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May 8, 2026
The moving cervical mass: A surprising discovery
S Ferchichi, K Gritli, G Kharrat, et al.
Pathologie-Biologie
|
November 15, 2011
Mucopolysaccharidosis IVA within Tunisian patients: Confirmation of the two novel GALNS gene mutations
S Khedhiri, L Chkioua, H Bouzidi, et al.
International Journal of Sports Medicine
|
July 14, 2012
High intensity exercise affects diurnal variation of some biological markers in trained subjects
O Hammouda, H Chtourou, H Chahed, et al.
BMC Medical Genetics
|
May 26, 2020
The mutational spectrum of hunter syndrome reveals correlation between biochemical and clinical profiles in Tunisian patients
L Chkioua, O Grissa, N Leban, et al.
Annales De Biologie Clinique
|
February 27, 2003
[Reactive hemophagocytic syndrome: about one case]
B Charfeddine, S Laradi, A Kassab, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
Mucopolysaccharidosis I: Alpha-L-Iduronidase mutations in three Tunisian families
S Laradi, T Tukel, M Erazo, et al.
Molecular Genetics and Metabolism
|
December 28, 2005
Mucopolysaccharidosis type IV: N-acetylgalactosamine-6-sulfatase mutations in Tunisian patients
S Laradi, T Tukel, S Khediri, et al.
Annales De Cardiologie Et D'Angeiologie
|
February 1, 2011
[Study of the intronic polymorphism of the angiotensin 1 converting enzyme among coronary Tunisians]
A Chalghoum, Y Noichri, L Chkioua, et al.
Annales De Biologie Clinique
|
April 19, 2003
[Diagnostic strategy of beta-thalassemic mutation in a Tunisian family, application in prenatal diagnosis]
A H Khelil, S Laradi, S Ferchichi, et al.
Pathologie-Biologie
|
January 8, 2008
[Molecular analysis of the p.Asn 370 Ser mutation in Gaucher disease]
A Dandana, S Ferchichi, S Ben Khelifa, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 29) with videos related to
Sort By:
Page
of 3
Idcases
|
May 8, 2026
The moving cervical mass: A surprising discovery
S Ferchichi, K Gritli, G Kharrat, et al.
Pathologie-Biologie
|
November 15, 2011
Mucopolysaccharidosis IVA within Tunisian patients: Confirmation of the two novel GALNS gene mutations
S Khedhiri, L Chkioua, H Bouzidi, et al.
International Journal of Sports Medicine
|
July 14, 2012
High intensity exercise affects diurnal variation of some biological markers in trained subjects
O Hammouda, H Chtourou, H Chahed, et al.
BMC Medical Genetics
|
May 26, 2020
The mutational spectrum of hunter syndrome reveals correlation between biochemical and clinical profiles in Tunisian patients
L Chkioua, O Grissa, N Leban, et al.
Annales De Biologie Clinique
|
February 27, 2003
[Reactive hemophagocytic syndrome: about one case]
B Charfeddine, S Laradi, A Kassab, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
Mucopolysaccharidosis I: Alpha-L-Iduronidase mutations in three Tunisian families
S Laradi, T Tukel, M Erazo, et al.
Molecular Genetics and Metabolism
|
December 28, 2005
Mucopolysaccharidosis type IV: N-acetylgalactosamine-6-sulfatase mutations in Tunisian patients
S Laradi, T Tukel, S Khediri, et al.
Annales De Cardiologie Et D'Angeiologie
|
February 1, 2011
[Study of the intronic polymorphism of the angiotensin 1 converting enzyme among coronary Tunisians]
A Chalghoum, Y Noichri, L Chkioua, et al.
Annales De Biologie Clinique
|
April 19, 2003
[Diagnostic strategy of beta-thalassemic mutation in a Tunisian family, application in prenatal diagnosis]
A H Khelil, S Laradi, S Ferchichi, et al.
Pathologie-Biologie
|
January 8, 2008
[Molecular analysis of the p.Asn 370 Ser mutation in Gaucher disease]
A Dandana, S Ferchichi, S Ben Khelifa, et al.
Page
of 3