U54 DK083908/DK/NIDDK NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2006	1
2008	1
2009	1
2010	6
2011	5
2012	4
2013	9
2014	18
2015	26
2016	22
2017	12
2018	15
2019	24
2020	15
2021	10
2022	7
2023	5
2024	1

1

Natural history of urine and plasma oxalate in children with primary hyperoxaluria type 1.

Sas DJ, Mara K, Mehta RA, Seide BM, Banks CJ, Danese DS, McGregor TL, Lieske JC, Milliner DS. Sas DJ, et al. Pediatr Nephrol. 2024 Jan;39(1):141-148. doi: 10.1007/s00467-023-06074-x. Epub 2023 Jul 17. Pediatr Nephrol. 2024. PMID: 37458799 Free PMC article.

2

End Point Considerations for Clinical Trials in Enteric Hyperoxaluria.

Langman CB, Assimos D, Blank M, Calle J, Grauer A, Kausz A, Milliner D, Nazzal L, Smith K, Tasian G, Thompson A, Wood KD, Worcester E, Yang S, Malley MA, Knauf F, Lieske JC; Rare Kidney Stone Consortium (RKSC) Kidney Health Initiative (KHI) Oxalosis and Hyperoxaluria Foundation Enteric Hyperoxaluria Workgroup (OHF EH Workgroup). Langman CB, et al. Clin J Am Soc Nephrol. 2023 Dec 1;18(12):1637-1644. doi: 10.2215/CJN.0000000000000234. Epub 2023 Jun 21. Clin J Am Soc Nephrol. 2023. PMID: 37342976

3

The Site and Type of CLCN5 Genetic Variation Impact the Resulting Dent Disease-1 Phenotype.

Arnous MG, Arroyo J, Cogal AG, Anglani F, Kang HG, Sas D, Harris PC, Lieske JC. Arnous MG, et al. Kidney Int Rep. 2023 Mar 23;8(6):1220-1230. doi: 10.1016/j.ekir.2023.03.012. eCollection 2023 Jun. Kidney Int Rep. 2023. PMID: 37284679 Free PMC article.

4

Characterization of Stone Events in Patients With Type 3 Primary Hyperoxaluria.

Arnous MG, Vaughan L, Mehta RA, Schulte PJ, Lieske JC, Milliner DS. Arnous MG, et al. J Urol. 2023 Jun;209(6):1141-1150. doi: 10.1097/JU.0000000000003400. Epub 2023 Mar 8. J Urol. 2023. PMID: 36888927 Free PMC article.

5

Emerging Perspectives on the Rare Tubulopathy Dent Disease: Is Glomerular Damage a Direct Consequence of ClC-5 Dysfunction?

Priante G, Ceol M, Gianesello L, Bizzotto D, Braghetta P, Calò LA, Del Prete D, Anglani F. Priante G, et al. Int J Mol Sci. 2023 Jan 9;24(2):1313. doi: 10.3390/ijms24021313. Int J Mol Sci. 2023. PMID: 36674829 Free PMC article.

6

Clinical and molecular characterization of primary hyperoxaluria in Egypt.

Soliman NA, Elmonem MA, Abdelrahman SM, Nabhan MM, Fahmy YA, Cogal A, Harris PC, Milliner DS. Soliman NA, et al. Sci Rep. 2022 Sep 23;12(1):15886. doi: 10.1038/s41598-022-17980-9. Sci Rep. 2022. PMID: 36151119 Free PMC article.

7

Estimated GFR Slope Across CKD Stages in Primary Hyperoxaluria Type 1.

Singh P, Vaughan LE, Schulte PJ, Sas DJ, Milliner DS, Lieske JC. Singh P, et al. Am J Kidney Dis. 2022 Sep;80(3):373-382. doi: 10.1053/j.ajkd.2022.01.428. Epub 2022 Mar 16. Am J Kidney Dis. 2022. PMID: 35306035 Free PMC article.

8

Comparison of clinical features of pregnant and non-pregnant females with primary hyperoxaluria.

Miao J, Mehta RA, Norby S, Seide B, Milliner DS, Lieske J, Kattah A. Miao J, et al. J Nephrol. 2022 Jul;35(6):1771-1774. doi: 10.1007/s40620-022-01253-9. Epub 2022 Jan 18. J Nephrol. 2022. PMID: 35041195 Free PMC article. No abstract available.

9

Comprehensive Genetic Analysis Reveals Complexity of Monogenic Urinary Stone Disease.

Cogal AG, Arroyo J, Shah RJ, Reese KJ, Walton BN, Reynolds LM, Kennedy GN, Seide BM, Senum SR, Baum M, Erickson SB, Jagadeesh S, Soliman NA, Goldfarb DS, Beara-Lasic L, Edvardsson VO, Palsson R, Milliner DS, Sas DJ, Lieske JC, Harris PC; Investigators of the Rare Kidney Stone Consortium. Cogal AG, et al. Kidney Int Rep. 2021 Sep 8;6(11):2862-2884. doi: 10.1016/j.ekir.2021.08.033. eCollection 2021 Nov. Kidney Int Rep. 2021. PMID: 34805638 Free PMC article.

10

Genotype Phenotype Correlation in Dent Disease 2 and Review of the Literature: OCRL Gene Pleiotropism or Extreme Phenotypic Variability of Lowe Syndrome?

Gianesello L, Arroyo J, Del Prete D, Priante G, Ceol M, Harris PC, Lieske JC, Anglani F. Gianesello L, et al. Genes (Basel). 2021 Oct 11;12(10):1597. doi: 10.3390/genes12101597. Genes (Basel). 2021. PMID: 34680992 Free PMC article.

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