Simmonds HA - Search Results

1

Aprt/Opn double knockout mice: osteopontin is a modifier of kidney stone disease severity.

Vernon HJ, Osborne C, Tzortzaki EG, Yang M, Chen J, Rittling SR, Denhardt DT, Buyske S, Bledsoe SB, Evan AP, Fairbanks L, Simmonds HA, Tischfield JA, Sahota A. Vernon HJ, et al. Among authors: simmonds ha. Kidney Int. 2005 Sep;68(3):938-47. doi: 10.1111/j.1523-1755.2005.00487.x. Kidney Int. 2005. PMID: 16105024 Free article.

2

Adenine phosphoribosyltransferase-deficient mice develop 2,8-dihydroxyadenine nephrolithiasis.

Engle SJ, Stockelman MG, Chen J, Boivin G, Yum MN, Davies PM, Ying MY, Sahota A, Simmonds HA, Stambrook PJ, Tischfield JA. Engle SJ, et al. Among authors: simmonds ha. Proc Natl Acad Sci U S A. 1996 May 28;93(11):5307-12. doi: 10.1073/pnas.93.11.5307. Proc Natl Acad Sci U S A. 1996. PMID: 8643571 Free PMC article.

3

Identification of a 7-basepair deletion in the adenine phosphoribosyltransferase gene as a cause of 2,8-dihydroxyadenine urolithiasis.

Bye S, Mallmann R, Duley J, Simmonds HA, Chen J, Tischfield JA, Sahota A. Bye S, et al. Among authors: simmonds ha. Clin Investig. 1994 Jul;72(7):550-3. doi: 10.1007/BF00207486. Clin Investig. 1994. PMID: 7981585

4

HPRT-APRT-deficient mice are not a model for lesch-nyhan syndrome.

Engle SJ, Womer DE, Davies PM, Boivin G, Sahota A, Simmonds HA, Stambrook PJ, Tischfield JA. Engle SJ, et al. Among authors: simmonds ha. Hum Mol Genet. 1996 Oct;5(10):1607-10. doi: 10.1093/hmg/5.10.1607. Hum Mol Genet. 1996. PMID: 8894695

5

Molecular characterization of a novel mutation in APRT heterozygotes.

Sahota A, Bye S, Chen J, Khattar NH, Turker MS, Moro F, Simmonds HA, Emmerson BT, Gordon RB, Tischfield JA. Sahota A, et al. Among authors: simmonds ha. Adv Exp Med Biol. 1994;370:675-8. doi: 10.1007/978-1-4615-2584-4_140. Adv Exp Med Biol. 1994. PMID: 7660994 No abstract available.

6

Combined adenine phosphoribosyltransferase and N-acetylgalactosamine-6-sulfate sulfatase deficiency.

Wang L, Ou X, Sebesta I, Vondrak K, Krijt J, Elleder M, Poupetova H, Ledvinova J, Zeman J, Simmonds HA, Tischfield JA, Sahota A. Wang L, et al. Among authors: simmonds ha. Mol Genet Metab. 1999 Sep;68(1):78-85. doi: 10.1006/mgme.1999.2893. Mol Genet Metab. 1999. PMID: 10479485

7

2,8-Dihydroxyadenine urolithiasis.

Simmonds H, Van Acker KJ, Sahota AS. Simmonds H, et al. Lancet. 1992 May 23;339(8804):1295-6. doi: 10.1016/0140-6736(92)91623-g. Lancet. 1992. PMID: 1349687 No abstract available.

8

An unusual patient with kidney stones composed of 1-methyluric acid.

Davies PM, Fairbanks LD, Safranow K, Bending MR, Simmonds HA. Davies PM, et al. Among authors: simmonds ha. Urol Res. 2006 Feb;34(1):58-60. doi: 10.1007/s00240-005-0002-8. Epub 2006 Jan 6. Urol Res. 2006. PMID: 16397778

9

Diagnosis of adenine phosphoribosyltransferase deficiency as the underlying cause of renal failure in a renal transplant recipient.

Cassidy MJ, McCulloch T, Fairbanks LD, Simmonds HA. Cassidy MJ, et al. Among authors: simmonds ha. Nephrol Dial Transplant. 2004 Mar;19(3):736-8. doi: 10.1093/ndt/gfg562. Nephrol Dial Transplant. 2004. PMID: 14767036 No abstract available.

10

Spectrum of 2,8-dihydroxyadenine urolithiasis in complete APRT deficiency.

Simmonds HA, Barratt TM, Webster DR, Sahota A, Van Acker KJ, Cameron JS, Dillon M. Simmonds HA, et al. Adv Exp Med Biol. 1980;122A:337-41. doi: 10.1007/978-1-4615-9140-5_55. Adv Exp Med Biol. 1980. PMID: 7424654

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

279 results

Search Page