Literature DB >> 25823987

An unusual cause of pink diapers in an infant: Questions and Answers.

Rasheda Amin1, Loai Eid2, Vidar O Edvardsson3,4, Lynette Fairbanks5, Asha Moudgil6.   

Abstract

Entities:  

Keywords:  Fractional excretion of uric acid; Hypouricemia; Pink-stained diapers; Urinary crystals

Mesh：

Substances：

Year:  2015        PMID： 25823987      PMCID： PMC4591217          DOI： 10.1007/s00467-015-3072-z

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN： 0931-041X            Impact factor:   3.714


× No keyword cloud information.
  14 in total

Review 1.  The clinical art and science of urine microscopy.

Authors:  Giovanni B Fogazzi; Giuseppe Garigali
Journal:  Curr Opin Nephrol Hypertens       Date:  2003-11       Impact factor: 2.894

2.  Xanthinuria type I: a rare cause of urolithiasis.

Authors:  Nina Arikyants; Ashot Sarkissian; Albrecht Hesse; Thomas Eggermann; Ernst Leumann; Beat Steinmann
Journal:  Pediatr Nephrol       Date:  2006-11-09       Impact factor: 3.714

3.  Adenine phosphoribosyltransferase deficiency in children.

Authors:  Jérôme Harambat; Guillaume Bollée; Michel Daudon; Irène Ceballos-Picot; Albert Bensman
Journal:  Pediatr Nephrol       Date:  2012-01-03       Impact factor: 3.714

4.  Identification of a new point mutation in the human xanthine dehydrogenase gene responsible for a case of classical type I xanthinuria.

Authors:  N Sakamoto; T Yamamoto; Y Moriwaki; T Teranishi; M Toyoda; Y Onishi; S Kuroda; K Sakaguchi; T Fujisawa; M Maeda; T Hada
Journal:  Hum Genet       Date:  2001-04       Impact factor: 4.132

Review 5.  Uric acid and the kidney.

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

6.  XDH gene mutation is the underlying cause of classical xanthinuria: a second report.

Authors:  D Levartovsky; A Lagziel; O Sperling; U Liberman; M Yaron; T Hosoya; K Ichida; H Peretz
Journal:  Kidney Int       Date:  2000-06       Impact factor: 10.612

7.  Mutational analysis of the xanthine dehydrogenase gene in a Turkish family with autosomal recessive classical xanthinuria.

Authors:  Faysal Gok; Kimiyoshi Ichida; Rezan Topaloglu
Journal:  Nephrol Dial Transplant       Date:  2003-11       Impact factor: 5.992

8.  Pediatric urolithiasis in Kuwait.

Authors:  A A Al-Eisa; A Al-Hunayyan; R Gupta
Journal:  Int Urol Nephrol       Date:  2002       Impact factor: 2.370

9.  Report on a new patient with combined deficiencies of sulphite oxidase and xanthine dehydrogenase due to molybdenum cofactor deficiency.

Authors:  W Endres; Y S Shin; R Günther; H Ibel; M Duran; S K Wadman
Journal:  Eur J Pediatr       Date:  1988-12       Impact factor: 3.183

Review 10.  Diagnostic examination of the child with urolithiasis or nephrocalcinosis.

Authors:  Bernd Hoppe; Markus J Kemper
Journal:  Pediatr Nephrol       Date:  2008-12-23       Impact factor: 3.714
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.