A Gerhard
Overview
Explore the profile of A Gerhard including associated specialties, affiliations and a list of published articles.
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Articles
25
Citations
649
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0
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Recent Articles
1.
Holmes S, Hinz R, Drake R, Gregory C, Conen S, Matthews J, et al.
Mol Psychiatry
. 2016 Oct;
21(12):1672-1679.
PMID: 27698434
Positron emission tomography (PET) imaging of the 18 kDa translocator protein (TSPO) has been used to investigate whether microglial activation, an indication of neuroinflammation, is evident in the brain of...
2.
Hunter H, Hinz R, Gerhard A, Talbot P, Su Z, Holland G, et al.
Br J Dermatol
. 2015 Mar;
175(5):1082-1084.
PMID: 25819441
No abstract available.
3.
Davidson Y, Robinson A, Hu Q, Mishra M, Baborie A, Jaros E, et al.
Neuropathol Appl Neurobiol
. 2012 Apr;
39(2):157-65.
PMID: 22497712
Aims: We aimed to investigate the role of the nuclear carrier and binding proteins, transportin 1 (TRN1) and transportin 2 (TRN2), TATA-binding protein-associated factor 15 (TAF15) and Ewing's sarcoma protein...
4.
Grover V, Pavese N, Koh S, Wylezinska M, Saxby B, Gerhard A, et al.
J Viral Hepat
. 2012 Jan;
19(2):e89-96.
PMID: 22239531
Patients with chronic hepatitis C infection may exhibit neuropsychological symptoms and cognitive impairment. Post-mortem studies of hepatitis C virus HCV quasispecies and replicative intermediates indicate that the brain might act...
5.
Foulds P, Yokota O, Thurston A, Davidson Y, Ahmed Z, Holton J, et al.
Neurobiol Dis
. 2011 Aug;
45(1):188-95.
PMID: 21856424
Differentiating clinically between Parkinson's disease (PD) and the atypical parkinsonian syndromes of Progressive supranuclear palsy (PSP), corticobasal syndrome (CBS) and multiple system atrophy (MSA) is challenging but crucial for patient...
6.
Trender-Gerhard I, Sweeney M, Schwingenschuh P, Mir P, Edwards M, Gerhard A, et al.
J Neurol Neurosurg Psychiatry
. 2009 Apr;
80(8):839-45.
PMID: 19332422
Background: An autosomal dominantly inherited defect in the GCH1 gene that encodes guanosine triphosphate cyclohydrolase 1 (GTPCH1) is the most common cause of dopa-responsive dystonia (DRD). A classic phenotype of...
7.
Albrecht J, Dellani P, Muller M, Schermuly I, Beck M, Stoeter P, et al.
J Neurol Neurosurg Psychiatry
. 2007 Apr;
78(9):964-9.
PMID: 17449543
Background: Fabry disease (FD) is a lysosomal storage disorder associated with marked cerebrovascular disease. Conventional MRI shows an extensive load of white matter lesions (WMLs) which may already be present...
8.
Pavese N, Gerhard A, Tai Y, Ho A, Turkheimer F, Barker R, et al.
Neurology
. 2006 Jun;
66(11):1638-43.
PMID: 16769933
Background: Huntington disease (HD) is characterized by the progressive death of medium spiny dopamine receptor bearing striatal GABAergic neurons. In addition, microglial activation in the areas of neuronal loss has...
9.
Turner M, Gerhard A, Al-Chalabi A, Shaw C, Hughes R, Banati R, et al.
J Neurol Neurosurg Psychiatry
. 2005 May;
76(6):871-4.
PMID: 15897516
(11)C-(R)-PK11195 positron emission tomography (PET) was used to explore and delineate in vivo the cortical lesion in three clinically isolated upper motor neurone syndromes of similar presentation, with reference to...
10.
Gerhard A, Banati R, Goerres G, Cagnin A, Myers R, Gunn R, et al.
Neurology
. 2003 Sep;
61(5):686-9.
PMID: 12963764
Microglia, the brain's intrinsic macrophages, bind (R)-PK11195 when activated by neuronal injury. The authors used [11C](R)-PK11195 PET to localize in vivo microglial activation in patients with multiple system atrophy (MSA)....