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Developmental Medicine and Child Neurology
|
December 1, 1986
Lipid abnormalities in serum in Batten's disease
M J Bennett, W S Gillis, G P Hosking, et al.
Pediatric Research
|
February 1, 1985
Urinary sediment dolichol excretion in patients with Batten disease and other neurodegenerative and storage disorders
M J Bennett, N J Mathers, F W Hemming, et al.
Human Molecular Genetics
|
April 6, 2000
Batten disease: evaluation of CLN3 mutations on protein localization and function
R E Haskell, C J Carr, D A Pearce, et al.
Mental Retardation
|
October 1, 1994
Detection of metabolic disorders among selectively screened people with idiopathic mental retardation
M B Kurtz, B Finucane, K Hyland, et al.
The Journal of Pediatrics
|
May 1, 1993
Detection of inborn errors of fatty acid oxidation from acylcarnitine analysis of plasma and blood spots with the radioisotopic exchange-high-performance liquid chromatographic method
E Schmidt-Sommerfeld, D Penn, M Duran, et al.
Neurology
|
February 5, 1999
Short-chain acyl-CoA dehydrogenase deficiency: a cause of ophthalmoplegia and multicore myopathy
I Tein, R H Haslam, W J Rhead, et al.
The Journal of Pediatrics
|
June 1, 1995
Clinical and biochemical characterization of short-chain acyl-coenzyme A dehydrogenase deficiency
A Bhala, S M Willi, P Rinaldo, et al.
American Journal of Medical Genetics. Supplement
|
January 1, 1988
Therapeutic modification of membrane lipid abnormalities in juvenile neuronal ceroid-lipofuscinosis (Batten disease)
M J Bennett, G P Hosking, R Gayton, et al.
The Plant Journal : for Cell and Molecular Biology
|
March 22, 2001
Novel auxin transport inhibitors phenocopy the auxin influx carrier mutation aux1
G Parry, A Delbarre, A Marchant, et al.
Annals of Emergency Medicine
|
August 25, 1999
Hypoketotic hypoglycemic coma in a 21-month-old child
M A Hostetler, G L Arnold, R Mooney, et al.
Page
of 36
Search research articles
Search
Showing results (251-260 of 351) with videos related to
Sort By:
Page
of 36
Developmental Medicine and Child Neurology
|
December 1, 1986
Lipid abnormalities in serum in Batten's disease
M J Bennett, W S Gillis, G P Hosking, et al.
Pediatric Research
|
February 1, 1985
Urinary sediment dolichol excretion in patients with Batten disease and other neurodegenerative and storage disorders
M J Bennett, N J Mathers, F W Hemming, et al.
Human Molecular Genetics
|
April 6, 2000
Batten disease: evaluation of CLN3 mutations on protein localization and function
R E Haskell, C J Carr, D A Pearce, et al.
Mental Retardation
|
October 1, 1994
Detection of metabolic disorders among selectively screened people with idiopathic mental retardation
M B Kurtz, B Finucane, K Hyland, et al.
The Journal of Pediatrics
|
May 1, 1993
Detection of inborn errors of fatty acid oxidation from acylcarnitine analysis of plasma and blood spots with the radioisotopic exchange-high-performance liquid chromatographic method
E Schmidt-Sommerfeld, D Penn, M Duran, et al.
Neurology
|
February 5, 1999
Short-chain acyl-CoA dehydrogenase deficiency: a cause of ophthalmoplegia and multicore myopathy
I Tein, R H Haslam, W J Rhead, et al.
The Journal of Pediatrics
|
June 1, 1995
Clinical and biochemical characterization of short-chain acyl-coenzyme A dehydrogenase deficiency
A Bhala, S M Willi, P Rinaldo, et al.
American Journal of Medical Genetics. Supplement
|
January 1, 1988
Therapeutic modification of membrane lipid abnormalities in juvenile neuronal ceroid-lipofuscinosis (Batten disease)
M J Bennett, G P Hosking, R Gayton, et al.
The Plant Journal : for Cell and Molecular Biology
|
March 22, 2001
Novel auxin transport inhibitors phenocopy the auxin influx carrier mutation aux1
G Parry, A Delbarre, A Marchant, et al.
Annals of Emergency Medicine
|
August 25, 1999
Hypoketotic hypoglycemic coma in a 21-month-old child
M A Hostetler, G L Arnold, R Mooney, et al.
Page
of 36