Page last updated: 2024-10-18

glycine and Hemophilia A

glycine has been researched along with Hemophilia A in 25 studies

Hemophilia A: The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage.

Research Excerpts

ExcerptRelevanceReference
"Bleeding episodes in patients with hemophilia A with anti-factor VII antibodies are frequently difficult to treat."1.26Treatment of anti-factor VIII antibodies. ( Blatt, PM; McMillan, CW; Roberts, HR; White, GC, 1977)

Research

Studies (25)

TimeframeStudies, this research(%)All Research%
pre-199022 (88.00)18.7374
1990's3 (12.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
FANTL, P1
Knevelman, A1
de Wit, HJ1
Potstra, P1
vd Does, JA1
Yamamoto, Y1
Yasuoka, A1
Tachikawa, N1
Teruya, K1
Genka, I1
Yamaguchi, M1
Yasuoka, C1
Kikuchi, Y1
Aoki, M1
Oka, S1
Legaz, ME1
Weinstein, MJ1
Heldebrant, CM1
Davie, EW1
Blatt, PM1
White, GC1
McMillan, CW1
Roberts, HR5
Ruggeri, ZM1
Mannucci, PM1
Allain, JP1
Frommel, D1
Bajaj, SP1
Spitzer, SG1
Welsh, WJ1
Warn-Cramer, BJ1
Kasper, CK1
Birktoft, JJ1
Youssoufian, H1
Wong, C1
Aronis, S1
Platokoukis, H1
Kazazian, HH1
Antonarakis, SE1
Rossman, RE1
Brody, JI1
Breckenridge, RT1
Ratnoff, OD1
Waterbury, L1
Frenkel, EP1
Lurie, A1
Peterson, CA1
Borucki, DT1
Austin, G1
Shanbrom, E4
Garvey, MB1
Tannenberg, WJ1
Necheles, TF1
Allen, DM1
Brinkhous, KM4
Webster, WP4
Fekete, L1
Wagner, RH4
Blombäck, M1
Blombäck, B1
Dallman, PR1
Pool, JG1
Verstraete, M1
Olislaegers, P1
Van Itterbeek, H1
Waumans, P1
Lust, A1
Thelin, GM2
Abildgaard, CF1
Simone, JV1
Corrigan, JJ1
Seeler, RA1
Edelstein, G1
Vanderheiden, J1
Schulman, I1

Reviews

3 reviews available for glycine and Hemophilia A

ArticleYear
Isolation, subunit structure, and proteolytic modification of bovine factor VIII.
    Annals of the New York Academy of Sciences, 1975, Jan-20, Volume: 240

    Topics: Aminocaproates; Anticoagulants; Blood Coagulation Tests; Calcium; Carbohydrates; Cellulose; Chromato

1975
Therapy of hereditary disorders of blood coagulation.
    Modern treatment, 1968, Volume: 5, Issue:1

    Topics: Abdomen, Acute; Afibrinogenemia; Blood Coagulation Disorders; Blood Transfusion; Cerebral Hemorrhage

1968
The treatment of classical hemophilia with factor 8 concentrates.
    Clinical anesthesia, 1968, Volume: 3

    Topics: Blood Coagulation Tests; Chemical Precipitation; Factor VIII; Fibrinogen; Freezing; Glycine; Hemophi

1968

Other Studies

22 other studies available for glycine and Hemophilia A

ArticleYear
CLOTTING IN HEPARINISED PLASMA. II. UNDERLYING REACTIONS.
    The Australian journal of experimental biology and medical science, 1965, Volume: 43

    Topics: Anticoagulants; Antithrombin III; Blood Coagulation; Blood Coagulation Disorders; Blood Platelets; C

1965
Development and small-scale production of a severely heated factor VIII concentrate.
    Vox sanguinis, 1994, Volume: 66, Issue:2

    Topics: Chemical Precipitation; Factor VIII; Freeze Drying; Glycine; Half-Life; Hemophilia A; HIV-1; Hot Tem

1994
Mitigation of hepato-cellular injury caused by HAART with glycyrrhizin compound in patients co-infected with HIV and HCV.
    Japanese journal of infectious diseases, 1999, Volume: 52, Issue:6

    Topics: Anti-HIV Agents; Chemical and Drug Induced Liver Injury; Cysteine; Drug Combinations; Drug Therapy,

1999
Treatment of anti-factor VIII antibodies.
    Thrombosis and haemostasis, 1977, Aug-31, Volume: 38, Issue:2

    Topics: Adult; Antibodies; Child; Child, Preschool; Factor VIII; Glycine; Hemophilia A; Humans; Male; Middle

1977
Preliminary trial of cyclophosphamide in the management of hemophiliacs with factor VIII inhibitors.
    Annals of the New York Academy of Sciences, 1975, Jan-20, Volume: 240

    Topics: Adolescent; Adult; Antibodies; Antibody Formation; Blood Platelets; Child; Child, Preschool; Cycloph

