uric acid has been researched along with Glycogenosis in 38 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.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Seven male members of one family had a form of glycogen storage disease that was inherited in an X-linked recessive pattern." | 7.67 | X-linked glycogen storage disease. A cause of hypotonia, hyperuricemia, and growth retardation. ( Brown, BI; DiMauro, S; Keating, JP; White, NH, 1985) |
| "Seven male members of one family had a form of glycogen storage disease that was inherited in an X-linked recessive pattern." | 3.67 | X-linked glycogen storage disease. A cause of hypotonia, hyperuricemia, and growth retardation. ( Brown, BI; DiMauro, S; Keating, JP; White, NH, 1985) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 33 (86.84) | 18.7374 |
| 1990's | 4 (10.53) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (2.63) | 2.80 |
| Authors | Studies |
|---|---|
| Xu, N | 1 |
| Han, X | 1 |
| Zhang, Y | 1 |
| Huang, X | 1 |
| Zhu, W | 1 |
| Shen, M | 1 |
| Zhang, W | 1 |
| Jialin, C | 1 |
| Wei, M | 1 |
| Qiu, Z | 1 |
| Zeng, X | 1 |
| JEANDET, J | 1 |
| LESTRADET, H | 1 |
| BROMBACHER, PJ | 1 |
| VANCREVELD, S | 1 |
| DAMME, JP | 1 |
| HUIJING, F | 1 |
| PLOEM, JE | 1 |
| Greene, HL | 3 |
| Kawaguchi, Y | 1 |
| Shirasawa, K | 1 |
| Yotsumoto, S | 1 |
| Nagahara, S | 1 |
| Mineo, I | 9 |
| Tarui, S | 6 |
| Yamasaki, T | 3 |
| Hamaguchi, T | 2 |
| Nakajima, H | 6 |
| Matsuzawa, Y | 1 |
| Schaub, J | 1 |
| Leonard, JV | 1 |
| Francis, DE | 1 |
| Dunger, DB | 1 |
| Kono, N | 8 |
| Hotta, K | 1 |
| Kawachi, M | 5 |
| Nishimura, T | 1 |
| Kuwajima, M | 3 |
| Noguchi, T | 2 |
| Tanaka, T | 1 |
| Shimizu, T | 4 |
| Kiyokawa, H | 3 |
| Yamada, Y | 4 |
| Hara, N | 4 |
| Wang, YL | 3 |
| Pronicka, E | 1 |
| Rowińska, E | 1 |
| Miłoszewska, E | 1 |
| Hardiman, O | 1 |
| Farrell, M | 1 |
| McElvaney, G | 1 |
| Tipton, K | 1 |
| Staunton, H | 1 |
| Fox, IH | 1 |
| Palella, TD | 1 |
| Kelley, WN | 2 |
| Keating, JP | 1 |
| Brown, BI | 2 |
| White, NH | 1 |
| DiMauro, S | 1 |
| Sumi, S | 1 |
| Nonaka, K | 1 |
| Holtzman, NA | 1 |
| Burr, IM | 1 |
| O'Neill, JA | 1 |
| Karzon, DT | 1 |
| Howard, LJ | 1 |
| Royer, P | 1 |
| Sorensen, LB | 1 |
| Pasero, GP | 1 |
| Ciompi, MI | 1 |
| Moses, SW | 1 |
| Starzl, TE | 1 |
| Putnam, CW | 1 |
| Porter, KA | 1 |
| Halgrimson, CG | 1 |
| Corman, J | 1 |
| Gotlin, RW | 1 |
| Rodgerson, DO | 1 |
| Dosman, J | 1 |
| Crawhall, JC | 1 |
| Klassen, GA | 2 |
| Mamer, OA | 2 |
| Neumann, P | 1 |
| Dosman, JA | 1 |
| Crawhill, JC | 1 |
| Fine, RN | 1 |
| Strauss, J | 1 |
| Donnell, GN | 1 |
| Smith, EE | 1 |
| Kurlander, GJ | 1 |
| Powell, RC | 1 |
| Rosenbloom, FM | 1 |
| Seegmiller, JE | 1 |
| Howell, RR | 1 |
| Benedetti, A | 1 |
| Bucciante, G | 1 |
| Cattano, G | 1 |
| Nardini, A | 1 |
| Ryckewaert, A | 1 |
| Preger, L | 1 |
| Sanders, GW | 1 |
| Gold, RH | 1 |
| Steinbach, HL | 1 |
| Pitman, P | 1 |
| Matschke, I | 1 |
| Neubaur, J | 1 |
| Willms, B | 1 |
| Wolf, H | 1 |
9 reviews available for uric acid and Glycogenosis
| Article | Year |
|---|---|
Clinical features of gout in adult patients with type Ia glycogen storage disease: a single-centre retrospective study and a review of literature.
