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Publications by Isao Yuasa
Three Japanese Patients With Beta-Ketothiolase Deficiency Who Share a Mutation, C.431A>C (H144P) in ACAT1
JIMD Reports
Internal Medicine
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes
Characterization of an Acidic Polysaccharide Isolated From the Leaves ofCorchorus Olitorius(Moroheiya)
Bioscience, Biotechnology and Biochemistry
Organic Chemistry
Applied Microbiology
Molecular Biology
Biochemistry
Analytical Chemistry
Medicine
Biotechnology
Related publications
Beta-Ketothiolase Deficiency
Beta-Ketothiolase Deficiency as a Treatable Neurometabolic Disorder: A Case Report Due to a Novel Compound Heterozygote Mutations in ACAT1 Gene
Biomedical Journal of Scientific & Technical Research
A Different SLC2A1 Gene Mutation in Glut 1 Deficiency Syndrome: C.734A>C
Balkan Medical Journal
Medicine
Donor Splice Site Mutation in the Apolipoprotein (Apo) C-Ii Gene (Apo C-IIHamburg) of a Patient With Apo C-Ii Deficiency.
Journal of Clinical Investigation
Medicine
Intermediate McAd Deficiency Associated With a Novel Mutation of theACADMGene: C.1052C>T
Case Reports in Genetics
Is Intravenous Vitamin C Contraindicated in Patients With G6PD Deficiency?
Critical Care
Critical Care
Intensive Care Medicine
No Effect of the Prothrombin G20210A Mutation on Protein C Activation in a Large Kindred With Type I Protein C Deficiency
Blood Coagulation and Fibrinolysis
Medicine
Hematology
Beta-Myosin Heavy Chain (Β-Mhc) and Myosin Binding Protein C (MyBP-C) Genes Mutation in Bangladeshi Hypertrophic Cardiomyopathy Patients: A Genotype-Phenotype Correlation
Canadian Journal of Biotechnology
Use of Human Protein C Concentrates in the Treatment of Patients With Severe Congenital Protein C Deficiency
Biologics: Targets and Therapy
Oncology
Immunology
Gastroenterology
Pharmacology
Rheumatology
Allergy
