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List of works by Tiziana Granata

A role for inflammation in status epilepticus is revealed by a review of current therapeutic approaches.

scientific article published on September 2013

Adult-onset Rasmussen's encephalitis: anatomical-electrographic-clinical features of 7 Italian cases

scientific article

An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy

scientific article published on 16 July 2007

Antagonism of peripheral inflammation reduces the severity of status epilepticus.

scientific article

Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsy

scientific article published in March 2011

Band heterotopia: Correlation of outcome with magnetic resonance imaging parameters ⬇️

scientific article published on October 1, 1994

Basal ganglia dysmorphism in patients with Aicardi syndrome

scientific article published on 04 December 2020

Blood–brain barrier dysfunction and epilepsy: Pathophysiologic role and therapeutic approaches ⬇️

scientific article published on August 20, 2012

Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations.

scientific article published on 22 March 2007

Clinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations

scientific article published on 15 February 2017

Clinical and genetic features of paroxysmal kinesigenic dyskinesia in Italian patients

article

Clinical course and variability of non-Rasmussen, nonstroke motor and sensory epilepsia partialis continua: a European survey and analysis of 65 cases

scientific article published on 14 February 2011

Cognitive and neuropsychological evolution in children with anti-NMDAR encephalitis.

scientific article published on 17 February 2016

Cognitive development in Dravet syndrome: A retrospective, multicenter study of 26 patients

scientific article published in January 2011

Comparative Pharmacokinetic Study of Chewable and Conventional Carbamazepine in Children

scientific article published in January 1993

Comprehensive care of children with Dravet syndrome ⬇️

scientific article (publication date: April 2011)

Congenital malformations due to antiepileptic drugs

scientific article published in February 1999

Defining the electroclinical phenotype and outcome of PCDH19-related epilepsy: A multicenter study

scientific article published on 19 November 2018

Double cortex syndrome: electroclinical study of three cases.

scientific article

Dravet syndrome: early clinical manifestations and cognitive outcome in 37 Italian patients.

scientific article published on 24 October 2009

Early add-on immunoglobulin administration in Rasmussen encephalitis: the hypothesis of neuroimmunomodulation.

scientific article published on 31 August 2011

Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world study

scientific article published on 18 September 2020

Electroclinical features and long-term outcome of cryptogenic epilepsy in children with Down syndrome.

scientific article published on 27 August 2013

Electroclinical spectrum of the neuronal ceroid lipofuscinoses associated with CLN6 mutations

scientific article published on 26 June 2015

Electroencephalographic (EEG) Photoparoxysmal Responses Under 5 Years of Age: Diagnostic Implications and Peculiarities.

scientific article

Epilepsy in type 1 Chiari malformation ⬇️

scientific article published on December 1, 2011

Epileptic and imaging findings in perinatal hypoxic-ischemic encephalopathy with ulegyria.

scientific article published in August 2003

Epileptic phenotypes in children with early-onset mitochondrial diseases

scientific article published on 06 June 2019

Familial Occurrence of Febrile Seizures and Epilepsy in Severe Myoclonic Epilepsy of Infancy (SMEI) Patients with SCN1A Mutations

Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype

scientific article published on 21 August 2015

Focal seizure, focal dyskinesia, or both? A complex motor phenomenon reveals anti-NMDAR encephalitis

scientific article published in April 2015

Focal seizures versus epileptic spasms in children with focal cortical dysplasia and epilepsy onset in the first year

scientific article published on 26 November 2014

Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy

scientific article

HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyond

scientific article published on 01 November 2018

Hemispherotomy and functional hemispherectomy: indications and outcome.

scientific article published in November 2009

Hemispherotomy in Rasmussen encephalitis: long-term outcome in an Italian series of 16 patients.

scientific article

ICTAL EEG Fast Activity in West Syndrome: From Onset to Outcome

scientific article published on 06 September 2007

Immune-mediated epilepsies.

scientific article

Impaired surface αβγ GABA(A) receptor expression in familial epilepsy due to a GABRG2 frameshift mutation

scientific article published on 13 October 2012

Inflammatory pathways of seizure disorders

scientific article published on 16 December 2013

Joubert syndrome with bilateral polymicrogyria: clinical and neuropathological findings in two brothers.

