D Halsall
Overview
Explore the profile of D Halsall including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
14
Citations
231
Followers
0
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Recent Articles
1.
Maddox C, Halsall D, Hall J, Tully M
Res Social Adm Pharm
. 2015 Jun;
12(1):41-55.
PMID: 26048711
Background: In the UK, the majority of non-medical prescribers (NMPs) are nurses or pharmacists working in community or primary care. However, little is known about what influences their decisions to...
2.
Frankenberger M, Heimbeck I, Moller W, Mamidi S, Kassner G, Pukelsheim K, et al.
Eur Respir J
. 2009 Dec;
34(6):1487-9.
PMID: 19948915
No abstract available.
3.
Owen P, Chatterjee V, John R, Halsall D, Lazarus J
Clin Endocrinol (Oxf)
. 2008 Sep;
70(4):650-4.
PMID: 18803680
Objective: Resistance to thyroid hormone (RTH) is associated with a varied clinical presentation. The cardiac effects of RTH have been described but vascular function has yet to be fully evaluated...
4.
Karabulut H, Halsall D, Sayin B, Tonyukuk V, Cox T, Bokesoy I
Genet Couns
. 2007 Mar;
17(4):457-60.
PMID: 17375533
No abstract available.
5.
Mellanby R, Mellor P, Villiers E, Herrtage M, Halsall D, ORahilly S, et al.
J Small Anim Pract
. 2006 Apr;
47(4):207-12.
PMID: 16573764
A seven-year-old Labrador was presented with weight loss and mild generalised lymphadenopathy. Histopathology of an excised lymph node by the referring veterinarian demonstrated granulomatous lymphadenitis. At the time of referral,...
6.
Whitfield P, Calvin J, Hogg S, ODriscoll E, Halsall D, Burling K, et al.
J Inherit Metab Dis
. 2005 Feb;
28(1):21-33.
PMID: 15702403
Anderson-Fabry disease (referred to as Fabry disease) is an X-linked disorder characterized by a deficiency of the lysosomal enzyme alpha-galactosidase A and the subsequent accumulation in various tissues of globotriaosylceramide...
7.
Lachmann R, Grant I, Halsall D, Cox T
QJM
. 2004 Mar;
97(4):199-204.
PMID: 15028849
Background: Non-neuronopathic (type 1) Gaucher's disease, a recessive disorder caused by glucocerebrosidase deficiency, shows marked variability in the severity and extent of clinical expression: many individuals who harbour two mutant...
8.
Meirhaeghe A, Luan J, Hennings S, Mitchell J, Halsall D, ORahilly S, et al.
J Clin Endocrinol Metab
. 2001 Dec;
86(12):5881-7.
PMID: 11739457
The lipolytic effects of catecholamines are mediated through members of the beta(2)-adrenergic receptor (BAR-2) family. Previous studies have suggested that genetic variants in the BAR-2 gene may be associated with...
9.
Taube J, Halsall D, Baglin T
Blood
. 2000 Aug;
96(5):1816-9.
PMID: 10961881
Cytochrome P-450 2C9 is the principle enzyme that terminates the anticoagulant effect of warfarin. Genetic polymorphisms in CYP2C9 producing variants with altered catalytic properties have been identified. Patients (n =...
10.
Byrne C, Maison P, Halsall D, Martensz N, Hales C, Wareham N
Diabet Med
. 2000 Feb;
16(12):1007-15.
PMID: 10656229
Aims: Cross-sectional studies have demonstrated an association between high non-esterified fatty acid (NEFA) concentrations and glucose intolerance. However, the direction of causality in these studies is uncertain. The aim of...