Detailansicht

Wissensnetz

Person

Renzo Guerrini

Neurologe

Name	Renzo Guerrini
Ort	Italien
Beruf	Neurologe (charakteristischer Beruf)
Beziehung	Kinderpsychiatrie (Thema)
Quelle	BN
Datensatztyp	Person
GND-Nummer	1189744295
Datensatz-ID	1189744295
Beteiligt an alle anzeigen Additional Results from Two Randomized, Placebo-Controlled Trials of Stiripentol in Dravet Syndrome Highlight a Rapid Antiseizure Efficacy with Longer Seizure-Free Periods Morphometric network-based abnormalities correlate with psychiatric comorbidities and gene expression in PCDH19-related developmental and epileptic encephalopathy Steps to Improve Precision Medicine in Epilepsy Additive effect of DNAJC30 and NDUFA9 mutations causing Leigh syndrome Efficacy and Safety of Long-Term Treatment with Stiripentol in Children and Adults with Drug-Resistant Epilepsies: A Retrospective Cohort Study of 196 Patients Defective IGF-1 prohormone N-glycosylation and reduced IGF-1 receptor signaling activation in congenital disorders of glycosylation Rare and Complex Epilepsies from Childhood to Adulthood: Requirements for Separate Management or Scope for a Lifespan Holistic Approach? International consensus recommendations on the diagnostic work-up for malformations of cortical development Multiple genomic copy number variants associated with periventricular nodular heterotopia indicate extreme genetic heterogeneity White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA Epilepsy study The landscape of epilepsy-related GATOR1 variants

Hinweis

Die Betaversion beinhaltet noch nicht alle Funktionen und Informationen des Katalogs des DNB-Portals. Falls Sie Informationen vermissen oder ein Medium bestellen wollen, besuchen Sie bitte die entsprechende Seite im Katalog des DNB-Portals über folgenden Link:

Katalog der Deutschen Nationalbibliothek

Renzo Guerrini

Additional Results from Two Randomized, Placebo-Controlled Trials of Stiripentol in Dravet Syndrome Highlight a Rapid Antiseizure Efficacy with Longer Seizure-Free Periods

Morphometric network-based abnormalities correlate with psychiatric comorbidities and gene expression in PCDH19-related developmental and epileptic encephalopathy

Steps to Improve Precision Medicine in Epilepsy

Additive effect of DNAJC30 and NDUFA9 mutations causing Leigh syndrome

Efficacy and Safety of Long-Term Treatment with Stiripentol in Children and Adults with Drug-Resistant Epilepsies: A Retrospective Cohort Study of 196 Patients

Defective IGF-1 prohormone N-glycosylation and reduced IGF-1 receptor signaling activation in congenital disorders of glycosylation

Rare and Complex Epilepsies from Childhood to Adulthood: Requirements for Separate Management or Scope for a Lifespan Holistic Approach?

International consensus recommendations on the diagnostic work-up for malformations of cortical development

Multiple genomic copy number variants associated with periventricular nodular heterotopia indicate extreme genetic heterogeneity

White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA Epilepsy study

The landscape of epilepsy-related GATOR1 variants