Current treatment for primary hyperoxaluria type 1: When should liver/kidney transplantation be considered
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| Veröffentlicht in: | Pediatric transplantation 2009-11, Vol.13 (7), p.805-807 |
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| container_end_page | 807 |
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| container_issue | 7 |
| container_start_page | 805 |
| container_title | Pediatric transplantation |
| container_volume | 13 |
| creator | Eytan Mor, M. D. Weismann, Irit |
| description | |
| doi_str_mv | 10.1111/j.1399-3046.2009.01230.x |
| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 1397-3142 |
| ispartof | Pediatric transplantation, 2009-11, Vol.13 (7), p.805-807 |
| issn | 1397-3142 1399-3046 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_734090728 |
| source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
| subjects | Adolescent Adult Age Factors Child Child, Preschool Female Humans Hyperoxaluria, Primary - genetics Hyperoxaluria, Primary - surgery Hyperoxaluria, Primary - therapy Infant Kidney Transplantation - methods Liver Transplantation - methods Male Renal Dialysis - methods Risk Treatment Outcome |
| title | Current treatment for primary hyperoxaluria type 1: When should liver/kidney transplantation be considered |
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