Ophthalmic features of primary oxalosis after combined liver/kidney transplantation [10]

British Journal of Ophthalmology

Volumn 84, Issue 11, 2000, Pages 1326-1327

  Alcorn, D M ^a   Frederick, D R ^a  

^a STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CHILD; CLINICAL FEATURE; EYE SURGERY; FEMALE; HUMAN; KIDNEY FAILURE; KIDNEY TRANSPLANTATION; LETTER; LIVER FAILURE; LIVER TRANSPLANTATION; MALE; OPHTHALMOSCOPY; OPTIC NERVE ATROPHY; OXALOSIS; PERITONEAL DIALYSIS; PIGMENT EPITHELIUM; PRIORITY JOURNAL; PROGNOSIS; RETINA MACULOPATHY; RETINOPATHY; SPECTACLES; TREATMENT OUTCOME; VISUAL IMPAIRMENT; BIOPSY; INFANT; KIDNEY CALCIFICATION; METABOLISM; NEWBORN; OXALOSIS 1; RETINA DISEASE; VISUAL ACUITY;

CALCIUM OXALATE;

BIOPSY; CALCIUM OXALATE; FEMALE; HUMANS; HYPEROXALURIA, PRIMARY; INFANT; INFANT, NEWBORN; KIDNEY TRANSPLANTATION; LIVER TRANSPLANTATION; MALE; NEPHROCALCINOSIS; PIGMENT EPITHELIUM OF EYE; RETINAL DISEASES; TREATMENT OUTCOME; VISUAL ACUITY;

EID: 0033623553     PISSN: 00071161     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (10)

1. Primary hyperoxaluria
2. The clinical spectrum of the primary hyperoxalurias and their treatment
3. Ophthalmic manifestation of primary oxalosis
4. Primary hyperoxaluria type 2
5. Primary hereditary oxalosis retinopathy
6. Ocular findings in primary hyperoxaluria
7. The retinopathy of primary hyperoxaluria
8. Primary hereditary oxalosis retinopathy
9. Primary hyperoxaluria type 1: A cluster of new mutations in exon 7 of the AGXT gene
10. Characterization and chromsomal mapping of a genomic clone encoding human alanine: Glyoxylate aminotransferase