threonine and von Willebrand Diseases

threonine has been researched along with von Willebrand Diseases 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
Ewenstein, BM; Gorlin, J; Handin, RI; Jesson, M; Narins, SC; Wise, RJ	1
Boehnke, M; Bruck, ME; Collins, FS; Ginsburg, D; Hanna, WT; Hidaka, N; Iannuzzi, MC	1

Reviews

1 review(s) available for threonine and von Willebrand Diseases

Article	Year
Autosomal recessive transmission of hemophilia A due to a von Willebrand factor mutation. Human genetics, 1993, Volume: 91, Issue:4 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

Article

Year

Autosomal recessive transmission of hemophilia A due to a von Willebrand factor mutation.

Human genetics, 1993, Volume: 91, Issue:4

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

Other Studies

1 other study(ies) available for threonine and von Willebrand Diseases

Article	Year
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

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