74 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 33945205 | Primary hyperoxaluria type 1 in children: Clinical classification, renal replacement therapy, and outcome in a single centre experience. | 2022 Feb | 1 |
2 | 35155860 | Long-Term Transplantation Outcomes in Patients With Primary Hyperoxaluria Type 1 Included in the European Hyperoxaluria Consortium (OxalEurope) Registry. | 2022 Feb | 1 |
3 | 35237473 | Infantile Primary Hyperoxaluria Type 1 Treated With Lumasiran in Twin Males. | 2022 Jan | 1 |
4 | 35257062 | Randomized Clinical Trial on the Long-Term Efficacy and Safety of Lumasiran in Patients With Primary Hyperoxaluria Type 1. | 2022 Mar | 1 |
5 | 35266883 | New therapeutics for primary hyperoxaluria type 1. | 2022 Jul 1 | 2 |
6 | 35592622 | Primary hyperoxaluria type 1 in developing countries: novel challenges in a new therapeutic era. | 2022 May | 4 |
7 | 32891627 | Recovery From Dialysis in Patients With Primary Hyperoxaluria Type 1 Treated With Pyridoxine: A Report of 3 Cases. | 2021 May | 2 |
8 | 33405070 | Lumasiran: First Approval. | 2021 Feb | 1 |
9 | 33789010 | Lumasiran, an RNAi Therapeutic for Primary Hyperoxaluria Type 1. | 2021 Apr 1 | 1 |
10 | 33898474 | Natural History of Clinical, Laboratory, and Echocardiographic Parameters of a Primary Hyperoxaluria Cohort on Long Term Hemodialysis. | 2021 | 1 |
11 | 33959570 | The Struggling Odyssey of Infantile Primary Hyperoxaluria. | 2021 | 2 |
12 | 34433051 | Epigenomic and transcriptional profiling identifies impaired glyoxylate detoxification in NAFLD as a risk factor for hyperoxaluria. | 2021 Aug 24 | 1 |
13 | 34686543 | Endogenous Oxalate Production in Primary Hyperoxaluria Type 1 Patients. | 2021 Oct 22 | 1 |
14 | 35071135 | Case Report: Sustained Efficacy of Lumasiran at 18 Months in Primary Hyperoxaluria Type 1. | 2021 | 1 |
15 | 32418144 | Stiripentol fails to lower plasma oxalate in a dialysis-dependent PH1 patient. | 2020 Sep | 1 |
16 | 32792227 | The ILE56 mutation on different genetic backgrounds of alanine:glyoxylate aminotransferase: Clinical features and biochemical characterization. | 2020 Sep - Oct | 4 |
17 | 33305106 | Transplantation for Primary Hyperoxaluria Type 1: Designing New Strategies in the Era of Promising Therapeutic Perspectives. | 2020 Dec | 2 |
18 | 30276532 | Skin microvascular dysfunction as an early cardiovascular marker in primary hyperoxaluria type I. | 2019 Feb | 1 |
19 | 30676254 | Systemic Alanine Glyoxylate Aminotransferase mRNA Improves Glyoxylate Metabolism in a Mouse Model of Primary Hyperoxaluria Type 1. | 2019 Apr | 1 |
20 | 31402115 | Targeted gene therapy in human-induced pluripotent stem cells from a patient with primary hyperoxaluria type 1 using CRISPR/Cas9 technology. | 2019 Oct 1 | 3 |
21 | 32003182 | [Genetic aspects of primary hyperoxaluria: epidemiology, ethiology, pathogenesis, and clinical signs of the disorder]. | 2019 Dec 31 | 1 |
22 | 29243158 | Bilateral native nephrectomy to reduce oxalate stores in children at the time of combined liver-kidney transplantation for primary hyperoxaluria type 1. | 2018 May | 2 |
23 | 29244539 | Genotype-phenotype variability of retinal manifestation in primary hyperoxaluria type 1. | 2018 Apr | 1 |
24 | 29588429 | Hydroxyproline Metabolism and Oxalate Synthesis in Primary Hyperoxaluria. | 2018 Jun | 2 |
25 | 28217701 | Gut microbiota and oxalate homeostasis. | 2017 Jan | 5 |
26 | 28261895 | Bilateral native nephrectomy reduces systemic oxalate level after combined liver-kidney transplant: A case report. | 2017 May | 2 |
