isoleucine and Angiohemophilia

isoleucine has been researched along with Angiohemophilia in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	2 (100.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Canciani, MT; Di Rocco, N; Federici, AB; Mannucci, PM; Miyata, S; Ruggeri, ZM; Stabile, F; Ware, J	1
Boehnke, M; Bruck, ME; Collins, FS; Ginsburg, D; Hanna, WT; Hidaka, N; Iannuzzi, MC	1

Other Studies

2 other study(ies) available for isoleucine and Angiohemophilia

Article	Year
A type 2b von Willebrand disease mutation (Ile546-->Val) associated with an unusual phenotype. Thrombosis and haemostasis, 1997, Volume: 78, Issue:3 Topics: Adult; Anti-Bacterial Agents; Child; Female; Humans; Isoleucine; Male; Middle Aged; Phenotype; Platelet Aggregation; Point Mutation; Restriction Mapping; Ristocetin; Sequence Analysis, DNA; Valine; von Willebrand Diseases; von Willebrand Factor	1997
Analysis of the relationship of von Willebrand disease (vWD) and hereditary hemorrhagic telangiectasia and identification of a potential type IIA vWD mutation (IIe865 to Thr). American journal of human genetics, 1991, Volume: 48, Issue:4 Topics: Alleles; Base Sequence; Chromosomes, Human, Pair 12; DNA; Female; Genetic Linkage; Humans; Isoleucine; Male; Molecular Sequence Data; Mutation; Pedigree; Polymorphism, Restriction Fragment Length; Telangiectasia, Hereditary Hemorrhagic; Threonine; von Willebrand Diseases; von Willebrand Factor	1991

Article

Year

A type 2b von Willebrand disease mutation (Ile546-->Val) associated with an unusual phenotype.

Thrombosis and haemostasis, 1997, Volume: 78, Issue:3

Topics: Adult; Anti-Bacterial Agents; Child; Female; Humans; Isoleucine; Male; Middle Aged; Phenotype; Platelet Aggregation; Point Mutation; Restriction Mapping; Ristocetin; Sequence Analysis, DNA; Valine; von Willebrand Diseases; von Willebrand Factor

1997

Analysis of the relationship of von Willebrand disease (vWD) and hereditary hemorrhagic telangiectasia and identification of a potential type IIA vWD mutation (IIe865 to Thr).

American journal of human genetics, 1991, Volume: 48, Issue:4

Topics: Alleles; Base Sequence; Chromosomes, Human, Pair 12; DNA; Female; Genetic Linkage; Humans; Isoleucine; Male; Molecular Sequence Data; Mutation; Pedigree; Polymorphism, Restriction Fragment Length; Telangiectasia, Hereditary Hemorrhagic; Threonine; von Willebrand Diseases; von Willebrand Factor

1991