K Narisawa Selected Research

Multiple Carboxylase Deficiency (Deficiency, Multiple Carboxylase)

11/2001

Structure of human holocarboxylase synthetase gene and mutation spectrum of holocarboxylase synthetase deficiency.

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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	GlycogenIBA 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	EnzymesIBA 11/2001
1	glycine cleavage systemIBA 01/2001
1	Proteins (Proteins, Gene)FDA Link 01/2001
1	Glucose (Dextrose)FDA LinkGeneric 11/2000
1	Galactose (Galactopyranose)FDA LinkGeneric 11/2000
1	Glucose-6-PhosphateIBA 08/2000
1	SolutionsIBA 04/2000
1	Messenger RNA (mRNA)IBA 03/2000
1	Glycine Dehydrogenase (Decarboxylating)IBA 03/2000
1	beta-methylcrotonylglycineIBA 02/2000
1	Connexin 26IBA 01/2000
1	ConnexinsIBA 01/2000
1	DNA (Deoxyribonucleic Acid)IBA 01/2000

Therapy/Procedure

1	Therapeutics 01/2000