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N Miladi

Showing results (11-20 of 23) with videos related to

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Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|September 1, 1985
[Polychlorobiphenyl (Phenoclor DP6) and the metabolism of xenobiotics: effect of a high lipid diet]M A Pélissier, N Miladi, S Attéba, et al.
La Tunisie Medicale|March 24, 2000
[Vermian agenesis: Report of a family and review of the literature]S Gabsi, N Gouider-Khouja, I Mili-Boussen, et al.
Human Genetics|July 1, 1994
Submicroscopic deletions of 17p13.3 in type 1 LissencephalyA Mantel, C Leonard, B Husson, et al.
La Tunisie Medicale|July 7, 1999
[Treatment of febrile convulsions]M Fredj, A Kacem-Ezzahi, M Kallel, et al.
Journal of Child Neurology|October 31, 1998
Dihydropteridine reductase deficiency in a large consanguineous Tunisian family: clinical, biochemical, and neuropathologic findingsN Miladi, A Larnaout, J L Dhondt, et al.
Annals of Nutrition & Metabolism|January 1, 1986
[Protein restriction and metabolism of xenobiotics]R Albrecht, M A Pelissier, N Miladi, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 5, 1997
[Primary immunodeficiency in Tunisia: study of 152 cases]M Bejaoui, M R Barbouche, A Sassi, et al.
Neuropediatrics|February 24, 1999
Juvenile form of dihydropteridine reductase deficiency in 2 Tunisian patientsA Larnaout, S Belal, N Miladi, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 2, 2011
[Strabismus, nystagmus, and generalized hypotonia in a 7-month-old child]S Nagi, I Brahim, N Hammami, et al.
La Tunisie Medicale|May 1, 2008
[Hepatomegaly and early cytolysis as presenting symptoms in CDG syndrome type Ia]M Ben Hariz, S Ben Mrad, S Halioui, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|September 1, 1985
[Polychlorobiphenyl (Phenoclor DP6) and the metabolism of xenobiotics: effect of a high lipid diet]M A Pélissier, N Miladi, S Attéba, et al.
La Tunisie Medicale|March 24, 2000
[Vermian agenesis: Report of a family and review of the literature]S Gabsi, N Gouider-Khouja, I Mili-Boussen, et al.
Human Genetics|July 1, 1994
Submicroscopic deletions of 17p13.3 in type 1 LissencephalyA Mantel, C Leonard, B Husson, et al.
La Tunisie Medicale|July 7, 1999
[Treatment of febrile convulsions]M Fredj, A Kacem-Ezzahi, M Kallel, et al.
Journal of Child Neurology|October 31, 1998
Dihydropteridine reductase deficiency in a large consanguineous Tunisian family: clinical, biochemical, and neuropathologic findingsN Miladi, A Larnaout, J L Dhondt, et al.
Annals of Nutrition & Metabolism|January 1, 1986
[Protein restriction and metabolism of xenobiotics]R Albrecht, M A Pelissier, N Miladi, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 5, 1997
[Primary immunodeficiency in Tunisia: study of 152 cases]M Bejaoui, M R Barbouche, A Sassi, et al.
Neuropediatrics|February 24, 1999
Juvenile form of dihydropteridine reductase deficiency in 2 Tunisian patientsA Larnaout, S Belal, N Miladi, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 2, 2011
[Strabismus, nystagmus, and generalized hypotonia in a 7-month-old child]S Nagi, I Brahim, N Hammami, et al.
La Tunisie Medicale|May 1, 2008
[Hepatomegaly and early cytolysis as presenting symptoms in CDG syndrome type Ia]M Ben Hariz, S Ben Mrad, S Halioui, et al.
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