422 research outputs found
Role of Chlamydia pneumoniae and Mycoplasma pneumoniae as Causative Agents of Community-Acquired Pneumonia in Hospitalised Children and Adolescents
The aim of the study presented here was to determine the prevalence of Chlamydia pneumoniae versus Mycoplasma pneumoniae infections in paediatric patients with community-acquired pneumonia. A total of 50 patients (mean age, 5.5 years; median, 3.9 years) with community-acquired pneumonia were enrolled. Four patients were found to have Chlamydia pneumoniae infection (1 culture positive, 1 PCR positive and 2 serology positive) and 16 patients had Mycoplasma pneumoniae infection (2 PCR positive, 4 PCR and serology positive, 10 serology positive), including three patients with coinfection. The rates of Mycoplasma pneumoniae infection were 22%, 35% and 40% in children aged 1-3, >3-7 and >7 years, respectively. Acute Chlamydia pneumoniae infection was substantially less common than Mycoplasma pneumoniae infection in our study cohor
Probable multiple system atrophy in a German family. J Neurol Neurosurg Psychiatry 75: 924–925
Abstract: Mutations in LRRK2 were first reported as causing Parkinson's disease (PD) in late 2004. Since then, approximately a dozen LRRK2 substitutions have been identified that are believed to be pathogenic mutations. The substitution of adenine for guanine at nucleotide 4541 (4541G>A) in LRRK2 was recently reported. This substitution resulted in the replacement of an arginine at position 1514 with a glutamine (R1514Q). Although this substitution was not found in a large cohort of controls, its pathogenicity could not be verified. We have now genotyped the R1514Q substitution in a sample of 954 PD patients from 429 multiplex PD families. This substitution was identified in 1.8% of the PD patients; however, the majority of the PD sibships segregating this substitution were discordant for this putative mutation. In addition, the R1514Q substitution was detected in 1.4% of neurologically evaluated, control individuals. These data suggest that the R1514Q variant is not a pathogenic LRRK2 mutation. We believe it is imperative that the causative nature of any newly identified genetic variant be determined before it is included in any panel for diagnostic testing. © 2006 Movement Disorder Society Key words: Parkinson's disease; genetics; LRRK2; mutation Parkinson's disease (PD) is the second most common neurodegenerative disorder. Clinical features of PD include resting tremor, rigidity, bradykinesia, and postural instability. Although quite variable, the average age of onset is 60 years. In addition, there is a slight preponderance of affected men. Pathologically, PD is characterized by the presence of Lewy bodies and progressive degeneration of neurons in the substantia nigra, pars compacta, and other brain regions. In our ongoing effort to identify additional PD susceptibility genes, we have recruited a large cohort of PD families. The control sample was collected through three sources and provided appropriate written informed consent. One sample of controls (n ϭ 52) was ascertained in Indiana, and all control subjects were examined by a single Parkinson Study Group movement disorder specialist. These control subjects completed the identical clinical evaluation as the PD sample. Individuals were considered controls if they met the following criteria: did not have a diagnosis or symptoms of PD, Alzheimer's disease (AD), stroke, or other neurological disorder; no tremor; no other first-degree family members reported to be diagnosed with PD; and no history of polio. The average age at examination of these first control subjects was 68.3 years, with a range of 55 to 82 years. All individuals were non-Hispanic Caucasians. A second control sample (n ϭ 40) was obtained from the National Cell Repository for Alzheimer's Disease. The subjects were recruited as part of an ongoing genetic initiative to make available to the research community a sample of rigorously evaluated individuals without any evidence of neurological disease. All control subjects were evaluated, and there was no evidence for either PD or dementia. The average age at examination of the second control cohort was 76.9 years, with a range of 58 to 91 years. As was the case with the first control set, all subjects from the second control set were non-Hispanic Caucasians. DNA was prepared from peripheral blood samples collected from the PD families and control subjects. The third control sample (n ϭ 276) is composed of three neurologically normal Caucasian control panels (NDPT002, NDPT006, NDPT009) obtained from the NINDS Human Genetics Resource Center at the Coriell Institute Coriell Cell Repositories (Camden, NJ). This third control sample contains 132 males and 144 females. The average age at examination of the subjects was 69.7 years, with a range of 55 to 88 years. In total, 368 neurologically normal control samples were evaluated. The guanine to adenine substitution at nucleotide 4541 of the LRRK2 cDNA that results in the R1514Q Lrrk2 (dardarin) protein variant was screened for using a newly developed TaqMan allelic-discrimination assay (Applied Biosystems). The assay was performed with 30 ng of genomic DNA from each PD subject and control individual using conditions recommended by the manufacturer and an Applied Biosystems 7300 Real Time PCR System. Of 954 affected individuals from 12 different families, 16 (1.8%) were shown to be heterozygous carriers of the R1514Q variant. In addition, 5 (1.4%) of 368 control subjects were also found to be heterozygous for the same variant similar to the frequency observed by Zimprich and associates. Discordance for the mutation among affected individuals was observed in 10 of the 13 families in which the variant was segregating. Of the 28 affected individuals in these 12 families for whom DNA was available for study, 12 of them do not carry the R1514Q variant. This finding suggests that the R1514Q variant is not segregating with PD in these families. No statistically significant difference between the R1514Q carrier group (16) and the noncarrier group (938) was detected in our analyses of numerous parameters, including age of disease onset (61.75 years in R1514Q carriers vs. 60.9 years in noncarriers), disease duration (7.18 years carriers vs. 9.53 years noncarriers), Mini-Mental State Examination score (25.62 carriers vs. 26.48 noncarriers), Blessed Functional Activity Scale (3.66 carriers vs. 4.41 noncarriers), Hoehn & Yahr (2.2 carriers vs. 2.48 noncarriers), and ethnicity. Taken together, these data suggest that the R1514Q variant is likely a nonpathogenic variant in Lrrk2 that does not contribute to the development of Parkinson disease, confirming the report of Zimprich and coworkers
Lattice calculation of hybrid mesons with improved Kogut-Susskind fermions
We report on a lattice determination of the mass of the exotic
hybrid meson using an improved Kogut-Susskind action. Results from both
quenched and dynamical quark simulations are presented. We also compare with
earlier results using Wilson quarks at heavier quark masses. The results on
lattices with three flavors of dynamical quarks show effects of sea quarks on
the hybrid propagators which probably result from coupling to two meson states.
