Lista de obras - Deepak Gill - Dominio Público Uruguay

Accelerated long-term forgetting and behavioural difficulties in children with epilepsy.

artículo científico publicado en 2018

Accelerated long-term forgetting in children with idiopathic generalized epilepsy

artículo científico publicado en 2012

Accelerated long-term forgetting in children with temporal lobe epilepsy.

artículo científico publicado en 2014

Attention deficits in children with epilepsy: Preliminary findings.

artículo científico publicado en 2017

Atypical multifocal Dravet syndrome lacks generalized seizures and may show later cognitive decline

artículo científico publicado en 2013

Autoantibodies to neuronal antigens in children with new-onset seizures classified according to the revised ILAE organization of seizures and epilepsies.

artículo científico publicado en 2013

Autobiographical memory in children with Idiopathic Generalised Epilepsy.

artículo científico publicado en 2014

Autobiographical memory in children with temporal lobe epilepsy.

artículo científico

BRAT1 encephalopathy: a recessive cause of epilepsy of infancy with migrating focal seizures

artículo científico publicado en 2019

CHD2 myoclonic encephalopathy is frequently associated with self-induced seizures

artículo científico publicado en 2015

Cannabidiol for treating drug-resistant epilepsy in children: the New South Wales experience

scientific article published on 13 August 2018

Cerebrospinal fluid cyto-/chemokine profile during acute herpes simplex virus induced anti-N-methyl-d-aspartate receptor encephalitis and in chronic neurological sequelae.

artículo científico publicado en 2017

Corpus callosotomy outcomes in pediatric patients: A systematic review.

artículo científico publicado en 2016

Cortical Hypometabolism Demonstrated by PET in Relapsing NMDA Receptor Encephalitis ⬇️

artículo científico publicado el 1 de septiembre de 2010

Damaging de novo missense variants in EEF1A2 lead to a developmental and degenerative epileptic-dyskinetic encephalopathy

scientific article published on 20 March 2020

De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective study

artículo científico publicado en 2006

Dealing with a first seizure: accurate diagnosis and good management

scientific article published on 07 October 2018

Diagnostic yield of targeted massively parallel sequencing in children with epileptic encephalopathy

scientific article published on 28 May 2018

EpApp: Development and evaluation of a smartphone/tablet app for adolescents with epilepsy

artículo científico publicado en 2018

Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families

artículo científico publicado en 2009

Etiological associations and outcome predictors of acute electroencephalography in childhood encephalitis

artículo científico publicado en 2016

Eye movement disorders are an early manifestation of CACNA1A mutations in children

artículo científico publicado en 2016

Febrile infection-related epilepsy syndrome is not caused by SCN1A mutations

artículo científico publicado en 2012

GABRA1 and STXBP1: novel genetic causes of Dravet syndrome

artículo científico publicado en 2014

Immune-mediated steroid-responsive epileptic spasms and epileptic encephalopathy associated with VGKC-complex antibodies ⬇️

artículo científico publicado el 30 de agosto de 2011

Infectious and autoantibody-associated encephalitis: clinical features and long-term outcome.

artículo científico

Longitudinal study of accelerated long-term forgetting in children with genetic generalized epilepsy: Evidence of ongoing deficits

artículo científico publicado en 2017

Mortality in Dravet syndrome

artículo científico publicado en 2016

NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns

artículo científico publicado en 2020

Not all SCN1A epileptic encephalopathies are Dravet syndrome: Early profound Thr226Met phenotype

artículo científico publicado en 2017

Outcome of Early Juvenile Onset Metachromatic Leukodystrophy After Unrelated Cord Blood Transplantation: A Case Series and Review of the Literature.

artículo científico

Postencephalitic epilepsy and drug-resistant epilepsy after infectious and antibody-associated encephalitis in childhood: Clinical and etiologic risk factors

artículo científico publicado en 2015

Psychogenic non-epileptic seizures in children and adolescents: Part I - Diagnostic formulations.

artículo científico publicado en 2017

Psychogenic non-epileptic seizures in children and adolescents: Part II - explanations to families, treatment, and group outcomes

artículo científico publicado en 2017

Rare copy number variants are an important cause of epileptic encephalopathies

artículo científico publicado en 2011

Reduced complications from intracranial grid insertion by using a small grid size and a precise protocol during monitoring.

artículo científico publicado en 2015

Reduction of seizure frequency after epilepsy surgery in a patient with STXBP1 encephalopathy and clinical description of six novel mutation carriers

artículo científico publicado en 2013

Risk factors for complications during intracranial electrode recording in presurgical evaluation of drug resistant partial epilepsy

artículo científico publicado en 2009

Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome

artículo científico publicado en 2013

Seizure outcome after corpus callosotomy in a large paediatric series

artículo científico publicado en 2017

T2 hyperintensities in children with neurofibromatosis type 1 and their relationship to cognitive functioning

artículo científico publicado en 2007

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.

