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Pediatric Pharmacology (New York, N.Y.)
|
January 1, 1984
Favorable effect of dimethyl sulfoxide on secondary amyloidosis in juvenile rheumatoid arthritis
K Yoshimitsu, N Koga, Y Kitamura, et al.
Biochemical and Biophysical Research Communications
|
July 24, 1998
Molecular analysis of glycogen storage disease type Ib: identification of a prevalent mutation among Japanese patients and assignment of a putative glucose-6-phosphate translocase gene to chromosome 11
S Kure, Y Suzuki, Y Matsubara, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
January 1, 1985
Cushing's disease: pituitary microadenoma demonstrated by high resolution computed tomography with thin slices
Y Ikemoto, Y Nishi, N Sakura, et al.
Biochemical and Biophysical Research Communications
|
November 28, 1980
Isolation of glutathione from bovine thymus and its significance to research relevant to immune systems
K Folkers, J Dahmen, M Ohta, et al.
Metabolism: Clinical and Experimental
|
May 1, 1997
Serum concentrations of cortisone and cortisol in premature infants
M Fujitaka, K Jinno, N Sakura, et al.
Progress in Clinical and Biological Research
|
January 1, 1990
3-Ketothiolase deficiency: molecular heterogeneity of the enzyme defect and cloning of the cDNA
S Yamaguchi, T Fukao, H Nagasawa, et al.
Journal of Inherited Metabolic Disease
|
May 10, 2002
Type II citrullinaemia (citrin deficiency) in a neonate with hypergalactosaemia detected by mass screening
E Naito, M Ito, S Matsuura, et al.
Journal of Drug Targeting
|
November 8, 2001
Novel drug delivery system to bone using acidic oligopeptide: pharmacokinetic characteristics and pharmacological potential
T Sekido, N Sakura, Y Higashi, et al.
Journal of Inherited Metabolic Disease
|
February 19, 2004
Differential diagnosis of neonatal mild hypergalactosaemia detected by mass screening: clinical significance of portal vein imaging
Y Nishimura, G Tajima, A Dwi Bahagia, et al.
Journal of Inherited Metabolic Disease
|
October 2, 2003
The mitochondrial acetoacetyl-CoA thiolase (T2) deficiency in Japanese patients: urinary organic acid and blood acylcarnitine profiles under stable conditions have subtle abnormalities in T2-deficient patients with some residual T2 activity
T Fukao, G X Zhang, N Sakura, et al.
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of 14
Search research articles
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Showing results (121-130 of 131) with videos related to
Sort By:
Page
of 14
Pediatric Pharmacology (New York, N.Y.)
|
January 1, 1984
Favorable effect of dimethyl sulfoxide on secondary amyloidosis in juvenile rheumatoid arthritis
K Yoshimitsu, N Koga, Y Kitamura, et al.
Biochemical and Biophysical Research Communications
|
July 24, 1998
Molecular analysis of glycogen storage disease type Ib: identification of a prevalent mutation among Japanese patients and assignment of a putative glucose-6-phosphate translocase gene to chromosome 11
S Kure, Y Suzuki, Y Matsubara, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
January 1, 1985
Cushing's disease: pituitary microadenoma demonstrated by high resolution computed tomography with thin slices
Y Ikemoto, Y Nishi, N Sakura, et al.
Biochemical and Biophysical Research Communications
|
November 28, 1980
Isolation of glutathione from bovine thymus and its significance to research relevant to immune systems
K Folkers, J Dahmen, M Ohta, et al.
Metabolism: Clinical and Experimental
|
May 1, 1997
Serum concentrations of cortisone and cortisol in premature infants
M Fujitaka, K Jinno, N Sakura, et al.
Progress in Clinical and Biological Research
|
January 1, 1990
3-Ketothiolase deficiency: molecular heterogeneity of the enzyme defect and cloning of the cDNA
S Yamaguchi, T Fukao, H Nagasawa, et al.
Journal of Inherited Metabolic Disease
|
May 10, 2002
Type II citrullinaemia (citrin deficiency) in a neonate with hypergalactosaemia detected by mass screening
E Naito, M Ito, S Matsuura, et al.
Journal of Drug Targeting
|
November 8, 2001
Novel drug delivery system to bone using acidic oligopeptide: pharmacokinetic characteristics and pharmacological potential
T Sekido, N Sakura, Y Higashi, et al.
Journal of Inherited Metabolic Disease
|
February 19, 2004
Differential diagnosis of neonatal mild hypergalactosaemia detected by mass screening: clinical significance of portal vein imaging
Y Nishimura, G Tajima, A Dwi Bahagia, et al.
Journal of Inherited Metabolic Disease
|
October 2, 2003
The mitochondrial acetoacetyl-CoA thiolase (T2) deficiency in Japanese patients: urinary organic acid and blood acylcarnitine profiles under stable conditions have subtle abnormalities in T2-deficient patients with some residual T2 activity
T Fukao, G X Zhang, N Sakura, et al.
Page
of 14