Results 61 to 70 of about 57,018 (256)
ABSTRACT Background Differentiating demyelinating from axonal polyneuropathies helps for accurate diagnosis and treatment. However, the current clinical tools lack sensitivity to confirm demyelination in peripheral nerves, particularly for proximal nerves.
Jesus E. Fajardo +8 more
wiley +1 more source
Parameters of stimulation electroneuromyography in patients with primary hypothyroidism
Background. The purpose of the work is to identify the parameters of stimulation electroneuromyography (ENMG) in patients with primary hypothyroidism against the background of autoimmune thyroiditis and postoperative hypothyroidism. Materials and methods.
I.I. Bilous
doaj +1 more source
Summary Two cases of polyneuropathy occurring after rubella infections are described, together with the nerve biopsy and serological findings.
openaire +2 more sources
The article discusses the role of vitamin & mineral supplements in nootropic therapy, treatment of hypovitaminosis, neurological disorders, as well as in maintaining the normal function of human health in high stress.
N. V. Vakhnina, E. Y. Kalimeeva
doaj +1 more source
Clinical, electrophysiological, and histopathological profile of biopsy-proven vasculitic neuropathy
Background: Vasculitic neuropathies are an uncommon heterogeneous group of nerve disorders characterized by inflammation of the vasa nervorum, which may be either systemic vasculitic neuropathy (SVN) or non-SVN (NSVN).
Suchitra Deolalikar +6 more
doaj +1 more source
Cardiac MIBG Scintigraphy in Neurodegenerative Parkinsonism: Limitations in Clinical Practice
Abstract Background Reduced cardiac uptake on 123Iodine‐metaiodobenzylguanidine (MIBG) scintigraphy is a valuable tool for differentiating neurodegenerative parkinsonism but interpretation can be difficult due to comorbidities and drug‐tracer interactions.
Frank Jagusch +9 more
wiley +1 more source
Exteroceptive Reflexes in Stiff Person Syndrome, Other Neurological Conditions and Healthy Controls
Abstract Background Stiff person syndrome (SPS) is a rare disabling neurological condition with overlapping symptomatology with more common neurological conditions. Exaggerated exteroceptive reflex mechanisms are thought to play a role in its pathophysiology.
Belinda Cruse +8 more
wiley +1 more source
Proteomic Signatures of Ectopic Fat Distribution: Tissue‐Specific Drivers and Clinical Implications
Integration of plasma proteomics and multi‐organ MRI in 666 UK Biobank participants, combined with a knockoff‐based causal inference and machine learning framework, reveals organ‐specific drivers of ectopic fat: PLA2G1B (pancreas), ERBB2/IGFBP2 (liver), CA14 (muscle), and NCAM2/TNFRSF10B (pericardium). These drivers engage distinct pathways (e.g., PI3K‐
Bing Zhang +9 more
wiley +1 more source
A Chromosomal Deletion and New Frameshift Mutation Cause ARSACS in an African-American
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) is a rare, progressive, neurodegenerative disease characterized by ataxia, spasticity and polyneuropathy.
Sean C. Dougherty +4 more
doaj +1 more source
Abstract Background NKX2‐1–related disorders (NKX2‐1‐RDs) classically present with a triad of neurological, endocrine, and pulmonary manifestations, including benign hereditary chorea. However, in a fraction of patients, NKX2‐1 coding variants are not detected, and variants outside the NKX2‐1 locus have been reported.
Robin Wijngaard +33 more
wiley +1 more source

