Concepedia

Nourhène Fendri-Kriaa

NF

Statistics

Publications

6

Citations

107

H-Index

6

Active since

2009

Affiliations

University of Sfax(Current)

Centre of Biotechnology of Sfax

Hopital Universitaire Hedi Chaker

Hopital Universitaire Habib Bourguiba

Nourhène Fendri-Kriaa is an author at University of Sfax specializing in molecular genetics, human genetics, and genetic disorders.

Publications per year

2009–2010

6

Publications

6

New mutation c.374C>T and a putative disease-associated haplotype within SCN1B gene in Tunisian families with febrile seizures

Nourhène Fendri-Kriaa, F. Kammoun, Ikhlass Hadj Salem et al. · European Journal of Neurology · 2010 · 26 citations

, , +17

Congenital factor XIII deficiency caused by two mutations in eight Tunisian families: molecular confirmation of a founder effect

Nacim Louhichi, Moez Medhaffar, Ikhlass Hadjsalem et al. · Annals of Hematology · 2009 · 21 citations

, , +15

A novel m.3395A>G missense mutation in the mitochondrial ND1 gene associated with the new tRNAIle m.4316A>G mutation in a patient with hypertrophic cardiomyopathy and profound hearing loss

Imen Chamkha, Emna Mkaouar‐Rebai, Hajer Aloulou et al. · Biochemical and Biophysical Research Communications · 2010 · 18 citations

, , +17

Genetic screening of two Tunisian families with generalized epilepsy with febrile seizures plus

Nourhène Fendri-Kriaa, F. Kammoun, Ahmed Rebaï et al. · European Journal of Neurology · 2009 · 18 citations

, , +17

A Novel <i>MECP2</i> Gene Mutation in a Tunisian Patient with Rett Syndrome

Nourhène Fendri-Kriaa, Zaineb Abdelkafi, Imen Ben Rebeh et al. · Genetic Testing and Molecular Biomarkers · 2009 · 14 citations

, , +17

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