We extrapolate the quenched results to the physical light quark mass to allow
comparison with experimental candidates for the hybrid meson. The
lattice result remains somewhat heavier than the experimental result, although
it may be consistent with the .Comment: 24 pages, 12 figures. Replaced to match published versio
Is the Unitarity of the quark-mixing-CKM-matrix violated in neutron -decay?
We report on a new measurement of neutron -decay asymmetry. From the
result \linebreak = -0.1189(7), we derive the ratio of the axial vector
to the vector coupling constant = = -1.2739(19). When
included in the world average for the neutron lifetime = 885.7(7)s, this
gives the first element of the Cabibbo-Kobayashi-Maskawa (CKM) matrix . With this value and the Particle Data Group values for and
, we find a deviation from the unitarity condition for the first row of
the CKM matrix of = 0.0083(28), which is 3.0 times the stated error
Mitochondrial characters do not correlate with maximum lifespan across populations of the bivalve Arctica islandica.
The mitochondrial oxidative stress theory of aging posits that membrane susceptibility to peroxidation and the organization of the electron transport system (ETS) linked with reactive oxygen species (ROS) generation are two main drivers of lifespan. While a clear correlation has been established from species comparative studies, the significance of these characteristics as potential modulators of lifespan divergences among populations of individual species is still to be tested. The bivalve Arctica islandica, the longest-lived non-colonial animal with a record lifespan of 507y, possesses a lower mitochondrial peroxidation index (PI) and reduced H2O2 efflux linked to complexes I and III activities than related species. Taking advantage of the wide variation in maximum reported longevities (MRL) among 6 European populations (36 to 507y), we examined whether these two mitochondrial properties could explain differences in longevity. We report no relationship between membrane PI and MRL in populations of A. islandica, as well as a lack of intraspecific relationship between ETS complex activities and MRL. Individuals from brackish sites characterized by wide temperature and salinity windows had, however, markedly lower ETS enzyme activities relative to citrate synthase activity. Our results highlight environment-dependent remodeling of mitochondrial phenotypes
Alpha scattering and capture reactions in the A = 7 system at low energies
Differential cross sections for He- scattering were measured in
the energy range up to 3 MeV. These data together with other available
experimental results for He and H scattering were
analyzed in the framework of the optical model using double-folded potentials.
The optical potentials obtained were used to calculate the astrophysical
S-factors of the capture reactions HeBe and
HLi, and the branching ratios for the transitions into
the two final Be and Li bound states, respectively. For
HeBe excellent agreement between calculated and
experimental data is obtained. For HLi a value
has been found which is a factor of about 1.5 larger than the adopted value.
For both capture reactions a similar branching ratio of has been obtained.Comment: submitted to Phys.Rev.C, 34 pages, figures available from one of the
authors, LaTeX with RevTeX, IK-TUW-Preprint 930540
alpha-nucleus potentials for the neutron-deficient p nuclei
alpha-nucleus potentials are one important ingredient for the understanding
of the nucleosynthesis of heavy neutron-deficient p nuclei in the astrophysical
gamma-process where these p nuclei are produced by a series of (gamma,n),
(gamma,p), and (gamma,alpha) reactions. I present an improved alpha-nucleus
potential at the astrophysically relevant sub-Coulomb energies which is derived
from the analysis of alpha decay data and from a previously established
systematic behavior of double-folding potentials.Comment: 6 pages, 3 figures, accepted for publication in Phys. Rev.
Enhancing the top signal at Tevatron using Neural Nets
We show that Neural Nets can be useful for top analysis at Tevatron. The main
features of and background events on a mixed sample are projected in
a single output, which controls the efficiency and purity of the
signal.Comment: 11 pages, 6 figures (not included and available from the authors),
Latex, UB-ECM-PF 94/1
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