Compounds > hypoxanthine

hypoxanthine and Glycogenosis

hypoxanthine has been researched along with Glycogenosis in 6 studies

Research

Studies (6)

Timeframe	Studies, this research(%)	All Research%
pre-1990	5 (83.33)	18.7374
1990's	1 (16.67)	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
Hamaguchi, T; Matsuzawa, Y; Nakajima, H; Yamasaki, T	1
Binkhorst, RA; Coerwinkel, MM; Joosten, EM; Oei, TL; Oerlemans, FT; Sinkeler, SP; van Bennekom, CA; Wevers, RA	1
Binkhorst, R; Joosten, E; Oei, L; Sinkeler, S; Wevers, R	1
Hara, N; Kawachi, M; Kiyokawa, H; Kono, N; Mineo, I; Shimizu, T; Tarui, S; Wang, YL; Yamada, Y	1
Brooke, MH; Hagberg, JM; Heller, SL; Kaiser, KK; Planer, GJ	1
Hara, N; Kono, N; Mineo, I; Nonaka, K; Shimizu, T; Sumi, S; Tarui, S; Yamada, Y	1

Reviews

1 review(s) available for hypoxanthine and Glycogenosis

Article	Year
[Myogenic hyperuricemia]. Nihon rinsho. Japanese journal of clinical medicine, 1996, Volume: 54, Issue:12 Topics: Adenosine Monophosphate; Adenosine Triphosphate; Energy Metabolism; Glycogen Storage Disease; Humans; Hypoxanthine; Muscles; Mutation; Purines; Uric Acid	1996

Other Studies

5 other study(ies) available for hypoxanthine and Glycogenosis

Article	Year
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