Exploring patient experiences of illness and diagnostic pathways in self-reported Q fever cases. [PDF]
Tan T, Heller J, Hayes L, Wiethoelter A.
europepmc +1 more source
Ictal semiology in precuneus seizures: A systematic review
Abstract Objective To evaluate the ictal semiology in seizures originating in the precuneus and to help guide seizure interpretation within the framework of presurgical evaluation. Methods This systematic review followed a Preferred Reporting Items for Systematic Reviews and Meta‐Analyses (PRISMA) and a Quality Assessment tool for Diagnostic Accuracy ...
Erika Ignatius +8 more
wiley +1 more source
Intravenous Immunoglobulin Resistant Incomplete Kawasaki Disease in a 4-Month-Old Infant: A Case Report. [PDF]
Yadav S +8 more
europepmc +1 more source
Abstract Background and Objectives Muscle‐Eye‐Brain disease (MEB) is a dystroglycanopathy that belongs to the congenital muscular dystrophies. Central nervous system manifestations include congenital brain abnormalities, neurodevelopmental delay, and epilepsy, making it a rare but important cause of developmental and epileptic encephalopathy.
Stefania Kalampokini +6 more
wiley +1 more source
Clinical Characteristics of <i>Mycoplasma pneumoniae</i> Pneumonia in Children and Analysis of the Risk Factors for Severe <i>Mycoplasma pneumoniae</i> Pneumonia. [PDF]
Yang G +6 more
europepmc +1 more source
Abstract Objective Addressing the poorly understood impact of pediatric epilepsy on neurodevelopment, this large‐scale study delineates age‐ and sex‐stratified neurostructural trajectories in magnetic resonance imaging (MRI)‐negative pediatric epilepsy to identify periods of maximal developmental divergence from healthy controls.
Yingfan Wang +10 more
wiley +1 more source
Antibiotic Prescribing Patterns in Hospitalized Pediatric Patients With Clinically Suspected Enteric Fever: A Descriptive Study. [PDF]
Khan GAK +4 more
europepmc +1 more source
Behavioral and epileptic phenotypes in a CHD2‐related developmental delay model
Abstract Objective Heterozygous loss‐of‐function mutations in the CHD2 gene, encoding chromodomain helicase DNA‐binding protein 2, are associated with severe childhood onset epilepsy, global developmental delay, and autistic features. Animal models that accurately recapitulate human phenotypes are crucial for understanding rare neurodevelopmental ...
Anat Mavashov +10 more
wiley +1 more source
Clinical Management of Severe <i>Cupriavidus gilardii</i> Superinfection After Influenza a Virus Pneumonia: A Case Report and Literature Review. [PDF]
Guo C, Sun C, Zheng J, Zhou Q, Liang Y.
europepmc +1 more source