27 | 28752386 | Glycolate oxidase deficiency in a patient with congenital hyperinsulinism and unexplained hyperoxaluria. | 2017 Nov | 1 |
28 | 28916765 | Radiation damage at the active site of human alanine:glyoxylate aminotransferase reveals that the cofactor position is finely tuned during catalysis. | 2017 Sep 15 | 2 |
29 | 29144803 | ENDOCRINE MANIFESTATIONS OF PRIMARY HYPEROXALURIA. | 2017 Dec | 1 |
30 | 26854734 | Effects of alanine:glyoxylate aminotransferase variants and pyridoxine sensitivity on oxalate metabolism in a cell-based cytotoxicity assay. | 2016 Jun | 3 |
31 | 27179589 | Caenorhabditis elegans AGXT-1 is a mitochondrial and temperature-adapted ortholog of peroxisomal human AGT1: New insights into between-species divergence in glyoxylate metabolism. | 2016 Sep | 3 |
32 | 27239044 | In Silico Modeling of Liver Metabolism in a Human Disease Reveals a Key Enzyme for Histidine and Histamine Homeostasis. | 2016 Jun 7 | 1 |
33 | 27644547 | Two novel AGXT mutations identified in primary hyperoxaluria type-1 and distinct morphological and structural difference in kidney stones. | 2016 Sep 20 | 1 |
34 | 24797341 | Sustained pyridoxine response in primary hyperoxaluria type 1 recipients of kidney alone transplant. | 2014 Jun | 2 |
35 | 25237136 | Pharmacologic rescue of an enzyme-trafficking defect in primary hyperoxaluria 1. | 2014 Oct 7 | 1 |
36 | 23494551 | Primary hyperoxaluria type 1: practical and ethical issues. | 2013 Dec | 2 |
37 | 23915277 | Native portal vein embolization for persistent hyperoxaluria following kidney and auxiliary partial liver transplantation. | 2013 Oct | 2 |
38 | 24029263 | Combined liver and kidney transplantation in primary hyperoxaluria: a report of three cases and review of the literature. | 2013 Sep | 4 |
39 | 24089413 | A test of the hypothesis that oxalate secretion produces proximal tubule crystallization in primary hyperoxaluria type I. | 2013 Dec 1 | 2 |
40 | 22319153 | Multiple adaptive losses of alanine-glyoxylate aminotransferase mitochondrial targeting in fruit-eating bats. | 2012 Jun | 1 |
41 | 22821680 | Primary hyperoxaluria type 1 and brachydactyly mental retardation syndrome caused by a novel mutation in AGXT and a terminal deletion of chromosome 2. | 2012 Sep | 1 |
42 | 22956877 | Extreme intrafamilial variability of Saudi brothers with primary hyperoxaluria type 1. | 2012 | 2 |
43 | 21119625 | Phenotypic correction of a mouse model for primary hyperoxaluria with adeno-associated virus gene transfer. | 2011 May | 1 |
44 | 21558762 | Studies on a unique organelle localization of a liver enzyme, serine:pyruvate (or alanine:glyoxylate) aminotransferase. | 2011 | 2 |
45 | 21748001 | Primary hyperoxaluria. | 2011 | 2 |
46 | 25013605 | Liver-kidney transplantation in primary hyperoxaluria type-1: case report and literature review. | 2011 | 2 |
47 | 25984128 | Intra-operative continuous renal replacement therapy during combined liver-kidney transplantation in two patients with primary hyperoxaluria type 1. | 2011 Apr | 4 |
48 | 19496983 | Successful outcome after early combined liver and en bloc-kidney transplant in an infant with primary hyperoxaluria type 1: a case report. | 2009 Nov | 1 |
49 | 18155525 | Primary hyperoxaluria: clinical course, diagnosis, and treatment after kidney failure. | 2008 Jan | 2 |
50 | 18985333 | Primary hyperoxaluria: report of an Italian family with clear sex conditioned penetrance. | 2008 Dec | 1 |