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Results: 1-25 | 26-26
Results: 1-25/26
Online medical genetics resources: a UK perspective
Authors: Stewart, A Haites, N Rose, P
Citation: A. Stewart et al., Online medical genetics resources: a UK perspective, BR MED J, 322(7293), 2001, pp. 1037-1039
Stored tissue may be important for the future care of families
Authors: Haites, N Miedzybrodzka, Z Dean, J
Citation: N. Haites et al., Stored tissue may be important for the future care of families, BR MED J, 322(7293), 2001, pp. 1060-1060
Sequential occurrence within three years in a premenopausal woman of cervical, ovarian, and endometrial cancers - Drug induced long QT syndrome.
Authors: Cumming, GP Narayansingh, GV Parkin, DE Haites, N
Citation: Gp. Cumming et al., Sequential occurrence within three years in a premenopausal woman of cervical, ovarian, and endometrial cancers - Drug induced long QT syndrome., POSTG MED J, 77(907), 2001, pp. 344
Thy1 glomerulonephritis induced in young Lewis rats accelerates age-related glomerulosclerosis
Authors: Stewart, K Wilson, P Wilson, H Minto, A Haites, N Whiting, P Macleod, A Brown, P
Citation: K. Stewart et al., Thy1 glomerulonephritis induced in young Lewis rats accelerates age-related glomerulosclerosis, NEPHRON, 88(1), 2001, pp. 57-64
Residual ataxia telangiectasia mutated protein function in cells from ataxia telangiectasia patients, with 5762ins137 and 7271T -> G mutations, showing a less severe phenotype
Authors: Stewart, GS Last, JIK Stankovic, T Haites, N Kidd, AMJ Byrd, PJ Taylor, AMR
Citation: Gs. Stewart et al., Residual ataxia telangiectasia mutated protein function in cells from ataxia telangiectasia patients, with 5762ins137 and 7271T -> G mutations, showing a less severe phenotype, J BIOL CHEM, 276(32), 2001, pp. 30133-30141
Impairment of colour vision in workers exposed to organic solvents
Authors: Semple, S Dick, F Osborne, A Cherrie, JW Soutar, A Seaton, A Haites, N
Citation: S. Semple et al., Impairment of colour vision in workers exposed to organic solvents, OCC ENVIR M, 57(9), 2000, pp. 582-587
The pathology of familial breast cancer: Histological features of cancers in families not attributable to mutations in BRCA1 or BRCA2
Authors: Lakhani, SR Gusterson, BA Jacquemier, J Sloane, JP Anderson, TJ van de Vijver, MJ Venter, D Freeman, A Antoniou, A McGuffog, L Smyth, E Steel, CM Haites, N Scott, RJ Goldgar, D Neuhausen, S Daly, PA Ormiston, W McManus, R Scherneck, S Ponder, BAJ Futreal, PA Peto, J Stoppa-Lyonnet, D Bignon, YJ Struewing, JP Bishop, DT Klijn, JGM Devilee, P Cornelisse, CJ Lasset, C Lenoir, G Barkardottir, RB Egilsson, V Hamann, U Chang-Claude, J Sobol, H Weber, B Easton, DF Stratton, MR
Citation: Sr. Lakhani et al., The pathology of familial breast cancer: Histological features of cancers in families not attributable to mutations in BRCA1 or BRCA2, CLIN CANC R, 6(3), 2000, pp. 782-789
Patenting genes: a dangerous EU directive
Authors: Vigen, T Haites, N Burn, J Moller, P Steel, M
Citation: T. Vigen et al., Patenting genes: a dangerous EU directive, BR J GEN PR, 50(453), 2000, pp. 337-337
Steroid responsive polyneuropathy in a family with a novel myelin protein zero mutation