artículo científico publicado en 2013

The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures

scientific article published on 01 December 2019

The phenotypic spectrum of SCN8A encephalopathy

artículo científico publicado en 2015

The respiratory control of carbon dioxide in children and adolescents referred for treatment of psychogenic non-epileptic seizures

artículo científico publicado en 2017

The spectrum of SCN1A-related infantile epileptic encephalopathies

artículo científico publicado en 2007

Theory of Mind and social competence in children and adolescents with genetic generalised epilepsy (GGE): Relationships to epilepsy severity and anti-epileptic drugs

artículo científico publicado en 2018

VGKC antibodies in pediatric encephalitis presenting with status epilepticus.

artículo científico publicado en 2011

Lista de obras de Deepak Gill

Accelerated long-term forgetting and behavioural difficulties in children with epilepsy.

Accelerated long-term forgetting in children with idiopathic generalized epilepsy

Accelerated long-term forgetting in children with temporal lobe epilepsy.

Attention deficits in children with epilepsy: Preliminary findings.

Atypical multifocal Dravet syndrome lacks generalized seizures and may show later cognitive decline

Autoantibodies to neuronal antigens in children with new-onset seizures classified according to the revised ILAE organization of seizures and epilepsies.

Autobiographical memory in children with Idiopathic Generalised Epilepsy.

Autobiographical memory in children with temporal lobe epilepsy.

BRAT1 encephalopathy: a recessive cause of epilepsy of infancy with migrating focal seizures

CHD2 myoclonic encephalopathy is frequently associated with self-induced seizures

Cannabidiol for treating drug-resistant epilepsy in children: the New South Wales experience

Cerebrospinal fluid cyto-/chemokine profile during acute herpes simplex virus induced anti-N-methyl-d-aspartate receptor encephalitis and in chronic neurological sequelae.

Corpus callosotomy outcomes in pediatric patients: A systematic review.

Cortical Hypometabolism Demonstrated by PET in Relapsing NMDA Receptor Encephalitis ⬇️

Damaging de novo missense variants in EEF1A2 lead to a developmental and degenerative epileptic-dyskinetic encephalopathy

De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective study

Dealing with a first seizure: accurate diagnosis and good management

Diagnostic yield of targeted massively parallel sequencing in children with epileptic encephalopathy

EpApp: Development and evaluation of a smartphone/tablet app for adolescents with epilepsy

Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families

Etiological associations and outcome predictors of acute electroencephalography in childhood encephalitis

Eye movement disorders are an early manifestation of CACNA1A mutations in children

Febrile infection-related epilepsy syndrome is not caused by SCN1A mutations

GABRA1 and STXBP1: novel genetic causes of Dravet syndrome

Immune-mediated steroid-responsive epileptic spasms and epileptic encephalopathy associated with VGKC-complex antibodies ⬇️

Infectious and autoantibody-associated encephalitis: clinical features and long-term outcome.

Longitudinal study of accelerated long-term forgetting in children with genetic generalized epilepsy: Evidence of ongoing deficits

Mortality in Dravet syndrome

NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns

Not all SCN1A epileptic encephalopathies are Dravet syndrome: Early profound Thr226Met phenotype

Outcome of Early Juvenile Onset Metachromatic Leukodystrophy After Unrelated Cord Blood Transplantation: A Case Series and Review of the Literature.

Postencephalitic epilepsy and drug-resistant epilepsy after infectious and antibody-associated encephalitis in childhood: Clinical and etiologic risk factors

Psychogenic non-epileptic seizures in children and adolescents: Part I - Diagnostic formulations.

Psychogenic non-epileptic seizures in children and adolescents: Part II - explanations to families, treatment, and group outcomes

Rare copy number variants are an important cause of epileptic encephalopathies

Reduced complications from intracranial grid insertion by using a small grid size and a precise protocol during monitoring.

Reduction of seizure frequency after epilepsy surgery in a patient with STXBP1 encephalopathy and clinical description of six novel mutation carriers

Risk factors for complications during intracranial electrode recording in presurgical evaluation of drug resistant partial epilepsy

Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome

Seizure outcome after corpus callosotomy in a large paediatric series

T2 hyperintensities in children with neurofibromatosis type 1 and their relationship to cognitive functioning

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.

The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures

The phenotypic spectrum of SCN8A encephalopathy

The respiratory control of carbon dioxide in children and adolescents referred for treatment of psychogenic non-epileptic seizures

The spectrum of SCN1A-related infantile epileptic encephalopathies

Theory of Mind and social competence in children and adolescents with genetic generalised epilepsy (GGE): Relationships to epilepsy severity and anti-epileptic drugs

VGKC antibodies in pediatric encephalitis presenting with status epilepticus.