| scholarly article | Q13442814 |
| P2093 | author name string | Yi-Bing Cheng | |
| Chun-Lan Song | |||
| Ya-Jie Cui | |||
| P2860 | cites work | Selected AGXT gene mutations analysis provides a genetic diagnosis in 28% of Tunisian patients with primary hyperoxaluria | Q33911824 |
| Hereditary causes of kidney stones and chronic kidney disease | Q34066169 | ||
| Sustained pyridoxine response in primary hyperoxaluria type 1 recipients of kidney alone transplant | Q35977167 | ||
| Phenotype-Genotype Correlations and Estimated Carrier Frequencies of Primary Hyperoxaluria | Q36104822 | ||
| International registry for primary hyperoxaluria | Q36165824 | ||
| Primary hyperoxaluria type 1: update and additional mutation analysis of the AGXT gene. | Q37500313 | ||
| Vitamin B6 in primary hyperoxaluria I: first prospective trial after 40 years of practice | Q37621553 | ||
| Primary hyperoxalurias: diagnosis and treatment | Q38292247 | ||
| Primary hyperoxaluria in infants | Q39743223 | ||
| Enzymological diagnosis of primary hyperoxaluria type 1 by measurement of hepatic alanine: glyoxylate aminotransferase activity | Q42001558 | ||
| Primary hyperoxaluria type 1, a too often missed diagnosis and potentially treatable cause of end-stage renal disease in adults: results of the Dutch cohort | Q43990085 | ||
| Preserving double equipoise in living donor liver-kidney transplantation for primary hyperoxaluria type 1. | Q48038330 | ||
| Primary hyperoxaluria in children in central Tunisia | Q54117570 | ||
| Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatment | Q63441478 | ||
| Hyperoxalurie primitive | Q63441480 | ||
| Primary hyperoxaluria type 1: An underestimated cause of nephrocalcinosis and chronic renal failure in Saudi Arabian children | Q79874859 | ||
| Pediatrics: Timely diagnosis of primary hyperoxaluria type 1 | Q84947187 | ||
| Sequential liver and kidney transplantation from a single living donor in two young adults with primary hyperoxaluria type 1 | Q86485408 | ||
| Primary hyperoxaluria | Q86855943 | ||
| The first experience of sequential liver-kidney transplantation for the treatment of primary hyperoxaluria type-1 in Iran as a developing country | Q87920808 | ||
| P433 | issue | 2 | |
| P304 | page(s) | 203-207 | |
| P577 | publication date | 2017-02-01 | |
| P1433 | published in | 880-01 Zhong Guo Dang Dai Er Ke Za Zhi | Q26853819 |
| P1476 | title | [Oliguria and acute renal dysfunction in a six-month-old infant] | |
| P478 | volume | 19 |
| Q61798741 | Two Novel AGXT Mutations Cause the Infantile Form of Primary Hyperoxaluria Type I in a Chinese Family: Research on Missed Mutation | cites work | P2860 |
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