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K Narisawa Selected Research
K Narisawa Research Topics
Disease
2
Nonketotic Hyperglycinemia
01/2001 - 03/2000
2
Hepatorenal form of glycogen storage disease
05/2000 - 03/2000
2
Inborn Genetic Diseases (Disease, Hereditary)
04/2000 - 01/2000
1
Multiple Carboxylase Deficiency (Deficiency, Multiple Carboxylase)
11/2001
1
Holocarboxylase Synthetase Deficiency
11/2001
1
Protein Deficiency
01/2001
1
Fanconi Syndrome (Syndrome, Fanconi)
11/2000
1
Glycogen Storage Disease (Glycogenosis)
08/2000
1
Hyperglycemia
02/2000
1
Lactic Acidosis
02/2000
1
Hyperammonemia
02/2000
1
Deafness (Deaf Mutism)
01/2000
1
Ketosis
01/2000
1
Acidosis
01/2000
Drug/Important Bio-Agent (IBA)
3
Glycogen
IBA
11/2000 - 03/2000
3
Glucose-6-Phosphatase (Glucose 6 Phosphatase)
IBA
08/2000 - 03/2000
2
Ligases (Synthetase)
IBA
11/2001 - 01/2000
2
Biotin (Vitamin H)
FDA Link
11/2001 - 01/2000
1
Enzymes
IBA
11/2001
1
glycine cleavage system
IBA
01/2001
1
Proteins (Proteins, Gene)
FDA Link
01/2001
1
Glucose (Dextrose)
FDA Link
Generic
11/2000
1
Galactose (Galactopyranose)
FDA Link
Generic
11/2000
1
Glucose-6-Phosphate
IBA
08/2000
1
Solutions
IBA
04/2000
1
Messenger RNA (mRNA)
IBA
03/2000
1
Glycine Dehydrogenase (Decarboxylating)
IBA
03/2000
1
beta-methylcrotonylglycine
IBA
02/2000
1
Connexin 26
IBA
01/2000
1
Connexins
IBA
01/2000
1
DNA (Deoxyribonucleic Acid)
IBA
01/2000
Therapy/Procedure
1
Therapeutics
01/2000