Search results for "Axia"

Atlantoaxial subluxation and congenital atlas arch defect

2014

17. Masseter reflex abnormalities with meso-diencephalic lesions

2012

different papers and some eponyms used to characterize a certain neurological state differ from the original description. Except for Wallenberg‘s syndrome, classical brainstem syndromes are rarely seen in clinical practice. Lacunar brainstem syndromes are the consequence of infarcts, which involve long tracts and spare intra-axial cranial nerve segments. This group includes pure motor or pure sensory stroke, dysarthriaclumsy hand syndrome, or ataxic hemiparesis. Such infarcts may also cause body lateropulsion with or without limb ataxia, internuclear ophthalmoplgia, skew-torsion sign, or ocular tilt reaction. Small deep infarcts, which solely affect certain nuclei, may be followed by horizo…

SPECIAL SPLINES OF HYPERBOLIC TYPE FOR THE SOLUTIONS OF HEAT AND MASS TRANSFER 3-D PROBLEMS IN POROUS MULTI-LAYERED AXIAL SYMMETRY DOMAIN

2017

In this paper we study the problem of the diffusion of one substance through the pores of a porous multi layered material which may absorb and immobilize some of the diffusing substances with the evolution or absorption of heat. As an example we consider circular cross section wood-block with two layers in the radial direction. We consider the transfer of heat process. We derive the system of two partial differential equations (PDEs) - one expressing the rate of change of concentration of water vapour in the air spaces and the other - the rate of change of temperature in every layer. The approximation of corresponding initial boundary value problem of the system of PDEs is based on the cons…

Measurement of the parity violating asymmetry in the quasielastic electron-deuteron scattering and improved determination of the magnetic strange for…

2016

A new measurement of the parity-violating asymmetry in the electron-deuteron quasielastic scattering for backward angles at $⟨{Q}^{2}⟩=0.224\text{ }\text{ }{(\mathrm{GeV}/c)}^{2}$, obtained in the A4 experiment at the Mainz Microtron accelerator (MAMI) facility, is presented. The measured asymmetry is ${A}_{PV}^{d}=(\ensuremath{-}20.11\ifmmode\pm\else\textpm\fi{}0.8{7}_{\mathrm{stat}}\ifmmode\pm\else\textpm\fi{}\phantom{\rule{0ex}{0ex}}1.0{3}_{\mathrm{sys}})\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}6}$. A combination of these data with the proton measurements of the parity-violating asymmetry in the A4 experiment yields a value for the effective isovector axial-vector form facto…

Density distributions in the $B$ meson

2016

We report on a two-flavor lattice QCD study of the axial, charge and matter distributions of the $B$ meson and its first radial excitation. As our framework is the static limit of Heavy Quark Effective Theory (HQET), taking their Fourier transform gives access to several form factors at the kinematical point $q^2=0$. Moreover they provide some useful information on the nature of an excited state, i.e. a radial excitation of a quark-antiquark bound state or a multihadron state.

V-Belt Winding along Archimedean Spirals During the Variator Speed Ratio Shift

2010

Starting from a previous model for the shift mechanics of rubber belt variators, this lecture elaborates practical design formulas for the torque and the axial thrust making use of the very close resemblance of the belt path to a linear spiral of Archimedes along a large part of the arc of contact. In addition, as an alternative to the modern calculus tools, it is shown how the drive variables can be equally calculated applying some propositions of Archimedes’ classical treatise πeρί ‘eλίκων (On Spirals).

Late-Onset Globoid Cell Leukodystrophy: Unusual Ultrastructural Pathology and Subtotal β-Galactocerebrosidase Deficiency

1990

An 11-year-old girl was found to have severely reduced β-galactocerebrosidase activity as evidence of late-onset globoid cell leukodystrophy, while her mother had almost normal enzyme activity in circulating white blood cells. Clinically, the patient showed a remitting course marked by seizures, ataxia, white-matter disease on computed tomographic scan, and reduced conduction velocities of peripheral nerves. Symptoms improved somewhat around the age of 10 years. Two sural nerve biopsies, performed 6 years apart, disclosed a demyelinating neuropathy. By electron microscopy, membrane-bound vacuolar lysosomes in Schwann cells of myelinated axons, unlike the typical needlelike inclusions seen …

Early-onset ataxia with cardiomyopathy and retained tendon reflexes maps to the friedreich's ataxia locus on chromosome 9q

1995

Absence of lower limb tendon reflexes has been considered an essential diagnostic criterion for Friedreich's ataxia (FA). However, preservation of knee and ankle jerks has been reported in a few patients. Linkage analysis to FA locus (FRDA) on chromosome 9q13-21.1 was performed in 11 patients from 6 families with FA phenotype, including cardiomyopathy, but retained reflexes (FARR). A maximal lod score of 3.38 at recombination fraction theta equal to 0.00 was obtained demonstrating that FARR maps to the FRDA locus. These results suggest that FARR is a variant phenotype of FA.

Paraneoplastic Focal Outer Retinitis and Optic Neuropathy in a Patient with Small Cell Lung Carcinoma and Anti-CRMP5, Anti-HU and Anti-Amphiphysin An…

2020

Our aim is to describe clinical and optical coherence tomographic features of acute paraneoplastic focal outer retinitis associated with optic neuropathy in a patient diagnosed with small cell lung carcinoma. Bilateral focal outer retinitis, bilateral optic disc oedema and vitritis were identified in a patient with progressive bilateral visual loss and ataxia. Spectral domain optical coherence tomography (SD-OCT) revealed various extents of granular hyperreflectivity and atrophy of the macular outer retinal layers. Serum and cerebrospinal fluid positivity for anti-CRMP5, anti-HU and anti-amphiphysin antibodies intensified the search for an underlying malignancy, and a small cell lung carcin…

Superficial Siderosis of the Central Nervous System associated with Hemophilia A: A case report

2021

Abstract Superficial Siderosis of the Central Nervous System (SSCNS) is a condition secondary to the deposition of hemosiderin within the subpial layers of central nervous system leading to its progressive degeneration, clinically responsible for hearing impairment, cerebellar ataxia and pyramidal syndrome. Here we report the case of a 61-year-old man with medical history of congenital hemophilia A presenting with typical clinical features of SSCNS associated with extensive hypo-intensity on fast 2D gradient-echo-weighted sequences, along the spinal cord, posterior fossa's structures and cerebral cortex. Interestingly, although his disorder was revealed by a lumbar spinal stenosis, presurgi…