uric acid has been researched along with Glycogen Storage Disease Type V in 11 studies
Uric Acid: An oxidation product, via XANTHINE OXIDASE, of oxypurines such as XANTHINE and HYPOXANTHINE. It is the final oxidation product of purine catabolism in humans and primates, whereas in most other mammals URATE OXIDASE further oxidizes it to ALLANTOIN.
uric acid : An oxopurine that is the final oxidation product of purine metabolism.
6-hydroxy-1H-purine-2,8(7H,9H)-dione : A tautomer of uric acid having oxo groups at C-2 and C-8 and a hydroxy group at C-6.
7,9-dihydro-1H-purine-2,6,8(3H)-trione : An oxopurine in which the purine ring is substituted by oxo groups at positions 2, 6, and 8.
Glycogen Storage Disease Type V: Glycogenosis due to muscle phosphorylase deficiency. Characterized by painful cramps following sustained exercise.
Excerpt | Relevance | Reference |
---|---|---|
"We report the first case of McArdle's disease (muscle phosphorylase deficiency) and tophaceous gout." | 1.28 | McArdle's disease and gout. ( de Miguel, E; Espinosa, A; Gijón, J; Mateos, FA; Miranda, E; Puig, JG; Romera, NM, 1992) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 6 (54.55) | 18.7374 |
1990's | 2 (18.18) | 18.2507 |
2000's | 1 (9.09) | 29.6817 |
2010's | 2 (18.18) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Üsküdar Cansu, D | 1 |
Erdoğan, B | 1 |
Korkmaz, C | 1 |
Kitaoka, Y | 1 |
Ogborn, DI | 1 |
Nilsson, MI | 1 |
Mocellin, NJ | 1 |
MacNeil, LG | 1 |
Tarnopolsky, MA | 1 |
Yamasaki, T | 1 |
Mineo, I | 5 |
Jinnai, K | 1 |
Kono, N | 5 |
Yamamoto, Y | 1 |
Kanda, F | 1 |
Ohno, S | 1 |
Tsutsumi, M | 1 |
Yamada, Y | 4 |
Kawachi, M | 3 |
Tarui, S | 4 |
Fujita, T | 1 |
Puig, JG | 1 |
de Miguel, E | 1 |
Mateos, FA | 1 |
Miranda, E | 1 |
Romera, NM | 1 |
Espinosa, A | 1 |
Gijón, J | 1 |
Hara, N | 3 |
Kiyokawa, H | 2 |
Nakajima, H | 2 |
Shimizu, T | 3 |
Kuwajima, M | 1 |
Wang, YL | 2 |
Hardiman, O | 1 |
Farrell, M | 1 |
McElvaney, G | 1 |
Tipton, K | 1 |
Staunton, H | 1 |
Fox, IH | 1 |
Sumi, S | 1 |
Nonaka, K | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
GDF-15 as a Biomarker for Mitochondrial Disease[NCT02745938] | 97 participants (Actual) | Observational | 2016-06-30 | Completed | |||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
2 reviews available for uric acid and Glycogen Storage Disease Type V
Article | Year |
---|---|
Can hyperuricemia predict glycogen storage disease (McArdle's disease) in rheumatology practice? (Myogenic hyperuricemia).
Topics: Adult; Antirheumatic Agents; Arthritis; Arthritis, Gouty; Diagnosis, Differential; Diagnostic Errors | 2019 |
[Secondary hyperuricemia in glycogen storage disease types I, III, V and VII].
Topics: Glycogen Storage Disease Type I; Glycogen Storage Disease Type III; Glycogen Storage Disease Type V; | 2003 |
9 other studies available for uric acid and Glycogen Storage Disease Type V
Article | Year |
---|---|
Oxidative stress and Nrf2 signaling in McArdle disease.
Topics: Aldehydes; Female; Gene Expression Regulation; Glucosyltransferases; Glycogen Storage Disease Type V | 2013 |
Glycogenosis type V (McArdle's disease) with hyperuricemia. A case report and clinical investigation.
Topics: Adult; Biopsy; Enzymes; Exercise Test; Glycogen Storage Disease Type V; Gout; Humans; Male; Muscles; | 1993 |
McArdle's disease and gout.
Topics: Adenine Nucleotides; Arthritis, Gouty; Exercise Test; Glycogen Storage Disease Type V; Humans; Male; | 1992 |
Myogenic hyperuricemia: a comparative study between type V and type VII glycogenosis.
Topics: Adolescent; Adult; Exercise; Female; Glycogen Storage Disease; Glycogen Storage Disease Type V; Glyc | 1989 |
[Glycogenosis (molecular mechanism of muscle glycogenosis)].
Topics: Adenosine Triphosphate; Amino Acid Sequence; Glycogen; Glycogen Storage Disease; Glycogen Storage Di | 1988 |
Hyperuricemia in type V glycogenosis.
Topics: Glycogen Storage Disease; Glycogen Storage Disease Type V; Humans; Male; Middle Aged; Muscles; Physi | 1987 |
Myogenic hyperuricemia. A common pathophysiologic feature of glycogenosis types III, V, and VII.
Topics: Adult; Ammonia; Glycogen Storage Disease; Glycogen Storage Disease Type III; Glycogen Storage Diseas | 1987 |
Adenosine triphosphate degradation in specific disease.
Topics: Adenine; Adenosine Triphosphate; Biotransformation; Carnitine O-Palmitoyltransferase; Ethanol; Fruct | 1985 |
Excess purine degradation in exercising muscles of patients with glycogen storage disease types V and VII.
Topics: Adult; Ammonia; Female; Glycogen Storage Disease; Glycogen Storage Disease Type V; Glycogen Storage | 1985 |