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R Lakhoua

Showing results (21-30 of 54) with videos related to

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Human Genetics|November 1, 1994
A unique mutation underlying carbonic anhydrase II deficiency syndrome in patients of Arab descentD M Fathallah, M Bejaoui, W S Sly, et al.
Bulletin De La Societe De Pathologie Exotique (1990)|January 1, 1993
[Non-typhoid Salmonella in pediatric patients in Tunis (Hospital Charles-Nicolle) from 1980 to 1991]A Ben Hassen, M Bejaoui, A Hichri, et al.
Annales De Pediatrie|June 1, 1992
[Lymphoid hyperplasia of the intestine in children. 15 cases]M Bejaoui, M Guezmir, M Hamdi, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 1, 1995
[Value of extracorporeal shockwave lithotripsy in primary hyperoxaluria type I]A Kamoun, M Chebil, L Ben Hassine, et al.
Archives Francaises De Pediatrie|November 1, 1992
[Nocardial subphrenic abscess after splenectomy in a child with sickle cell-thalassemia]M Bejaoui, C Zarrouk, A Ben Hassen, et al.
La Tunisie Medicale|March 1, 1992
[Hyperactivation of the mononuclear phagocyte system and typhoid fever]M Bejaoui, A Dadi, A Kamoun, et al.
Annales De Pediatrie|September 1, 1989
[Hydatid cysts in children. Diagnostic and therapeutic aspects. Apropos of 1195 cases]B Chaouachi, S Ben Salah, R Lakhoua, et al.
Pediatric Rheumatology Online Journal|July 27, 2010
First case of childhood Takayasu arteritis with renal artery aneurysmsTahar Gargah, Mouna Ben Harrath, Haythem Bachrouche, et al.
Nephrologie|January 1, 1997
[Primary hyperoxaluria: Tunisian experience apropos of 24 pediatric cases]A Kamoun, M Daudon, A Zghal, et al.
Archives De L'Institut Pasteur De Tunis|July 1, 1994
[Hereditary immune deficiency in Tunisia]M R Barbouche, M Béjaoui, B Larguèche, et al.
Pageof 6

Showing results (21-30 of 54) with videos related to

Sort By:
Pageof 6
Human Genetics|November 1, 1994
A unique mutation underlying carbonic anhydrase II deficiency syndrome in patients of Arab descentD M Fathallah, M Bejaoui, W S Sly, et al.
Bulletin De La Societe De Pathologie Exotique (1990)|January 1, 1993
[Non-typhoid Salmonella in pediatric patients in Tunis (Hospital Charles-Nicolle) from 1980 to 1991]A Ben Hassen, M Bejaoui, A Hichri, et al.
Annales De Pediatrie|June 1, 1992
[Lymphoid hyperplasia of the intestine in children. 15 cases]M Bejaoui, M Guezmir, M Hamdi, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 1, 1995
[Value of extracorporeal shockwave lithotripsy in primary hyperoxaluria type I]A Kamoun, M Chebil, L Ben Hassine, et al.
Archives Francaises De Pediatrie|November 1, 1992
[Nocardial subphrenic abscess after splenectomy in a child with sickle cell-thalassemia]M Bejaoui, C Zarrouk, A Ben Hassen, et al.
La Tunisie Medicale|March 1, 1992
[Hyperactivation of the mononuclear phagocyte system and typhoid fever]M Bejaoui, A Dadi, A Kamoun, et al.
Annales De Pediatrie|September 1, 1989
[Hydatid cysts in children. Diagnostic and therapeutic aspects. Apropos of 1195 cases]B Chaouachi, S Ben Salah, R Lakhoua, et al.
Pediatric Rheumatology Online Journal|July 27, 2010
First case of childhood Takayasu arteritis with renal artery aneurysmsTahar Gargah, Mouna Ben Harrath, Haythem Bachrouche, et al.
Nephrologie|January 1, 1997
[Primary hyperoxaluria: Tunisian experience apropos of 24 pediatric cases]A Kamoun, M Daudon, A Zghal, et al.
Archives De L'Institut Pasteur De Tunis|July 1, 1994
[Hereditary immune deficiency in Tunisia]M R Barbouche, M Béjaoui, B Larguèche, et al.
Pageof 6