Search research articles
Contact Us
Filters
Showing results (1-10 of 15) with videos related to
Page
of 2
Sort By:
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 10, 2013
[Hemolytic uremic syndrome as of 2013]
C Loirat, P Mariani-Kurkdjian, V Fremeaux-Bacchi
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine
|
March 19, 2019
Complement activation during intravascular hemolysis: Implication for sickle cell disease and hemolytic transfusion reactions
N S Merle, I Boudhabhay, J Leon, et al.
Annales De Medecine Interne
|
January 1, 1996
High frequency of C4 "null" alleles in primary antiphospholipid syndrome
S Bentolila, V Fremeaux-Bacchi, L Weiss, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 24, 2014
[Complement terminal fraction deficiency revealed at first invasive meningococcal infection]
C de Marcellus, M-K Taha, J Gaudelus, et al.
Presse Medicale (Paris, France : 1983)
|
May 21, 2005
[Neisseria meningitidis infection. Clinical criteria orienting towards a deficiency in the proteins of the complement]
M A Rameix-Welti, H Chedani, J Blouin, et al.
Clinical and Experimental Immunology
|
March 26, 2003
Restricted genetic defects underlie human complement C6 deficiency
M A Dragon-Durey, V Fremeaux-Bacchi, J Blouin, et al.
Journal of Clinical Immunology
|
March 1, 1997
Combined heterozygous deficiency of the classical complement pathway proteins C2 and C4
D Hartmann, V Fremeaux-Bacchi, L Weiss, et al.
BMC Nephrology
|
March 14, 2020
Cobalamin c deficiency associated with antifactor h antibody-associated hemolytic uremic syndrome in a young adult
C Philipponnet, J Desenclos, M Brailova, et al.
Journal of Clinical Immunology
|
September 1, 1994
Complete inherited deficiency of the fourth complement component in a child with systemic lupus erythematosus and his disease-free brother in a north African family
V Fremeaux-Bacchi, B Uring-Lambert, L Weiss, et al.
Archives De L'Institut Pasteur De Tunis
|
April 25, 2009
[Complement protein hereditary deficits during purulent meningitis: study of 61 adult Tunisian patients]
M Kallel-Sellami, R Abdelmalek, Y Zerzeri, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 10, 2013
[Hemolytic uremic syndrome as of 2013]
C Loirat, P Mariani-Kurkdjian, V Fremeaux-Bacchi
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine
|
March 19, 2019
Complement activation during intravascular hemolysis: Implication for sickle cell disease and hemolytic transfusion reactions
N S Merle, I Boudhabhay, J Leon, et al.
Annales De Medecine Interne
|
January 1, 1996
High frequency of C4 "null" alleles in primary antiphospholipid syndrome
S Bentolila, V Fremeaux-Bacchi, L Weiss, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 24, 2014
[Complement terminal fraction deficiency revealed at first invasive meningococcal infection]
C de Marcellus, M-K Taha, J Gaudelus, et al.
Presse Medicale (Paris, France : 1983)
|
May 21, 2005
[Neisseria meningitidis infection. Clinical criteria orienting towards a deficiency in the proteins of the complement]
M A Rameix-Welti, H Chedani, J Blouin, et al.
Clinical and Experimental Immunology
|
March 26, 2003
Restricted genetic defects underlie human complement C6 deficiency
M A Dragon-Durey, V Fremeaux-Bacchi, J Blouin, et al.
Journal of Clinical Immunology
|
March 1, 1997
Combined heterozygous deficiency of the classical complement pathway proteins C2 and C4
D Hartmann, V Fremeaux-Bacchi, L Weiss, et al.
BMC Nephrology
|
March 14, 2020
Cobalamin c deficiency associated with antifactor h antibody-associated hemolytic uremic syndrome in a young adult
C Philipponnet, J Desenclos, M Brailova, et al.
Journal of Clinical Immunology
|
September 1, 1994
Complete inherited deficiency of the fourth complement component in a child with systemic lupus erythematosus and his disease-free brother in a north African family
V Fremeaux-Bacchi, B Uring-Lambert, L Weiss, et al.
Archives De L'Institut Pasteur De Tunis
|
April 25, 2009
[Complement protein hereditary deficits during purulent meningitis: study of 61 adult Tunisian patients]
M Kallel-Sellami, R Abdelmalek, Y Zerzeri, et al.
Page
of 2