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Mongia Hachicha

Showing results (21-30 of 78) with videos related to

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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.
Acta Clinica Belgica|August 13, 2019
Copy-number variation of the NPHP1 gene in patients with juvenile NephronophthisisMayssa Abdelwahed, Ines Maaloul, Valerie Benoit, et al.
Fetal and Pediatric Pathology|May 21, 2014
Hemolytic anemia and progressive neurologic impairment: think about triosephosphate isomerase deficiencyKhaoula Aissa, Fatma Kamoun, Lamia Sfaihi, et al.
Journal of Diabetes Research|June 3, 2022
Autoantibodies to Zinc Transporter 8 and <i>SLC30A8</i> Genotype in Type 1 Diabetes Childhood: A Pioneering Study in North AfricaRaouia Fakhfakh, Sana Kmiha, Safa Tahri, et al.
Nephrologie & Therapeutique|July 31, 2007
[Vasculitis with renal involvement and antineutrophil cytoplasmic antibodies (ANCA) in a child receiving benzylthiouracil]Mongia Hachicha, Thouraya Kammoun, Wafa Ben Romdhane, et al.
La Tunisie Medicale|April 1, 2003
[Hypothyroidism in children. 82 cases]Mongia Hachicha, Abdelmajid Mahfoudh, Fatma Loulou, 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|June 22, 2005
[The cortico-resistent idiopathic nephrotic syndrome of child. Study of 14 observations]Mongia Hachicha, Thouraya Kammoun, Abdelmajid Mahfoudh, et al.
Molecular Biology Reports|June 5, 2021
Mitochondrial disease patients with novel ND4 12058A > C and ND1 m.3911A > G variations: implications for a role in the phenotype following a bioinformatic investigationEmna Mkaouar-Rebai, Marwa Ammar, Lamia Sfaihi, et al.
La Tunisie Medicale|November 16, 2018
Hypoparathyroidism in children: a study of eight casesInes Maaloul, Hajer Aloulou, Sana Kmiha, et al.
Pageof 8

Showing results (21-30 of 78) with videos related to

Sort By:
Pageof 8
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.
Acta Clinica Belgica|August 13, 2019
Copy-number variation of the NPHP1 gene in patients with juvenile NephronophthisisMayssa Abdelwahed, Ines Maaloul, Valerie Benoit, et al.
Fetal and Pediatric Pathology|May 21, 2014
Hemolytic anemia and progressive neurologic impairment: think about triosephosphate isomerase deficiencyKhaoula Aissa, Fatma Kamoun, Lamia Sfaihi, et al.
Journal of Diabetes Research|June 3, 2022
Autoantibodies to Zinc Transporter 8 and <i>SLC30A8</i> Genotype in Type 1 Diabetes Childhood: A Pioneering Study in North AfricaRaouia Fakhfakh, Sana Kmiha, Safa Tahri, et al.
Nephrologie & Therapeutique|July 31, 2007
[Vasculitis with renal involvement and antineutrophil cytoplasmic antibodies (ANCA) in a child receiving benzylthiouracil]Mongia Hachicha, Thouraya Kammoun, Wafa Ben Romdhane, et al.
La Tunisie Medicale|April 1, 2003
[Hypothyroidism in children. 82 cases]Mongia Hachicha, Abdelmajid Mahfoudh, Fatma Loulou, 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|June 22, 2005
[The cortico-resistent idiopathic nephrotic syndrome of child. Study of 14 observations]Mongia Hachicha, Thouraya Kammoun, Abdelmajid Mahfoudh, et al.
Molecular Biology Reports|June 5, 2021
Mitochondrial disease patients with novel ND4 12058A > C and ND1 m.3911A > G variations: implications for a role in the phenotype following a bioinformatic investigationEmna Mkaouar-Rebai, Marwa Ammar, Lamia Sfaihi, et al.
La Tunisie Medicale|November 16, 2018
Hypoparathyroidism in children: a study of eight casesInes Maaloul, Hajer Aloulou, Sana Kmiha, et al.
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