List of works - Hadassa Goldberg-Stern

PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome

scientific article published on January 2012

Genotype-phenotype analysis of human frontoparietal polymicrogyria syndromes

scientific article

Attention-deficit disorders and epilepsy in childhood: incidence, causative relations and treatment possibilities

scientific article published on June 2009

Glucose transporter 1 deficiency in the idiopathic generalized epilepsies

scientific journal article

Early onset epileptic encephalopathy caused by de novo SCN8A mutations

scientific article published on 2 June 2014

Clinical spectrum and medical treatment of children with electrical status epilepticus in sleep (ESES).

scientific article

PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizures

scientific article

Severe refractory status epilepticus owing to presumed encephalitis

scientific article published on March 2005

Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome

scientific article published on 15 May 2015

De novo KCNB1 mutations in infantile epilepsy inhibit repetitive neuronal firing

scientific article

Autoimmune epilepsy: distinct subpopulations of epilepsy patients harbor serum autoantibodies to either glutamate/AMPA receptor GluR3, glutamate/NMDA receptor subunit NR2A or double-stranded DNA.

scientific article published in June 2005

Broad phenotypic heterogeneity due to a novel SCN1A mutation in a family with genetic epilepsy with febrile seizures plus

scientific article published on 20 November 2013

Autoimmune epilepsy: some epilepsy patients harbor autoantibodies to glutamate receptors and dsDNA on both sides of the blood-brain barrier, which may kill neurons and decrease in brain fluids after hemispherotomy

scientific article published on September 2004

Outcome of children with juvenile absence epilepsy

scientific article

Does a normalizing electroencephalogram in benign childhood epilepsy with centrotemporal spikes abort attention deficit hyperactivity disorder?

scientific article published on October 2012

Paternal germline mosaicism of a SCN2A mutation results in Ohtahara syndrome in half siblings

scientific article published on 18 April 2014

RARS2 mutations cause early onset epileptic encephalopathy without ponto-cerebellar hypoplasia

scientific article published on 2 March 2016

Multiplex families with epilepsy: Success of clinical and molecular genetic characterization

scientific article published on 22 January 2016

Late infantile neuronal ceroid lipofuscinosis: a new mutation in Arabs

scientific article published in October 2009

Idiopathic photosensitive occipital epilepsy: clinical and electroencephalographic (EEG) features

scientific article

GnRH agonist treatment in girls with precocious puberty does not compromise post-pubertal uterine size

scientific article published on 15 December 2006

The mystery of electroencephalography in acute lymphoblastic leukemia

scientific article published on 2 February 2011

List of works by Hadassa Goldberg-Stern

PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome

Genotype-phenotype analysis of human frontoparietal polymicrogyria syndromes

Attention-deficit disorders and epilepsy in childhood: incidence, causative relations and treatment possibilities

Glucose transporter 1 deficiency in the idiopathic generalized epilepsies

Early onset epileptic encephalopathy caused by de novo SCN8A mutations

Clinical spectrum and medical treatment of children with electrical status epilepticus in sleep (ESES).

PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizures

Severe refractory status epilepticus owing to presumed encephalitis

Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome

De novo KCNB1 mutations in infantile epilepsy inhibit repetitive neuronal firing

Autoimmune epilepsy: distinct subpopulations of epilepsy patients harbor serum autoantibodies to either glutamate/AMPA receptor GluR3, glutamate/NMDA receptor subunit NR2A or double-stranded DNA.

Broad phenotypic heterogeneity due to a novel SCN1A mutation in a family with genetic epilepsy with febrile seizures plus

Autoimmune epilepsy: some epilepsy patients harbor autoantibodies to glutamate receptors and dsDNA on both sides of the blood-brain barrier, which may kill neurons and decrease in brain fluids after hemispherotomy

Outcome of children with juvenile absence epilepsy

Does a normalizing electroencephalogram in benign childhood epilepsy with centrotemporal spikes abort attention deficit hyperactivity disorder?

Paternal germline mosaicism of a SCN2A mutation results in Ohtahara syndrome in half siblings

RARS2 mutations cause early onset epileptic encephalopathy without ponto-cerebellar hypoplasia

Multiplex families with epilepsy: Success of clinical and molecular genetic characterization

Late infantile neuronal ceroid lipofuscinosis: a new mutation in Arabs

Idiopathic photosensitive occipital epilepsy: clinical and electroencephalographic (EEG) features

GnRH agonist treatment in girls with precocious puberty does not compromise post-pubertal uterine size

The mystery of electroencephalography in acute lymphoblastic leukemia