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Author/Creator Hachicha, Mongia

12. Hemophagocytic Lymphohistiocytosis: A Rare Complication of an Ultrarare Lysosomal Storage Disease. Issue 4 (May 2020)

Authors:
Chabchoub, Imen; Boudabbous, Hela; Maaloul, Ines; Ben Abdelaziz, Rim; Ben Chehida, Amel; Ayadi, Lobna; Kamoun, Thouraya; Tebib, Neji; Boudaouara, Tahia; Bekri, Soumeya; Hachicha, Mongia
Journal:
Journal of pediatric hematology/oncology
Issue:
Volume 42:Issue 4(2020)
Page Start:
310
Record Type:
Journal Article
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13. Hemophagocytic Lymphohistiocytosis: A Rare Complication of an Ultrarare Lysosomal Storage Disease. Issue 4 (May 2020)

Authors:
Chabchoub, Imen; Boudabbous, Hela; Maaloul, Ines; Ben Abdelaziz, Rim; Ben Chehida, Amel; Ayadi, Lobna; Kamoun, Thouraya; Tebib, Neji; Boudaouara, Tahia; Bekri, Soumeya; Hachicha, Mongia
Journal:
Journal of pediatric hematology/oncology
Issue:
Volume 42:Issue 4(2020)
Page Start:
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

14. High frequency of exon 15 deletion in the FANCA gene in Tunisian patients affected with Fanconi anemia disease: implication for diagnosis. Issue 2 (5th February 2014)

Authors:
Amouri, Ahlem; Talmoudi, Faten; Messaoud, Olfa; d'Enghien, Catherine D.; Rekaya, Mariem B.; Allegui, Ines; Azaiez, Héla; Kefi, Rym; Abdelhak, Ahlem; Meseddi, Sondes H.; Torjemane, Lamia; Ouederni, Monia; Mellouli, Fethi; Abid, Héla B.; Aissaoui, Lamia; Bejaoui, Mohamed; Othmen, Tarek B.; Lyonnet,...
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 2:Issue 2(2014:Mar.)
Page Start:
160
Record Type:
Journal Article
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15. In silico investigation of the impact of synonymous variants in ABCB4 gene on mRNA stability/structure, splicing accuracy and codon usage: Potential contribution to PFIC3 disease. (December 2016)

Authors:
Khabou, Boudour; Siala-Sahnoun, Olfa; Gargouri, Lamia; Mkaouar-Rebai, Emna; Keskes, Leila; Hachicha, Mongia; Fakhfakh, Faiza
Journal:
Computational biology and chemistry
Issue:
Volume 65(2016)
Page Start:
103
Record Type:
Journal Article
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17. Primary ciliary dyskinesia gene contribution in Tunisia: Identification of a major Mediterranean allele. Issue 1 (15th September 2019)

Authors:
Mani, Rahma; Belkacem, Sabrina; Soua, Zohra; Chantot, Sandra; Montantin, Guy; Tissier, Sylvie; Copin, Bruno; Bouguila, Jihene; Rive Le Gouard, Nicolas; Boughamoura, Lamia; Ben Ameur, Salma; Hachicha, Mongia; Boussoffara, Raoudha; Boussetta, Khadija; Hammouda, Samia; Bedoui, Abir; Besbes, Habib; M...
Journal:
Human mutation
Issue:
Volume 41:Issue 1(2020)
Page Start:
115
Record Type:
Journal Article
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