Results 41 to 50 of about 14,013 (211)
KBG syndrome: A scoping review of electroclinical features of patients with epilepsy
Epileptic Disorders, EarlyView.Abstract Background and Objectives KBG syndrome is a rare autosomal developmental disorder caused by pathogenic variants of the ANKRD11 gene. This scoping review aimed to explore all current literature data regarding clinical and electroencephalographic features of patients with KBG syndrome and epilepsy. Materials and Methods We conducted a literature
Stefania Kalampokini +6 more
wiley +1 more source
Behavior problems associated with brain heterotopia
European Psychiatry, 2021 Introduction Brain heterotopia represent a group of rare malformations with a heterogeneous phenotype, ranging from asymptomatic to severe clinical picture (resistant epilepsy, severe developmental delay). The etiology is multifactorial, including both
M. Budisteanu +12 more
doaj +1 more source
Epilepsia, EarlyView.Abstract Objective Detection of epilepsy‐causing structural brain lesions on magnetic resonance imaging (MRI) is critical for diagnosis, prognosis, and treatment planning in people with epilepsy. We aimed to establish an epilepsy‐directed multisite harmonized 3‐T MRI acquisition protocol for the Australian Epilepsy Project (AEP) and describe the ...
David N. Vaughan +19 more
wiley +1 more source
Epilepsia, EarlyView.Abstract Objective Subclinical seizures (SCSs) remain an understudied aspect of presurgical evaluation in patients with drug‐resistant epilepsy (DRE), with uncertain prevalence, distribution among epilepsy types, and predictive value for surgical outcomes.
Pilar Bosque‐Varela +6 more
wiley +1 more source
Congenital geniculate quadruple sectoranopia with occipital heterotopia
American Journal of Ophthalmology Case Reports, 2020 Purpose: To report a case of congenital geniculate quadruple sectoranopia associated with occipital heterotopia. Observations: A 51-year-old healthy woman was incidentally found to have a left incongruous quadruple sectoranopia.
Kaori Hanai +3 more
doaj +1 more source
Epilepsia, EarlyView.Abstract Objective Quantitative assessment of extent of tissue resection following epilepsy surgery requires accurate delineation of the resection cavity on postoperative magnetic resonance imaging (MRI). Current methods for resection cavity masking are time‐consuming and labor‐intensive, and existing automated approaches exhibit variable segmentation ...
Jieun Seo +91 more
wiley +1 more source
Epilepsia Open, EarlyView.Abstract Objectives Adults with developmental and epileptic encephalopathies (DEEs) often enter adult neurology care without etiologic clarification because of incomplete transition from pediatric services, outdated investigations, and attenuation of childhood electro‐clinical features over time.
Giuseppe d’Orsi +10 more
wiley +1 more source
Congenital short bowel syndrome: Clinical aspects by systematic review
JPGN Reports, EarlyView.Abstract Objectives Congenital short bowel syndrome (CSBS) is a rare intestinal disorder characterized by inborn shortening of the bowel with mainly mutations in Coxsackie and Adenovirus receptor‐like membrane protein (CLMP) and Filamin A (FLNA) genes.
Barblin Remund +2 more
wiley +1 more source
ACM SIGGRAPH 2019 Virtual, Augmented, and Mixed Reality, 2019 Entre o texto (BARTHES, 1988, 2003) e sua individuação (SIMONDON, 2005; DELEUZE, 1980, 1988, 2002; BARTHES, 2005; MACÉ, 2018) biografa-se o pátio da universidade, rabiscando com as cadências de quem passa. Com os deveres e as obrigações em meio às bicicletas em ziguezague. Com motores. Entre vãos. Ordens. Velocidades e lentidões.
Noa Kaplan, Szilvia Ruszev
openaire +5 more sources