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N Kaabachi

Showing results (1-10 of 59) with videos related to

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Annales De Biologie Clinique|December 13, 2006
[Iron metabolism, overview and recent insights]S Omar, M Feki, N Kaabachi
La Tunisie Medicale|January 1, 1989
[A critique of chemical methods of analyzing urinary calculi]H Fallah, N Kaabachi, A Mebazaa
La Tunisie Medicale|April 1, 1990
[Fibronectin: biologic properties and clinical significance]J Abdelmoula, N Kaabachi, A Mebazaa
La Tunisie Medicale|May 1, 1991
[Biochemical approaches in states of urinary proteins]J Abdelmoula, N Kaabachi, H Fellah, et al.
La Tunisie Medicale|September 1, 1984
[The first Tunisian case of familial bisalbuminemia]A Mebazaa, N Kaabachi, S Zmandar, et al.
La Tunisie Medicale|January 1, 1984
[Study of plasma bile acids in fasting state and following a test meal, using gas chromatography]A Mebazaa, L Mamlouk, Ben Slama, et al.
La Tunisie Medicale|November 1, 1989
[Organized detection of hereditary metabolic diseases. Amino acidopathies and organic acidurias]N Kaabachi, A Mebazaa, L Hamza, et al.
Journal of Child Neurology|January 1, 1992
Phenylketonuria: an underlying etiology of autistic syndrome. A case reportN Miladi, A Larnaout, N Kaabachi, et al.
Journal of Inherited Metabolic Disease|December 22, 1999
beta-Ketothiolase (2-methylacetoacetyl-CoA thiolase) deficiency: a frequent disease in Tunisia?K Monastiri, F Amri, K Limam, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1992
[Lipid evolution during normal pregnancy]N Kaabachi, H Fellah, J Abdelmoula, et al.
Pageof 6

Showing results (1-10 of 59) with videos related to

Sort By:
Pageof 6
Annales De Biologie Clinique|December 13, 2006
[Iron metabolism, overview and recent insights]S Omar, M Feki, N Kaabachi
La Tunisie Medicale|January 1, 1989
[A critique of chemical methods of analyzing urinary calculi]H Fallah, N Kaabachi, A Mebazaa
La Tunisie Medicale|April 1, 1990
[Fibronectin: biologic properties and clinical significance]J Abdelmoula, N Kaabachi, A Mebazaa
La Tunisie Medicale|May 1, 1991
[Biochemical approaches in states of urinary proteins]J Abdelmoula, N Kaabachi, H Fellah, et al.
La Tunisie Medicale|September 1, 1984
[The first Tunisian case of familial bisalbuminemia]A Mebazaa, N Kaabachi, S Zmandar, et al.
La Tunisie Medicale|January 1, 1984
[Study of plasma bile acids in fasting state and following a test meal, using gas chromatography]A Mebazaa, L Mamlouk, Ben Slama, et al.
La Tunisie Medicale|November 1, 1989
[Organized detection of hereditary metabolic diseases. Amino acidopathies and organic acidurias]N Kaabachi, A Mebazaa, L Hamza, et al.
Journal of Child Neurology|January 1, 1992
Phenylketonuria: an underlying etiology of autistic syndrome. A case reportN Miladi, A Larnaout, N Kaabachi, et al.
Journal of Inherited Metabolic Disease|December 22, 1999
beta-Ketothiolase (2-methylacetoacetyl-CoA thiolase) deficiency: a frequent disease in Tunisia?K Monastiri, F Amri, K Limam, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1992
[Lipid evolution during normal pregnancy]N Kaabachi, H Fellah, J Abdelmoula, et al.
Pageof 6