Carmen Campana

Congenital Hyperinsulinism of a Large Italian Cohort: A Retrospective Study

Francesco Tagliaferri, Roberta Iannuzzi, Gabriele Canciani, Silvia Maria Bernabei et autres

INTRODUCTION: To evaluate and describe the diagnostic process, medical, nutritional, and surgical approach, and neurological outcome, we report data from a large Italian cohort of patients with congenital hyperinsulinism (CHI). METHODS: We retrospectively analyzed 154 CHI patients admitted to Ospedale Pediatrico Bambino …

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Enteral formula compared to Nissen-Fundoplication: Data from a retrospective analysis on tolerance, utility, applicability, and safeness in children with neurological diseases

Chiara Maria Trovato, Teresa Capriati, Giulia Bolasco, Carla Brusco et autres

Objectives and study Approximately 46–90% of children with neurological disorders (NDs) suffer from gastrointestinal diseases, such as gastro-esophageal reflux disease (GERD), constipation, or malnutrition. Therefore, enteral feeding is often necessary to achieve nutritional requirements. The treatment of GERD could be based on …

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A new phenotype of aldolase a deficiency in a 14 year-old boy with epilepsy and rhabdomyolysis – case report

Lucia Santoro, Dorina Pjetraj, Virtut Velmishi, Carmen Campana et autres

BACKGROUND: Glycogen storage disease type XII is a rare metabolic disease resulting from Aldolase A deficiency that causes muscle glycogen accumulation, with crisis of rhabdomyolysis and hemolytic anemia. In the very few cases described, rhabdomyolysis crises are caused by fever and/or exercise …

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Ketogenic diet as elective treatment in patients with drug-unresponsive hyperinsulinemic hypoglycemia caused by glucokinase mutations

Arianna Maiorana, Stefania Caviglia, Benedetta Greco, Paolo Alfieri et autres

BACKGROUND: Hyperinsulinemic hypoglycemia (HI) is the most frequent cause of recurrent hypoglycemia in children. Despite diagnostic and therapeutic advances, it remains an important cause of morbidity, leading to neurological complications, such as psychomotor retardation and epilepsy. Patients with diffuse drug-unresponsive HI manifest …

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Dietary lipids in glycogen storage disease type III: A systematic literature study, case studies, and future recommendations

Alessandro Rossi, Irene J. Hoogeveen, Vanessa B. Bastek, Foekje de Boer et autres

A potential role of dietary lipids in the management of hepatic glycogen storage diseases (GSDs) has been proposed, but no consensus on management guidelines exists. The aim of this study was to describe current experiences with dietary lipid manipulations in hepatic GSD …

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P170 Ketogenic diet: new applications beyond epilepsy

Domenica Elia, Carmen Campana, Damiano De Giorgio, Silvia Maria Bernabei et autres

7. Cathodal transcranial direct current stimulation reduces seizure frequency and modulates brain functional connectivity with drug-resistant temporal lobe epilepsy: A sham controlled study

Giovanni Assenza, Carlo Domenico Cottone, Franca Tecchio, Giovanni Pellegrino et autres

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11. Clinical usefulness of synchronous tilt testing and video-EEG monitoring in patients diagnosed with epilepsy

Giovanni Assenza, Antonella Benvenga, Carmen Campana, Federica Assenza et autres

Inflammation and iron metabolism in adult patients with epilepsy: Does a link exist?

Mario Tombini, Rosanna Squitti, Fabio Cacciapaglia, Mariacarla Ventriglia et autres

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131. Antiepileptic drugs and risk of suicide in patients with epilepsy

Carmen Campana, Matteo Caporro, A. Saglimbene, M. Tasillo et autres

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[Clinical course of epileptic seizures in Rett's syndrome].

M Nieto-Barrera, M Nieto-Jiménez, Fernando López Díaz, Carmen Campana et autres

INTRODUCTION: Seventeen girls diagnosed as Rett syndrome (RS) patients suffer or have suffered epileptic fits; we have analyzed the evolution of these seizures. The RS diagnosis is based on criteria established by the Rett Syndrome Diagnostic Criteria Working Group in 1988. PATIENTS …

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