Literature DB >> 8648529

Abnormal serum uric acid levels in children.

W D Wilcox1.   

Abstract

Measurement of the serum uric acid level, most commonly considered in adult patients, is frequently obtained inadvertently for pediatric patients because it is a standard component of many multichannel chemistry profiles offered by clinical laboratories. Most standard references for normal uric acid values do not take into account the impact of the metabolic changes in children at different ages on the uric acid level. A substantial number of childhood conditions may produce perturbations in the serum uric acid level. Knowledge of normal serum uric acid levels and of the conditions affecting those levels in children enables a more focused pursuit of underlying abnormalities.

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Year:  1996        PMID: 8648529     DOI: 10.1016/s0022-3476(96)70322-0

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  27 in total

1.  Uromodulin is expressed in renal primary cilia and UMOD mutations result in decreased ciliary uromodulin expression.

Authors:  Frank Zaucke; Joana M Boehnlein; Sarah Steffens; Roman S Polishchuk; Luca Rampoldi; Andreas Fischer; Andreas Pasch; Christoph W A Boehm; Anne Baasner; Massimo Attanasio; Bernd Hoppe; Helmut Hopfer; Bodo B Beck; John A Sayer; Friedhelm Hildebrandt; Matthias T F Wolf
Journal:  Hum Mol Genet       Date:  2010-02-18       Impact factor: 6.150

Review 2.  Perinatal biomarkers in prematurity: early identification of neurologic injury.

Authors:  Maria Andrikopoulou; Ahmad Almalki; Azadeh Farzin; Christina N Cordeiro; Michael V Johnston; Irina Burd
Journal:  Int J Dev Neurosci       Date:  2014-04-24       Impact factor: 2.457

Review 3.  Inherited defects of purine and pyrimidine metabolism: laboratory methods for diagnosis.

Authors:  M Duran; L Dorland; E E Meuleman; P Allers; R Berger
Journal:  J Inherit Metab Dis       Date:  1997-06       Impact factor: 4.982

4.  Medullary cystic kidney disease type 1: mutational analysis in 37 genes based on haplotype sharing.

Authors:  Matthias T F Wolf; Bettina E Mucha; Hans C Hennies; Massimo Attanasio; Franziska Panther; Isabella Zalewski; Stephanie M Karle; Edgar A Otto; C Constantinou Deltas; Arno Fuchshuber; Friedhelm Hildebrandt
Journal:  Hum Genet       Date:  2006-04-26       Impact factor: 4.132

5.  Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy.

Authors:  T C Hart; M C Gorry; P S Hart; A S Woodard; Z Shihabi; J Sandhu; B Shirts; L Xu; H Zhu; M M Barmada; A J Bleyer
Journal:  J Med Genet       Date:  2002-12       Impact factor: 6.318

6.  Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic kidney failure.

Authors:  Martina Zivná; Helena Hůlková; Marie Matignon; Katerina Hodanová; Petr Vylet'al; Marie Kalbácová; Veronika Baresová; Jakub Sikora; Hana Blazková; Jan Zivný; Robert Ivánek; Viktor Stránecký; Jana Sovová; Kathleen Claes; Evelyne Lerut; Jean-Pierre Fryns; P Suzanne Hart; Thomas C Hart; Jeremy N Adams; Audrey Pawtowski; Maud Clemessy; Jean-Marie Gasc; Marie-Claire Gübler; Corinne Antignac; Milan Elleder; Katja Kapp; Philippe Grimbert; Anthony J Bleyer; Stanislav Kmoch
Journal:  Am J Hum Genet       Date:  2009-08-06       Impact factor: 11.025

7.  Partial hypoxanthine-guanine phosphoribosyltransferase deficiency presenting as acute renal failure.

Authors:  Sarah Cherian; Charles H Crompton
Journal:  Pediatr Nephrol       Date:  2005-10-21       Impact factor: 3.714

Review 8.  Uric acid and the kidney.

Authors:  Sahar A Fathallah-Shaykh; Monica T Cramer
Journal:  Pediatr Nephrol       Date:  2013-07-04       Impact factor: 3.714

9.  Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD.

Authors:  Bodo B Beck; Howard Trachtman; Michael Gitman; Ilene Miller; John A Sayer; Andrea Pannes; Anne Baasner; Friedhelm Hildebrandt; Matthias T F Wolf
Journal:  Am J Kidney Dis       Date:  2011-09-08       Impact factor: 8.860

10.  Lesch-Nyhan syndrome presenting with acute renal failure in a 3-day-old newborn.

Authors:  Ivana Pela; Maria Alice Donati; Elena Procopio; Patrizio Fiorini
Journal:  Pediatr Nephrol       Date:  2007-08-16       Impact factor: 3.714

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