Compounds > glutamine

glutamine and Phlegmasia Alba Dolens

glutamine has been researched along with Phlegmasia Alba Dolens in 7 studies

Research

Studies (7)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	7 (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
Dahlbäck, B; He, X; Svensson, PJ; Zöller, B	1
Borchiellini, A; Montaruli, B; Muleo, G; Pannocchia, A; Schinco, P; Tamponi, G; van Mourik, JA; Voorberg, J	1
Alving, BM; Carrington, LR; Gillespie, DL; Griffin, JH	1
Grohmann, J; Koch, HG; Nowak-Göttl, U; Schneppenheim, R; Vielhaber, H	1
Binder, M; Dübbers, A; Kehrel, B; Koch, HG; Nowak-Göttl, U; Veltmann, H; Vielhaber, H	1
Griffin, JH; Petäjä, JM	1
Bathelier, C; Champenois, T; Lucotte, G	1

Other Studies

7 other study(ies) available for glutamine and Phlegmasia Alba Dolens

Article	Year
Identification of the same factor V gene mutation in 47 out of 50 thrombosis-prone families with inherited resistance to activated protein C. The Journal of clinical investigation, 1994, Volume: 94, Issue:6 Topics: Arginine; Base Sequence; Drug Resistance; Enzyme Activation; Factor V; Female; Genetic Predisposition to Disease; Glutamine; Heterozygote; Homozygote; Humans; Male; Molecular Sequence Data; Point Mutation; Protein C; Risk Factors; Survival Analysis; Sweden; Thrombophlebitis	1994
Arterial and venous thrombosis in two Italian families with the factor V Arg506-->Gln mutation. European journal of haematology, 1996, Volume: 57, Issue:1 Topics: Adult; Arginine; Base Sequence; Factor V; Female; Glutamine; Heterozygote; Homozygote; Humans; Italy; Male; Molecular Sequence Data; Mutation; Myocardial Infarction; Pedigree; Thrombophlebitis; Thrombosis	1996
Resistance to activated protein C: a common inherited cause of venous thrombosis. Annals of vascular surgery, 1996, Volume: 10, Issue:2 Topics: Adolescent; Adult; Anticoagulants; Antithrombin III; Arginine; Contraceptives, Oral; DNA; Drug Resistance; Factor V; Female; Glutamine; Humans; Male; Middle Aged; Mutation; Obesity; Pregnancy; Protein C; Protein C Deficiency; Protein S Deficiency; Recurrence; Risk Factors; Thromboembolism; Thrombophlebitis	1996
Arginine506 to glutamin mutation in the factor V gene in infancy and childhood: evidence of fibrinolytic impairment. European journal of pediatrics, 1997, Volume: 156, Issue:3 Topics: Adolescent; Arginine; Child; Child, Preschool; DNA Mutational Analysis; Factor V; Female; Fibrin Fibrinogen Degradation Products; Fibrinolysis; Genetic Carrier Screening; Genetic Predisposition to Disease; Glutamine; Homozygote; Humans; Infant; Infant, Newborn; Male; Oligopeptides; Protein C; Thrombin; Thrombophlebitis	1997
Arg506 to Gln mutation in the factor V gene causes poor fibrinolytic response in children after venous occlusion. Thrombosis and haemostasis, 1997, Volume: 78, Issue:3 Topics: Arginine; Child; Factor V; Fibrinolysis; Glutamine; Humans; Plasminogen Activator Inhibitor 1; Point Mutation; Protein C; Thrombophlebitis; Tissue Plasminogen Activator	1997
Activated protein C resistance: What have we learned now that the dust has settled? Annals of medicine, 1997, Volume: 29, Issue:6 Topics: Adult; Aged; Aged, 80 and over; Anticoagulants; Arginine; Blood Coagulation Disorders; Cerebrovascular Disorders; Drug Resistance; Factor V; Female; Glutamine; Humans; Male; Middle Aged; Myocardial Infarction; Point Mutation; Protein C; Risk Factors; Thrombophlebitis; Thrombosis	1997
ARMS test for diagnosis of factor V Leiden mutation and allele frequencies in France. Molecular and cellular probes, 1998, Volume: 12, Issue:2 Topics: Alleles; Amino Acid Substitution; Arginine; Factor V; France; Gene Frequency; Glutamine; Humans; Point Mutation; Thrombophlebitis	1998