Pollak MR - Search Results

1

NPHS2 R229Q functional variant is associated with microalbuminuria in the general population.

Pereira AC, Pereira AB, Mota GF, Cunha RS, Herkenhoff FL, Pollak MR, Mill JG, Krieger JE. Pereira AC, et al. Among authors: pollak mr. Kidney Int. 2004 Mar;65(3):1026-30. doi: 10.1111/j.1523-1755.2004.00479.x. Kidney Int. 2004. PMID: 14871423 Free article.

2

A locus for adolescent and adult onset familial focal segmental glomerulosclerosis on chromosome 1q25-31.

Tsukaguchi H, Yager H, Dawborn J, Jost L, Cohlmia J, Abreu PF, Pereira AB, Pollak MR. Tsukaguchi H, et al. Among authors: pollak mr. J Am Soc Nephrol. 2000 Sep;11(9):1674-1680. doi: 10.1681/ASN.V1191674. J Am Soc Nephrol. 2000. PMID: 10966492

3

NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele.

Tsukaguchi H, Sudhakar A, Le TC, Nguyen T, Yao J, Schwimmer JA, Schachter AD, Poch E, Abreu PF, Appel GB, Pereira AB, Kalluri R, Pollak MR. Tsukaguchi H, et al. Among authors: pollak mr. J Clin Invest. 2002 Dec;110(11):1659-66. doi: 10.1172/JCI16242. J Clin Invest. 2002. PMID: 12464671 Free PMC article.

4

Expanding the spectrum of NPHS1-associated disease.

Pollak MR. Pollak MR. Kidney Int. 2009 Dec;76(12):1221-3. doi: 10.1038/ki.2009.391. Kidney Int. 2009. PMID: 19946311 Free article. Review.

5

APOL1-Associated Kidney Disease in Brazil.

Riella C, Siemens TA, Wang M, Campos RP, Moraes TP, Riella LV, Friedman DJ, Riella MC, Pollak MR. Riella C, et al. Among authors: pollak mr. Kidney Int Rep. 2019 Mar 20;4(7):923-929. doi: 10.1016/j.ekir.2019.03.006. eCollection 2019 Jul. Kidney Int Rep. 2019. PMID: 31317114 Free PMC article.

6

NPHS2 variation in focal and segmental glomerulosclerosis.

Tonna SJ, Needham A, Polu K, Uscinski A, Appel GB, Falk RJ, Katz A, Al-Waheeb S, Kaplan BS, Jerums G, Savige J, Harmon J, Zhang K, Curhan GC, Pollak MR. Tonna SJ, et al. Among authors: pollak mr. BMC Nephrol. 2008 Sep 29;9:13. doi: 10.1186/1471-2369-9-13. BMC Nephrol. 2008. PMID: 18823551 Free PMC article.

7

Genetic testing for nephrotic syndrome and FSGS in the era of next-generation sequencing.

Brown EJ, Pollak MR, Barua M. Brown EJ, et al. Among authors: pollak mr. Kidney Int. 2014 May;85(5):1030-8. doi: 10.1038/ki.2014.48. Epub 2014 Mar 5. Kidney Int. 2014. PMID: 24599252 Free PMC article. Review.

8

Exome sequencing and in vitro studies identified podocalyxin as a candidate gene for focal and segmental glomerulosclerosis.

Barua M, Shieh E, Schlondorff J, Genovese G, Kaplan BS, Pollak MR. Barua M, et al. Among authors: pollak mr. Kidney Int. 2014 Jan;85(1):124-33. doi: 10.1038/ki.2013.354. Epub 2013 Sep 18. Kidney Int. 2014. PMID: 24048372 Free PMC article.

9

Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference.

KDIGO Conference Participants. KDIGO Conference Participants. Kidney Int. 2022 Jun;101(6):1126-1141. doi: 10.1016/j.kint.2022.03.019. Epub 2022 Apr 20. Kidney Int. 2022. PMID: 35460632 Free PMC article.

10

The glomerular filter: Biologic and genetic complexity.

Dandapani SV, Pollak MR. Dandapani SV, et al. Among authors: pollak mr. Kidney Int. 2006 Sep;70(6):980-2. doi: 10.1038/sj.ki.5001801. Kidney Int. 2006. PMID: 16957744 Free article.

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