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La Revue De Medecine Interne
|
June 25, 2022
[Contribution of antiphosphatidylserine/prothrombin (anti-PS/PT) antibody detection in the diagnosis and management of antiphospholipid syndrome (APS)]
A Delarue, M-A Dragon-Durey, L Darnige
La Revue De Medecine Interne
|
March 18, 2017
[Laboratory diagnosis of antiphospholipid syndrome: From criteria to practice]
V Joste, M-A Dragon-Durey, L Darnige
La Revue De Medecine Interne
|
March 8, 2011
[Atypical hemolytic-uremic syndrome related to abnormalities within the complement system]
V Frémeaux-Bacchi, F Fakhouri, L Roumenina, 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.
Immunology Letters
|
February 13, 2001
Expression of low-affinity Fc gamma receptor by a human metastatic melanoma line
L Cassard, M A Dragon-Durey, A Ralli, et al.
Leukemia
|
July 17, 1998
Non-Hodgkin's lymphomas and myeloid disorders: deletions associated with t(2;5) and t(3;5) detected by FISH
M A Dragon-Durey, A F Goguel, C Leonard, et al.
Indian Journal of Nephrology
|
March 31, 2017
Targeting renin-angiotensin system in malignant hypertension in atypical hemolytic uremic syndrome
V Raghunathan, S K Sethi, M A Dragon-Durey, et al.
Journal of Medical Genetics
|
May 14, 2009
The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome
M-A Dragon-Durey, C Blanc, F Marliot, et al.
Journal of Immunology Research
|
June 12, 2015
Increased Performances of the Biological Diagnosis of the Antiphospholipid Syndrome by the Use of a Multiplex Assay
M Sénant, H Rostane, F Fernani-Oukil, et al.
The British Journal of Dermatology
|
September 21, 2004
Hereditary angio-oedema: effective treatment with the progestogen-only pill in a young woman
L Amar, O Lidove, J E Kahn, et al.
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of 2
Search research articles
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Showing results (1-10 of 18) with videos related to
Sort By:
Page
of 2
La Revue De Medecine Interne
|
June 25, 2022
[Contribution of antiphosphatidylserine/prothrombin (anti-PS/PT) antibody detection in the diagnosis and management of antiphospholipid syndrome (APS)]
A Delarue, M-A Dragon-Durey, L Darnige
La Revue De Medecine Interne
|
March 18, 2017
[Laboratory diagnosis of antiphospholipid syndrome: From criteria to practice]
V Joste, M-A Dragon-Durey, L Darnige
La Revue De Medecine Interne
|
March 8, 2011
[Atypical hemolytic-uremic syndrome related to abnormalities within the complement system]
V Frémeaux-Bacchi, F Fakhouri, L Roumenina, 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.
Immunology Letters
|
February 13, 2001
Expression of low-affinity Fc gamma receptor by a human metastatic melanoma line
L Cassard, M A Dragon-Durey, A Ralli, et al.
Leukemia
|
July 17, 1998
Non-Hodgkin's lymphomas and myeloid disorders: deletions associated with t(2;5) and t(3;5) detected by FISH
M A Dragon-Durey, A F Goguel, C Leonard, et al.
Indian Journal of Nephrology
|
March 31, 2017
Targeting renin-angiotensin system in malignant hypertension in atypical hemolytic uremic syndrome
V Raghunathan, S K Sethi, M A Dragon-Durey, et al.
Journal of Medical Genetics
|
May 14, 2009
The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome
M-A Dragon-Durey, C Blanc, F Marliot, et al.
Journal of Immunology Research
|
June 12, 2015
Increased Performances of the Biological Diagnosis of the Antiphospholipid Syndrome by the Use of a Multiplex Assay
M Sénant, H Rostane, F Fernani-Oukil, et al.
The British Journal of Dermatology
|
September 21, 2004
Hereditary angio-oedema: effective treatment with the progestogen-only pill in a young woman
L Amar, O Lidove, J E Kahn, et al.
Page
of 2