vitamin k1 oxide has been researched along with Hemorrhagic Disorders in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Fregin, A; Krebsova, A; Muller, CR; Oldenburg, J; Rost, S; Wolz, W | 1 |
| Ghosh, K; Mohanty, D; Shetty, S | 1 |
| Brenner, B; Keller, CB; Seligsohn, U; Suttie, JW; Tatarsky, I; Tavori, S; Zivelin, A | 1 |
3 other study(ies) available for vitamin k1 oxide and Hemorrhagic Disorders
| Article | Year |
|---|---|
Homozygosity mapping of a second gene locus for hereditary combined deficiency of vitamin K-dependent clotting factors to the centromeric region of chromosome 16.
Topics: Animals; Blood Coagulation Factors; Centromere; Child; Chromosome Mapping; Chromosomes, Human, Pair 16; DNA Mutational Analysis; Drug Resistance; Female; Genes, Recessive; Genetic Markers; Genotype; Germany; Glutathione Transferase; Hemorrhagic Disorders; Humans; Infant, Newborn; Lebanon; Lod Score; Male; Mice; Microsatellite Repeats; Mixed Function Oxygenases; Multienzyme Complexes; Pedigree; Rats; Species Specificity; Vitamin K; Vitamin K 1; Vitamin K Epoxide Reductases; Warfarin | 2002 |
Congenital deficiency of vitamin K dependent coagulation factors--its rarity and need for an international registry.
Topics: Carbon-Carbon Ligases; Consanguinity; Global Health; Hemorrhagic Disorders; Humans; India; Infant, Newborn; Mixed Function Oxygenases; Registries; Vitamin K 1; Vitamin K Epoxide Reductases | 2001 |
Hereditary deficiency of all vitamin K-dependent procoagulants and anticoagulants.
Topics: Blood Coagulation Disorders; Child; Factor VII Deficiency; Factor X Deficiency; Female; Glycoproteins; Hemophilia B; Hemorrhagic Disorders; Humans; Hypoprothrombinemias; Male; Pedigree; Protein C Deficiency; Protein S; Vitamin K; Vitamin K 1 | 1990 |