Halsall DJ - 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: halsall dj. 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: halsall dj. 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: halsall dj. 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

Hemochromatosis--neonatal and young subjects.

Cox TM, Halsall DJ. Cox TM, et al. Among authors: halsall dj. Blood Cells Mol Dis. 2002 Nov-Dec;29(3):411-7. doi: 10.1006/bcmd.2002.0580. Blood Cells Mol Dis. 2002. PMID: 12547231 Review.

5

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. Hum Mol Genet. 2003 Jun 15;12(12):1361-5. doi: 10.1093/hmg/ddg149. Hum Mol Genet. 2003. PMID: 12783844

6

Metachromatic leucodystrophy: a newly identified mutation in arylsulphatase A, D281Y, found as a compound heterozygote with I179L in an adult onset case.

Halsall DJ, Halligan EP, Elsey TS, Cox TM. Halsall DJ, et al. Hum Mutat. 1999 Nov;14(5):447. doi: 10.1002/(SICI)1098-1004(199911)14:5<447::AID-HUMU12>3.0.CO;2-1. Hum Mutat. 1999. PMID: 10533072

7

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: halsall dj. Ann Clin Biochem. 2007 May;44(Pt 3):297-9. doi: 10.1258/000456307780480927. Ann Clin Biochem. 2007. PMID: 17456300

8

Twin pairs showing discordance of phenotype in adult Gaucher's disease.

Lachmann RH, Grant IR, Halsall D, Cox TM. Lachmann RH, et al. QJM. 2004 Apr;97(4):199-204. doi: 10.1093/qjmed/hch036. QJM. 2004. PMID: 15028849

9

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. 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

10

Aldolase B mutations in Turkish families from central Anatolia.

Karabulut HG, Halsall D, Sayin BD, Tonyukuk V, Cox TM, Bökesoy I. Karabulut HG, et al. Genet Couns. 2006;17(4):457-60. Genet Couns. 2006. PMID: 17375533 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

117 results

Search Page

Filters