, pp 1166-1177, issn 0022-3069, 12 p.Article

Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72COOPER-KNOCK, Johnathan; HEWITT, Christopher; BAXTER, Lynne et al.Brain. 2012, Vol 135, pp 751-764, issn 0006-8950, 14 p., 3Article

A robust assay for alternative lengthening of telomeres in tumors shows the significance of alternative lengthening of telomeres in sarcomas and astrocytomasHENSON, Jeremy D; HANNAY, Jonathan A; ROBINSON, Bruce G et al.Clinical cancer research. 2005, Vol 11, Num 1, pp 217-225, issn 1078-0432, 9 p.Article

Fatal spontaneous thrombosis of a cerebral arteriovenous malformation in a young patient with a rare heterozygous prothrombin gene mutation : Case reportTAHA, Mahmoud; PATEL, Umang; WHARTON, Stephen B et al.Journal of neurosurgery. Pediatrics. 2007, Vol 106, Num 2, pp 143-146, issn 1933-0707, 4 p.Article

Expression of vascular endothelial growth factor and its receptors in the central nervous system in amyotrophic lateral sclerosisBROCKINGTON, Alice; WHARTON, Stephen B; FERNANDO, Malee et al.Journal of neuropathology and experimental neurology. 2006, Vol 65, Num 1, pp 26-36, issn 0022-3069, 11 p.Article

Progressive loss of motor neuron function in wasted mice : Effects of a spontaneous null mutation in the gene for the eFF1 A2 translation factorNEWBERY, Helen J; GILLINGWATER, Thomas H; DHARMASAROJA, Permphan et al.Journal of neuropathology and experimental neurology. 2005, Vol 64, Num 4, pp 295-303, issn 0022-3069, 9 p.Article

Alterations in the blood brain barrier in ageing cerebral cortex in relationship to Alzheimer-type pathology: A study in the MRC-CFAS population neuropathology cohortVIGGARS, Andrew P; WHARTON, Stephen B; SIMPSON, Julie E et al.Neuroscience letters. 2011, Vol 505, Num 1, pp 25-30, issn 0304-3940, 6 p.Article

Phosphatase and tensin homologue/protein kinase B pathway linked to motor neuron survival in human superoxide dismutase 1-related amyotrophic lateral sclerosisKIRBY, Janine; KE NING; INCE, Paul G et al.Brain. 2011, Vol 134, pp 506-517, issn 0006-8950, 12 p., 2Article

Broad clinical phenotypes associated with TAR-DNA binding protein (TARDBP) mutations in amyotrophic lateral sclerosisKIRBY, Janine; GOODALL, Emily F; INCE, Paul G et al.Neurogenetics (Oxford. Print). 2010, Vol 11, Num 2, pp 217-225, issn 1364-6745, 9 p.Article

White matter lesions in an unselected cohort of the elderly : Molecular pathology suggests origin from chronic hypoperfusion injuryFERNANDO, Malee S; SIMPSON, Julie E; SHAW, Pamela J et al.Stroke (1970). 2006, Vol 37, Num 6, pp 1391-1398, issn 0039-2499, 8 p.Article

Alterations of the blood―brain barrier in cerebral white matter lesions in the ageing brainSIMPSON, Julie E; WHARTON, Stephen B; INCE, Paul G et al.Neuroscience letters. 2010, Vol 486, Num 3, pp 246-251, issn 0304-3940, 6 p.Article

Expression of Ki67, PCNA and the chromosome replication licensing protein Mcm2 in glial cells of the ageing human hippocampus increases with the burden of Alzheimer-type pathologyWHARTON, Stephen B; WILLIAMS, Gareth H; STOEBER, Kai et al.Neuroscience letters. 2005, Vol 383, Num 1-2, pp 33-38, issn 0304-3940, 6 p.Article

Production of monocyte chemoattractant protein-1 in amyotrophic lateral sclerosisBARON, Pierluigi; BUSSINI, Simona; SILANI, Vincenzo et al.Muscle & nerve. 2005, Vol 32, Num 4, pp 541-544, issn 0148-639X, 4 p.Article

Hereditary spastic paraparesis: Disrupted intracellular transport associated with spastin mutationMCDERMOTT, Christopher J; GRIERSON, Andrew J; WOOD, Jonathan D et al.Annals of neurology. 2003, Vol 54, Num 6, pp 748-759, issn 0364-5134, 12 p.Article

Sequestration of multiple RNA recognition motif-containing proteins by C9orf72 repeat expansionsCOOPER-KNOCK, Johnathan; WALSH, Matthew J; HAUTBERGUE, Guillaume M et al.Brain. 2014, Vol 137, pp 2040-2051, issn 0006-8950, 12 p., 7Article

Age, Neuropathology, and DementiaSAVVA, George M; WHARTON, Stephen B; INCE, Paul G et al.The New England journal of medicine. 2009, Vol 360, Num 22, pp 2302-2309, issn 0028-4793, 8 p.Article

Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patientsKASHER, Paul R; DE VOS, Kurt J; SHAW, Pamela J et al.Journal of neurochemistry. 2009, Vol 110, Num 1, pp 34-44, issn 0022-3042, 11 p.Article

Microarray RNA Expression Analysis of Cerebral White Matter Lesions Reveals Changes in Multiple Functional PathwaysSIMPSON, Julie E; HOSNY, Ola; KALARIA, Raj N et al.Stroke (1970). 2009, Vol 40, Num 2, pp 369-375, issn 0039-2499, 7 p.Article

  • Page / 1