Skip to main content

STRENGTHENING THE SFAX UNIVERSITY EXPERTISE FOR DIAGNOSIS AND MANAGEMENT OF EPILEPTIC ENCEPHALOPATHIES

Deliverables

Communication and Dissemination Plan

The plan shall define the target groups, key messages, media channels and responsibilities. Measurable criteria of the dissemination efforts shall be selected in order to effectively evaluate each dissemination activity. Satisfaction and evaluation questionnaires after each events will be collected. The dissemination plan shall define principles to be followed by all dissemination activities in order to avoid confusion and misconceptions and to foster the quality of project communication. It will submitted in M6 and then updated on an annual basis. (M12, M24, M36)

Project Website and dissemination material

D 5.2 Project Website and dissemination material

Peer-reviewed publications of the coordinating entity during the three years preceding the start date of the project

Introduce in the Continuous reporting tool on the Funding and Tenders portal before the end of month 2 of the project peer-reviewed publications (in the particular field of research) of the coordinating entity during the three years preceding the start date of the project.

Objectives and teaching tools of the training

D 2.1 Objectives and teaching tools of the training

Searching for OpenAIRE data...

Publications

Novel pathogenic mutations and further evidence for clinical relevance of genes and variants causing hearing impairment in Tunisian population

Author(s): Amal Souissi, Mariem Ben Said, Ikhlas Ben Ayed, Ines Elloumi, Amal Bouzid, Mohamed Ali Mosrati, Mehdi Hasnaoui, Malek Belcadhi, Nabil Idriss, Hassen Kamoun, Nourhene Gharbi, Abdullah A. Gibriel, Abdelaziz Tlili, Saber Masmoudi
Published in: Journal of Advanced Research, 2021, ISSN 2090-1232
Publisher: Cairo University
DOI: 10.1016/j.jare.2021.01.005

Phenotypic variability in two infants sharing the same MECP2 mutation: evidence of chromosomal rearrangements and high sister-chromatid exchange levels in Rett syndrome

Author(s): Marwa Kharrat, Ines Hsairi, Hajer Doukali, Nourhene Fendri-Kriaa, Hassen Kammoun, Leila Ammar-keskes, Chahnez Triki, Faiza Fakhfakh
Published in: Acta Neurologica Belgica, 117/1, 2017, Page(s) 251-258, ISSN 0300-9009
Publisher: Acta Medica Belgica
DOI: 10.1007/s13760-016-0667-5

Clinical, Molecular, and Computational Analysis in Patients With a Novel Double Mutation and a New Synonymous Variant in MeCP2: Report of the First Missense Mutation Within the AT-hook1 Cluster in Rett Syndrome

Author(s): Marwa Kharrat, Yosra Kamoun, Fatma Kamoun, Emna Ellouze, Marwa Maalej, Nourhene Fendri-Kriaa, Leila Ammar-Keskes, Neila Belghith, Ali Gargouri, Chahnez Triki, Faiza Fakhfakh
Published in: Journal of Child Neurology, 32/8, 2017, Page(s) 694-703, ISSN 0883-0738
Publisher: SAGE Publications
DOI: 10.1177/0883073817701622

A novel C-terminal truncated mutation in hCDKL5 protein causing a severe West syndrome: Comparison with previous truncated mutations and genotype/phenotype correlation

Author(s): Marwa Ben Jdila, Chahnez Triki, Bochra Ben Rhouma, Rihab Ben Jomaa, Abir Ben Issa, Leila Ammar-Keskes, Fatma Kamoun, Faiza Fakhfakh
Published in: International Journal of Developmental Neuroscience, 72, 2019, Page(s) 22-30, ISSN 0736-5748
Publisher: Pergamon Press Ltd.
DOI: 10.1016/j.ijdevneu.2018.09.006

Novel mutations in the CDKL5 gene in complex genotypes associated with West syndrome with variable phenotype: First description of somatic mosaic state

Author(s): Marwa Ben Jdila, Abir Ben Issa, Boudour Khabou, Bochra Ben Rhouma, Fatma Kamoun, Leila Ammar-Keskes, Chahnez Triki, Faiza Fakhfakh
Published in: Clinica Chimica Acta, 473, 2017, Page(s) 51-59, ISSN 0009-8981
Publisher: Elsevier BV
DOI: 10.1016/j.cca.2017.08.001

First description of an unusual novel double mutation in MECP2 co-occurring with the m.827A>G mutation in the MT-RNR1 gene associated with angelman-like syndrome

Author(s): Marwa Kharrat, Chahnez Triki, Marwa Maalej, Sihem Ncir, Marwa Ammar, Fatma Kammoun, Faiza Fakhfakh
Published in: International Journal of Developmental Neuroscience, 79, 2019, Page(s) 37-44, ISSN 0736-5748
Publisher: Pergamon Press Ltd.
DOI: 10.1016/j.ijdevneu.2019.10.002