Compounds > hypoxanthine

hypoxanthine and Glycogen Storage Disease Type V

hypoxanthine has been researched along with Glycogen Storage Disease Type V in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19905 (83.33)18.7374
1990's1 (16.67)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hamaguchi, T; Hara, N; Kawachi, M; Kiyokawa, H; Kono, N; Kuwajima, M; Mineo, I; Nakajima, H; Yamada, Y; Yamasaki, T1
Binkhorst, RA; Coerwinkel, MM; Joosten, EM; Oei, TL; Oerlemans, FT; Sinkeler, SP; van Bennekom, CA; Wevers, RA1
Binkhorst, R; Joosten, E; Oei, L; Sinkeler, S; Wevers, R1
Hara, N; Kawachi, M; Kiyokawa, H; Kono, N; Mineo, I; Shimizu, T; Tarui, S; Wang, YL; Yamada, Y1
Brooke, MH; Hagberg, JM; Heller, SL; Kaiser, KK; Planer, GJ1
Hara, N; Kono, N; Mineo, I; Nonaka, K; Shimizu, T; Sumi, S; Tarui, S; Yamada, Y1

Other Studies

6 other study(ies) available for hypoxanthine and Glycogen Storage Disease Type V

ArticleYear
Glucose infusion abolishes the excessive ATP degradation in working muscles of a patient with McArdle's disease.
    Muscle & nerve, 1990, Volume: 13, Issue:7

    Topics: Adenosine Triphosphate; Adult; Ammonia; Creatine Kinase; Exercise Test; Female; Glucose; Glycogen Storage Disease Type V; Humans; Hypoxanthine; Hypoxanthines; Infusions, Intravenous; Muscle Contraction; Muscles; Physical Exertion

1990
Ischaemic exercise test in myoadenylate deaminase deficiency and McArdle's disease: measurement of plasma adenosine, inosine and hypoxanthine.
    Clinical science (London, England : 1979), 1986, Volume: 70, Issue:4

    Topics: Adult; AMP Deaminase; Exercise Test; Female; Glycogen Storage Disease; Glycogen Storage Disease Type V; Humans; Hypoxanthine; Hypoxanthines; Male; Middle Aged; Muscles; Nucleotide Deaminases; Purine Nucleotides

1986
Skeletal muscle adenosine, inosine and hypoxanthine release following ischaemic forearm exercise in myoadenylate deaminase deficiency and McArdle's disease.
    Advances in experimental medicine and biology, 1986, Volume: 195 Pt B

    Topics: Adenosine; AMP Deaminase; Female; Glycogen Storage Disease; Glycogen Storage Disease Type V; Humans; Hypoxanthine; Hypoxanthines; Inosine; Ischemia; Male; Middle Aged; Muscles; Nucleotide Deaminases; Physical Exertion; Purine Nucleosides

1986
Myogenic hyperuricemia. A common pathophysiologic feature of glycogenosis types III, V, and VII.
    The New England journal of medicine, 1987, Jul-09, Volume: 317, Issue:2

    Topics: Adult; Ammonia; Glycogen Storage Disease; Glycogen Storage Disease Type III; Glycogen Storage Disease Type V; Glycogen Storage Disease Type VII; Humans; Hypoxanthine; Hypoxanthines; Inosine; Male; Middle Aged; Muscles; Physical Exertion; Rest; Uric Acid

1987
McArdle's disease with myoadenylate deaminase deficiency: observations in a combined enzyme deficiency.
    Neurology, 1987, Volume: 37, Issue:6

    Topics: Adult; Ammonia; AMP Deaminase; Female; Glycogen Storage Disease; Glycogen Storage Disease Type V; Humans; Hypoxanthine; Hypoxanthines; Male; Metabolic Diseases; Nucleotide Deaminases; Physical Exertion

1987
Excess purine degradation in exercising muscles of patients with glycogen storage disease types V and VII.
    The Journal of clinical investigation, 1985, Volume: 76, Issue:2

    Topics: Adult; Ammonia; Female; Glycogen Storage Disease; Glycogen Storage Disease Type V; Glycogen Storage Disease Type VII; Glycolysis; Humans; Hypoxanthine; Hypoxanthines; Inosine; Lactates; Lactic Acid; Male; Models, Biological; Muscles; Physical Exertion; Purines; Uric Acid

1985