uric acid has been researched along with Enlarged Liver in 20 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) |
| "The development of hepatomegaly and liver tumors in mice lacking Urah suggests that uric acid metabolites may be toxic and that urate oxidase activity without HIU hydrolase function may affect liver growth and transformation." | 1.36 | Deficiency of 5-hydroxyisourate hydrolase causes hepatomegaly and hepatocellular carcinoma in mice. ( Alexander, WS; Bahlo, M; Gill, A; Hennebry, S; Hilton, AA; Hilton, DJ; Hyland, CD; Masters, SL; Metcalf, D; Morgan, PO; Nicola, NA; Richardson, SJ; Roberts, AW; Stevenson, WS; Viney, EM; Willson, TA; Zhang, JG, 2010) |
| "Hepatomegaly was present in 39 out of 40, while 11 out of 27 reported patients had marked hepatomegaly (> 10 cm below the costal margin in the midclavicular line)." | 1.29 | The long-term outcome of patients with glycogen storage disease type Ia. ( Smit, GP, 1993) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 16 (80.00) | 18.7374 |
| 1990's | 2 (10.00) | 18.2507 |
| 2000's | 1 (5.00) | 29.6817 |
| 2010's | 1 (5.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Stevenson, WS | 1 |
| Hyland, CD | 1 |
| Zhang, JG | 1 |
| Morgan, PO | 1 |
| Willson, TA | 1 |
| Gill, A | 1 |
| Hilton, AA | 1 |
| Viney, EM | 1 |
| Bahlo, M | 1 |
| Masters, SL | 1 |
| Hennebry, S | 1 |
| Richardson, SJ | 1 |
| Nicola, NA | 1 |
| Metcalf, D | 1 |
| Hilton, DJ | 1 |
| Roberts, AW | 1 |
| Alexander, WS | 1 |
| BROMBACHER, PJ | 1 |
| VANCREVELD, S | 1 |
| DAMME, JP | 1 |
| HUIJING, F | 1 |
| PLOEM, JE | 1 |
| Jakovcic, S | 1 |
| Sorensen, LB | 1 |
| Smit, GP | 1 |
| Sugita, K | 1 |
| Hagisawa, S | 1 |
| Satoh, Y | 1 |
| Eguchi, M | 1 |
| Furukawa, T | 1 |
| Gonzalez Ruíz, A | 1 |
| Bernal Ruíz, AI | 1 |
| Aragoneses Fraile, H | 1 |
| Peral Martinez, I | 1 |
| García Muñoz, M | 1 |
| Schaub, J | 1 |
| Fevery, J | 1 |
| You, W | 1 |
| Weisbrot, IM | 1 |
| Corneo, G | 1 |
| Galli, C | 1 |
| Airoldi, M | 1 |
| Ceccherini Nelli, L | 1 |
| Ogea García, JL | 1 |
| Villanueva Marcos, JL | 1 |
| Jurado, R | 1 |
| Rivero, S | 1 |
| Orchard, PJ | 1 |
| Moffet, HL | 1 |
| Hafez, GR | 1 |
| Sondel, PM | 1 |
| Keating, JP | 1 |
| Brown, BI | 1 |
| White, NH | 1 |
| DiMauro, S | 1 |
| Prokocimer, M | 1 |
| Modan, M | 1 |
| Lusky, A | 1 |
| Hershko, C | 1 |
| Peschel, G | 1 |
| Scheffler, W | 1 |
| Burr, IM | 1 |
| O'Neill, JA | 1 |
| Karzon, DT | 1 |
| Howard, LJ | 1 |
| Greene, HL | 1 |
| de Gennes, JL | 1 |
| Thomopoulos, P | 1 |
| Truffert, J | 1 |
| Labrousse de Tregomain, B | 1 |
| Kay, NE | 1 |
| Nelson, DA | 1 |
| Gottlieb, AJ | 1 |
| Myrhed, M | 1 |
| Benedetti, A | 1 |
| Bucciante, G | 1 |
| Cattano, G | 1 |
| Nardini, A | 1 |
2 reviews available for uric acid and Enlarged Liver
| Article | Year |
|---|---|
[The glycogenoses. Fundamentals of clinical and biochemical diagnosis].
Topics: Acidosis; Cardiomegaly; Dietary Carbohydrates; Dietary Fats; Dietary Proteins; Glycogen Storage Dise | 1978 |
[Biochemical basis of the effects of alcohol].
