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Mongia Hachicha

Showing results (11-20 of 78) with videos related to

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The Pan African Medical Journal|September 7, 2019
[Epidemiology of home accidents in childhood: experience in the Division of General Pediatrics in Southern Tunisia]Ines Maaloul, Sana Kmiha, Sourour Yaich, et al.
La Tunisie Medicale|August 2, 2007
[Hepatopulmonary syndrome and portal hypertension]Thouraya Kammoun, Rim Ben Abdallah, Imen Chabchoub, et al.
La Tunisie Medicale|June 1, 2014
[Cerebral imaging in epileptic children: study of 140 cases]Salma Ben Ameur, Hajer Aloulou, Lamia Sfaihi, et al.
La Tunisie Medicale|January 22, 2003
[Delayed growth due to growth hormone deficiency (study of 16 cases)]Mongia Hachicha, Thouraya Kammoun, Sémia Kolsi, et al.
La Tunisie Medicale|June 8, 2006
[Beneficial effects of antimalarials in the treatment of generalized granuloma annular in children]Abderrahman Masmoudi, Wafa Abdelmaksoud, Hamida Turki, et al.
Biochemical and Biophysical Research Communications|November 8, 2012
A novel m.12908T>a mutation in the mitochondrial ND5 gene in patient with infantile-onset Pompe diseaseImen Chamkha, Olfa Alila-Fersi, Emna Mkaouar-Rebai, et al.
Computational Biology and Chemistry|October 28, 2016
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 diseaseBoudour Khabou, Olfa Siala-Sahnoun, Lamia Gargouri, et al.
Mitochondrial DNA|July 12, 2013
A novel MT-CO2 m.8249G>A pathogenic variation and the MT-TW m.5521G>A mutation in patients with mitochondrial myopathyEmna Mkaouar-Rebai, Afif Ben Mahmoud, Imen Chamkha, et al.
Biochemical and Biophysical Research Communications|December 11, 2012
A novel MT-CO1 m.6498C>A variation associated with the m.7444G>A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes in a patient with hearing impairment, diabetes and congenital visual lossEmna Mkaouar-Rebai, Imen Chamkha, Thouraya Kammoun, et al.
Molecular Genetics and Metabolism|April 8, 2009
Two new mutations in the MT-TW gene leading to the disruption of the secondary structure of the tRNA(Trp) in patients with Leigh syndromeEmna Mkaouar-Rebai, Imen Chamkha, Fatma Kammoun, et al.
Pageof 8

Showing results (11-20 of 78) with videos related to

Sort By:
Pageof 8
The Pan African Medical Journal|September 7, 2019
[Epidemiology of home accidents in childhood: experience in the Division of General Pediatrics in Southern Tunisia]Ines Maaloul, Sana Kmiha, Sourour Yaich, et al.
La Tunisie Medicale|August 2, 2007
[Hepatopulmonary syndrome and portal hypertension]Thouraya Kammoun, Rim Ben Abdallah, Imen Chabchoub, et al.
La Tunisie Medicale|June 1, 2014
[Cerebral imaging in epileptic children: study of 140 cases]Salma Ben Ameur, Hajer Aloulou, Lamia Sfaihi, et al.
La Tunisie Medicale|January 22, 2003
[Delayed growth due to growth hormone deficiency (study of 16 cases)]Mongia Hachicha, Thouraya Kammoun, Sémia Kolsi, et al.
La Tunisie Medicale|June 8, 2006
[Beneficial effects of antimalarials in the treatment of generalized granuloma annular in children]Abderrahman Masmoudi, Wafa Abdelmaksoud, Hamida Turki, et al.
Biochemical and Biophysical Research Communications|November 8, 2012
A novel m.12908T>a mutation in the mitochondrial ND5 gene in patient with infantile-onset Pompe diseaseImen Chamkha, Olfa Alila-Fersi, Emna Mkaouar-Rebai, et al.
Computational Biology and Chemistry|October 28, 2016
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 diseaseBoudour Khabou, Olfa Siala-Sahnoun, Lamia Gargouri, et al.
Mitochondrial DNA|July 12, 2013
A novel MT-CO2 m.8249G>A pathogenic variation and the MT-TW m.5521G>A mutation in patients with mitochondrial myopathyEmna Mkaouar-Rebai, Afif Ben Mahmoud, Imen Chamkha, et al.
Biochemical and Biophysical Research Communications|December 11, 2012
A novel MT-CO1 m.6498C>A variation associated with the m.7444G>A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes in a patient with hearing impairment, diabetes and congenital visual lossEmna Mkaouar-Rebai, Imen Chamkha, Thouraya Kammoun, et al.
Molecular Genetics and Metabolism|April 8, 2009
Two new mutations in the MT-TW gene leading to the disruption of the secondary structure of the tRNA(Trp) in patients with Leigh syndromeEmna Mkaouar-Rebai, Imen Chamkha, Fatma Kammoun, et al.
Pageof 8