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Pediatrics
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November 1, 1976
Ketonic diet in the management of pyruvate dehydrogenase deficiency
R E Falk, S D Cederbaum, J P Blass, et al.
Pediatric Research
|
June 11, 1992
Deletion in blood mitochondrial DNA in Kearns-Sayre syndrome
N Fischel-Ghodsian, M C Bohlman, T R Prezant, et al.
Molecular Genetics and Metabolism
|
October 6, 1998
Molecular basis of hyperargininemia: structure-function consequences of mutations in human liver arginase
D E Ash, L R Scolnick, Z F Kanyo, et al.
Archives of Biochemistry and Biophysics
|
July 1, 1987
Regulation of mRNA levels for five urea cycle enzymes in rat liver by diet, cyclic AMP, and glucocorticoids
S M Morris, C L Moncman, K D Rand, et al.
Pediatric Research
|
July 1, 1979
Hyperargininemia with arginase deficiency
S D Cederbaum, K N Shaw, E B Spector, et al.
The New England Journal of Medicine
|
July 2, 1992
Brief report: renal tubular acidosis in carnitine palmitoyltransferase type 1 deficiency
Z C Falik-Borenstein, S C Jordan, J M Saudubray, et al.
Gene Therapy
|
February 6, 2015
Minimal ureagenesis is necessary for survival in the murine model of hyperargininemia treated by AAV-based gene therapy
C Hu, D S Tai, H Park, et al.
Human Genetics
|
March 1, 1993
Arginase deficiency manifesting delayed clinical sequelae and induction of a kidney arginase isozyme
W W Grody, R M Kern, D Klein, et al.
Biochemical and Molecular Medicine
|
October 1, 1996
Loss of function mutations in conserved regions of the human arginase I gene
J G Vockley, B K Goodman, D E Tabor, et al.
The American Journal of Physiology
|
November 1, 1996
Arginase activity in endothelial cells: inhibition by NG-hydroxy-L-arginine during high-output NO production
G M Buga, R Singh, S Pervin, et al.
Page
of 10
Search research articles
Search
Showing results (71-80 of 93) with videos related to
Sort By:
Page
of 10
Pediatrics
|
November 1, 1976
Ketonic diet in the management of pyruvate dehydrogenase deficiency
R E Falk, S D Cederbaum, J P Blass, et al.
Pediatric Research
|
June 11, 1992
Deletion in blood mitochondrial DNA in Kearns-Sayre syndrome
N Fischel-Ghodsian, M C Bohlman, T R Prezant, et al.
Molecular Genetics and Metabolism
|
October 6, 1998
Molecular basis of hyperargininemia: structure-function consequences of mutations in human liver arginase
D E Ash, L R Scolnick, Z F Kanyo, et al.
Archives of Biochemistry and Biophysics
|
July 1, 1987
Regulation of mRNA levels for five urea cycle enzymes in rat liver by diet, cyclic AMP, and glucocorticoids
S M Morris, C L Moncman, K D Rand, et al.
Pediatric Research
|
July 1, 1979
Hyperargininemia with arginase deficiency
S D Cederbaum, K N Shaw, E B Spector, et al.
The New England Journal of Medicine
|
July 2, 1992
Brief report: renal tubular acidosis in carnitine palmitoyltransferase type 1 deficiency
Z C Falik-Borenstein, S C Jordan, J M Saudubray, et al.
Gene Therapy
|
February 6, 2015
Minimal ureagenesis is necessary for survival in the murine model of hyperargininemia treated by AAV-based gene therapy
C Hu, D S Tai, H Park, et al.
Human Genetics
|
March 1, 1993
Arginase deficiency manifesting delayed clinical sequelae and induction of a kidney arginase isozyme
W W Grody, R M Kern, D Klein, et al.
Biochemical and Molecular Medicine
|
October 1, 1996
Loss of function mutations in conserved regions of the human arginase I gene
J G Vockley, B K Goodman, D E Tabor, et al.
The American Journal of Physiology
|
November 1, 1996
Arginase activity in endothelial cells: inhibition by NG-hydroxy-L-arginine during high-output NO production
G M Buga, R Singh, S Pervin, et al.
Page
of 10