Authors: Donaghy, M Sisodiya, SM Kennett, R McDonald, B Haites, N Bell, C
Citation: M. Donaghy et al., Steroid responsive polyneuropathy in a family with a novel myelin protein zero mutation, J NE NE PSY, 69(6), 2000, pp. 799-805
Human fetal testis: Second trimester proliferative and steroidogenic capacities
Authors: Murray, TJ Fowler, PA Abramovich, DR Haites, N Lea, RG
Citation: Tj. Murray et al., Human fetal testis: Second trimester proliferative and steroidogenic capacities, J CLIN END, 85(12), 2000, pp. 4812-4817
Mutations in the peripheral myelin genes and associated genes in inheritedperipheral neuropathies
Authors: Nelis, E Haites, N Van Broeckhoven, C
Citation: E. Nelis et al., Mutations in the peripheral myelin genes and associated genes in inheritedperipheral neuropathies, HUM MUTAT, 13(1), 1999, pp. 11-28
Non-penetrance in a MODY 3 family with a mutation in the hepatic nuclear factor 1 alpha gene: implications for predictive testing
Authors: Miedzybrodzka, Z Hattersley, AT Ellard, S Pearson, D de Silva, D Harvey, R Haites, N
Citation: Z. Miedzybrodzka et al., Non-penetrance in a MODY 3 family with a mutation in the hepatic nuclear factor 1 alpha gene: implications for predictive testing, EUR J HUM G, 7(6), 1999, pp. 729-732
Untitled
Authors: Haites, N Brown, I Milner, B Steel, M
Citation: N. Haites et al., Untitled, DIS MARKER, 15(1-3), 1999, pp. 1-1
Cancer genetics services in Europe
Authors: Hodgson, S Milner, B Brown, I Bevilacqua, G Chang-Claude, J Eccles, D Evans, G Gregory, H Moller, P Morrison, P Steel, M Stoppa-Lyonnet, D Vasen, H Haites, N
Citation: S. Hodgson et al., Cancer genetics services in Europe, DIS MARKER, 15(1-3), 1999, pp. 3-13
Risk estimation as a decision-making tool for genetic analysis of the breast cancer susceptibility genes
Authors: Chang-Claude, J Becher, H Caligo, M Eccles, D Evans, G Haites, N Hodgson, S Moller, P Weber, BHF Stoppa-Lyonnet, D
Citation: J. Chang-claude et al., Risk estimation as a decision-making tool for genetic analysis of the breast cancer susceptibility genes, DIS MARKER, 15(1-3), 1999, pp. 53-65
Ethical, social and economic issues in familial breast cancer: a compilation of views from the EC biomed II demonstration project
Authors: Steel, M Smyth, E Vasen, H Eccles, D Evans, G Moller, P Hodgson, S Stoppa-Lyonnet, D Chang-Claude, J Caligo, M Morrison, P Haites, N
Citation: M. Steel et al., Ethical, social and economic issues in familial breast cancer: a compilation of views from the EC biomed II demonstration project, DIS MARKER, 15(1-3), 1999, pp. 125-131
Utilisation of prophylactic mastectomy in 10 European centers
Authors: Evans, DGR Anderson, E Lalloo, F Vasen, H Beckmann, M Eccles, D Hodgson, S Moller, P Chang-Claude, J Morrison, P Stoppa-Lyonnet, D Steel, M Haites, N
Citation: Dgr. Evans et al., Utilisation of prophylactic mastectomy in 10 European centers, DIS MARKER, 15(1-3), 1999, pp. 148-151
Teaching breast cancer genetics to medical students: Evaluation of a computer assister learning (CAL) package
Authors: Miedzybrodzka, Z Hamilton, NM Gregory, H Milner, B Frade, I Sinclair, T Mollison, J Haites, N
Citation: Z. Miedzybrodzka et al., Teaching breast cancer genetics to medical students: Evaluation of a computer assister learning (CAL) package, DIS MARKER, 15(1-3), 1999, pp. 157-157
