Barratt TM - Search Results

1

Incompletely penetrant PKD1 alleles suggest a role for gene dosage in cyst initiation in polycystic kidney disease.

Rossetti S, Kubly VJ, Consugar MB, Hopp K, Roy S, Horsley SW, Chauveau D, Rees L, Barratt TM, van't Hoff WG, Niaudet P, Torres VE, Harris PC. Rossetti S, et al. Among authors: barratt tm. Kidney Int. 2009 Apr;75(8):848-55. doi: 10.1038/ki.2008.686. Epub 2009 Jan 21. Kidney Int. 2009. PMID: 19165178 Free PMC article.

2

The position of the polycystic kidney disease 1 (PKD1) gene mutation correlates with the severity of renal disease.

Rossetti S, Burton S, Strmecki L, Pond GR, San Millán JL, Zerres K, Barratt TM, Ozen S, Torres VE, Bergstralh EJ, Winearls CG, Harris PC. Rossetti S, et al. Among authors: barratt tm. J Am Soc Nephrol. 2002 May;13(5):1230-7. doi: 10.1097/01.asn.0000013300.11876.37. J Am Soc Nephrol. 2002. PMID: 11961010

3

Are there guidelines for a strategy according to glomerular filtration rate, plasma oxalate determination and the risk of oxalate accumulation?

Barratt TM, van't Hoff WG. Barratt TM, et al. Nephrol Dial Transplant. 1995;10 Suppl 8:22-3. doi: 10.1093/ndt/10.supp8.22. Nephrol Dial Transplant. 1995. PMID: 8592620 No abstract available.

4

Autosomal recessive polycystic kidney disease: long-term outcome of neonatal survivors.

Roy S, Dillon MJ, Trompeter RS, Barratt TM. Roy S, et al. Among authors: barratt tm. Pediatr Nephrol. 1997 Jun;11(3):302-6. doi: 10.1007/s004670050281. Pediatr Nephrol. 1997. PMID: 9203177 Clinical Trial.

5

Cadaveric renal transplantation in children under 5 years of age.

Fitzpatrick MM, Duffy PG, Fernando ON, Barratt TM, Dillon MJ, Trompeter RS. Fitzpatrick MM, et al. Among authors: barratt tm. Pediatr Nephrol. 1992 Mar;6(2):166-71. doi: 10.1007/BF00866302. Pediatr Nephrol. 1992. PMID: 1571214

6

Autosomal recessive polycystic kidney disease.

Kaplan BS, Fay J, Shah V, Dillon MJ, Barratt TM. Kaplan BS, et al. Among authors: barratt tm. Pediatr Nephrol. 1989 Jan;3(1):43-9. doi: 10.1007/BF00859625. Pediatr Nephrol. 1989. PMID: 2702087

7

Clinical quiz. Acute renal failure in a 2-week-old infant.

Barratt TM, Dillon MJ, Gordon I, Ransley PG. Barratt TM, et al. Pediatr Nephrol. 1987 Jul;1(3):379-80. doi: 10.1007/BF00849238. Pediatr Nephrol. 1987. PMID: 3153303 No abstract available.

8

Serum intact parathyroid hormone and ionised calcium concentration in children with renal insufficiency.

Ledermann SE, Johnson A, Dillon MJ, Trompeter RS, Barratt TM. Ledermann SE, et al. Among authors: barratt tm. Pediatr Nephrol. 1994 Oct;8(5):561-5. doi: 10.1007/BF00858126. Pediatr Nephrol. 1994. PMID: 7819001

9

Long-term cyclosporin A treatment of minimal-change nephrotic syndrome of childhood.

Hulton SA, Neuhaus TJ, Dillon MJ, Barratt TM. Hulton SA, et al. Among authors: barratt tm. Pediatr Nephrol. 1994 Aug;8(4):401-3. doi: 10.1007/BF00856511. Pediatr Nephrol. 1994. PMID: 7947023

10

Effect of cyclosporin A on glomerular filtration rate in children with minimal change nephrotic syndrome.

Hulton SA, Jadresic L, Shah V, Trompeter RS, Dillon MJ, Barratt TM. Hulton SA, et al. Among authors: barratt tm. Pediatr Nephrol. 1994 Aug;8(4):404-7. doi: 10.1007/BF00856512. Pediatr Nephrol. 1994. PMID: 7947024

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