C. Iliescu

发表

Intellectual disability and epilepsy in down syndrome.

M. Budisteanu, D. Barca, O. Tarta-Arsene, 2014, Maedica.

Exploring the prevalence and profile of epilepsy across Europe using a standard retrospective chart review: Challenges and opportunities

T. Tomson, L. Forsgren, N. Delanty, 2021, Epilepsia.

De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome.

Holger Lerche, Renzo Guerrini, Christel Depienne, 2013, American journal of human genetics.

Clinical and genomic findings in brain heterotopia: Report of a pediatric patient cohort from Romania

M. Budisteanu, S. Papuc, D. Barca, 2021, Experimental and therapeutic medicine.

Phenotypic and Genotypic Spectrum of Early-Onset Developmental and Epileptic Encephalopathies—Data from a Romanian Cohort

M. Budisteanu, C. Iliescu, C. Burloiu, 2022, Genes.

Loss of function of the retinoid-related nuclear receptor (RORB) gene and epilepsy

G. Carvill, I. Scheffer, H. Mefford, 2016, European Journal of Human Genetics.

Angelman syndrome patient management: 5 years of clinical experience

M. Budisteanu, S. Papuc, C. Iliescu, 2013 .

Rett-like onset in late-infantile neuronal ceroid lipofuscinosis (CLN7) caused by compound heterozygous mutation in the MFSD8 gene and review of the literature data on clinical onset signs.

A. Rolfs, A. Dica, C. Iliescu, 2014, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

The Phenotypic Spectrum of 15q13.3 Region Duplications: Report of 5 Patients

M. Budisteanu, S. Papuc, C. Iliescu, 2021, Genes.

Diagnostic approach of epilepsy in childhood and adolescence.

C. Iliescu, D. Craiu, 2013, Maedica.

DMD and West syndrome

L. Servais, J. Nectoux, C. Iliescu, 2017, Neuromuscular Disorders.

A Multinational Survey on Actual Diagnostics and Treatment of Subacute Sclerosing Panencephalitis

B. Anlar, C. Iliescu, D. Craiu, 2015, Neuropediatrics.

Rett-like onset in late-infantile neuronal ceroid lipofuscinosis (CLN7) caused by compound heterozygous mutation in the MFSD8 gene and review of the literature data on clinical onset signs.

A. Rolfs, A. Dica, C. Iliescu, 2015, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.