394 research outputs found
De Internationale van Amsterdam : de wereld van het Internationaal Vakverbond (IVV), 1913-1945
Biodiversiteit in België: van vitaal belang = La biodiversité en Belgique: une question vitale
POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotype
<p>Abstract</p> <p>Background</p> <p>The c.2447G>A (p.R722H) mutation in the gene <it>POLG1 </it>of the catalytic subunit of human mitochondrial polymerase gamma has been previously found in a few occasions but its pathogenicity has remained uncertain. We set out to ascertain its contribution to neuromuscular disease.</p> <p>Methods</p> <p>Probands from two families with probable mitochondrial disease were examined clinically, muscle and buccal epithelial DNA were analyzed for mtDNA deletions, and the <it>POLG1, POLG2, ANT1 </it>and <it>Twinkle </it>genes were sequenced.</p> <p>Results</p> <p>An adult proband presented with progressive external ophthalmoplegia, sensorineural hearing impairment, diabetes mellitus, dysphagia, a limb myopathy and dementia. Brain MRI showed central and cortical atrophy, and <sup>18</sup>F-deoxyglucose PET revealed reduced glucose uptake. Histochemical analysis of muscle disclosed ragged red fibers and cytochrome c oxidase-negative fibers. Electron microscopy showed subsarcolemmal aggregates of morphologically normal mitochondria. Multiple mtDNA deletions were found in the muscle, and sequencing of the <it>POLG1 </it>gene revealed a homozygous c.2447G>A (p.R722H) mutation. His two siblings were also homozygous with respect to the p.R722H mutation and presented with dementia and sensorineural hearing impairment. In another family the p.R722H mutation was found as compound heterozygosity with the common p.W748S mutation in two siblings with mental retardation, ptosis, epilepsy and psychiatric symptoms. The estimated carrier frequency of the p.R722H mutation was 1:135 in the Finnish population. No mutations in <it>POLG2</it>, <it>ANT1 </it>and <it>Twinkle </it>genes were found. Analysis of the POLG1 sequence by homology modeling supported the notion that the p.R722H mutation is pathogenic.</p> <p>Conclusions</p> <p>The recessive c.2447G>A (p.R722H) mutation in the linker region of the <it>POLG1 </it>gene is pathogenic for multiple mtDNA deletions in muscle and is associated with a late-onset neurological phenotype as a homozygous state. The onset of the disease can be earlier in compound heterozygotes.</p
Mother-to-child transmission of human immunodeficiency virus type 1 (HIV-1) and its determinants : a cohort study in Kigali, Rwanda
Magnesium treatment for patients with refractory status epilepticus due to POLG1-mutations
Mutations in the gene encoding of the catalytic subunit of mtDNA polymerase gamma (POLG1) can cause typical Alpers' syndrome. Recently, a new POLG1 mutation phenotype was described, the so-called juvenile-onset Alpers' syndrome. This POLG1 mutation phenotype is characterized by refractory epilepsy with recurrent status epilepticus and episodes of epilepsia partialis continua, which often necessitate admission to the intensive care unit (ICU) and pose an important mortality risk. We describe two previously healthy unrelated teenage girls, who both were admitted with generalized tonic-clonic seizures and visual symptoms leading to a DNA-supported diagnosis of juvenile-onset Alpers' syndrome. Despite combined treatment with anti-epileptic drugs, both patients developed status epilepticus requiring admission to the ICU. Intravenous magnesium as anti-convulsant therapy was initiated, resulting in clinical and neurophysiological improvement and rapid extubation of both patients. Treating status epilepticus in juvenile-onset Alpers' syndrome with magnesium has not been described previously. Given the difficulties encountered while treating epilepsy in patients with this syndrome, magnesium therapy might be considered
Experimental assessment of relative stopping power prediction by single energy and dual energy CT
Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia
Thermal bremsstrahlung probing the thermodynamical state of multifragmenting systems
Inclusive and exclusive hard-photon (E 30 MeV) production in five
different heavy-ion reactions (Ar+Au, Ag, Ni,
C at 60{\it A} MeV and Xe+Sn at 50{\it A} MeV) has been
studied coupling the TAPS photon spectrometer with several charged-particle
multidetectors covering more than 80% of 4. The measured spectra, slope
parameters and source velocities as well as their target-dependence, confirm
the existence of thermal bremsstrahlung emission from secondary nucleon-nucleon
collisions that accounts for roughly 20% of the total hard-photon yield. The
thermal slopes are a direct measure of the temperature of the excited nuclear
systems produced during the reaction.Comment: 4 pages, 3 figures, Proceedings CRIS 2000, 3rd Catania Relativistic
Ion Studies, "Phase Transitions in Strong Interactions: Status and
Perspectives", Acicastello, Italy, May 22-26, 2000 (to be published in Nuc.
Phys. A
La mer du Nord belge - Une eau vive! Biodiversité et Natura 2000 dans la partie belge de la mer du Nord
Evidence for Thermal Equilibration in Multifragmentation Reactions probed with Bremsstrahlung Photons
The production of nuclear bremsstrahlung photons (E 30 MeV) has
been studied in inclusive and exclusive measurements in four heavy-ion
reactions at 60{\it A} MeV. The measured photon spectra, angular distributions
and multiplicities indicate that a significant part of the hard-photons are
emitted in secondary nucleon-nucleon collisions from a thermally equilibrated
system. The observation of the thermal component in multi-fragment
Ar+Au reactions suggests that the breakup of the thermalized
source produced in this system occurs on a rather long time-scale.Comment: Revised version, accepted for publication in Physical Review Letters.
4 pages, 4 fig
- âŠ