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Author/Creator Chargui, Mariem

1. A Founder Large Deletion Mutation in Xeroderma Pigmentosum-Variant Form in Tunisia: Implication for Molecular Diagnosis and Therapy. (3rd May 2014)

Authors:
Ben Rekaya, Mariem; Laroussi, Nadia; Messaoud, Olfa; Jones, Mariem; Jerbi, Manel; Naouali, Chokri; Bouyacoub, Yosra; Chargui, Mariem; Kefi, Rym; Fazaa, Becima; Boubaker, Mohamed Samir; Boussen, Hamouda; Mokni, Mourad; Abdelhak, Sonia; Zghal, Mohamed; Khaled, Aida; Yacoub-Youssef, Houda
Other Names:
Burmeister Margit Academic Editor.
Journal:
BioMed research international
Issue:
Volume 2014(2014)
Page Start:
Record Type:
Journal Article
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2. Gender-specific associations of genetic variants with metabolic syndrome components in the Tunisian population. (1st October 2016)

Authors:
Elouej, Sahar; Rejeb, Insaf; Attaoua, Redha; Nagara, Majdi; Sallem, Om Kalthoum; Kamoun, Ines; Chargui, Mariem; Jamoussi, Henda; Turki, Zinet; Abid, Abdelmajid; Ben Slama, Claude; Bahri, Sonia; Ben Romdhane, Habiba; Abdelhak, Sonia; Kefi, Rym; Grigorescu, Florin
Journal:
Endocrine research
Issue:
Volume 41:Number 4(2016:Nov.)
Page Start:
300
Record Type:
Journal Article
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3. Granular type I corneal dystrophy in a large consanguineous Tunisian family with homozygous p.R124S mutation in the TGFBI gene. (4th July 2019)

Authors:
Bouyacoub, Yosra; Falfoul, Yousra; Ouederni, Mariem; Sayeb, Marwa; Chedli, Aschraf; Chargui, Mariem; Sassi, Hela; Chakroun Chenguel, Ilhem; Munier, Francis L.; El Matri, Leila; Abdelhak, Sonia; Cheour, Monia
Journal:
Ophthalmic genetics
Issue:
Volume 40:Number 4(2019)
Page Start:
329
Record Type:
Journal Article
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4. H syndrome: Clinical, histological and genetic investigation in Tunisian patients. Issue 8 (29th May 2018)

Authors:
Jaouadi, Hager; Zaouak, Anissa; Sellami, Khadija; Messaoud, Olfa; Chargui, Mariem; Hammami, Houda; Jones, Meriem; Jouini, Raja; Chadli Debbiche, Achraf; Chraiet, Karima; Fenniche, Sami; Mrad, Ridha; Mokni, Mourad; Turki, Hamida; Benkhalifa, Rym; Abdelhak, Sonia
Journal:
Journal of dermatology
Issue:
Volume 45:Issue 8(2018)
Page Start:
978
Record Type:
Journal Article
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6. Whole Exome Sequencing allows the identification of two novel groups of Xeroderma pigmentosum in Tunisia, XP-D and XP-E: Impact on molecular diagnosis. Issue 2 (February 2018)

Authors:
Ben Rekaya, Mariem; Naouali, Chokri; Messaoud, Olfa; Jones, Meriem; Bouyacoub, Yosra; Nagara, Majdi; Pippucci, Tommaso; Jmel, Haifa; Chargui, Mariem; Jerbi, Manel; Alibi, Mohamed; Dallali, Hamza; Bashamboo, Anu; McElreavey, Kenneth; Romeo, Giovanni; Barakat, Abdelhamid; Zghal, Mohamed; Yacoub-You...
Journal:
Journal of dermatological science
Issue:
Volume 89:Issue 2(2018)
Page Start:
172
Record Type:
Journal Article
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