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Taieb Messaoud

Showing results (1-10 of 75) with videos related to

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Hemoglobin|June 27, 2006
Haplotypes linked to three rare beta-thalassemia mutations, originally reported in TunisiaAmina Bibi, Taieb Messaoud, Slaheddine Fattoum
Neurocase|April 4, 2020
Refractory epilepsy in PSEN 1 mutation (I83T)Saloua Fray, Afef Rassas, Taieb Messaoud, et al.
Hemoglobin|September 22, 2006
Detection of two rare beta-thalassemia alleles found in the Tunisian population: codon 47 (+A) and codons 106/107 (+G)Amina Bibi, Taieb Messaoud, Cherif Beldjord, et al.
Journal of Genetics|October 13, 2022
Missing apolipoprotein E ε4 allele associated with nonamnestic Alzheimer's disease in a Tunisian populationSaloua Fray, Afef Achouri-Rassas, Samir Belal, et al.
Annals of Human Biology|February 19, 2011
First report of cystic fibrosis mutations in Libyan cystic fibrosis patientsSondess Hadj Fredj, Slaheddine Fattoum, Abdelraouf Chabchoub, et al.
Hemoglobin|December 24, 2005
First description in Tunisia of a point mutation at codon 119 (CCT-->TCT) in the alpha1-globin gene: Hb Groene Hart in association with the -alpha3.7 deletionHajer Siala, Faida Ouali, Taieb Messaoud, et al.
Gene|July 10, 2012
Identification of candidate genes involved in clinical variability among Tunisian patients with β-thalassemiaAwatef Mejri, Hajer Siala, Faida Ouali, et al.
La Tunisie Medicale|June 18, 2011
[Profile of biochemical markers in cystic fibrosis. Prospective study about 13 cases]Raja Belhaj, Wided Souissi, Sondes Hadj frej, et al.
Annales De Biologie Clinique|April 8, 2015
Autosomal dominant polycystic kidney disease: identification of two polymorphismsSafa Sahnoun, Samia Barbouch, Sondess Hadj Fredj, et al.
Annales De Biologie Clinique|April 17, 2013
Identification of a cystic fibrosis mutation W19X in TunisiaMonia Boudaya, Sondess Hadj Fredj, Hajer Siala, et al.
Pageof 8

Showing results (1-10 of 75) with videos related to

Sort By:
Pageof 8
Hemoglobin|June 27, 2006
Haplotypes linked to three rare beta-thalassemia mutations, originally reported in TunisiaAmina Bibi, Taieb Messaoud, Slaheddine Fattoum
Neurocase|April 4, 2020
Refractory epilepsy in PSEN 1 mutation (I83T)Saloua Fray, Afef Rassas, Taieb Messaoud, et al.
Hemoglobin|September 22, 2006
Detection of two rare beta-thalassemia alleles found in the Tunisian population: codon 47 (+A) and codons 106/107 (+G)Amina Bibi, Taieb Messaoud, Cherif Beldjord, et al.
Journal of Genetics|October 13, 2022
Missing apolipoprotein E ε4 allele associated with nonamnestic Alzheimer's disease in a Tunisian populationSaloua Fray, Afef Achouri-Rassas, Samir Belal, et al.
Annals of Human Biology|February 19, 2011
First report of cystic fibrosis mutations in Libyan cystic fibrosis patientsSondess Hadj Fredj, Slaheddine Fattoum, Abdelraouf Chabchoub, et al.
Hemoglobin|December 24, 2005
First description in Tunisia of a point mutation at codon 119 (CCT-->TCT) in the alpha1-globin gene: Hb Groene Hart in association with the -alpha3.7 deletionHajer Siala, Faida Ouali, Taieb Messaoud, et al.
Gene|July 10, 2012
Identification of candidate genes involved in clinical variability among Tunisian patients with β-thalassemiaAwatef Mejri, Hajer Siala, Faida Ouali, et al.
La Tunisie Medicale|June 18, 2011
[Profile of biochemical markers in cystic fibrosis. Prospective study about 13 cases]Raja Belhaj, Wided Souissi, Sondes Hadj frej, et al.
Annales De Biologie Clinique|April 8, 2015
Autosomal dominant polycystic kidney disease: identification of two polymorphismsSafa Sahnoun, Samia Barbouch, Sondess Hadj Fredj, et al.
Annales De Biologie Clinique|April 17, 2013
Identification of a cystic fibrosis mutation W19X in TunisiaMonia Boudaya, Sondess Hadj Fredj, Hajer Siala, et al.
Pageof 8