McFarlane I - Search Results

1

Primary iron overload with inappropriate hepcidin expression in V162del ferroportin disease.

Zoller H, McFarlane I, Theurl I, Stadlmann S, Nemeth E, Oxley D, Ganz T, Halsall DJ, Cox TM, Vogel W. Zoller H, et al. Among authors: mcfarlane i. Hepatology. 2005 Aug;42(2):466-72. doi: 10.1002/hep.20775. Hepatology. 2005. PMID: 15986403

2

Clinical presentation and molecular pathophysiology of autosomal dominant hemochromatosis caused by a novel ferroportin mutation.

Griffiths WJ, Mayr R, McFarlane I, Hermann M, Halsall DJ, Zoller H, Cox TM. Griffiths WJ, et al. Among authors: mcfarlane i. Hepatology. 2010 Mar;51(3):788-95. doi: 10.1002/hep.23377. Hepatology. 2010. PMID: 19937651

3

Identification of mutations in SLC40A1 that affect ferroportin function and phenotype of human ferroportin iron overload.

Mayr R, Griffiths WJ, Hermann M, McFarlane I, Halsall DJ, Finkenstedt A, Douds A, Davies SE, Janecke AR, Vogel W, Cox TM, Zoller H. Mayr R, et al. Among authors: mcfarlane i. Gastroenterology. 2011 Jun;140(7):2056-63, 2063.e1. doi: 10.1053/j.gastro.2011.02.064. Epub 2011 Mar 9. Gastroenterology. 2011. PMID: 21396368

4

Typical type 2 diabetes mellitus and HFE gene mutations: a population-based case - control study.

Halsall DJ, McFarlane I, Luan J, Cox TM, Wareham NJ. Halsall DJ, et al. Among authors: mcfarlane i. Hum Mol Genet. 2003 Jun 15;12(12):1361-5. doi: 10.1093/hmg/ddg149. Hum Mol Genet. 2003. PMID: 12783844

5

The effect of potassium EDTA on the stability of parathyroid hormone in whole blood.

English E, McFarlane I, Taylor KP, Halsall DJ. English E, et al. Among authors: mcfarlane i. Ann Clin Biochem. 2007 May;44(Pt 3):297-9. doi: 10.1258/000456307780480927. Ann Clin Biochem. 2007. PMID: 17456300

6

Clinical evaluation of chemokine and enzymatic biomarkers of Gaucher disease.

Deegan PB, Moran MT, McFarlane I, Schofield JP, Boot RG, Aerts JM, Cox TM. Deegan PB, et al. Among authors: mcfarlane i. Blood Cells Mol Dis. 2005 Sep-Oct;35(2):259-67. doi: 10.1016/j.bcmd.2005.05.005. Blood Cells Mol Dis. 2005. PMID: 16125420

7

Potential biomarkers of osteonecrosis in Gaucher disease.

Pavlova EV, Deegan PB, Tindall J, McFarlane I, Mehta A, Hughes D, Wraith JE, Cox TM. Pavlova EV, et al. Among authors: mcfarlane i. Blood Cells Mol Dis. 2011 Jan 15;46(1):27-33. doi: 10.1016/j.bcmd.2010.10.010. Epub 2010 Nov 13. Blood Cells Mol Dis. 2011. PMID: 21075651

8

A novel CYP11B2 gene mutation in an Asian family with aldosterone synthase deficiency.

Løvås K, McFarlane I, Nguyen HH, Curran S, Schwabe J, Halsall D, Bernhardt R, Wallace AM, Chatterjee VK. Løvås K, et al. Among authors: mcfarlane i. J Clin Endocrinol Metab. 2009 Mar;94(3):914-9. doi: 10.1210/jc.2008-1524. Epub 2008 Dec 30. J Clin Endocrinol Metab. 2009. PMID: 19116236

9

Focused parathyroid surgery with intraoperative parathyroid hormone measurement as a day-case procedure.

Gurnell EM, Thomas SK, McFarlane I, Munday I, Balan KK, Berman L, Chatterjee VK, Wishart GC. Gurnell EM, et al. Among authors: mcfarlane i. Br J Surg. 2004 Jan;91(1):78-82. doi: 10.1002/bjs.4463. Br J Surg. 2004. PMID: 14716798 Free PMC article.

10

Long-term outcome of permanent urethral stents in the treatment of detrusor-sphincter dyssynergia.

McFarlane IP, Foley SJ, Shah PJ. McFarlane IP, et al. Br J Urol. 1996 Nov;78(5):729-32. doi: 10.1046/j.1464-410x.1996.11911.x. Br J Urol. 1996. PMID: 8976768

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