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Molecular Genetics and Metabolism
|
May 30, 2007
Unusually mild phenotype of AADC deficiency in 2 siblings
S K H Tay, K S Poh, K Hyland, et al.
European Journal of Pediatrics
|
January 1, 1989
Neurodevelopmental delay and focal seizures as presenting symptoms of human immunodeficiency virus I infection
P Habibi, S Strobel, I Smith, et al.
Brain Research. Molecular Brain Research
|
April 29, 2005
Effects of AAV-2-mediated aspartoacylase gene transfer in the tremor rat model of Canavan disease
S W J McPhee, J Francis, C G Janson, et al.
Journal of Inherited Metabolic Disease
|
December 31, 1998
One-methyl group metabolism in non-ketotic hyperglycinaemia: mildly elevated cerebrospinal fluid homocysteine levels
J L Van Hove, F Lazeyras, S H Zeisel, et al.
Journal of Inherited Metabolic Disease
|
October 25, 2008
Tetrahydrobiopterin deficiency in human rabies
R E Willoughby, T Opladen, T Maier, et al.
Journal of Chiropractic Humanities
|
August 23, 2013
Multiple views to address diversity issues: an initial dialog to advance the chiropractic profession
Claire Johnson, Lisa Zaynab Killinger, Mark G Christensen, et al.
Annals of Neurology
|
July 17, 1998
Dystonia with motor delay in compound heterozygotes for GTP-cyclohydrolase I gene mutations
Y Furukawa, S J Kish, E M Bebin, et al.
Developments in Biologicals
|
July 19, 2008
Generalised cranial artery spasm in human rabies
R E Willoughby, A Roy-Burman, K W Martin, et al.
Annals of Neurology
|
April 13, 2000
Dopa-responsive dystonia due to a large deletion in the GTP cyclohydrolase I gene
Y Furukawa, M Guttman, S P Sparagana, et al.
Neurology
|
May 1, 1997
Oral phenylalanine loading in dopa-responsive dystonia: a possible diagnostic test
K Hyland, J S Fryburg, W G Wilson, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 95) with videos related to
Sort By:
Page
of 10
Molecular Genetics and Metabolism
|
May 30, 2007
Unusually mild phenotype of AADC deficiency in 2 siblings
S K H Tay, K S Poh, K Hyland, et al.
European Journal of Pediatrics
|
January 1, 1989
Neurodevelopmental delay and focal seizures as presenting symptoms of human immunodeficiency virus I infection
P Habibi, S Strobel, I Smith, et al.
Brain Research. Molecular Brain Research
|
April 29, 2005
Effects of AAV-2-mediated aspartoacylase gene transfer in the tremor rat model of Canavan disease
S W J McPhee, J Francis, C G Janson, et al.
Journal of Inherited Metabolic Disease
|
December 31, 1998
One-methyl group metabolism in non-ketotic hyperglycinaemia: mildly elevated cerebrospinal fluid homocysteine levels
J L Van Hove, F Lazeyras, S H Zeisel, et al.
Journal of Inherited Metabolic Disease
|
October 25, 2008
Tetrahydrobiopterin deficiency in human rabies
R E Willoughby, T Opladen, T Maier, et al.
Journal of Chiropractic Humanities
|
August 23, 2013
Multiple views to address diversity issues: an initial dialog to advance the chiropractic profession
Claire Johnson, Lisa Zaynab Killinger, Mark G Christensen, et al.
Annals of Neurology
|
July 17, 1998
Dystonia with motor delay in compound heterozygotes for GTP-cyclohydrolase I gene mutations
Y Furukawa, S J Kish, E M Bebin, et al.
Developments in Biologicals
|
July 19, 2008
Generalised cranial artery spasm in human rabies
R E Willoughby, A Roy-Burman, K W Martin, et al.
Annals of Neurology
|
April 13, 2000
Dopa-responsive dystonia due to a large deletion in the GTP cyclohydrolase I gene
Y Furukawa, M Guttman, S P Sparagana, et al.
Neurology
|
May 1, 1997
Oral phenylalanine loading in dopa-responsive dystonia: a possible diagnostic test
K Hyland, J S Fryburg, W G Wilson, et al.
Page
of 10