S E Marshall
Overview
Explore the profile of S E Marshall including associated specialties, affiliations and a list of published articles.
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Articles
70
Citations
833
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Recent Articles
1.
Wadelius M, Marshall S, Islander G, Nordang L, Karawajczyk M, Yue Q, et al.
Clin Pharmacol Ther
. 2014 Jun;
96(4):477-81.
PMID: 24960520
Angioedema is a potentially life-threatening adverse reaction to angiotensin-converting enzyme inhibitors and angiotensin receptor blockers. To study the genetic etiology of this rare adverse event, international consortia and multicenter recruitment...
2.
D M Edgar J, Buckland M, Guzman D, Conlon N, Knerr V, Bangs C, et al.
Clin Exp Immunol
. 2013 Jul;
175(1):68-78.
PMID: 23841717
This report summarizes the establishment of the first national online registry of primary immune deficency in the United Kingdom, the United Kingdom Primary Immunodeficiency (UKPID Registry). This UKPID Registry is...
3.
Carew M, Marshall S, Hoffmann A
Bull Entomol Res
. 2011 Mar;
101(5):505-19.
PMID: 21388576
Molecular approaches for identifying aquatic macroinvertebrate species are increasingly being used but there is ongoing debate about the number of DNA markers needed to differentiate species accurately. Here, we use...
4.
Spagnolo P, Sato H, Grutters J, Renzoni E, Marshall S, Ruven H, et al.
Tissue Antigens
. 2007 Jul;
70(3):219-27.
PMID: 17661910
Sarcoidosis is a heterogeneous disorder, both phenotypically and genetically. Two independent studies have recently shown that a functional polymorphism within butyrophilin-like 2 (BTNL2) gene predisposes to sarcoidosis independently of the...
5.
AbdAllah A, Renzoni E, Anevlavis S, Lagan A, Munkonge F, Fonseca C, et al.
Int J Immunogenet
. 2006 May;
33(3):155-61.
PMID: 16712644
Systemic sclerosis (SSc) is a connective tissue disease of unknown aetiology characterized by fibrosis of the skin and internal organs, vascular abnormalities and humoral autoimmunity. Strong T-cell-dependent autoantibody and HLA...
6.
Ahmad T, Zhang L, Gogus F, Verity D, Wallace G, Madanat W, et al.
Scand J Rheumatol
. 2005 Sep;
34(3):233-7.
PMID: 16134731
Background: Behçet's disease (BD) is a chronic multi-system inflammatory disorder of unknown aetiology, which shares many features of the inflammatory bowel diseases (IBDs). CARD15 has recently been identified as the...
7.
Loucaidou M, Stitchbury J, Lee J, Borrows R, Marshall S, Mclean A, et al.
Transplant Proc
. 2005 May;
37(4):1760-1.
PMID: 15919456
Introduction: Acute rejection remains an important cause of graft loss after renal transplantation. It has been suggested that cytokine genotyping may play a predictive role in identifying individuals who are...
8.
Yang X, Ahmad T, Gogus F, Verity D, Wallace G, Madanat W, et al.
Eur J Immunogenet
. 2004 Mar;
31(1):11-4.
PMID: 15009175
Chemokines are important determinants of the early inflammatory response. The CC chemokine receptor 5 (CCR5) Delta32 variant results in a non-functional form of the chemokine receptor, and has been implicated...
9.
Jones D, Bunce M, Fuggle S, Young N, Marshall S
Eur J Immunogenet
. 2003 Dec;
30(6):415-9.
PMID: 14675395
Alloimmunization to human platelet alloantigens (HPAs) is responsible for neonatal alloimmune thrombocytopenia (NAIT), post-transfusional purpura (PTP) and platelet transfusion refractoriness. HPAs may also have a role as histocompatibility antigens in...
10.
The contribution of human leucocyte antigen complex genes to disease phenotype in ulcerative colitis
Ahmad T, Armuzzi A, Neville M, Bunce M, Ling K, Welsh K, et al.
Tissue Antigens
. 2003 Nov;
62(6):527-35.
PMID: 14617036
Linkage and association studies implicate the human leucocyte antigen (HLA) region in genetic susceptibility to ulcerative colitis (UC). However, associations with specific variants have been inconsistent, even within defined ethnic...