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Pediatric Research
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May 19, 1998
Molecular characterization of pyruvate carboxylase deficiency in two consanguineous families
I D Wexler, D S Kerr, Y Du, et al.
Journal of Medical Genetics
|
September 5, 2006
A novel mutation in the mitochondrial tRNA(Ser(AGY)) gene associated with mitochondrial myopathy, encephalopathy, and complex I deficiency
L-J C Wong, D Yim, R-K Bai, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
July 1, 1996
Parathyroid hormone resistance and B cell lymphopenia in propionic acidemia
T A Griffin, R W Hostoffer, K Y Tserng, et al.
Human Molecular Genetics
|
February 1, 1995
Pyruvate dehydrogenase complex deficiency due to a point mutation (P188L) within the thiamine pyrophosphate binding loop of the E1 alpha subunit
S G Hemalatha, D S Kerr, I D Wexler, et al.
Neurology
|
July 23, 2003
Autosomal dominant acute necrotizing encephalopathy
D E Neilson, R M Eiben, S Waniewski, et al.
Pediatric Research
|
September 1, 1987
Systemic deficiency of the first component of the pyruvate dehydrogenase complex
D S Kerr, L Ho, C M Berlin, et al.
Neurology
|
December 31, 1997
Outcome of pyruvate dehydrogenase deficiency treated with ketogenic diets. Studies in patients with identical mutations
I D Wexler, S G Hemalatha, J McConnell, et al.
Toxicon : Official Journal of the International Society on Toxinology
|
July 21, 2007
Isodomoic acids A and C exhibit low KA receptor affinity and reduced in vitro potency relative to domoic acid in region CA1 of rat hippocampus
P M Sawant, B A Weare, P T Holland, et al.
Amino Acids
|
October 10, 2002
Comparison of the in vitro and in vivo neurotoxicity of three new sources of kainic acid
R A R Tasker, P B Bernard, T A Doucette, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 1, 1988
Heterogeneous expression of protein and mRNA in pyruvate dehydrogenase deficiency
I D Wexler, D S Kerr, L Ho, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 86) with videos related to
Sort By:
Page
of 9
Pediatric Research
|
May 19, 1998
Molecular characterization of pyruvate carboxylase deficiency in two consanguineous families
I D Wexler, D S Kerr, Y Du, et al.
Journal of Medical Genetics
|
September 5, 2006
A novel mutation in the mitochondrial tRNA(Ser(AGY)) gene associated with mitochondrial myopathy, encephalopathy, and complex I deficiency
L-J C Wong, D Yim, R-K Bai, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
July 1, 1996
Parathyroid hormone resistance and B cell lymphopenia in propionic acidemia
T A Griffin, R W Hostoffer, K Y Tserng, et al.
Human Molecular Genetics
|
February 1, 1995
Pyruvate dehydrogenase complex deficiency due to a point mutation (P188L) within the thiamine pyrophosphate binding loop of the E1 alpha subunit
S G Hemalatha, D S Kerr, I D Wexler, et al.
Neurology
|
July 23, 2003
Autosomal dominant acute necrotizing encephalopathy
D E Neilson, R M Eiben, S Waniewski, et al.
Pediatric Research
|
September 1, 1987
Systemic deficiency of the first component of the pyruvate dehydrogenase complex
D S Kerr, L Ho, C M Berlin, et al.
Neurology
|
December 31, 1997
Outcome of pyruvate dehydrogenase deficiency treated with ketogenic diets. Studies in patients with identical mutations
I D Wexler, S G Hemalatha, J McConnell, et al.
Toxicon : Official Journal of the International Society on Toxinology
|
July 21, 2007
Isodomoic acids A and C exhibit low KA receptor affinity and reduced in vitro potency relative to domoic acid in region CA1 of rat hippocampus
P M Sawant, B A Weare, P T Holland, et al.
Amino Acids
|
October 10, 2002
Comparison of the in vitro and in vivo neurotoxicity of three new sources of kainic acid
R A R Tasker, P B Bernard, T A Doucette, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 1, 1988
Heterogeneous expression of protein and mRNA in pyruvate dehydrogenase deficiency
I D Wexler, D S Kerr, L Ho, et al.
Page
of 9