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Results: 1-16 |
Results: 16
Genes for left-handedness: How to search for the needle in the haystack?
Authors: Van Agtmael, T Forrest, SM Williamson, R
Citation: T. Van Agtmael et al., Genes for left-handedness: How to search for the needle in the haystack?, LATERALITY, 6(2), 2001, pp. 149-164
Atomic force microscopy imaging of DNA - cationic liposome complexes optimised for gene transfection into neuronal cells
Authors: Wangerek, LA Dahl, HHM Senden, TJ Carlin, JB Jans, DA Dunstan, DE Ioannou, PA Williamson, R Forrest, SM
Citation: La. Wangerek et al., Atomic force microscopy imaging of DNA - cationic liposome complexes optimised for gene transfection into neuronal cells, J GENE MED, 3(1), 2001, pp. 72-81
A novel deletion in the flavin-containing monooxygenase gene (FMO3) in a Greek patient with trimethylaminuria
Authors: Forrest, SM Knight, M Akerman, BR Cashman, JR Treacy, EP
Citation: Sm. Forrest et al., A novel deletion in the flavin-containing monooxygenase gene (FMO3) in a Greek patient with trimethylaminuria, PHARMACOGEN, 11(2), 2001, pp. 169-174
Clinical features of a large Australian pedigree with episodic ataxia type1
Authors: Hand, PJ Gardner, RJM Knight, MA Forrest, SM Storey, E
Citation: Pj. Hand et al., Clinical features of a large Australian pedigree with episodic ataxia type1, MOVEMENT D, 16(5), 2001, pp. 938-939
A new autosomal dominant pure cerebellar ataxia
Authors: Storey, E Gardner, RJM Knight, MA Kennerson, ML Tuck, RR Forrest, SM Nicholson, GA
Citation: E. Storey et al., A new autosomal dominant pure cerebellar ataxia, NEUROLOGY, 57(10), 2001, pp. 1913-1915
Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxia
Authors: Storey, E du Sart, D Shaw, JH Lorentzos, P Kelly, L Gardner, RJM Forrest, SM Biros, I Nicholson, GA
Citation: E. Storey et al., Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxia, AM J MED G, 95(4), 2000, pp. 351-357
Population-specific polymorphisms of the human FMO3 gene: Significance fordetoxication
Authors: Cashman, JR Akerman, BR Forrest, SM Treacy, EP
Citation: Jr. Cashman et al., Population-specific polymorphisms of the human FMO3 gene: Significance fordetoxication, DRUG META D, 28(2), 2000, pp. 169-173
The relationship between neonatal immunoreactive trypsinogen, Delta F508, and IVS8-5T
Authors: Massie, J du Sart, D Forshaw, K Carlin, J Forrest, SM
Citation: J. Massie et al., The relationship between neonatal immunoreactive trypsinogen, Delta F508, and IVS8-5T, J MED GENET, 37(8), 2000, pp. 629-632
Friedreich ataxia: an overview
Authors: Delatycki, MB Williamson, R Forrest, SM
Citation: Mb. Delatycki et al., Friedreich ataxia: an overview, J MED GENET, 37(1), 2000, pp. 1-8
Early-onset Alzheimer's disease caused by a novel mutation at codon 219 ofthe presenilin-1 gene
Authors: Smith, MJ Gardner, RJM Knight, MA Forrest, SM Beyreuther, K Storey, E McLean, CA Cotton, RGH Cappal, R Masters, CL
Citation: Mj. Smith et al., Early-onset Alzheimer's disease caused by a novel mutation at codon 219 ofthe presenilin-1 gene, NEUROREPORT, 10(3), 1999, pp. 503-507
Direct evidence that mitochondrial iron accumulation occurs in Friedreich ataxia
Authors: Delatycki, MB Camakaris, J Brooks, H Evans-Whipp, T Thorburn, DR Williamson, R Forrest, SM
Citation: Mb. Delatycki et al., Direct evidence that mitochondrial iron accumulation occurs in Friedreich ataxia, ANN NEUROL, 45(5), 1999, pp. 673-675
G130V, a common FRDA point mutation, appears to have arisen from a common founder
Authors: Delatycki, MB Knight, M Koenig, M Cossee, M Williamson, R Forrest, SM
Citation: Mb. Delatycki et al., G130V, a common FRDA point mutation, appears to have arisen from a common founder, HUM GENET, 105(4), 1999, pp. 343-346
Clinical and genetic study of Friedreich ataxia in an Australian population
Authors: Delatycki, MB Paris, DBBP Gardner, RJM Nicholson, GA Nassif, N Storey, E MacMillan, JC Collins, V Williamson, R Forrest, SM
Citation: Mb. Delatycki et al., Clinical and genetic study of Friedreich ataxia in an Australian population, AM J MED G, 87(2), 1999, pp. 168-174
Genotype and intellectual phenotype in untreated phenylketonuria patients
Authors: Ramus, SJ Forrest, SM Pitt, DD Cotton, RGH
Citation: Sj. Ramus et al., Genotype and intellectual phenotype in untreated phenylketonuria patients, PEDIAT RES, 45(4), 1999, pp. 474-481
Spinocerebellar ataxia type 2 - Clinical features of a pedigree displayingprominent frontal-executive dysfunction
Authors: Storey, E Forrest, SM Shaw, JH Mitchell, P Gardner, RJM
Citation: E. Storey et al., Spinocerebellar ataxia type 2 - Clinical features of a pedigree displayingprominent frontal-executive dysfunction, ARCH NEUROL, 56(1), 1999, pp. 43-50
Duplex PCR for autosomal dominant spinocerebellar ataxia testing: A nonradioactive rapid screening method
Authors: Biros, I Forrest, SM
Citation: I. Biros et Sm. Forrest, Duplex PCR for autosomal dominant spinocerebellar ataxia testing: A nonradioactive rapid screening method, MOL DIAGN, 3(4), 1998, pp. 223-228
Risultati: 1-16 |