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Scandinavian Journal of Rheumatology
|
September 2, 2017
Relationship between glucocorticoid dose and adverse events in systemic lupus erythematosus: data from a randomized clinical trial
S Emamikia, C Gentline, K Chatzidionysiou, et al.
Clinical Genetics
|
October 16, 2007
Crouzon with acanthosis nigricans. Further delineation of the syndrome
L Arnaud-López, R Fragoso, J Mantilla-Capacho, et al.
La Revue De Medecine Interne
|
September 23, 2008
[Pathogenesis of primary large vessel arteritis]
L Arnaud, J Haroche, P Duhaut, et al.
Heredity
|
December 6, 2002
Increased fecundity of malathion-specific resistant beetles in absence of insecticide pressure
L Arnaud, Y Brostaux, L K Assié, et al.
Electrophoresis
|
October 10, 2002
Finite element simulation of Off-Gel trade mark buffering
Isabelle L Arnaud, Jacques Josserand, Joël S Rossier, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine
|
June 4, 2013
[A KEL*02mod allele responsible for an apparent maternity exclusion]
M Monfort, T Peyrard, L Arnaud, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 31, 2006
Apert syndrome with preaxial polydactyly showing the typical mutation Ser252Trp in the FGFR2 gene
J M Mantilla-Capacho, L Arnaud, M Díaz-Rodriguez, et al.
Optics Express
|
April 1, 2009
An enhanced contrast to detect bulk objects under arbitrary rough surfaces
L Arnaud, G Georges, J Sorrentini, et al.
The British Journal of Dermatology
|
January 24, 2017
Efficacy and comparison of antimalarials in cutaneous lupus erythematosus subtypes: a systematic review and meta-analysis
F Chasset, J-D Bouaziz, N Costedoat-Chalumeau, et al.
Vox Sanguinis
|
September 11, 2012
The ABCB6 mutation p.Arg192Trp is a recessive mutation causing the Lan- blood type
C Saison, V Helias, T Peyrard, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 79) with videos related to
Sort By:
Page
of 8
Scandinavian Journal of Rheumatology
|
September 2, 2017
Relationship between glucocorticoid dose and adverse events in systemic lupus erythematosus: data from a randomized clinical trial
S Emamikia, C Gentline, K Chatzidionysiou, et al.
Clinical Genetics
|
October 16, 2007
Crouzon with acanthosis nigricans. Further delineation of the syndrome
L Arnaud-López, R Fragoso, J Mantilla-Capacho, et al.
La Revue De Medecine Interne
|
September 23, 2008
[Pathogenesis of primary large vessel arteritis]
L Arnaud, J Haroche, P Duhaut, et al.
Heredity
|
December 6, 2002
Increased fecundity of malathion-specific resistant beetles in absence of insecticide pressure
L Arnaud, Y Brostaux, L K Assié, et al.
Electrophoresis
|
October 10, 2002
Finite element simulation of Off-Gel trade mark buffering
Isabelle L Arnaud, Jacques Josserand, Joël S Rossier, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine
|
June 4, 2013
[A KEL*02mod allele responsible for an apparent maternity exclusion]
M Monfort, T Peyrard, L Arnaud, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 31, 2006
Apert syndrome with preaxial polydactyly showing the typical mutation Ser252Trp in the FGFR2 gene
J M Mantilla-Capacho, L Arnaud, M Díaz-Rodriguez, et al.
Optics Express
|
April 1, 2009
An enhanced contrast to detect bulk objects under arbitrary rough surfaces
L Arnaud, G Georges, J Sorrentini, et al.
The British Journal of Dermatology
|
January 24, 2017
Efficacy and comparison of antimalarials in cutaneous lupus erythematosus subtypes: a systematic review and meta-analysis
F Chasset, J-D Bouaziz, N Costedoat-Chalumeau, et al.
Vox Sanguinis
|
September 11, 2012
The ABCB6 mutation p.Arg192Trp is a recessive mutation causing the Lan- blood type
C Saison, V Helias, T Peyrard, et al.
Page
of 8