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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 1, 2024. (Total: 233962Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Urolithiasis and AGXT[original query]
Phenotypic and functional analysis of human SLC26A6 variants in patients with familial hyperoxaluria and calcium oxalate nephrolithiasis.
American journal of kidney diseases : the official journal of the National Kidney Foundation 2008 Dec 52 (6): 1096-103.
Monico Carla G, Weinstein Adam, Jiang Zhirong, Rohlinger Audrey L, Cogal Andrea G, Bjornson Beth B, Olson Julie B, Bergstralh Eric J, Milliner Dawn S, Aronson Peter
Characteristics of the genotype and phenotype in Chinese primary hyperoxaluria type 1 populations.
Urolithiasis 2020 6 49 (1): 17-25.
Zhao Fangzhou, Li Jun, Tang Lei, Li Chunming, Wang Wenying, Ning Ch
Molecular Diagnosis of Primary Hyperoxaluria Type 1 and Distal Renal Tubular Acidosis in Moroccan Patients With Nephrolithiasis and/or Nephrocalcinosis.
Cureus 2022 5 14 (3): e23616.
Fatima Abdouss, Mohamed Ahakoud, Moustapha Hida, Karim Ould
Determinants of Kidney Failure in Primary Hyperoxaluria Type 1: Findings of the European Hyperoxaluria Consortium.
Kidney international reports 2023 10 8 (10): 2029-2042.
Elisabeth L Metry, Sander F Garrelfs, Lisa J Deesker, Cecile Acquaviva, Viola D'Ambrosio, Justine Bacchetta, Bodo B Beck, Pierre Cochat, Laure Collard, Julien Hogan, Pietro Manuel Ferraro, Casper F M Franssen, Jérôme Harambat, Sally-Anne Hulton, Graham W Lipkin, Giorgia Mandrile, Cristina Martin-Higueras, Nilufar Mohebbi, Shabbir H Moochhala, Thomas J Neuhaus, Larisa Prikhodina, Eduardo Salido, Rezan Topaloglu, Michiel J S Oosterveld, Jaap W Groothoff, Hessel Peters-Senge
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