| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/S10545-007-0455-8 |
| P8608 | Fatcat ID | release_kmwviqdikbekbkgl2vblxmuhfa |
| P698 | PubMed publication ID | 17520339 |
| P50 | author | Francisco Radler de Aquino Neto | Q54147375 |
| P2093 | author name string | R E Simoni | |
| C P H Oliveira | |||
| F B Scalco | |||
| L N L Ferreira Gomes | |||
| M L Costa de Oliveira | |||
| P2860 | cites work | Uric acid: A new look at an old risk marker for cardiovascular disease, metabolic syndrome, and type 2 diabetes mellitus: The urate redox shuttle | Q24559986 |
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| Serum uric acid and coronary heart disease in 9,458 incident cases and 155,084 controls: prospective study and meta-analysis | Q24805426 | ||
| The genetics of autism | Q28259677 | ||
| Adenine phosphoribosyltransferase deficiency identified by urinary sediment analysis: cellular and molecular confirmation | Q28291233 | ||
| Myoadenylate deaminase deficiency does not affect muscle anaplerosis during exhaustive exercise in humans | Q28366955 | ||
| A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype | Q28609693 | ||
| Ethanol metabolism, cirrhosis and alcoholism | Q28610013 | ||
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| Is there a pathogenetic role for uric acid in hypertension and cardiovascular and renal disease? | Q35111714 | ||
| Recent developments in our understanding of the renal basis of hyperuricemia and the development of novel antihyperuricemic therapeutics | Q35578918 | ||
| Hyperuricaemia does not impair cardiovascular function in healthy adults | Q35582012 | ||
| Rhabdomyolysis. Pathophysiology, recognition, and management | Q35614254 | ||
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| Uric acid, endothelial dysfunction and pre-eclampsia: searching for a pathogenetic link | Q35742936 | ||
| Natural history of autosomal dominant polycystic kidney disease | Q40759629 | ||
| The management of gout | Q40940712 | ||
| When to investigate for purine and pyrimidine disorders. Introduction and review of clinical and laboratory indications | Q41521428 | ||
| Inherited defects of purine and pyrimidine metabolism: Laboratory methods for diagnosis | Q41521436 | ||
| Purine metabolism abnormalities in a hyperuricosuric subclass of autism | Q41722721 | ||
| Metabolic myopathies and physical activity: when fatigue is more than simple exertion | Q43189456 | ||
| Urate and arteriosclerosis in primary hyperparathyroidism | Q43650572 | ||
| Hyperuricemia and gout in thyroid endocrine disorders. | Q43854809 | ||
| Persistent developmental delay despite successful bone marrow transplantation for purine nucleoside phosphorylase deficiency | Q43922657 | ||
| Hypouricaemia as a marker of a generalized proximal tubular damage in alcoholic patients | Q44129388 | ||
| Leptin might be a regulator of serum uric acid concentrations in humans | Q44541346 | ||
| Hypouricemia, an old subject and new concepts | Q44964872 | ||
| Myoadenylate deaminase deficiency in a child with myalgias induced by physical exercise | Q45066146 | ||
| Renal involvement in Down syndrome | Q46399526 | ||
| Mutational analysis of idiopathic renal hypouricemia in Korea | Q46506213 | ||
| Hypouricemia, abnormal renal tubular urate transport, and plasma natriuretic factor(s) in patients with Alzheimer's disease | Q48290756 | ||
| Hyperuricaemia and medium-chain acyl-CoA dehydrogenase deficiency | Q48565979 | ||
| Cerebral salt wasting syndrome following brain injury in three pediatric patients: suggestions for rapid diagnosis and therapy | Q48662100 | ||
| Gout: the last 50 years. | Q53613615 | ||
| Serum lipid resistance to oxidation and uric acid levels in subjects with Down's syndrome. | Q54037214 | ||
| Serum uric acid levels in patients with cirrhosis: a reevaluation. | Q54076997 | ||
| Sarcoidosis | Q56656053 | ||
| [Renal hypouricemia in juvenile diabetes mellitus] | Q71800817 | ||
| [Myogenic hyperuricemia] | Q71926702 | ||
| [Abnormal serum uric acid level in endocrine disorders] | Q71926716 | ||
| Differences in purine metabolism in patients with Down's syndrome | Q72283162 | ||
| Urolithiasis related to laxative abuse | Q72677087 | ||
| [Clinical significance of hyperuricemia in psoriasis] | Q72881246 | ||
| Urinary uric acid/creatinine ratio as an additional marker of perinatal asphyxia | Q73147204 | ||
| Sequential evaluation of serum urate concentrations in AIDS patients with infections of the central nervous system | Q73506512 | ||
| Renal metabolism of uric acid in type I insulin-dependent diabetic patients: relation to metabolic compensation | Q73957407 | ||
| Renal Transport of Urate in Humans | Q73967377 | ||
| Rhabdomyolysis | Q74037069 | ||
| Genotype-phenotype correlations in normotensive patients with primary renal tubular hypokalemic metabolic alkalosis | Q74554952 | ||
| Metabolic liver disease: Working Group Report of the First World Congress of Pediatric Gastroenterology, Hepatology, and Nutrition | Q74645016 | ||
| [Hereditary xanthinuria, rare cause of hypo-uric acidemia. 2 cases] | Q77395949 | ||
| Cerebral salt-wasting syndrome: does it exist? | Q77867048 | ||
| Hemolytic anemia | Q80212472 | ||
| Tamm-Horsfall protein or uromodulin: new ideas about an old molecule | Q81666610 | ||
| Hyperuricemia in psoriatic arthritis: prevalence and associated features | Q82945480 | ||
| P433 | issue | 3 | |
| P304 | page(s) | 295-309 | |
| P577 | publication date | 2007-05-19 | |
| P1433 | published in | Journal of Inherited Metabolic Disease | Q6295359 |
| P1476 | title | Uric acid changes in urine and plasma: an effective tool in screening for purine inborn errors of metabolism and other pathological conditions | |
| P478 | volume | 30 |
| Q42572005 | (1)H NMR-based metabolomic analysis for identifying serum biomarkers to evaluate methotrexate treatment in patients with early rheumatoid arthritis |
| Q36113752 | An unusual cause of "pink diaper" in an infant: Answers. |
| Q102152302 | Association of hyperuricemia and gamma glutamyl transferase as a marker of metabolic risk in alcohol use disorder |
| Q104136127 | Atypical presentation of Arts syndrome due to a novel hemizygous loss-of-function variant in the PRPS1 gene |
| Q35775904 | Comparison of mouse urinary metabolic profiles after exposure to the inflammatory stressors γ radiation and lipopolysaccharide |
| Q37416449 | Inborn errors of purine and pyrimidine metabolism. |
| Q60133323 | Metabolic profile of amniotic fluid as a biochemical tool to screen for inborn errors of metabolism and fetal anomalies |
| Q64949815 | Temporal Effects on Radiation Responses in Nonhuman Primates: Identification of Biofluid Small Molecule Signatures by Gas Chromatography⁻Mass Spectrometry Metabolomics. |
| Q41594620 | Uric acid, an important screening tool to detect inborn errors of metabolism: a case series. |
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