371 research outputs found
Neurocysticercosis as a first presentation of tonic-clonic seizures: a case report
We report the case of a 28 year-old immigrant Asian man from the Punjab region with a first presentation of seizures. This patient had no significant past medical history, but suffered several headaches in the preceding week and was pyrexial on presentation. A CT scan of his head showed a single area of subcortical low attenuation initially suggesting ischaemia. A lumbar puncture and CSF examination was unremarkable. Further investigation revealed discrete calcified gluteal lesions on pelvic X-ray, and serum immunology positive for cysticercosis. The diagnosis of neurocysticercosis was made, and the patient improved on dexamethasone and a short course of vermicide, to be discharged a week later. With increasing global migration, the prevalence of neurological parasitic infections seen in the UK is likely to rise. This case highlights the importance of careful interpretation of non-specific head CTs in the context of first presentation of seizures in a susceptible population
Phase I dose escalation study of vinorelbine and topotecan combination chemotherapy in patients with recurrent lung cancer
Effective connectivity measured using optogenetically evoked hemodynamic signals exhibits topography distinct from resting state functional connectivity in the mouse
Brain connectomics has expanded from histological assessment of axonal projection connectivity (APC) to encompass resting state functional connectivity (RS-FC). RS-FC analyses are efficient for whole-brain mapping, but attempts to explain aspects of RS-FC (e.g., interhemispheric RS-FC) based on APC have been only partially successful. Neuroimaging with hemoglobin alone lacks specificity for determining how activity in a population of cells contributes to RS-FC. Wide-field mapping of optogenetically defined connectivity could provide insights into the brain\u27s structure-function relationship. We combined optogenetics with optical intrinsic signal imaging to create an efficient, optogenetic effective connectivity (Opto-EC) mapping assay. We examined EC patterns of excitatory neurons in awake, Thy1-ChR2 transgenic mice. These Thy1-based EC (Thy1-EC) patterns were evaluated against RS-FC over the cortex. Compared to RS-FC, Thy1-EC exhibited increased spatial specificity, reduced interhemispheric connectivity in regions with strong RS-FC, and appreciable connection strength asymmetry. Comparing the topography of Thy1-EC and RS-FC patterns to maps of APC revealed that Thy1-EC more closely resembled APC than did RS-FC. The more general method of Opto-EC mapping with hemoglobin can be determined for 100 sites in single animals in under an hour, and is amenable to other neuroimaging modalities. Opto-EC mapping represents a powerful strategy for examining evolving connectivity-related circuit plasticity
New Analyses of Star-to-Star Abundance Variations Among Bright Giants in the Mildly Metal-Poor Globular Cluster M5
We present a chemical composition analysis of 36 giant stars in the mildly
metal-poor globular cluster M5 (NGC 5904). The analysis makes use of high
resolution data acquired at the Keck I telescope as well as a re-analysis of
high resolution spectra acquired for an earlier study at Lick Observatory. We
employed two analysis techniques: one, adopting standard spectroscopic
constraints, and two, adopting an analysis consistent with the non-LTE precepts
as recently described by Thevenin & Idiart. The abundance ratios we derive for
magnesium, silicon, calcium, scandium, titanium, vanadium, nickel, barium and
europium in M5 show no significant abundance variations and the ratios are
comparable to those of halo field stars. However, large variations are seen in
the abundances of oxygen, sodium and aluminum, the elements that are sensitive
to proton-capture nucleosynthesis. In comparing the abundances of M5 and M4
(NGC 6121), another mildly metal-poor globular cluster, we find that silicon,
aluminum, barium and lanthanum are overabundant in M4 with respect to what is
seen in M5, confirming and expanding the results of previous studies. In
comparing the abundances between these two clusters and others having
comparable metallicities, we find that the anti-correlations observed in M5 are
similar to those found in more metal-poor clusters, M3, M10 and M13, whereas
the behavior in M4 is more like that of the more metal-rich globular cluster
