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M Bejaoui

Showing results (21-30 of 55) with videos related to

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Physical Chemistry Chemical Physics : PCCP|May 14, 2026
<i>Ab initio</i> study of the ground and excited electronic states of the SiNa<sup>+</sup> molecular ionN Abbassi, J Dhiflaoui, M Bejaoui, et al.
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.
Pathologie-Biologie|May 6, 2008
Detection of SHV-1 beta-lactamase in Pseudomonas aeruginosa strains by genetic methodsS Kalai Blagui, W Achour, M Bejaoui, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 6, 2011
[Cryptosporidium infection in patients with major histocompatibility complex class II deficiency syndrome in Tunisia: description of five cases]I Ben Abda, R Essid, F Mellouli, et al.
Pediatric Transplantation|January 28, 2009
Successful treatment of influenza A virus by oseltamivir in bone marrow transplant recipientsF Mellouli, M Ouederni, N Dhouib, 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.
Archives Francaises De Pediatrie|December 1, 1989
[The accelerated phase of Chediak-Higashi syndrome]M Bejaoui, F Veber, D Girault, et al.
Human Genetics|May 1, 1997
Carbonic anhydrase II (CA II) deficiency in Maghrebian patients: evidence for founder effect and genomic recombination at the CA II locusD M Fathallah, M Bejaoui, D Lepaslier, et al.
La Tunisie Medicale|June 3, 2010
Early onset of cerebrovascular accident in a thalassemia major childN Dhouib, F Mellouli, M Ouederni, et al.
Pageof 6

Showing results (21-30 of 55) with videos related to

Sort By:
Pageof 6
Physical Chemistry Chemical Physics : PCCP|May 14, 2026
<i>Ab initio</i> study of the ground and excited electronic states of the SiNa<sup>+</sup> molecular ionN Abbassi, J Dhiflaoui, M Bejaoui, et al.
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.
Pathologie-Biologie|May 6, 2008
Detection of SHV-1 beta-lactamase in Pseudomonas aeruginosa strains by genetic methodsS Kalai Blagui, W Achour, M Bejaoui, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 6, 2011
[Cryptosporidium infection in patients with major histocompatibility complex class II deficiency syndrome in Tunisia: description of five cases]I Ben Abda, R Essid, F Mellouli, et al.
Pediatric Transplantation|January 28, 2009
Successful treatment of influenza A virus by oseltamivir in bone marrow transplant recipientsF Mellouli, M Ouederni, N Dhouib, 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.
Archives Francaises De Pediatrie|December 1, 1989
[The accelerated phase of Chediak-Higashi syndrome]M Bejaoui, F Veber, D Girault, et al.
Human Genetics|May 1, 1997
Carbonic anhydrase II (CA II) deficiency in Maghrebian patients: evidence for founder effect and genomic recombination at the CA II locusD M Fathallah, M Bejaoui, D Lepaslier, et al.
La Tunisie Medicale|June 3, 2010
Early onset of cerebrovascular accident in a thalassemia major childN Dhouib, F Mellouli, M Ouederni, et al.
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