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Imen Chabchoub

Showing results (11-20 of 55) with videos related to

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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.
La Tunisie Medicale|June 1, 2026
Psychosocial and academic impact of blood transfusion-dependent diseases on childrenInes Maaloul, Majida Nakti, Taicir Rekik, et al.
Therapie|April 13, 2025
Rapid desensitization to insulin in a patient with diabetic ketoacidosis and insulin allergyEmna Chtourou, Fatma Charfi, Imen Chabchoub, et al.
Mitochondrion|April 15, 2010
A case of Kearns-Sayre syndrome with two novel deletions (9.768 and 7.253 kb) of the mtDNA associated with the common deletion in blood leukocytes, buccal mucosa and hair folliclesEmna Mkaouar-Rebai, Imen Chamkha, Thouraya Kammoun, et al.
La Tunisie Medicale|November 16, 2018
Hypoparathyroidism in children: a study of eight casesInes Maaloul, Hajer Aloulou, Sana Kmiha, et al.
La Tunisie Medicale|January 27, 2011
[Bardet - Biedl syndrome in the child. A study of 11 cases]Hajer Aloulou, Hela Cheikhrouhou, Neila Belguith, et al.
La Tunisie Medicale|October 5, 2010
[Type I Crigler Najjar syndrome in Tunisia: a study of 30 cases]Hajer Aloulou, Afef Ben Thabet, Sonia Khanfir, et al.
La Tunisie Medicale|December 8, 2010
[Reasons of diagnostic delay of breast cancer in Tunisian women (160 patients in the central region of Tunisia)]Amel Landolsi, Selma Gahbiche, Rym Chaafii, et al.
Romanian Journal of Internal Medicine = Revue Roumaine De Medecine Interne|November 10, 2023
Clinical features and outcomes in patients with human immunodeficiency virus-negative, Castleman's disease: a single medical center study in TunisiaImen Chabchoub, Raida Ben Salah, Rim Kallel, et al.
BMC Pediatrics|February 22, 2025
Dihydrolipoamide dehydrogenase deficiency in two unrelated Tunisian childrenHajer Aloulou, Fatma Charfi, Rim Charfi, et al.
Pageof 6

Showing results (11-20 of 55) with videos related to

Sort By:
Pageof 6
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.
La Tunisie Medicale|June 1, 2026
Psychosocial and academic impact of blood transfusion-dependent diseases on childrenInes Maaloul, Majida Nakti, Taicir Rekik, et al.
Therapie|April 13, 2025
Rapid desensitization to insulin in a patient with diabetic ketoacidosis and insulin allergyEmna Chtourou, Fatma Charfi, Imen Chabchoub, et al.
Mitochondrion|April 15, 2010
A case of Kearns-Sayre syndrome with two novel deletions (9.768 and 7.253 kb) of the mtDNA associated with the common deletion in blood leukocytes, buccal mucosa and hair folliclesEmna Mkaouar-Rebai, Imen Chamkha, Thouraya Kammoun, et al.
La Tunisie Medicale|November 16, 2018
Hypoparathyroidism in children: a study of eight casesInes Maaloul, Hajer Aloulou, Sana Kmiha, et al.
La Tunisie Medicale|January 27, 2011
[Bardet - Biedl syndrome in the child. A study of 11 cases]Hajer Aloulou, Hela Cheikhrouhou, Neila Belguith, et al.
La Tunisie Medicale|October 5, 2010
[Type I Crigler Najjar syndrome in Tunisia: a study of 30 cases]Hajer Aloulou, Afef Ben Thabet, Sonia Khanfir, et al.
La Tunisie Medicale|December 8, 2010
[Reasons of diagnostic delay of breast cancer in Tunisian women (160 patients in the central region of Tunisia)]Amel Landolsi, Selma Gahbiche, Rym Chaafii, et al.
Romanian Journal of Internal Medicine = Revue Roumaine De Medecine Interne|November 10, 2023
Clinical features and outcomes in patients with human immunodeficiency virus-negative, Castleman's disease: a single medical center study in TunisiaImen Chabchoub, Raida Ben Salah, Rim Kallel, et al.
BMC Pediatrics|February 22, 2025
Dihydrolipoamide dehydrogenase deficiency in two unrelated Tunisian childrenHajer Aloulou, Fatma Charfi, Rim Charfi, et al.
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