Search Results - "STANFORD, P. M."

Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene: Expansion of the disease phenotype caused by tau gene mutations by STANFORD, P. M, HALLIDAY, G. M, BROOKS, W. S, KWOK, J. B. J, STOREY, C. E, CREASEY, H, MORRIS, J. G. L, FULHAM, M. J, SCHOFIELD, P. R

“…Genetic mutations in the tau gene on chromosome 17 are known to cause frontotemporal dementias. We have identified a novel silent mutation (S305S) in the tau…”
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Mutations in the tau gene that cause an increase in three repeat tau and frontotemporal dementia by Stanford, Prudence M., Shepherd, Claire E., Halliday, Glenda M., Brooks, William S., Schofield, Peter W., Brodaty, Henry, Martins, Ralph N., Kwok, John B. J., Schofield, Peter R.

“…The majority of cases with frontotemporal dementia (FTD) have no tau deposition in the brain, yet mutations in the tau gene lead to a similar clinical…”
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Similar early clinical presentations in familial and non-familial frontotemporal dementia by Piguet, O, Brooks, W S, Halliday, G M, Schofield, P R, Stanford, P M, Kwok, J B J, Spillantini, M-G, Yancopoulou, D, Nestor, P J, Broe, G A, Hodges, J R

“…Background: It is unclear whether there are early clinical features that can distinguish between patients with familial and non-familial frontotemporal…”
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Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16 by CAVANAUGH, J. A., CALLEN, D. F., WILSON, S. R., STANFORD, P. M., SRAML, M. E., GORSKA, M., CRAWFORD, J., WHITMORE, S. A., SHLEGEL, C., FOOTE, S., KOHONEN-CORISH, M., PAVLI, P.

“…A number of localizations for the putative susceptibility gene(s) have been identified for both Crohn's disease and ulcerative colitis. In a genome wide scan,…”
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Hepatitis B vaccination rates among staff at a district general hospital by Stanford, M P, Black, T R, March, L M, Holt, D A, Campbell, D H

“…To evaluate the uptake of hepatitis B vaccination by staff of a metropolitan district general hospital and associated community health service in order to…”
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Of ends and means by Stanford, M P

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International Collaboration Provides Convincing Linkage Replication in Complex Disease through Analysis of a Large Pooled Data Set: Crohn Disease and Chromosome 16 by Cavanaugh, Juleen

“…Numerous familial, non-Mendelian (i.e., complex) diseases have been screened by linkage analysis for regions harboring susceptibility genes. Except for rare,…”
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More incentives needed for doctor managers by Stanford, M P

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"Operation Cataract" by Stanford, M. P., Kaushik, Nikhil C.

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Socs2 and Elf5 Mediate Prolactin-Induced Mammary Gland Development by Harris, Jessica, Stanford, Prudence M, Sutherland, Kate, Oakes, Samantha R, Naylor, Matthew J, Robertson, Fiona G, Blazek, Katrina D, Kazlauskas, Michael, Hilton, Heidi N, Wittlin, Sergio, Alexander, Warren S, Lindeman, Geoffrey J, Visvader, Jane E, Ormandy, Christopher J

“…The proliferative phase of mammary alveolar morphogenesis is initiated during early pregnancy by rising levels of serum prolactin and progesterone,…”
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Multiaxial pedicle screw designs: Static and dynamic mechanical testing by STANFORD, Ralph Edward, LOEFLER, Andreas Herman, STANFORD, Philip Mark, WALSH, William R

“…Randomized investigation of multiaxial pedicle screw mechanical properties. Measure static yield and ultimate strengths, yield stiffness, and fatigue…”
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Prolactin and the prolactin receptor: new targets of an old hormone by Harris, Jessica, Stanford, Prudence M, Oakes, Samantha R, Ormandy, Christopher J

“…Prolactin (PRL) is one of a family of related hormones including growth hormone (GH) and placental lactogen (PL) that are hypothesized to have arisen from a…”
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Frequency of tau mutations in familial and sporadic frontotemporal dementia and other tauopathies by STANFORD, Prudence M, BROOKS, William S, TEBER, Erdahl T, HALLUPP, Marianne, MCLEAN, Catriona, HALLIDAY, Glenda M, MARTINS, Ralph N, KWOK, John B. J, SCHOFIELD, Peter R

“…Tau gene mutations with insoluble Tau neuropathology have been identified in pedigrees with frontotemporal dementia with parkinsonism linked to chromosome 17…”
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Laparoscopic cholecystectomy by Stanford, Michael P., Espiner, H. J., Eltringham, W. K., Rowe, A., Miller, R., Eyre-Brook, I. A., Barlow, A. P.

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