Haq MR - Search Results

1

Hemolytic uremic syndrome associated with invasive pneumococcal disease: the United kingdom experience.

Waters AM, Kerecuk L, Luk D, Haq MR, Fitzpatrick MM, Gilbert RD, Inward C, Jones C, Pichon B, Reid C, Slack MP, Van't Hoff W, Dillon MJ, Taylor CM, Tullus K. Waters AM, et al. Among authors: haq mr. J Pediatr. 2007 Aug;151(2):140-4. doi: 10.1016/j.jpeds.2007.03.055. J Pediatr. 2007. PMID: 17643764

2

Does dysregulated complement activation contribute to haemolytic uraemic syndrome secondary to Streptococcus pneumoniae?

Gilbert RD, Nagra A, Haq MR. Gilbert RD, et al. Among authors: haq mr. Med Hypotheses. 2013 Sep;81(3):400-3. doi: 10.1016/j.mehy.2013.05.030. Epub 2013 Jun 17. Med Hypotheses. 2013. PMID: 23786906

3

Exfoliated human proximal tubular cells: a model of cystinosis and Fanconi syndrome.

Laube GF, Haq MR, van't Hoff WG. Laube GF, et al. Among authors: haq mr. Pediatr Nephrol. 2005 Feb;20(2):136-40. doi: 10.1007/s00467-004-1703-x. Epub 2004 Dec 31. Pediatr Nephrol. 2005. PMID: 15627171

4

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: haq mr. Pediatr Nephrol. 2014 Jun;29(6):1103-6. doi: 10.1007/s00467-013-2709-z. Epub 2013 Dec 8. Pediatr Nephrol. 2014. PMID: 24317637

5

Glutathione depletion and increased apoptosis rate in human cystinotic proximal tubular cells.

Laube GF, Shah V, Stewart VC, Hargreaves IP, Haq MR, Heales SJ, van't Hoff WG. Laube GF, et al. Among authors: haq mr. Pediatr Nephrol. 2006 Apr;21(4):503-9. doi: 10.1007/s00467-006-0005-x. Epub 2006 Mar 1. Pediatr Nephrol. 2006. PMID: 16508773 Free article.

6

Autosomal dominant inheritance of non-syndromic renal hypoplasia and dysplasia: dramatic variation in clinical severity in a single kindred.

Kerecuk L, Sajoo A, McGregor L, Berg J, Haq MR, Sebire NJ, Bingham C, Edghill EL, Ellard S, Taylor J, Rigden S, Flinter FA, Woolf AS. Kerecuk L, et al. Among authors: haq mr. Nephrol Dial Transplant. 2007 Jan;22(1):259-63. doi: 10.1093/ndt/gfl531. Epub 2006 Sep 23. Nephrol Dial Transplant. 2007. PMID: 16998226 No abstract available.

7

Tolvaptan treatment for severe neonatal autosomal-dominant polycystic kidney disease.

Gilbert RD, Evans H, Olalekan K, Nagra A, Haq MR, Griffiths M. Gilbert RD, et al. Among authors: haq mr. Pediatr Nephrol. 2017 May;32(5):893-896. doi: 10.1007/s00467-017-3584-9. Epub 2017 Feb 13. Pediatr Nephrol. 2017. PMID: 28194574 Free PMC article.

8

Immunolocalization of cystinosin, the protein defective in cystinosis.

Haq MR, Kalatzis V, Gubler MC, Town MM, Antignac C, Van't Hoff WG, Woolf AS. Haq MR, et al. J Am Soc Nephrol. 2002 Aug;13(8):2046-51. doi: 10.1097/01.asn.0000022012.95680.ba. J Am Soc Nephrol. 2002. PMID: 12138135

9

Mutations in phospholipase C epsilon 1 are not sufficient to cause diffuse mesangial sclerosis.

Gilbert RD, Turner CL, Gibson J, Bass PS, Haq MR, Cross E, Bunyan DJ, Collins AR, Tapper WJ, Needell JC, Dell B, Morton NE, Temple IK, Robinson DO. Gilbert RD, et al. Among authors: haq mr. Kidney Int. 2009 Feb;75(4):415-9. doi: 10.1038/ki.2008.573. Epub 2008 Nov 26. Kidney Int. 2009. PMID: 19037252 Free article.

10

Mutations in PIK3R1 cause SHORT syndrome.

Dyment DA, Smith AC, Alcantara D, Schwartzentruber JA, Basel-Vanagaite L, Curry CJ, Temple IK, Reardon W, Mansour S, Haq MR, Gilbert R, Lehmann OJ, Vanstone MR, Beaulieu CL; FORGE Canada Consortium; Majewski J, Bulman DE, O'Driscoll M, Boycott KM, Innes AM. Dyment DA, et al. Among authors: haq mr. Am J Hum Genet. 2013 Jul 11;93(1):158-66. doi: 10.1016/j.ajhg.2013.06.005. Epub 2013 Jun 27. Am J Hum Genet. 2013. PMID: 23810382 Free PMC article.

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