Topics: Acetaldehyde; Alcoholism; Arrhythmias, Cardiac; Carbohydrate Metabolism; Citrates; Citric Acid Cycle | 1976 |
18 other studies available for uric acid and Enlarged Liver
| Article | Year |
|---|---|
Deficiency of 5-hydroxyisourate hydrolase causes hepatomegaly and hepatocellular carcinoma in mice.
Topics: Amidohydrolases; Amino Acid Sequence; Animals; Female; Genes, Tumor Suppressor; Hepatocytes; Hepatom | 2010 |
A REPORT OF TWO ADULT PATIENTS WITH GLYCOGEN STORAGE DISEASE.
Topics: Acetone; Adult; Blood Glucose; Carbohydrate Metabolism; Child; Epinephrine; Galactose; Glucagon; Glu | 1964 |
Studies of uric acid metabolism in glycogen storage disease associated with gouty arthritis.
Topics: Adolescent; Allopurinol; Body Height; Body Weight; Carbon Isotopes; Enzyme Therapy; Glucosephosphate | 1967 |
The long-term outcome of patients with glycogen storage disease type Ia.
Topics: Adenoma; Adolescent; Adult; Aged; Apolipoproteins; Blood Glucose; Child; Cholesterol; Female; Glycog | 1993 |
Recurrent hepatosplenomegaly and peripheral blood cytopenia, persistent Epstein-Barr virus infection and central nervous system manifestation in a patient with lymphadenopathy and low serum uric acid.
Topics: Central Nervous System Diseases; Child, Preschool; Hepatomegaly; Herpesviridae Infections; Herpesvir | 1998 |
Progressive nodular histiocytosis accompanied by systemic disorders.
Topics: Cholesterol; Hepatomegaly; Histiocytosis, Non-Langerhans-Cell; Humans; Hypothyroidism; Leukemia, Mye | 2000 |
Chronic neutrophilic leukemia. Report of two cases and review of the literature.
Topics: Adult; Aged; Alkaline Phosphatase; Bone Marrow; Chromosomes, Human, 21-22 and Y; Hemorrhagic Disorde | 1979 |
[Clinical and therapeutic aspects of polycythemia vera].
Topics: Adult; Age Factors; Aged; Bilirubin; Blood Cell Count; Blood Urea Nitrogen; Bloodletting; Busulfan; | 1978 |
[Burkitt's lymphoma and AIDS. Their presentation as tumoral hepatomegaly and acute kidney failure due to the tubular deposit of urates].
Topics: Acquired Immunodeficiency Syndrome; Acute Kidney Injury; Adult; Burkitt Lymphoma; Diagnosis, Differe | 1989 |
Pseudomonas sepsis simulating acute promyelocytic leukemia.
Topics: Bone Marrow Examination; Hemoglobins; Hepatomegaly; Humans; Infant; Leukemia, Myeloid, Acute; Leukoc | 1988 |
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 |
Multivariate analysis of prognostic factors in chronic lymphocytic leukemia.
Topics: Adult; Aged; Anemia; Ethnicity; Female; Hemoglobins; Hepatomegaly; Humans; Leukemia, Lymphoid; Leuko | 1985 |
[8 years of SGPT screening at the District Institute for Blood Donation and Transfusion Services in Karl-Marx-Stadt].
Topics: Adult; Alanine Transaminase; Biopsy; Blood Donors; Clinical Enzyme Tests; Diabetes Mellitus; Fatty L | 1973 |
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 |
[Hyperlipemias due to alcohol].
Topics: Adult; Alcoholism; Body Weight; Cardiovascular Diseases; Cholesterol; Dietary Carbohydrates; Ethanol | 1972 |
Eosinophilic Pelger-Huët anomaly with myeloproliferative disorder.
Topics: Aged; Eosinophilia; Eosinophils; Hepatomegaly; Histocytochemistry; Humans; Inclusion Bodies; Leukocy | 1973 |
Alcohol consumption in relation to factors associated with ischemic heart disease. A co-twin control study.
Topics: Aged; Alanine Transaminase; Alcohol Drinking; Alcoholism; Alkaline Phosphatase; Aspartate Aminotrans | 1974 |
[Gout in the evolution of Von Gierke's disease].
Topics: Adolescent; Adult; Allopurinol; Child; Female; Glycogen Storage Disease; Glycogen Storage Disease Ty | 1969 |