Milliner DS - Search Results

1

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: milliner ds. 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.

2

Long-term prognosis in primary hyperoxaluria type II (L-glyceric aciduria).

Chlebeck PT, Milliner DS, Smith LH. Chlebeck PT, et al. Among authors: milliner ds. Am J Kidney Dis. 1994 Feb;23(2):255-9. doi: 10.1016/s0272-6386(12)80981-4. Am J Kidney Dis. 1994. PMID: 8311084 Review.

3

Clinical expression and long-term outcomes of primary hyperoxaluria types 1 and 2.

Milliner DS, Wilson DM, Smith LH. Milliner DS, et al. J Nephrol. 1998 Mar-Apr;11 Suppl 1:56-9. J Nephrol. 1998. PMID: 9604813

4

Hyperoxaluria and urolithiasis in young children: an atypical presentation.

Monico CG, Milliner DS. Monico CG, et al. Among authors: milliner ds. J Endourol. 1999 Nov;13(9):633-6. doi: 10.1089/end.1999.13.633. J Endourol. 1999. PMID: 10608514

5

Phenotypic expression of primary hyperoxaluria: comparative features of types I and II.

Milliner DS, Wilson DM, Smith LH. Milliner DS, et al. Kidney Int. 2001 Jan;59(1):31-6. doi: 10.1046/j.1523-1755.2001.00462.x. Kidney Int. 2001. PMID: 11135054 Free article.

6

Combined liver-kidney and kidney-alone transplantation in primary hyperoxaluria.

Monico CG, Milliner DS. Monico CG, et al. Among authors: milliner ds. Liver Transpl. 2001 Nov;7(11):954-63. doi: 10.1053/jlts.2001.28741. Liver Transpl. 2001. PMID: 11699031 Free article.

7

The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein.

Ward CJ, Hogan MC, Rossetti S, Walker D, Sneddon T, Wang X, Kubly V, Cunningham JM, Bacallao R, Ishibashi M, Milliner DS, Torres VE, Harris PC. Ward CJ, et al. Among authors: milliner ds. Nat Genet. 2002 Mar;30(3):259-69. doi: 10.1038/ng833. Epub 2002 Feb 4. Nat Genet. 2002. PMID: 11919560

8

Potential mechanisms of marked hyperoxaluria not due to primary hyperoxaluria I or II.

Monico CG, Persson M, Ford GC, Rumsby G, Milliner DS. Monico CG, et al. Among authors: milliner ds. Kidney Int. 2002 Aug;62(2):392-400. doi: 10.1046/j.1523-1755.2002.00468.x. Kidney Int. 2002. PMID: 12110000 Free article.

9

Outcomes and complications of pregnancy in women with primary hyperoxaluria.

Norby SM, Milliner DS. Norby SM, et al. Among authors: milliner ds. Am J Kidney Dis. 2004 Feb;43(2):277-85. doi: 10.1053/j.ajkd.2003.10.034. Am J Kidney Dis. 2004. PMID: 14750093

10

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: milliner ds. Kidney Int. 2005 May;67(5):1704-9. doi: 10.1111/j.1523-1755.2005.00267.x. Kidney Int. 2005. PMID: 15840016 Free article.

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