methionine has been researched along with Angiohemophilia in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (22.22) | 18.7374 |
| 1990's | 5 (55.56) | 18.2507 |
| 2000's | 1 (11.11) | 29.6817 |
| 2010's | 1 (11.11) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cloutier, S; Duan, Z; Jackson, SC; Poon, MC; Rand, ML; Sinclair, GD | 1 |
| De Cristofaro, R; De Filippis, V; Lancellotti, S; Mannucci, PM; Palla, R; Peyvandi, F; Pitocco, D; Pozzi, N; Rocca, B; Rutella, S | 1 |
| Anbo, H; Furukawa, T; Handa, M; Kawai, Y; Moriki, T; Murata, M; Nikkuni, K; Shibata, A; Takahashi, H; Watanabe, K | 1 |
| Ewenstein, BM; Gorlin, J; Handin, RI; Jesson, M; Narins, SC; Wise, RJ | 1 |
| Anbo, H; Handa, M; Ikeda, Y; Kitaguchi, T; Moriki, T; Murata, M; Takahashi, H; Watanabe, K | 1 |
| Dodds, WJ | 1 |
| Giles, AR; Lillicrap, D; Murray, EW | 1 |
| Bahnak, BR; Derlon, A; Lavergne, JM; Meyer, D; Piétu, G; Ribba, AS | 1 |
| Benoit, FL; Fry, GL; Hoak, JC; Theilen, EO; Warner, ED; Wilson, WR | 1 |
1 review(s) available for methionine and Angiohemophilia
| 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 |
8 other study(ies) available for methionine and Angiohemophilia
| Article | Year |
|---|---|
The Montreal platelet syndrome kindred has type 2B von Willebrand disease with the VWF V1316M mutation.
Topics: Amino Acid Substitution; Blood Coagulation Tests; Blood Platelet Disorders; Blood Platelets; DNA Mutational Analysis; Family; Female; Humans; Male; Methionine; Mutation, Missense; Pedigree; Platelet Aggregation; Syndrome; Valine; von Willebrand Diseases; von Willebrand Factor | 2009 |
Formation of methionine sulfoxide by peroxynitrite at position 1606 of von Willebrand factor inhibits its cleavage by ADAMTS-13: A new prothrombotic mechanism in diseases associated with oxidative stress.
Topics: ADAM Proteins; ADAMTS13 Protein; Adult; Binding Sites; Blood Platelets; Case-Control Studies; Diabetes Mellitus, Type 2; Female; Humans; Hydrolysis; Male; Methionine; Middle Aged; Oxidative Stress; Peptide Fragments; Peroxynitrous Acid; Platelet Aggregation; Protein Multimerization; Ristocetin; Tyrosine; von Willebrand Diseases; von Willebrand Factor | 2010 |
Substitution of Val for Met at residue 239 of platelet glycoprotein Ib alpha in Japanese patients with platelet-type von Willebrand disease.
Topics: Amino Acid Sequence; Base Sequence; Blood Platelets; Codon; DNA Primers; Female; Genetic Carrier Screening; Humans; Japan; Male; Methionine; Molecular Sequence Data; Pedigree; Platelet Aggregation; Platelet Membrane Glycoproteins; Point Mutation; Polymerase Chain Reaction; Valine; von Willebrand Diseases | 1995 |
Expression and functional characterization of an abnormal platelet membrane glycoprotein Ib alpha (Met239 --> Val) reported in patients with platelet-type von Willebrand disease.
Topics: Analysis of Variance; Humans; Methionine; Platelet Aggregation; Platelet Aggregation Inhibitors; Platelet Glycoprotein GPIb-IX Complex; Point Mutation; Recombinant Proteins; Ristocetin; Transfection; Valine; von Willebrand Diseases | 1997 |
Further studies of canine von Willebrand's disease.
Topics: Acute Kidney Injury; Age Factors; Animals; Blood Coagulation Tests; Blood Platelets; Colitis; Dog Diseases; Dogs; Eosinophilia; Factor VIII; Female; Fibrinogen; Glomerulonephritis; Intestinal Obstruction; Lymphedema; Lymphoma; Male; Melena; Methionine; Osteitis; Pregnancy; Rabbits; von Willebrand Diseases | 1975 |
Germ-line mosaicism for a valine-to-methionine substitution at residue 553 in the glycoprotein Ib-binding domain of von Willebrand factor, causing type IIB von Willebrand disease.
Topics: Autoradiography; Base Sequence; Blood Coagulation Tests; DNA; Electrophoresis, Polyacrylamide Gel; Humans; Leukocytes; Male; Methionine; Molecular Sequence Data; Mosaicism; Mutation; Pedigree; Platelet Membrane Glycoproteins; Polymerase Chain Reaction; Polymorphism, Genetic; Spermatozoa; Valine; von Willebrand Diseases; von Willebrand Factor | 1992 |
Duplication of a methionine within the glycoprotein Ib binding domain of von Willebrand factor detected by denaturing gradient gel electrophoresis in a patient with type IIB von Willebrand disease.
Topics: Base Sequence; Binding Sites; Codon; Electrophoresis, Polyacrylamide Gel; Exons; Female; Humans; Methionine; Molecular Sequence Data; Mutation; Nucleic Acid Hybridization; Pedigree; Platelet Membrane Glycoproteins; Polymerase Chain Reaction; von Willebrand Diseases | 1991 |
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 |