List of works by Antonietta Coppola

17q21.31 microdeletion syndrome: Description of a case further contributing to the delineation of Koolen-de Vries syndrome.

scientific article published on 17 February 2016

A clinical and genetic study of 33 new cases with early-onset absence epilepsy

scientific article

A pilot open-label trial of zonisamide in Unverricht-Lundborg disease

scientific article published on 11 October 2010

A pilot trial of levetiracetam in eyelid myoclonia with absences (Jeavons syndrome).

scientific article

Advances in genetic testing and optimization of clinical management in children and adults with epilepsy

scientific article published on 27 January 2020

CHD2 mutations: Only epilepsy? Description of cognitive and behavioral profile in a case with a new mutation

scientific article

Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new cases.

scientific article published in September 2006

Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization

scientific article published on 14 November 2011

Comparative effectiveness of antiepileptic drugs in patients with mesial temporal lobe epilepsy with hippocampal sclerosis

scientific article published on 31 August 2017

Diagnosis and Management of Type 1 Sialidosis: Clinical Insights from Long-Term Care of Four Unrelated Patients

scientific article published on 01 August 2020

Diagnostic implications of genetic copy number variation in epilepsy plus

scientific article published on 13 March 2019

Different electroclinical picture of generalized epilepsy in two families with 15q13.3 microdeletion

scientific article published on 28 February 2013

Dramatic response to levetiracetam in post-ischaemic Holmes' tremor.

scientific article published on 23 January 2009

Dramatic response to levetiracetam in post-ischaemic Holmes' tremor.

scientific article published on April 2007

Epileptic myoclonus as ciprofloxacin-associated adverse effect

scientific article published on 01 August 2007

Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies

article

Inherited neuromyotonia: a clinical and genetic study of a family

scientific article published on 30 November 2006

Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2

scientific article published on 29 October 2019

Life-threatening status epilepticus following gabapentin administration in a patient with benign adult familial myoclonic epilepsy.

scientific article

Natural history and long-term evolution in families with autosomal dominant cortical tremor, myoclonus, and epilepsy.

scientific article published on 22 March 2011

Neurological features and long-term follow-up in 15q11.2-13.1 duplication

scientific article

Psychiatric comorbidities in patients from seven families with autosomal dominant cortical tremor, myoclonus, and epilepsy

scientific article published on 28 January 2016

Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study

article

The spectrum of intermediate SCN8A-related epilepsy

scientific article published on 10 April 2019

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