M71. We conclude that among stars in Galactic globular clusters, there is no
definitive ``single'' value of [el/Fe] at a given [Fe/H] for at least some
alpha-capture, odd-Z and slow neutron-capture process elements, in this case,
silicon, aluminum, barium and lanthanum.Comment: 31 pages + 16 figures + 11 tables; accepted for publication in
Sept.2001 Astronomical Journa
Physics of cosmic plasmas from high angular resolution X-ray imaging of galaxy clusters
Galaxy clusters are massive dark matter-dominated systems filled with X-ray
emitting, optically thin plasma. Their large size and relative simplicity (at
least as astrophysical objects go) make them a unique laboratory to measure
some of the interesting plasma properties that are inaccessible by other means
but fundamentally important for understanding and modeling many astrophysical
phenomena -- from solar flares to black hole accretion to galaxy formation and
the emergence of the cosmological Large Scale Structure. While every cluster
astrophysicist is eagerly anticipating the direct gas velocity measurements
from the forthcoming microcalorimeters onboard XRISM, Athena and future
missions such as Lynx, a number of those plasma properties can best be probed
by high-resolution X-ray imaging of galaxy clusters. Chandra has obtained some
trailblazing results, but only grazed the surface of such studies. In this
white paper, we discuss why we need arcsecond-resolution, high collecting area,
low relative background X-ray imagers (with modest spectral resolution), such
as the proposed AXIS and the imaging detector of Lynx.Comment: Science white paper submitted for Astro2020 Decadal survey. 9 pages,
4 figure
A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia
Numerous single nucleotide polymorphisms (SNPs) have been found in recent genome wide association studies (GWAS) to be associated with subtle plasma triglyceride (TG) variation in normolipidemic subjects. However, since these GWAS did not specifically evaluate patients with rare disorders of lipoprotein metabolism—‘hyperlipoproteinemia’ (HLP)—it remains largely unresolved whether any of these SNP determinants of modest physiological changes in TG are necessarily also determinants of most HLP phenotypes. To address this question, we evaluated 28 TG-associated SNPs from GWAS in 386 unrelated adult patients with one of five Fredrickson phenotypes (HLP types 2A, 2B, 3, 4 and 5) and 242 matched normolipidemic controls. We found that several SNPs associated with TG in normolipidemic samples, including APOA5 p.S19W and -1131T>C, TRIB1 rs17321515, TBL2 rs17145738, GCKR rs780094, GALNT2 rs4846914 and ANGPTL3 rs12130333, were significantly associated with HLP types 2B, 3, 4 and 5. The findings indicate that: (i) the TG-associated Fredrickson HLP types 2B, 3, 4 and 5 are polygenic traits; (ii) these Fredrickson HLP types share numerous genetic determinants among themselves; and (iii) genetic determinants of modest TG variation in normolipidemic population samples also underlie—to an apparently even greater degree—susceptibility to these rare HLP phenotypes. Thus, the TG-associated Fredrickson HLP types 2B, 3, 4 and 5, although historically considered to be distinct are actually complex traits sharing among them several common genetic determinants seen in GWAS of normolipidemic population samples
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use.
Tobacco and alcohol use are leading causes of mortality that influence risk for many complex diseases and disorders1. They are heritable2,3 and etiologically related4,5 behaviors that have been resistant to gene discovery efforts6-11. In sample sizes up to 1.2 million individuals, we discovered 566 genetic variants in 406 loci associated with multiple stages of tobacco use (initiation, cessation, and heaviness) as well as alcohol use, with 150 loci evidencing pleiotropic association. Smoking phenotypes were positively genetically correlated with many health conditions, whereas alcohol use was negatively correlated with these conditions, such that increased genetic risk for alcohol use is associated with lower disease risk. We report evidence for the involvement of many systems in tobacco and alcohol use, including genes involved in nicotinic, dopaminergic, and glutamatergic neurotransmission. The results provide a solid starting point to evaluate the effects of these loci in model organisms and more precise substance use measures
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