Progressive Changes in Brain Morphology in People With Idiopathic Generalized Epilepsy. [PDF]
Xiao F +14 more
europepmc +1 more source
Alterations of Cerebral Perfusion and Functional Connectivity in Children With Idiopathic Generalized Epilepsy. [PDF]
Chen G +12 more
europepmc +1 more source
Progressive Parkinsonism in PPP2R5D‐Related Neurodevelopmental Disorder
ABSTRACT PPP2R5D‐related neurodevelopmental disorder (Houge–Janssens syndrome type 1) is a rare autosomal dominant condition characterized by macrocephaly, intellectual disability, and epilepsy. Progressive parkinsonism is an emerging adult phenotype that neurologists should be aware of since timely genetic diagnosis opens the door to disease‐modifying
Katerina Bernardi +6 more
wiley +1 more source
Ictal eructation in a case of idiopathic generalized epilepsy. [PDF]
Shekar A, Koneru S, Szabó CÁ.
europepmc +1 more source
Replacement of Valproic Acid with New Anti-Seizure Medications in Idiopathic Generalized Epilepsy. [PDF]
Fujimoto A +4 more
europepmc +1 more source
The Impact of Caring for a Child With Juvenile Idiopathic Arthritis on Caregiver Quality of Life
Objective Juvenile idiopathic arthritis (JIA) impacts children and their families, often increasing caregiver burden and diminishing quality of life. This study assessed the care‐related quality of life of parent‐caregivers of children with JIA using the Care‐Related Quality of Life instrument (CarerQol), identified the most affected caregiving ...
Deborah A. Marshall +105 more
wiley +1 more source
Increased volumes of the precuneus and the pallidum in idiopathic generalized epilepsy. [PDF]
Hannoun S +6 more
europepmc +1 more source
Seizure control in mono- and combination therapy in a cohort of patients with Idiopathic Generalized Epilepsy. [PDF]
Pipek LZ, Pipek HZ, Castro LHM.
europepmc +1 more source
Glymphatic System Dysfunction and its Associated Factors in Wilson's Disease: A DTI–ALPS Study
Glymphatic function, assessed by DTI‐ALPS index, was impaired in neurological Wilson's disease compared with hepatic phenotype and controls. Age, AST, and UWDRS‐I score independently predicted dysfunction, linking neurodegeneration, liver injury, and altered glymphatic activity. ABSTRACT Background Wilson's disease (WD) is a genetic disorder of copper (
Ling Zhu +14 more
wiley +1 more source
Association of GABRG2 gene polymorphisms with idiopathic generalized epilepsy in Egyptian children: a case-control study. [PDF]
Wahba Y +8 more
europepmc +1 more source

