Olson JB - Search Results

1

Comprehensive mutation screening in 55 probands with type 1 primary hyperoxaluria shows feasibility of a gene-based diagnosis.

Monico CG, Rossetti S, Schwanz HA, Olson JB, Lundquist PA, Dawson DB, Harris PC, Milliner DS. Monico CG, et al. Among authors: olson jb. J Am Soc Nephrol. 2007 Jun;18(6):1905-14. doi: 10.1681/ASN.2006111230. Epub 2007 Apr 25. J Am Soc Nephrol. 2007. PMID: 17460142

2

Pyridoxine effect in type I primary hyperoxaluria is associated with the most common mutant allele.

Monico CG, Rossetti S, Olson JB, Milliner DS. Monico CG, et al. Among authors: olson jb. Kidney Int. 2005 May;67(5):1704-9. doi: 10.1111/j.1523-1755.2005.00267.x. Kidney Int. 2005. PMID: 15840016 Free article.

3

Implications of genotype and enzyme phenotype in pyridoxine response of patients with type I primary hyperoxaluria.

Monico CG, Olson JB, Milliner DS. Monico CG, et al. Among authors: olson jb. Am J Nephrol. 2005 Mar-Apr;25(2):183-8. doi: 10.1159/000085411. Epub 2005 Apr 21. Am J Nephrol. 2005. PMID: 15849466

4

International registry for primary hyperoxaluria.

Lieske JC, Monico CG, Holmes WS, Bergstralh EJ, Slezak JM, Rohlinger AL, Olson JB, Milliner DS. Lieske JC, et al. Among authors: olson jb. Am J Nephrol. 2005 May-Jun;25(3):290-6. doi: 10.1159/000086360. Epub 2005 Jun 15. Am J Nephrol. 2005. PMID: 15961949

5

Primary hyperoxaluria type III gene HOGA1 (formerly DHDPSL) as a possible risk factor for idiopathic calcium oxalate urolithiasis.

Monico CG, Rossetti S, Belostotsky R, Cogal AG, Herges RM, Seide BM, Olson JB, Bergstrahl EJ, Williams HJ, Haley WE, Frishberg Y, Milliner DS. Monico CG, et al. Among authors: olson jb. Clin J Am Soc Nephrol. 2011 Sep;6(9):2289-95. doi: 10.2215/CJN.02760311. Clin J Am Soc Nephrol. 2011. PMID: 21896830 Free PMC article.

6

Phenotype-Genotype Correlations and Estimated Carrier Frequencies of Primary Hyperoxaluria.

Hopp K, Cogal AG, Bergstralh EJ, Seide BM, Olson JB, Meek AM, Lieske JC, Milliner DS, Harris PC; Rare Kidney Stone Consortium. Hopp K, et al. Among authors: olson jb. J Am Soc Nephrol. 2015 Oct;26(10):2559-70. doi: 10.1681/ASN.2014070698. Epub 2015 Feb 2. J Am Soc Nephrol. 2015. PMID: 25644115 Free PMC article.

7

Hydroxyproline Metabolism and Oxalate Synthesis in Primary Hyperoxaluria.

Fargue S, Milliner DS, Knight J, Olson JB, Lowther WT, Holmes RP. Fargue S, et al. Among authors: olson jb. J Am Soc Nephrol. 2018 Jun;29(6):1615-1623. doi: 10.1681/ASN.2017040390. Epub 2018 Mar 27. J Am Soc Nephrol. 2018. PMID: 29588429 Free PMC article.

8

Clinical characterization of primary hyperoxaluria type 3 in comparison with types 1 and 2.

Singh P, Viehman JK, Mehta RA, Cogal AG, Hasadsri L, Oglesbee D, Olson JB, Seide BM, Sas DJ, Harris PC, Lieske JC, Milliner DS. Singh P, et al. Among authors: olson jb. Nephrol Dial Transplant. 2022 Apr 25;37(5):869-875. doi: 10.1093/ndt/gfab027. Nephrol Dial Transplant. 2022. PMID: 33543760 Free PMC article.

9

Sustained pyridoxine response in primary hyperoxaluria type 1 recipients of kidney alone transplant.

Lorenz EC, Lieske JC, Seide BM, Meek AM, Olson JB, Bergstralh EJ, Milliner DS. Lorenz EC, et al. Among authors: olson jb. Am J Transplant. 2014 Jun;14(6):1433-8. doi: 10.1111/ajt.12706. Epub 2014 May 2. Am J Transplant. 2014. PMID: 24797341 Free PMC article.

10

Phenotypic and functional analysis of human SLC26A6 variants in patients with familial hyperoxaluria and calcium oxalate nephrolithiasis.

Monico CG, Weinstein A, Jiang Z, Rohlinger AL, Cogal AG, Bjornson BB, Olson JB, Bergstralh EJ, Milliner DS, Aronson PS. Monico CG, et al. Among authors: olson jb. Am J Kidney Dis. 2008 Dec;52(6):1096-103. doi: 10.1053/j.ajkd.2008.07.041. Epub 2008 Oct 31. Am J Kidney Dis. 2008. PMID: 18951670 Free PMC article.

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