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M R Barbouche

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

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Archives De L'Institut Pasteur De Tunis|December 12, 2003
Genetic and immunological assessment of a bone marrow transplantation in a patient with a primary immune defect: leukocyte adhesion deficiencyT Jamal, M R Barbouche, M Ben Hariz, et al.
Molecular Biotechnology|April 3, 2007
High level expression of recombinant Mycobacterium tuberculosis culture filtrate protein CFP32 in Pichia pastorisC Benabdesselem, M R Barbouche, M A Jarboui, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 18, 2017
Staphylococcal scalded skin syndrome: An uncommon symptomatology revealing an immune deficiencyH Ajmi, N Jemmali, S Mabrouk, et al.
Clinical and Diagnostic Laboratory Immunology|December 13, 2005
Gamma interferon is dispensable for neopterin production in vivoR Sghiri, J Feinberg, F Thabet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 25, 2015
[Auto-immune hepatitis in chronic granulomatous disease in a 2-year-old girl]L Gargouri, F Safi, I Mejdoub, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|April 14, 2020
Diagnosis and management of autoimmune hemolytic anemia in childrenM Weli, A Ben Hlima, R Belhadj, et al.
Bulletin De La Societe De Pathologie Exotique (1990)|December 22, 2010
[Listeriosis in Tunis: seven cases reports]A Elbeldi, H Smaoui, S Hamouda, et al.
Journal of Immunology (Baltimore, Md. : 1950)|April 21, 2001
Uncoordinated HLA-D gene expression in a RFXANK-defective patient with MHC class II deficiencyA M Lennon-Duménil, M R Barbouche, J Vedrenne, et al.
Clinical Immunology (Orlando, Fla.)|July 3, 2017
Rare splicing defects of FAS underly severe recessive autoimmune lymphoproliferative syndromeN Agrebi, I Ben-Mustapha, N Matoussi, et al.
Journal of Human Genetics|August 29, 2006
Genetic and mutational heterogeneity of autosomal recessive chronic granulomatous disease in TunisiaR El Kares, M R Barbouche, H Elloumi-Zghal, et al.
Pageof 2

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

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Archives De L'Institut Pasteur De Tunis|December 12, 2003
Genetic and immunological assessment of a bone marrow transplantation in a patient with a primary immune defect: leukocyte adhesion deficiencyT Jamal, M R Barbouche, M Ben Hariz, et al.
Molecular Biotechnology|April 3, 2007
High level expression of recombinant Mycobacterium tuberculosis culture filtrate protein CFP32 in Pichia pastorisC Benabdesselem, M R Barbouche, M A Jarboui, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 18, 2017
Staphylococcal scalded skin syndrome: An uncommon symptomatology revealing an immune deficiencyH Ajmi, N Jemmali, S Mabrouk, et al.
Clinical and Diagnostic Laboratory Immunology|December 13, 2005
Gamma interferon is dispensable for neopterin production in vivoR Sghiri, J Feinberg, F Thabet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 25, 2015
[Auto-immune hepatitis in chronic granulomatous disease in a 2-year-old girl]L Gargouri, F Safi, I Mejdoub, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|April 14, 2020
Diagnosis and management of autoimmune hemolytic anemia in childrenM Weli, A Ben Hlima, R Belhadj, et al.
Bulletin De La Societe De Pathologie Exotique (1990)|December 22, 2010
[Listeriosis in Tunis: seven cases reports]A Elbeldi, H Smaoui, S Hamouda, et al.
Journal of Immunology (Baltimore, Md. : 1950)|April 21, 2001
Uncoordinated HLA-D gene expression in a RFXANK-defective patient with MHC class II deficiencyA M Lennon-Duménil, M R Barbouche, J Vedrenne, et al.
Clinical Immunology (Orlando, Fla.)|July 3, 2017
Rare splicing defects of FAS underly severe recessive autoimmune lymphoproliferative syndromeN Agrebi, I Ben-Mustapha, N Matoussi, et al.
Journal of Human Genetics|August 29, 2006
Genetic and mutational heterogeneity of autosomal recessive chronic granulomatous disease in TunisiaR El Kares, M R Barbouche, H Elloumi-Zghal, et al.
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