Efficacy of early diagnosis and treatment in women with a family history of breast cancer
Authors: Moller, P Reis, MM Evans, G Vasen, H Haites, N Anderson, E Steel, CM Apold, J Lalloo, F Maehle, L Preece, P Gregory, H Heimdal, K
Citation: P. Moller et al., Efficacy of early diagnosis and treatment in women with a family history of breast cancer, DIS MARKER, 15(1-3), 1999, pp. 179-186
Management of hereditary breast cancer
Authors: Eccles, DM Simmonds, P Goddard, J Coultas, M Lalloo, F Evans, G Haites, N
Citation: Dm. Eccles et al., Management of hereditary breast cancer, DIS MARKER, 15(1-3), 1999, pp. 187-189
Audit of women attending the Aberdeen Genetic Clinic with a family historyof breast cancer who subsequently develop cancer
Authors: Gregory, H Gibbons, B Haites, N
Citation: H. Gregory et al., Audit of women attending the Aberdeen Genetic Clinic with a family historyof breast cancer who subsequently develop cancer, DIS MARKER, 15(1-3), 1999, pp. 201-203
Mutation-specific survival of inherited breast cancer
Authors: Moller, P Borg, A Evans, G Haites, N Steel, CM Vasen, H Gregory, H Hodgson, S Apold, J Lalloo, F Maehle, L Anderson, E Heimdal, K
Citation: P. Moller et al., Mutation-specific survival of inherited breast cancer, DIS MARKER, 15(1-3), 1999, pp. 205-205
Guidelines for follow-up of women at high risk for inherited breast cancer: Consensus statement from the Biomed 2 Demonstration Programme on Inherited Breast Cancer
Authors: Moller, P Evans, G Haites, N Vasen, H Reis, MM Anderson, E Apold, J Hodgson, S Eccles, D Olsson, H Stoppa-Lyonnet, D Chang-Claude, J Morrison, PJ Bevilacqua, G Heimdal, K Maehle, L Lalloo, F Gregory, H Preece, P Borg, A Nevin, NC Caligo, M Steel, CM
Citation: P. Moller et al., Guidelines for follow-up of women at high risk for inherited breast cancer: Consensus statement from the Biomed 2 Demonstration Programme on Inherited Breast Cancer, DIS MARKER, 15(1-3), 1999, pp. 207-211
Haemochromatosis mutations in North-East Scotland
Authors: Miedzybrodzka, Z Loughlin, S Baty, D Terron, A Kelly, K Dean, J Greaves, M Pippard, M Haites, N
Citation: Z. Miedzybrodzka et al., Haemochromatosis mutations in North-East Scotland, BR J HAEM, 106(2), 1999, pp. 385-387
Concerted action polyp prevention, CAPP2: A trial of aspirin and/or resistant starch in people at risk of hereditary non-polyposis colon cancer (HNPCC)
Authors: Burn, J Alonso, A Bertario, L Bishop, T Bisgaard, ML Cummings, J Davidson, R Delhanty, J Demant, P Dunlop, M Eccles, D Ellis, A Evans, G Fidalgo, P Fodde, R Haites, N Hodgson, S Hultcrantz, R Huson, S Jarvinen, H Kartheuser, A Kleibeuker, J Lenaerts, C Lucasson, A Lunt, P McDermot, K McKay, J McKeown, C Maher, E Mathers, J Mecklin, JP Moslein, G Murday, V Nagengast, F Northover, JMA Obrador, A Parks, TG Paraskeva, C Phillips, R San Roman, C Ruscheoff, J Sampson, J Shepherd, N Tempesta, A Trembath, R Turnpenny, P Vasen, HFA
Citation: J. Burn et al., Concerted action polyp prevention, CAPP2: A trial of aspirin and/or resistant starch in people at risk of hereditary non-polyposis colon cancer (HNPCC), BIOM HLTH R, 24, 1998, pp. 17-23
Risultati: 1-25 | 26-26