Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

D Vallance

Showing results (41-50 of 61) with videos related to

Pageof 7
Sort By:
British Journal of Haematology|February 28, 2015
A phase II trial of AZD1152 in relapsed/refractory diffuse large B-cell lymphomaGraham P Collins, Toby A Eyre, Kim M Linton, et al.
Clinical Journal of the American Society of Nephrology : CJASN|November 16, 2007
Screening for Fabry disease in patients with chronic kidney disease: limitations of plasma alpha-galactosidase assay as a screening testJason Andrade, Paula J Waters, R Suneet Singh, et al.
Molecular Genetics and Metabolism Reports|July 20, 2018
Marked elevation in plasma trimethylamine-N-oxide (TMAO) in patients with mitochondrial disorders treated with oral l-carnitineH D Vallance, A Koochin, J Branov, et al.
Human Mutation|April 29, 1999
Identification of 6 new mutations in the iduronate sulfatase gene. Mutation in brief no. 233. OnlineH D Vallance, L Bernard, M Rashed, et al.
Clinical Science (London, England : 1979)|December 1, 1993
Brisk walking and serum lipoprotein variables in formerly sedentary men aged 42-59 yearsD J Stensel, A E Hardman, K Brooke-Wavell, et al.
Annals of Neurology|June 29, 2005
6-pyruvoyl-tetrahydropterin synthase deficiency with mild hyperphenylalaninemiaMichelle K Demos, Paula J Waters, Hilary D Vallance, et al.
Heart (British Cardiac Society)|November 18, 2004
Relation between coronary pressure derived collateral flow, myocardial perfusion grade, and outcome in left ventricular function after rescue percutaneous coronary interventionK P Balachandran, C Berry, J Norrie, et al.
American Journal of Medical Genetics. Part A|March 18, 2011
Infantile cardioencephalopathy due to a COX15 gene defect: report and reviewMajid Alfadhel, Yolanda P Lillquist, Paula J Waters, et al.
Atherosclerosis|August 1, 1994
Effects of ciprofibrate on LDL metabolism in manA Gaw, C J Packard, M J Caslake, et al.
Molecular Genetics and Metabolism|September 27, 2005
Neonatal hyperphenylalaninemia, perinatal hemochromatosis, and renal tubulopathy: a unique patient or a novel metabolic disorder?Paula J Waters, Minesh Khashu, Yolanda Lillquist, et al.
Pageof 7

Showing results (41-50 of 61) with videos related to

Sort By:
Pageof 7
British Journal of Haematology|February 28, 2015
A phase II trial of AZD1152 in relapsed/refractory diffuse large B-cell lymphomaGraham P Collins, Toby A Eyre, Kim M Linton, et al.
Clinical Journal of the American Society of Nephrology : CJASN|November 16, 2007
Screening for Fabry disease in patients with chronic kidney disease: limitations of plasma alpha-galactosidase assay as a screening testJason Andrade, Paula J Waters, R Suneet Singh, et al.
Molecular Genetics and Metabolism Reports|July 20, 2018
Marked elevation in plasma trimethylamine-N-oxide (TMAO) in patients with mitochondrial disorders treated with oral l-carnitineH D Vallance, A Koochin, J Branov, et al.
Human Mutation|April 29, 1999
Identification of 6 new mutations in the iduronate sulfatase gene. Mutation in brief no. 233. OnlineH D Vallance, L Bernard, M Rashed, et al.
Clinical Science (London, England : 1979)|December 1, 1993
Brisk walking and serum lipoprotein variables in formerly sedentary men aged 42-59 yearsD J Stensel, A E Hardman, K Brooke-Wavell, et al.
Annals of Neurology|June 29, 2005
6-pyruvoyl-tetrahydropterin synthase deficiency with mild hyperphenylalaninemiaMichelle K Demos, Paula J Waters, Hilary D Vallance, et al.
Heart (British Cardiac Society)|November 18, 2004
Relation between coronary pressure derived collateral flow, myocardial perfusion grade, and outcome in left ventricular function after rescue percutaneous coronary interventionK P Balachandran, C Berry, J Norrie, et al.
American Journal of Medical Genetics. Part A|March 18, 2011
Infantile cardioencephalopathy due to a COX15 gene defect: report and reviewMajid Alfadhel, Yolanda P Lillquist, Paula J Waters, et al.
Atherosclerosis|August 1, 1994
Effects of ciprofibrate on LDL metabolism in manA Gaw, C J Packard, M J Caslake, et al.
Molecular Genetics and Metabolism|September 27, 2005
Neonatal hyperphenylalaninemia, perinatal hemochromatosis, and renal tubulopathy: a unique patient or a novel metabolic disorder?Paula J Waters, Minesh Khashu, Yolanda Lillquist, et al.
Pageof 7