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N Kaabachi

Showing results (11-20 of 59) with videos related to

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Journal of Inherited Metabolic Disease|October 6, 2007
Osteoma of the calvaria in L-2-hydroxyglutaric aciduriaA Larnaout, R Amouri, S Neji, et al.
La Tunisie Medicale|October 1, 1988
[Current value of gamma-glutamyltransferase levels]S Ben Ammar, N Kaabachi, R Djait, et al.
La Tunisie Medicale|May 1, 1995
[The contribution of the laboratory in the diagnosis of hereditary intermediate metabolism disorders]D Khiari, N Tebib, N Kaabachi, et al.
La Tunisie Medicale|February 1, 1990
[Biochemical balance in the differential diagnosis of ascites]J Abdelmoula, N Kaabachi, N Ben Amor, et al.
L' Eurobiologiste|July 1, 1991
[Iron status and pregnancy in Tunisian women]N Kaabachi, J Abdelmoula, O Marrakchi, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 1, 1999
[Reference values of urinary orotic acid in a healthy Tunisian population]D el Khiari, N Tebib, N Kaabachi, et al.
La Tunisie Medicale|March 1, 1992
[Results of protein profile in glomerulopathies]H Fellahh, N Kaabachi, J Abdelmoula, 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.
Acta Neuropathologica|January 1, 1994
Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduriaA Larnaout, F Hentati, S Belal, et al.
Prostaglandins, Leukotrienes, and Essential Fatty Acids|September 18, 2016
Fatty acids profile in preterm Colostrum of Tunisian women. Association with selected maternal characteristicsS Fares, M M Sethom, M Feki, et al.
Pageof 6

Showing results (11-20 of 59) with videos related to

Sort By:
Pageof 6
Journal of Inherited Metabolic Disease|October 6, 2007
Osteoma of the calvaria in L-2-hydroxyglutaric aciduriaA Larnaout, R Amouri, S Neji, et al.
La Tunisie Medicale|October 1, 1988
[Current value of gamma-glutamyltransferase levels]S Ben Ammar, N Kaabachi, R Djait, et al.
La Tunisie Medicale|May 1, 1995
[The contribution of the laboratory in the diagnosis of hereditary intermediate metabolism disorders]D Khiari, N Tebib, N Kaabachi, et al.
La Tunisie Medicale|February 1, 1990
[Biochemical balance in the differential diagnosis of ascites]J Abdelmoula, N Kaabachi, N Ben Amor, et al.
L' Eurobiologiste|July 1, 1991
[Iron status and pregnancy in Tunisian women]N Kaabachi, J Abdelmoula, O Marrakchi, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 1, 1999
[Reference values of urinary orotic acid in a healthy Tunisian population]D el Khiari, N Tebib, N Kaabachi, et al.
La Tunisie Medicale|March 1, 1992
[Results of protein profile in glomerulopathies]H Fellahh, N Kaabachi, J Abdelmoula, 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.
Acta Neuropathologica|January 1, 1994
Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduriaA Larnaout, F Hentati, S Belal, et al.
Prostaglandins, Leukotrienes, and Essential Fatty Acids|September 18, 2016
Fatty acids profile in preterm Colostrum of Tunisian women. Association with selected maternal characteristicsS Fares, M M Sethom, M Feki, et al.
Pageof 6