Topics: Adolescent; Adult; Child; Female; Glycogen Storage Disease; Gout; Humans; Retrospective Studies; Sym | 2022 |
Glycogen storage disease.
Topics: Blood Glucose; Glucosephosphate Dehydrogenase Deficiency; Glycogen; Glycogen Storage Disease; Glycog | 1982 |
Myogenic hyperuricemia: what can we learn from metabolic myopathies?
Topics: Adenosine Diphosphate; Adenosine Triphosphate; Adult; AMP Deaminase; Energy Metabolism; Exercise; Ge | 1995 |
[Myogenic hyperuricemia].
Topics: Adenosine Monophosphate; Adenosine Triphosphate; Energy Metabolism; Glycogen Storage Disease; Humans | 1996 |
[The glycogenoses. Fundamentals of clinical and biochemical diagnosis].
Topics: Acidosis; Cardiomegaly; Dietary Carbohydrates; Dietary Fats; Dietary Proteins; Glycogen Storage Dise | 1978 |
[Myogenic hyperuricemia].
Topics: Glycogen Storage Disease; Humans; Muscles; Purines; Uric Acid | 1991 |
Dietary treatment of inborn errors of metabolism.
Topics: Ammonia; Carbohydrate Metabolism, Inborn Errors; Diet Therapy; Female; Fructose; Galactosemias; Glyc | 1970 |
Hyperuricemia and gout.
Topics: Biological Transport; Carbohydrate Metabolism, Inborn Errors; Down Syndrome; Fructose; Glucosyltrans | 1969 |
[Hyperuricemia in childhood].
Topics: Anemia, Hemolytic; Child; Down Syndrome; Glycogen Storage Disease; Gout; Humans; Kidney Calculi; Kid | 1973 |
29 other studies available for uric acid and Glycogenosis
| Article | Year |
|---|---|
[Hyperlactacidemia, probable cause of hyperuricemia, in hepatic glycogenosis].
Topics: Glycogen Storage Disease; Humans; Hyperuricemia; Lactates; Liver; Uric Acid | 1961 |
A REPORT OF TWO ADULT PATIENTS WITH GLYCOGEN STORAGE DISEASE.
Topics: Acetone; Adult; Blood Glucose; Carbohydrate Metabolism; Child; Epinephrine; Galactose; Glucagon; Glu | 1964 |
Type III glycogenosis with deposition of urate and amyloid.
Topics: Adult; Amyloid; Fructose Intolerance; Glycogen Storage Disease; Glycogen Storage Disease Type IV; Go | 1980 |
The dietary management of hepatic glycogen storage disease.
Topics: Blood Glucose; Cholesterol; Glucose; Glycogen Storage Disease; Glycogen Storage Disease Type I; Huma | 1979 |
A genetic defect in muscle phosphofructokinase deficiency, a typical clinical entity presenting myogenic hyperuricemia.
Topics: Base Sequence; DNA Mutational Analysis; Glycogen Storage Disease; Humans; Male; Molecular Sequence D | 1991 |
Molecular aspect of myogenic hyperuricemia: cloning of human muscle phosphofructokinase cDNA.
Topics: Amino Acid Sequence; Base Sequence; Cloning, Molecular; DNA; Glycogen Storage Disease; Humans; Molec | 1989 |
Exercise induced alteration of erythrocyte glycolysis associated with myogenic hyperuricemia.
