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Page 1
Urinary tract effects of HPSE2 mutations.
J Am Soc Nephrol. 2015 Apr;26(4):797-804. doi: 10.1681/ASN.2013090961. Epub 2014 Aug 21.
J Am Soc Nephrol. 2015.
PMID: 25145936
Free PMC article.
Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux.
Cordell HJ, Darlay R, Charoen P, Stewart A, Gullett AM, Lambert HJ, Malcolm S, Feather SA, Goodship TH, Woolf AS, Kenda RB, Goodship JA; UK VUR Study Group.
Cordell HJ, et al. Among authors: gullett am.
J Am Soc Nephrol. 2010 Jan;21(1):113-23. doi: 10.1681/ASN.2009060624. Epub 2009 Dec 3.
J Am Soc Nephrol. 2010.
PMID: 19959718
Free PMC article.
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Primary, nonsyndromic vesicoureteric reflux and nephropathy in sibling pairs: a United Kingdom cohort for a DNA bank.
Lambert HJ, Stewart A, Gullett AM, Cordell HJ, Malcolm S, Feather SA, Goodship JA, Goodship TH, Woolf AS; UK VUR Study Group.
Lambert HJ, et al. Among authors: gullett am.
Clin J Am Soc Nephrol. 2011 Apr;6(4):760-6. doi: 10.2215/CJN.04580510. Epub 2011 Mar 24.
Clin J Am Soc Nephrol. 2011.
PMID: 21441121
Free PMC article.
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De novo Uroplakin IIIa heterozygous mutations cause human renal adysplasia leading to severe kidney failure.
Jenkins D, Bitner-Glindzicz M, Malcolm S, Hu CC, Allison J, Winyard PJ, Gullett AM, Thomas DF, Belk RA, Feather SA, Sun TT, Woolf AS.
Jenkins D, et al. Among authors: gullett am.
J Am Soc Nephrol. 2005 Jul;16(7):2141-9. doi: 10.1681/ASN.2004090776. Epub 2005 May 11.
J Am Soc Nephrol. 2005.
PMID: 15888565
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Renal FMD may not confer a familial hypertensive risk nor is it caused by ACTA2 mutations.
Marks SD, Gullett AM, Brennan E, Tullus K, Jaureguiberry G, Klootwijk E, Stanescu HC, Kleta R, Woolf AS.
Marks SD, et al. Among authors: gullett am.
Pediatr Nephrol. 2011 Oct;26(10):1857-61. doi: 10.1007/s00467-011-1891-0. Epub 2011 May 8.
Pediatr Nephrol. 2011.
PMID: 21553326
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