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Neuropsychologia
|
July 10, 2003
Differential deficits in expression recognition in gene-carriers and patients with Huntington's disease
M Milders, J R Crawford, A Lamb, et al.
American Journal of Human Genetics
|
November 1, 1996
A specific superoxide dismutase mutation is on the same genetic background in sporadic and familial cases of amyotrophic lateral sclerosis
C Hayward, R J Swingler, S A Simpson, et al.
Australasian Radiology
|
May 1, 1996
Low dose rate teletherapy: updated tumour response
J W Denham, C S Hamilton, S A Simpson, et al.
Toxicology
|
April 20, 2000
A rat nasal epithelial model for predicting upper respiratory tract toxicity: in vivo-in vitro correlations
J D Kilgour, S A Simpson, D J Alexander, et al.
Journal of Medical Genetics
|
April 1, 1995
Superoxide dismutase mutations in an unselected cohort of Scottish amyotrophic lateral sclerosis patients
C T Jones, R J Swingler, S A Simpson, et al.
Clinical Genetics
|
June 1, 1992
One hundred requests for predictive testing for Huntington's disease
S A Simpson, J Besson, D Alexander, et al.
Clinical Genetics
|
January 26, 2007
Young people's experiences of growing up in a family affected by Huntington's disease
K Forrest Keenan, Z Miedzybrodzka, E van Teijlingen, et al.
Life Sciences
|
June 25, 1984
Canine postradiation plasma glucose variations
L G Cockerham, S A Simpson, T F Doyle, et al.
Journal of Psychopharmacology (Oxford, England)
|
October 6, 2005
A community based investigation of the association between cannabis use, injuries and accidents
E J K Wadsworth, S C Moss, S A Simpson, et al.
Thorax
|
June 13, 1998
Withdrawn: Opitz oculo-genito-laryngeal syndrome: a rare cause of recurrent aspiration pneumonia in an adult
D de Silva, A Osborne, S A Simpson, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 50) with videos related to
Sort By:
Page
of 5
Neuropsychologia
|
July 10, 2003
Differential deficits in expression recognition in gene-carriers and patients with Huntington's disease
M Milders, J R Crawford, A Lamb, et al.
American Journal of Human Genetics
|
November 1, 1996
A specific superoxide dismutase mutation is on the same genetic background in sporadic and familial cases of amyotrophic lateral sclerosis
C Hayward, R J Swingler, S A Simpson, et al.
Australasian Radiology
|
May 1, 1996
Low dose rate teletherapy: updated tumour response
J W Denham, C S Hamilton, S A Simpson, et al.
Toxicology
|
April 20, 2000
A rat nasal epithelial model for predicting upper respiratory tract toxicity: in vivo-in vitro correlations
J D Kilgour, S A Simpson, D J Alexander, et al.
Journal of Medical Genetics
|
April 1, 1995
Superoxide dismutase mutations in an unselected cohort of Scottish amyotrophic lateral sclerosis patients
C T Jones, R J Swingler, S A Simpson, et al.
Clinical Genetics
|
June 1, 1992
One hundred requests for predictive testing for Huntington's disease
S A Simpson, J Besson, D Alexander, et al.
Clinical Genetics
|
January 26, 2007
Young people's experiences of growing up in a family affected by Huntington's disease
K Forrest Keenan, Z Miedzybrodzka, E van Teijlingen, et al.
Life Sciences
|
June 25, 1984
Canine postradiation plasma glucose variations
L G Cockerham, S A Simpson, T F Doyle, et al.
Journal of Psychopharmacology (Oxford, England)
|
October 6, 2005
A community based investigation of the association between cannabis use, injuries and accidents
E J K Wadsworth, S C Moss, S A Simpson, et al.
Thorax
|
June 13, 1998
Withdrawn: Opitz oculo-genito-laryngeal syndrome: a rare cause of recurrent aspiration pneumonia in an adult
D de Silva, A Osborne, S A Simpson, et al.
Page
of 5