Gilbert RD - Search Results

1

Thrombotic microangiopathy following haematopoietic stem cell transplant.

Seaby EG, Gilbert RD. Seaby EG, et al. Among authors: gilbert rd. Pediatr Nephrol. 2018 Sep;33(9):1489-1500. doi: 10.1007/s00467-017-3803-4. Epub 2017 Oct 9. Pediatr Nephrol. 2018. PMID: 28993886 Free PMC article. Review.

2

Tubulointerstitial nephritis and uveitis in monozygotic twin boys.

Howarth L, Gilbert RD, Bass P, Deshpande PV. Howarth L, et al. Among authors: gilbert rd. Pediatr Nephrol. 2004 Aug;19(8):917-9. doi: 10.1007/s00467-004-1518-9. Epub 2004 Jun 17. Pediatr Nephrol. 2004. PMID: 15206033

3

Laparoscopic renal biopsy in obese children.

Mukhtar Z, Steinbrecher H, Gilbert RD, Deshpande PV. Mukhtar Z, et al. Among authors: gilbert rd. Pediatr Nephrol. 2005 Apr;20(4):495-8. doi: 10.1007/s00467-004-1768-6. Epub 2005 Jan 27. Pediatr Nephrol. 2005. PMID: 15747162

4

Rituximab therapy for steroid-dependent minimal change nephrotic syndrome.

Gilbert RD, Hulse E, Rigden S. Gilbert RD, et al. Pediatr Nephrol. 2006 Nov;21(11):1698-700. doi: 10.1007/s00467-006-0228-x. Epub 2006 Aug 24. Pediatr Nephrol. 2006. PMID: 16932900

5

Acute renal failure in a patient with paroxysmal cold hemoglobinuria.

Hothi DK, Bass P, Morgan M, Acharya J, Humphries SE, Gilbert RD. Hothi DK, et al. Among authors: gilbert rd. Pediatr Nephrol. 2007 Apr;22(4):593-6. doi: 10.1007/s00467-006-0352-7. Epub 2006 Nov 23. Pediatr Nephrol. 2007. PMID: 17123118

6

Bilineal inheritance of PKD1 abnormalities mimicking autosomal recessive polycystic disease.

Gilbert RD, Sukhtankar P, Lachlan K, Fowler DJ. Gilbert RD, et al. Pediatr Nephrol. 2013 Nov;28(11):2217-20. doi: 10.1007/s00467-013-2484-x. Epub 2013 Apr 28. Pediatr Nephrol. 2013. PMID: 23624871

7

Eculizumab therapy for atypical haemolytic uraemic syndrome due to a gain-of-function mutation of complement factor B.

Gilbert RD, Fowler DJ, Angus E, Hardy SA, Stanley L, Goodship TH. Gilbert RD, et al. Pediatr Nephrol. 2013 Aug;28(8):1315-8. doi: 10.1007/s00467-013-2492-x. Epub 2013 Apr 28. Pediatr Nephrol. 2013. PMID: 23624872

8

Eculizumab in atypical haemolytic uraemic syndrome with severe cardiac and neurological involvement.

Hu H, Nagra A, Haq MR, Gilbert RD. Hu H, et al. Among authors: gilbert rd. Pediatr Nephrol. 2014 Jun;29(6):1103-6. doi: 10.1007/s00467-013-2709-z. Epub 2013 Dec 8. Pediatr Nephrol. 2014. PMID: 24317637

9

Progressive myoclonic epilepsy with Fanconi syndrome.

Seaby EG, Gilbert RD, Pengelly RJ, Andreoletti G, Clarke A, Ennis S. Seaby EG, et al. Among authors: gilbert rd. JRSM Open. 2016 Jun 6;7(6):2054270415623145. doi: 10.1177/2054270415623145. eCollection 2016 Jun. JRSM Open. 2016. PMID: 27293772 Free PMC article.

10

AMMECR1: a single point mutation causes developmental delay, midface hypoplasia and elliptocytosis.

Andreoletti G, Seaby EG, Dewing JM, O'Kelly I, Lachlan K, Gilbert RD, Ennis S. Andreoletti G, et al. Among authors: gilbert rd. J Med Genet. 2017 Apr;54(4):269-277. doi: 10.1136/jmedgenet-2016-104100. Epub 2016 Nov 3. J Med Genet. 2017. PMID: 27811305 Free PMC article.

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