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Results:
1-24
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Results: 24
Authors:
Chapman, BA
Burt, MJ
Frampton, CMA
Chapman, TM
Whitehead, MR
Upton, JD
George, PM
Citation: Ba. Chapman et al., Influence of haemochromatosis gene mutations on treatment outcomes in patients with hepatitis C, INTERN M J, 31(4), 2001, pp. 254-255
Authors:
Brennan, SO
Wyatt, JM
May, S
De Caigney, S
George, PM
Citation: So. Brennan et al., Hypofibrinogenemia due to novel 316 Asp -> Tyr substitution in the fibrinogen B beta chain, THROMB HAEM, 85(3), 2001, pp. 450-453
Authors:
McGregor, DO
Dellow, WJ
Lever, M
George, PM
Robson, RA
Chambers, ST
Citation: Do. Mcgregor et al., Dimethylglycine accumulates in uremia and predicts elevated plasma homocysteine concentrations, KIDNEY INT, 59(6), 2001, pp. 2267-2272
Authors:
Crossen, K
Scott, RS
McGeoch, GRB
George, PM
Citation: K. Crossen et al., Implementation of evidence based cardiovascular risk treatments by generalpractitioners, NZ MED J, 114(1133), 2001, pp. 260-262
Authors:
George, PM
Citation: Pm. George, Care and maintenance of the successful career: How experienced law librarians make their work rewarding, LAW LIBR J, 93(4), 2001, pp. 535-539
Authors:
Raizis, AM
Ferguson, MM
George, PM
Citation: Am. Raizis et al., Effect of nonsense mutations on PTEN mRNA stability, HUM GENET, 107(1), 2000, pp. 24-27
Authors:
Wyatt, J
Brennan, SO
May, S
George, PM
Citation: J. Wyatt et al., Hypofibrinogenaemia with compound heterozygosity for two gamma chain mutations-gamma 82 Ala -> Gly and an intron two GT -> AT splice site mutation, THROMB HAEM, 84(3), 2000, pp. 449-452
Authors:
Brennan, SO
George, PM
Citation: So. Brennan et Pm. George, Three truncated forms of serum albumin associated with pancreatic pseudocyst, BBA-PROT ST, 1481(2), 2000, pp. 337-343
Authors:
Chapman, BA
Burt, MJ
Frampton, CMA
Collett, JA
Yeo, KHJ
Wilkinson, ID
Cook, HB
Barclay, MJ
Ross, AG
George, PM
Citation: Ba. Chapman et al., The prevalence of viral hepatitis (HAV, HBV and HCV) in the Christchurch community, NZ MED J, 113(1118), 2000, pp. 394-396
Authors:
Raizis, AM
Ferguson, MM
Nicholls, DT
Goodisson, GW
George, PM
Citation: Am. Raizis et al., A novel 5 ' (40 41insA) mutation in a patient with numerous manifestationsof Cowden disease, J INVES DER, 114(3), 2000, pp. 597-598
Authors:
Stott, MK
Fellowes, AP
Upton, JD
Burt, MJ
George, PM
Citation: Mk. Stott et al., Simple multiplex PCR for the simultaneous detection of the C282Y and H63D hemochromatosis (HFE) gene mutations (vol 45, pg 426, 1999), CLIN CHEM, 46(2), 2000, pp. 308-309
Authors:
Brennan, SO
Wyatt, JM
Ockelford, P
George, PM
Citation: So. Brennan et al., Defective fibrinogen polymerization associated with a novel gamma 279Ala -> Asp mutation, BR J HAEM, 108(2), 2000, pp. 236-240
Authors:
Fellowes, AP
Brennan, SO
Holme, R
Stormorken, H
Brosstad, FR
George, PM
Citation: Ap. Fellowes et al., Homozygous truncation of the fibrinogen A alpha chain within the coiled coil causes congenital afibrinogenemia, BLOOD, 96(2), 2000, pp. 773-775
Authors:
Brennan, SO
Fellowes, AP
Faed, JM
George, PM
Citation: So. Brennan et al., Hypofibrinogenemia in an individual with 2 coding (gamma 82 A -> G and B beta 235 P -> L) and 2 noncoding mutations, BLOOD, 95(5), 2000, pp. 1709-1713
Authors:
Brennan, SO
Wyatt, J
Medicina, D
Callea, F
George, PM
Citation: So. Brennan et al., Fibrinogen brescia - Hepatic endoplasmic reticulum storage and hypofibrinogenemia because of a gamma 284 Gly -> Arg mutation, AM J PATH, 157(1), 2000, pp. 189-196
Authors:
Wilkinson, TJ
Hanger, HC
George, PM
Sainsbury, R
Citation: Tj. Wilkinson et al., Is thiamine deficiency in elderly people related to age or co-morbidity?, AGE AGEING, 29(2), 2000, pp. 111-116
Authors:
Aitken, GD
Raizis, AM
Yandle, TG
George, PM
Espiner, EA
Cameron, VA
Citation: Gd. Aitken et al., The characterization of ovine genes for atrial, brain, and C-type natriuretic peptides, DOM ANIM EN, 16(2), 1999, pp. 115-121
Authors:
Metcalf, VJ
Brennan, SO
George, PM
Citation: Vj. Metcalf et al., The Antarctic toothfish (Dissostichus mawsoni) lacks plasma albumin and utilises high density lipoprotein as its major palmitate binding protein, COMP BIOC B, 124(2), 1999, pp. 147-155
Authors:
Florkowski, CM
George, PM
Willis, JA
Stott, MK
Burt, MJ
Upton, JD
Nesbit, J
Walmsley, TA
Scott, RS
Citation: Cm. Florkowski et al., Haemochromatosis gene mutations Cys282Tyr and His63Asp are not increased in Type 2 diabetic patients compared with the Canterbury (New Zealand) general population, DIABET RE C, 43(3), 1999, pp. 199-203
Authors:
Brennan, SO
Fellowes, AP
George, PM
Citation: So. Brennan et al., Albumin Banks Peninsula: a new termination variant characterised by electrospray mass spectrometry, BBA-PROT ST, 1433(1-2), 1999, pp. 321-326
Authors:
Metcalf, VJ
Brennan, SO
Chambers, G
George, PM
Citation: Vj. Metcalf et al., High density lipoprotein (HDL), and not albumin, is the major palmitate binding protein in New Zealand long-finned (Anguilla dieffenbachii) and short-finned eel (Anguilla australis schmidtii) plasma, BBA-PROT ST, 1429(2), 1999, pp. 467-475
Authors:
Stott, MK
Fellowes, AP
Upton, JD
Burt, MJ
George, PM
Citation: Mk. Stott et al., Simple multiplex PCR for the simultaneous detection of the C282Y and H63D hemochromatosis (HFE) gene mutations, CLIN CHEM, 45(3), 1999, pp. 426-428
Authors:
Simeon-Rudolf, V
Reiner, E
Evans, RT
George, PM
Potter, HC
Citation: V. Simeon-rudolf et al., Catalytic parameters for the hydrolysis of butyrylthiocholine by human serum butyrylcholinesterase variants, CHEM-BIO IN, 120, 1999, pp. 165-171
Authors:
Raizis, AM
Ferguson, MM
Robinson, BA
Atkinson, CH
George, PM
Citation: Am. Raizis et al., Identification of a novel PTEN mutation (L139X) in a patient with Cowden disease and Sjogren's syndrome, J CL PATH-M, 51(6), 1998, pp. 339-341
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