Primary hyperoxaluria type 1

Archives of Disease in Childhood

Volumn 92, Issue 3, 2007, Pages 197-

  Ajzensztejn, Michal J ^a   Sebire, Neil J ^a   Trompeter, Richard S ^a   Marks, Stephen D ^a,b  

^a GREAT ORMOND STREET HOSPITAL   (United Kingdom)

^b Great Ormond Street Hospital for Children NHS Trust ^*  (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

OXALIC ACID;

ARTICLE; BONE MARROW BIOPSY; CASE REPORT; CLINICAL FEATURE; ECHOCARDIOGRAPHY; GENE MUTATION; GENETIC SCREENING; HEMODIALYSIS; HETEROZYGOTE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; KIDNEY BIOPSY; LIVER GRAFT; MALE; OPHTHALMOSCOPY; OXALOSIS 1; PERCUTANEOUS BIOPSY; PRESCHOOL CHILD; PRIORITY JOURNAL; ULTRASOUND;

HUMANS; HYPEROXALURIA, PRIMARY; INFANT; MALE;

EID: 33947274305     PISSN: 00039888     EISSN: 14682044     Source Type: Journal    
DOI: 10.1136/adc.2006.107334     Document Type: Article

References (5)

1. Jones C, Mughal Z. Disorders of mineral metabolism and nephrolithiasis: primary hyperoxaluria type I. In: Webb N, Postlethwaite R, eds. Clinical paediatric nephrology 3rd edn. Oxford: Oxford Medical Publications, 2003:91-3.
2. Karel VAJ, Wolff ED. Hyperoxaluria and oxalosis. In: Chester M, Edelmann JR, eds. Paediatric kidney disease, 2nd edn. Boston: Little Brown & Company, 1992:1687-93.
3. Cochat P, Collard LBDE. Primary hyperoxaluria. In: Avner ED, Harmon WE, Niaudet P, eds. Pediatric nephrology. 5th edn. Section VI: tubular disease, Chapter 42, Philadelphia: Lippincott Williams & Wilkins, 2003:807-16.
4. Danpure CJ. Molecular etiology of primary hyperoxaluria type 1: new directions for treatment. Am J Nephrol 2005;25:303-10.
5. Kemper MJ. Concurrent or sequential liver and kidney transplantation in children with primary hyperoxaluria type 1? Pediatr Transplant 2005;9:693-6.