Topics: Adolescent; Erythrocytes; Exercise; Glycogen Storage Disease; Glycolysis; Humans; Male; Muscles; Uri | 1989 |
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 |
Tubular function of kidney after galactose loading in two patients with glycogen storage disease type XL.
Topics: Adolescent; Adult; Bicarbonates; Fanconi Syndrome; Galactose; Galactosemias; Glycogen Storage Diseas | 1987 |
[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 |
Hyperuricemia: a marker for cell energy crisis.
Topics: Adenosine Triphosphate; Glycogen Storage Disease; Humans; Uric Acid | 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 |
X-linked glycogen storage disease. A cause of hypotonia, hyperuricemia, and growth retardation.
Topics: Adolescent; Adult; Biopsy; Child; Glycogen; Glycogen Debranching Enzyme System; Glycogen Storage Dis | 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 |
Comparison of the effects of total parenteral nutrition, continuous intragastric feeding, and portacaval shunt on a patient with type I glycogen storage disease.
Topics: Adolescent; Amino Acids; Enteral Nutrition; Glucose; Glycogen Storage Disease; Hepatomegaly; Humans; | 1974 |
Hyperuricemia in children, with the exception of the Lesch-Nyhan syndrome.
Topics: Acidosis; Acute Disease; Acute Kidney Injury; Adult; Child; Child, Preschool; Chronic Disease; Femal | 1974 |
An unusual case of glycogen storage disease.
Topics: Alanine Transaminase; Allopurinol; Aspartate Aminotransferases; Blood Glucose; Carbon Radioisotopes; | 1973 |
Portal diversion for the treatment of glycogen storage disease in humans.
Topics: Acidosis; Biopsy; Blood Glucose; Child; Glycogen Storage Disease; Humans; Liver; Liver Cirrhosis; Li | 1973 |
Urinary excretion of C6-C10 dicarboxylic acids in glycogen storage disease types I and 3.
Topics: Adolescent; Blood Glucose; Body Height; Body Weight; Carbon Radioisotopes; Child; Cholesterol; Chrom | 1974 |
Hyperuricemia and dicarboxylicaciduria in glycogen storage disease.
Topics: Body Height; Body Weight; Carbon Radioisotopes; Child; Cholesterol; Chromatography, Gas; Creatinine; | 1973 |
Hyperuricemia in glycogen-storage disease type 1.
Topics: Adolescent; Adult; Child; Child, Preschool; Glucose; Glycogen Storage Disease; Glycogen Storage Dise | 1966 |
Lactic acid and hyperuricemia of faulty renal urate transport.
Topics: Female; Glycogen Storage Disease; Gout; Humans; Hypertension; Kidney Diseases; Lactates; Pre-Eclamps | 1967 |
Two rare causes of secondary gouty arthritis.
Topics: Adult; Glomerulonephritis; Glycogen Storage Disease; Gout; Humans; Male; Phosphates; Radiography; Re | 1967 |
Excessive production of uric acid in type I glycogen storage disease.
Topics: Adolescent; Carbon Isotopes; Female; Glucosephosphate Dehydrogenase Deficiency; Glucosyltransferases | 1968 |
[Gout in the evolution of Von Gierke's disease].
Topics: Adolescent; Adult; Allopurinol; Child; Female; Glycogen Storage Disease; Glycogen Storage Disease Ty | 1969 |
[Diagnostic value of hyperuricemia].
Topics: Adult; Allopurinol; Child; Diabetes Mellitus; Female; Glycogen Storage Disease; Gout; Humans; Hypert | 1968 |
Roentgenographic skeletal changes in the glycogen storage diseases.
Topics: Adolescent; Adult; Age Factors; Body Height; Bone and Bones; Child; Child, Preschool; Female; Glycog | 1969 |
[Metabolism studies in children and young adults with glycogenoses].
Topics: Adolescent; Adult; Child; Fatty Acids; Glucagon; Glucosidases; Glucosyltransferases; Glycogen Storag | 1969 |