Results 131 to 140 of about 281,352 (313)
Management of ring chromosome 20 syndrome: Narrative review and consensus recommendations
Epilepsia, EarlyView.Abstract Ring chromosome 20 (ring 20) is a rare genetic condition usually presenting as developmental and epileptic encephalopathy. The disease is caused by fusion of the long and short arms of chromosome 20. Patients are symptomatic even if there is no loss of genetic material.
Asma Khamis +8 more
wiley +1 more source
The dynamic functional connectivity peak index: Detection of interictal epileptic activity with fMRI
Epilepsia, EarlyView.Abstract Objective Epileptogenic zone (EZ) localization is crucial for surgical treatment of patients with medication‐resistant epilepsy. Although simultaneous electroencephalography (EEG) and functional magnetic resonance imaging (fMRI) can detect interictal discharges for EZ localization, clinical adoption is limited by the need for specialized ...
Lucas E. Sainburg +9 more
wiley +1 more source
, 2009 Riconosciuta la via Emilia come un gigantesco decumano sul quale l'intera regione si appoggia, si illustrano le sue caratteristiche dfal punto di vista dello sviluppo dell'insediamento e delle strutture ...
FARINELLI, FRANCO
core
Epilepsia Open, EarlyView.Abstract Objectives Temporal lobe epilepsy (TLE) impacts multiple brain networks. Aberrant functional connectivity has been demonstrated in resting‐state networks (RSNs) that mediate higher brain functions in TLE. This study aimed to identify the reproducible patterns of altered functional connectivity in TLE in a large, international cohort through ...
Victoria Ives‐Deliperi +28 more
wiley +1 more source
Genetic landscape of patients with atypical absence status epilepticus: A systematic review
Epilepsia Open, EarlyView.Abstract Atypical absence status epilepticus (AASE) is a rare subtype of nonconvulsive status epilepticus (NCSE), characterized by clouding of consciousness and continuous or fluctuating epileptiform activity, generally at a frequency below 3 Hz. Only sparse literature exists on the genetic conditions associated with it.
Maria Cristina Cioclu +2 more
wiley +1 more source
El Argonauta EspañolThe objective of this study is to edit and study the unpublished correspondence of Emilia Pardo Bazán Munilla Jose Ortega, editor of The Fair and its literary supplement.
Dolores Thion Soriano-Mollá
doaj +1 more source
Gli amministratori della Provincia. Intervista a Giuseppe Gherpelli e Ione Bartoli [PDF]
, 2014 - Intervista a Ione Bartoli, Reggio Emilia, 15/02/2011.
Federico Ferretti, Alberto Ferraboschi
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European Eating Disorders Review, EarlyView.ABSTRACT Objective Approximately 25% of individuals with eating disorders develop severe and enduring eating disorders (SEEDs); yet effective treatments remain limited. This study explored lived experiences of SEEDs, focussing on past treatments, as well as current needs and hopes. Method Twenty participants with eating disorders of ≥ 7 years and prior
Emilia Kotilahti +3 more
wiley +1 more source
Emilia Pardo Bazán e Italia [PDF]
, 2009 The comparison with European nations in the late nineteenth century (crisis of ’98) constituted an imperative for the majority of Spanish intellectuals trying to help a solution of socio-ecomic problems and problems of identity of their homeland.
PABA, ANTONINA
core
BMJ Paediatrics OpenEase of access to primary care may be inversely related to non-emergency access to emergency room services (ERS). We assessed whether patients of general paediatricians working in networks have reduced the use of ERS in an Italian province.
Giulio Formoso +7 more
doaj +1 more source