1975
Experimental and theoretical evidence supporting the role of Gly363 in blood coagulation factor IXa (Gly193 in chymotrypsin) for proper activation of the proenzyme.
    The Journal of biological chemistry, 1990, Feb-15, Volume: 265, Issue:5

    Topics: Computer Graphics; Enzyme Activation; Enzyme Precursors; Factor IXa; Factor X; Glycine; Hemophilia A

1990
Moderately severe hemophilia A resulting from Glu----Gly substitution in exon 7 of the factor VIII gene.
    American journal of human genetics, 1988, Volume: 42, Issue:6

    Topics: Adolescent; Deoxyribonucleases, Type II Site-Specific; DNA Restriction Enzymes; Exons; Factor VIII;

1988
Even more concentrated antihaemophilic globulin.
    Lancet (London, England), 1968, Nov-30, Volume: 2, Issue:7579

    Topics: Factor VIII; Glycine; Hemarthrosis; Hemophilia A; Humans; Methods

1968
Reactivity to factor-VIII concentrates of lymphocytes from patients with haemophilia and von Willebrand's disease.
    British journal of haematology, 1974, Volume: 28, Issue:1

    Topics: Adolescent; Adult; Albumins; Antigens; Carbon Radioisotopes; Cells, Cultured; Chemical Precipitation

1974
The laboratory assessment of the efficacy of antihaemophilic therapy.
    South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde, 1972, Aug-19, Volume: 46, Issue:33

    Topics: Blood Coagulation Factors; Blood Preservation; Blood Transfusion; Factor VIII; Freezing; Glycine; He

1972
Pre-assayed AHF concentrate therapy for hemophilia.
    Bibliotheca haematologica, 1968, Volume: 29

    Topics: Adolescent; Adult; Antibodies; Blood Transfusion; Chemical Precipitation; Child, Preschool; Cold Tem

1968
Rapid correction of AHF deficiency by antihemophilic factor-method four, with special reference to inhibitors.
    Bibliotheca haematologica, 1970, Volume: 34

    Topics: Blood Coagulation Tests; Drug Hypersensitivity; Factor VIII; Glycine; Glycols; Hemophilia A; Humans;

1970
The use of glycine-precipitated antihemophilic factor during surgery in the hemophilic patient.
    The Journal of pediatrics, 1968, Volume: 72, Issue:3

    Topics: Child; Craniotomy; Esophageal and Gastric Varices; Factor VIII; Glycine; Hematoma, Subdural; Hemophi

1968
A new high-potency glycine-precipitated antihemophilic factor (AHF) concentrate. Treatment of classical hemophilia and hemophilia with inhibitors.
    JAMA, 1968, Aug-26, Volume: 205, Issue:9

    Topics: Adult; Blood Coagulation Tests; Chemical Precipitation; Factor VIII; Fibrinogen; Glycine; Hemophilia

1968
Use of aliphatic amino acid precipitated antihemophilic factor in therapy of hemophilia.
    Bibliotheca haematologica, 1968, Volume: 29

    Topics: Adult; Alanine; Amino Acids; Chemical Precipitation; Factor VIII; Glycine; Hemophilia A; Humans; Mal

1968
Fractions rich in factor VIII.
    Bibliotheca haematologica, 1968, Volume: 29

    Topics: Chemical Phenomena; Chemistry; Factor VIII; Fibrinogen; Glycine; Hemophilia A; Humans; Methods; Solu

1968
Treatment of hemophilia with factor 8 concentrates.
    The New England journal of medicine, 1968, Jan-25, Volume: 278, Issue:4

    Topics: Adult; Child; Cryoglobulins; Factor VIII; Glycine; Hemophilia A; Humans

1968
Glycine-precipitated antihemophilic factor concentrates and their clinical use.
    Thrombosis et diathesis haemorrhagica. Supplementum, 1968, Volume: 35

    Topics: Chemical Precipitation; Cryoglobulins; Factor VIII; Freeze Drying; Glycine; Hemophilia A; Humans; Me

1968
Human plasma and plasma fractions as sources of factor VIII (antihaemophilic factor).
    Vox sanguinis, 1969, Volume: 16, Issue:4

    Topics: Antigens; Blood Preservation; Blood Volume; Chemical Precipitation; Citrates; Factor IX; Factor VIII

1969
Experimental prophylaxis of severe hemophilia with a factor VIII concentrate.
    JAMA, 1969, Jun-09, Volume: 208, Issue:10

    Topics: Acute Disease; Adult; Blood Pressure; Chemical Precipitation; Factor VIII; Fibrinogen; Glycine; Hemo

1969
Clinical use of a new glycine-precipitated antihemophilic fraction.
    The American journal of the medical sciences, 1965, Volume: 250, Issue:6

    Topics: Adult; Chemical Precipitation; Factor VIII; Female; Glycine; Hemophilia A; Humans; Male

1965
Treatment of hemophilia with glycine-precipitated factor 8.
    The New England journal of medicine, 1966, Sep-01, Volume: 275, Issue:9

    Topics: Adolescent; Blood Proteins; Blood Transfusion; Child; Child, Preschool; Factor VIII; Fibrinogen; Gly

1966