Search Results - "Naziha, Khouja"

Novel double deletions in the MECP2 gene in Tunisian Rett patient by Fendri-Kriaa, Nourhene, Rouissi, Aida, Ghorbel, Rania, Mkaouar-Rebai, Emna, Belguith, Neila, Gouider-Khouja, Naziha, Fakhfakh, Faiza

“…Rett syndrome (RTT) is a severe neurodevelopmental disorder affecting almost exclusively girls. Rett patients present an apparently normal psychomotor…”
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Novel Mutations in the C-Terminal Region of the MECP2 Gene in Tunisian Rett Syndrome Patients by Fendri-Kriaa, Nourhene, Rouissi, Aida, Ghorbel, Rania, Mkaouar-Rebai, Emna, Belguith, Neila, Gouider-Khouja, Naziha, Fakhfakh, Faiza

“…Rett syndrome (RTT), an X-linked dominant neurodevelopmental disorder in females, is caused mainly by de novo mutations in the methyl-CpG-binding protein 2…”
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Screening of three Mediterranean phenylketonuria mutations in Tunisian families by KHEMIR, SAMEH, SIALA, HAJER, TAIEB, SAMEH HADJ, CHERIF, WAFA, AZZOUZ, HATEM, KÉFI, RYM, ABDELHAK, SONIA, KHOUJA, NAZIHA, TEBIB, NEJI, MASSAOUD, TAIEB, DRIDI, MARIE FRANÇOISE BEN, KAABACHI, NAZIHA

“…research note…”
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Study of dyslexia within school kids that suffer from epilepsia by Charfi, Afifa, Ben Hadj Yahia, Sihem, Kharrat, Salima, Zouari, Mourad, Bouchama, Jihen, Naziha, Khouja, Abdelmajid, Larnaout, Hentati, Fayçal, Hachicha, Slah

“…Dyslexia is a reading problem disorder. It can be a direct result of epilepsia for some kids. The researchers have done the study on 30 school kids that suffer…”
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