Page last updated: 2024-08-26

vitamin b 6 and Oxaluria, Primary

vitamin b 6 has been researched along with Oxaluria, Primary in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's5 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Cellini, B; Dell'Orco, D; Dindo, M; Montone, R; Oppici, E1
Beck, BB; Franklin, J; Hero, B; Hoppe, B; Hoyer-Kuhn, H; Kohbrok, S; Volland, R1
Bouzidi, H; Daudon, M; Majdoub, A; Najjar, MF1
García de la Oliva, T; García, I; Hernández, D; Jironda, C; Martín Reyes, G; Martín, M; Pérez Vaca, ML; Toledo Rojas, R; Torres de Rueda, A1
Acquaviva, C; Cochat, P; Danpure, CJ; Daudon, M; De Marchi, M; Fargue, S; Groothoff, J; Harambat, J; Hoppe, B; Hulton, SA; Jamieson, NV; Kemper, MJ; Mandrile, G; Marangella, M; Picca, S; Rumsby, G; Salido, E; Straub, M; van Woerden, CS1

Reviews

1 review(s) available for vitamin b 6 and Oxaluria, Primary

ArticleYear
[Primary hyperoxaluria: A review].
    Nephrologie & therapeutique, 2016, Volume: 12, Issue:6

    Topics: Disease Progression; Fluid Therapy; Humans; Hyperoxaluria; Hyperoxaluria, Primary; Kidney Failure, Chronic; Kidney Transplantation; Liver Transplantation; Nephrocalcinosis; Peritoneal Dialysis; Treatment Outcome; Vitamin B 6; Vitamin B Complex

2016

Trials

1 trial(s) available for vitamin b 6 and Oxaluria, Primary

ArticleYear
Vitamin B6 in primary hyperoxaluria I: first prospective trial after 40 years of practice.
    Clinical journal of the American Society of Nephrology : CJASN, 2014, Volume: 9, Issue:3

    Topics: Administration, Oral; Adolescent; Biomarkers; Child; Female; Genetic Predisposition to Disease; Germany; Heterozygote; Homozygote; Humans; Hyperoxaluria, Primary; Male; Mutation; Oxalic Acid; Phenotype; Prospective Studies; Time Factors; Transaminases; Treatment Outcome; Vitamin B 6

2014

Other Studies

3 other study(ies) available for vitamin b 6 and Oxaluria, Primary

ArticleYear
Correlation between the molecular effects of mutations at the dimer interface of alanine-glyoxylate aminotransferase leading to primary hyperoxaluria type I and the cellular response to vitamin B
    Journal of inherited metabolic disease, 2018, Volume: 41, Issue:2

    Topics: Animals; CHO Cells; Cricetulus; Genetic Predisposition to Disease; Humans; Hyperoxaluria, Primary; Mutation; Phenotype; Protein Folding; Protein Multimerization; Structure-Activity Relationship; Transaminases; Vitamin B 6

2018
[Delayed diagnosis of primary hyperoxaluria in a young patient with advanced chronic renal failure].
    Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia, 2011, Volume: 31, Issue:2

    Topics: Africa, Northern; Arthritis, Infectious; Bone Marrow Examination; Catheter-Related Infections; Combined Modality Therapy; Decompression, Surgical; Delayed Diagnosis; Discitis; Fatal Outcome; Humans; Hyperoxaluria; Hyperoxaluria, Primary; Hyperthyroidism; Incidental Findings; Kidney Failure, Chronic; Laminectomy; Male; Nephrocalcinosis; Renal Dialysis; Thrombophilia; Transaminases; Vitamin B 6; Young Adult

2011
Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatment.
    Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2012, Volume: 27, Issue:5

    Topics: Fluid Therapy; Genetic Testing; Humans; Hyperoxaluria, Primary; Kidney; Kidney Transplantation; Mutation; Oxalates; Potassium Citrate; Transaminases; Ultrasonography; Vitamin B 6

2012