Results 141 to 150 of about 76,096 (261)

Data‐Driven Insights into Hyperkinetic Disorders in Neurodevelopmental Syndromes and Epileptic Encephalopathies

Movement Disorders Clinical Practice, EarlyView.
Abstract Background Childhood‐onset hyperkinetic movement disorders occur in a range of genetic conditions. Recently, there has been an increase in recognition of hyperkinetic movement disorders, mainly dystonia, chorea and dyskinesia, with monogenic conditions associated with neurodevelopmental delay (NDD) and also with developmental and epileptic ...
Hugo Morales‐Briceño, Shekeeb S. Mohammad, Rajeshwar Reddy Angiti, Velda Han, Michel Tchan, Russell C. Dale, Victor S.C. Fung   +6 more
wiley   +1 more source

Right Atrial Myxoma Presenting as Fever of Unknown Origin: A Rare Case Report. [PDF]

Clin Case Rep
Basnet A, Maskey A, Koirala P, Joshi S, Mainali G.   +4 more
europepmc   +1 more source

Rare Presentation of Fever of Unknown Origin: A Diagnostic Challenge. [PDF]

Cureus
Kondolay T, Samifanni R, Wang G, Abraham J, Shahzad MA.   +4 more
europepmc   +1 more source

The Potential for Absolute Temperature Imaging Based on Brain Metabolites Using an FID‐Shifting Approach in Gradient Echo Planar Spectroscopic Imaging (GREPSI)

Magnetic Resonance in Medicine, EarlyView.
ABSTRACT Purpose To implement and evaluate an efficient method for absolute temperature measurement using a gradient echo implementation of the echo planar spectroscopic imaging (EPSI) sequence. Methods The gradient echo EPSI sequence (GREPSI) utilizes an oscillating readout gradient together with continuous signal readout after slab selective ...
Dennis L. Parker, Henrik Odéen, Peyton Wong, Seong‐Eun Kim, Wesley Judd, Duane D. Blatter   +5 more
wiley   +1 more source

Unsupervised clustering of PET/CT features in fever of unknown origin (FUO) and inflammation of unknown origin (IUO). [PDF]

Front Med (Lausanne)
Ceylan S, Ceylan B, Olmuscelik O, Cakir T.   +3 more
europepmc   +1 more source

Real‐World Safety and Effectiveness of Glatiramer Acetate in Patients With Multiple Sclerosis: Final Results of Post‐Marketing Surveillance in Japan

Neurology and Clinical Neuroscience, EarlyView.
ABSTRACT Background Glatiramer acetate is an injectable disease‐modifying therapy indicated for multiple sclerosis (MS). Aim To evaluate the real‐world safety and effectiveness of glatiramer acetate for MS in Japan. Methods A prospective, multicenter, observational, all‐case post‐marketing survey was conducted in Japan between November 2015 and March ...
Masaaki Niino, Eriko Hayashi, Mai Itani, Jun‐ichi Kira   +3 more
wiley   +1 more source

Diagnostic Value of Lymph Node Biopsy in Adult Patients with Classic Fever of Unknown Origin Accompanied by Lymphadenopathy. [PDF]

J Clin Med
Liu H, Ruan G, Shi X, Liu X, Ge Y.
europepmc   +1 more source

Clinical Value of Metagenomic Next‐Generation Sequencing Versus Conventional Methods in Diagnosing Cryptococcal Infection After Kidney Transplantation

Organ Medicine, EarlyView.
This retrospective study evaluated metagenomic next‑generation sequencing (mNGS) against conventional methods (India ink, culture, antigen) for diagnosing cryptococcal infection in 16 kidney transplant recipients. mNGS showed a significantly higher positivity rate (93.8% vs 62.5%, p = 0.031) and shorter turnaround time (24 vs. 120 h, p < 0.001).
Luhao Liu, Rongxin Chen, Haonan Lin, Yuhe Guo, Guanghui Li, Jiali Fang, Zheng Chen   +6 more
wiley   +1 more source

Gastrointestinal-Predominant ALK-Negative Systemic Anaplastic Large Cell Lymphoma Presenting as Fever of Unknown Origin: Case Report. [PDF]

Korean J Helicobacter Up Gastrointest Res
Kim CH, Lee SH.
europepmc   +1 more source

Perianesthetic Complications in Genetic Mitochondrial Disease: A Review of Case Reports

Pediatric Anesthesia, EarlyView.
ABSTRACT Background Genetic mitochondrial diseases (GMDs) are a large group of genetically and clinically heterogeneous disorders caused by defects in genes encoding mitochondrial components. GMDs are grouped into named syndromes based on clinical presentation, for example, Leigh syndrome (LS).
Brittany M. Johnson, Simon C. Johnson
wiley   +1 more source