methionine has been researched along with Autosomal Hemophilia A in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (50.00) | 18.7374 |
1990's | 1 (50.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Ewenstein, BM; Gorlin, J; Handin, RI; Jesson, M; Narins, SC; Wise, RJ | 1 |
Benoit, FL; Fry, GL; Hoak, JC; Theilen, EO; Warner, ED; Wilson, WR | 1 |
1 review(s) available for methionine and Autosomal Hemophilia A
Article | Year |
---|---|
Autosomal recessive transmission of hemophilia A due to a von Willebrand factor mutation.
Topics: Base Sequence; Diagnosis, Differential; DNA Mutational Analysis; Factor VIII; Female; Genes, Recessive; Hemophilia A; Humans; Infant; Methionine; Molecular Sequence Data; Pedigree; Point Mutation; Precipitin Tests; Protein Binding; Threonine; von Willebrand Diseases; von Willebrand Factor | 1993 |
1 other study(ies) available for methionine and Autosomal Hemophilia A
Article | Year |
---|---|
Effects of triiodothyronine-induced hypermetabolism on factor 8 and fibrinogen in man.
Topics: Basal Metabolism; Epinephrine; Factor VIII; Fibrinogen; Hemophilia A; Humans; Hyperthyroidism; Male; Methionine; Propranolol; Selenium; Sensory Receptor Cells; Thyroxine; Triiodothyronine; von Willebrand Diseases | 1969 |