scientific article published in July 2009

Lamotrigine Plasma Concentrations in Children and Adults

scientific article published in December 1997

Long-term outcome after limited cortical resections in two cases of adult-onset Rasmussen encephalitis

scientific article published on 04 April 2014

Malformations in Offspring of Women with Epilepsy: A Prospective Study

scientific article published on 01 September 1999

Malformations in offspring of 305 epileptic women: a prospective study

scientific article published on March 1, 1992

Management of the patient with medically refractory epilepsy.

scientific article published on December 2009

Metabolic and degenerative disorders.

scientific article published on January 2012

Neonatal developmental and epileptic encephalopathy due to autosomal recessive variants in SLC13A5 gene

scientific article published on 16 October 2020

Neuromuscular syndrome associated with the 3291T→C mutation of mitochondrial DNA: a second case

scientific article published in August 2000

Neuronal migration disorders and epilepsy: a morphological analysis of three surgically treated patients.

scientific article published on December 1996

No evidence of GABRG2 mutations in severe myoclonic epilepsy of infancy

scientific article published in March 2003

Overview of presurgical assessment and surgical treatment of epilepsy from the Italian League Against Epilepsy.

scientific article published on October 2013

Paroxysmal dyskinesias in childhood

scientific article published in March 2003

Partial Seizures Associated with Antiphospholipid Antibodies in Childhood

scientific article published in October 1998

Periventricular nodular heterotopia

scientific article published in 2007

Periventricular nodular heterotopia: epileptogenic findings.

scientific article published in November 1997

Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation

scientific article published in November 2006

Rasmussen encephalitis tissue transfer program

scientific article published in June 2016

Rasmussen?s syndrome ⬇️

scientific article published on October 1, 2003

Rasmussen’s encephalitis: update on pathogenesis and treatment

scientific article published on 01 November 2003

Reflex myoclonic epilepsy in infancy: a multicenter clinical study.

scientific article

Refractory absence epilepsy and glut1 deficiency syndrome: a new case report and literature review

scientific article published on 03 June 2014

Revelation of a novel CLN5 mutation in early juvenile neuronal ceroid lipofuscinosis.

scientific article

Schizencephaly

scientific article published in 2007

Screening of SLC2A1 in a large cohort of patients suspected for Glut1 deficiency syndrome: identification of novel variants and associated phenotypes

scientific article published on 20 March 2019

Seizure-promoting effect of blood-brain barrier disruption

scientific article

Single-dose pharmacokinetics of lamotrigine in children: influence of age and antiepileptic comedication.

scientific article published in June 2001

Small 6q16.1 Deletions Encompassing POU3F2 Cause Susceptibility to Obesity and Variable Developmental Delay with Intellectual Disability

scientific article

Somatic and germline mosaicisms in Severe Myoclonic Epilepsy of Infancy

scientific article published in 2006

Spectral properties of EEG fast activity ictal discharges associated with infantile spasms.

scientific article

Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With <i>KCNC2</i> Pathogenic Variants

scientific article published on 21 March 2022

Suppressive efficacy by a commercially available blue lens on PPR in 610 photosensitive epilepsy patients

scientific article

Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective multicentre study

scientific article published on 20 October 2016

The blood-brain barrier hypothesis in drug resistant epilepsy

scientific article published on 16 January 2012

Transition into adulthood: tuberous sclerosis complex, Sturge-Weber syndrome, and Rasmussen encephalitis.

scientific article published on August 2014

Transporters in drug-refractory epilepsy: clinical significance.

scientific article published on January 2010

VARS2 and TARS2 mutations in patients with mitochondrial encephalomyopathies

scientific article published on 24 June 2014

Vagus nerve stimulation for drug-resistant Epilepsia Partialis Continua: report of four cases.

scientific article published on 8 September 2013

Variant late infantile ceroid lipofuscinoses associated with novel mutations in CLN6

scientific article published on 07 January 2009

West syndrome associated with 14q12 duplications harboring FOXG1

scientific article published on 2 May 2011

Xp22.3 genomic deletions involving the CDKL5 gene in girls with early onset epileptic encephalopathy

scientific article

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