Results 61 to 70 of about 4,373 (200)
Nanoflowers Templated CuO/Cu Hybrid Metasurface for Sensitive THz‐TDS Detection of Acetylcholine
This research focuses on sensitively detecting acetylcholine in the terahertz range through the integration of CuO nanoflowers with Cu nanoslots. The terahertz transmittance measurements are recalibrated by incorporating acidic components hydrolyzed from acetylcholine.
Soo Hyun Lee, Taeyeon Kim, Minah Seo
wiley +1 more source
International audienceLambert-Eaton myasthenic syndrome is an autoimmune disease that impairs neuromuscular transmission. Several studies suggest that neurotransmitter release is reduced by an immune response directed against the calcium channel complex ...
M De Waard +13 more
core +1 more source
SOX1 antibodies are markers of paraneoplastic Lambert-Eaton myasthenic syndrome [PDF]
BACKGROUND/OBJECTIVE: We reported that 43% of patients with Lambert-Eaton myasthenic syndrome (LEMS) and small cell lung cancer (SCLC) had an antibody called anti-glial nuclear antibody (AGNA), defined by the immunoreaction with the nuclei of the ...
Saiz, A. +5 more
core +1 more source
Diaphragmatic Palsy Due to a Paraneoplastic Autoimmune Syndrome Revealed by Checkpoint Inhibitors
Background and Clinical Significance: Immune checkpoint inhibitors (ICIs) have revolutionized cancer treatment but may underlie diverse and potentially life-threatening immune-related adverse events (irAEs).
Jean-Baptiste Destival +6 more
doaj +1 more source
Patients diagnosed with small‐cell lung cancer (SCLC) at a single center between August 2007 and April 2021 were retrospectively analyzed. A total of 318 patients were evaluated; paraneoplastic neurological syndrome (PNS) was present in 2.8% (n = 9) of the overall population.
Yuki Sato +7 more
wiley +1 more source
Pseudomyopathic Changes in Needle Electromyography in Lambert-Eaton Myasthenic Syndrome
Lambert-Eaton myasthenic syndrome (LEMS) is a rare presynaptic disorder of the neuromuscular junction in association with cancer and subsequently in cases in which no neoplasm has been detected (O’Neill et al., 1988).
Teppei Komatsu +4 more
doaj +1 more source
Antibodies against endogenous retroviruses
Summary The human genome harbors hundreds of thousands of integrations of ancient retroviruses, amassed over millions of years of evolution. To reduce further amplification in the genome, the host prevents transcription of these now endogenous retroviruses (ERVs) through epigenetic repression and, with evolutionary time, ERVs are incapacitated by ...
Mihaela Chisca +3 more
wiley +1 more source
The impact of diagnosis delay on European patients with generalised myasthenia gravis
Abstract Objective The objective was to determine the mean duration of diagnosis delay for patients with myasthenia gravis from five European countries and explore the impact of >1 year diagnosis delay. Methods Patients with myasthenia gravis (N = 387) from Europe (France/Germany/Italy/Spain/United Kingdom) and their physicians participated in the ...
Elena Cortés‐Vicente +12 more
wiley +1 more source
Calcium channel autoantibodies in the lambert‐eaton myasthenic syndrome
We have tested 36 patients with the Lambert‐Eaton myasthenic syndrome for serum antibodies to voltage‐gated calcium channels by using an immunoprecipitation assay with [125I] ω‐conotoxin–labeled voltage‐gated calcium channels extracted from a human ...
Newsom-Davis, John +7 more
core +1 more source
Clinical and genetic basis of congenital myasthenic syndromes
Neuromuscular junction disorders represent a wide group of neurological diseases characterized by weakness, fatigability and variable degrees of appendicular, ocular and bulbar musculature involvement.
Paulo Victor Sgobbi de Souza +5 more
doaj +1 more source

