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Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics
|
December 31, 2005
Propagation and localization of electromagnetic waves in quasiperiodic serial loop structures
H Aynaou, E H El Boudouti, Y El Hassouani, et al.
Pathologie-Biologie
|
July 16, 2013
Genetic factors and multiple sclerosis in the Moroccan population: a role for HLA class II
S Ouadghiri, K El Alaoui Toussi, C Brick, et al.
Nature Genetics
|
May 1, 1995
The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1
A Benomar, L Krols, G Stevanin, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
April 1, 1987
Chemotactic factor and P15E-related chemotaxis inhibitor in human melanoma cell lines with different macrophage content and tumorigenicity in nude mice
A Benomar, W J Ming, G Taraboletti, et al.
Revue Neurologique
|
June 13, 2009
[Efficacy and safety of cyclophosphamide treatment in progressive multiple sclerosis]
E Ait Ben Haddou, A Benomar, S Ahid, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
November 22, 2005
[Q fever: a rare cause of endocarditis]
M El Kouache, L Marmade, M Laaroussi, et al.
Journal of Medical Genetics
|
April 16, 1998
The first de novo mutation of the connexin 32 gene associated with X linked Charcot-Marie-Tooth disease
F Meggouh, A Benomar, H Rouger, et al.
Journal of Neuroradiology = Journal De Neuroradiologie
|
September 1, 1996
[Cerebral vascular accidents due to hydatid embolisms. Apropos of 2 cases]
A el Quessar, M Benabdejlil, A Mansouri, et al.
Human Genetics
|
February 1, 1997
Refinement of the locus for autosomal dominant cerebellar ataxia type II to chromosome 3p21.1-14.1
L Krols, J J Martin, G David, et al.
La Revue De Medecine Interne
|
January 1, 1997
[Cerebral infarction, pseudolupic syndrome and myxoma of the left atrium]
K Benbouazza, M el Alaoui Faris, A Benomar, et al.
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of 8
Search research articles
Search
Showing results (51-60 of 77) with videos related to
Sort By:
Page
of 8
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics
|
December 31, 2005
Propagation and localization of electromagnetic waves in quasiperiodic serial loop structures
H Aynaou, E H El Boudouti, Y El Hassouani, et al.
Pathologie-Biologie
|
July 16, 2013
Genetic factors and multiple sclerosis in the Moroccan population: a role for HLA class II
S Ouadghiri, K El Alaoui Toussi, C Brick, et al.
Nature Genetics
|
May 1, 1995
The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1
A Benomar, L Krols, G Stevanin, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
April 1, 1987
Chemotactic factor and P15E-related chemotaxis inhibitor in human melanoma cell lines with different macrophage content and tumorigenicity in nude mice
A Benomar, W J Ming, G Taraboletti, et al.
Revue Neurologique
|
June 13, 2009
[Efficacy and safety of cyclophosphamide treatment in progressive multiple sclerosis]
E Ait Ben Haddou, A Benomar, S Ahid, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
November 22, 2005
[Q fever: a rare cause of endocarditis]
M El Kouache, L Marmade, M Laaroussi, et al.
Journal of Medical Genetics
|
April 16, 1998
The first de novo mutation of the connexin 32 gene associated with X linked Charcot-Marie-Tooth disease
F Meggouh, A Benomar, H Rouger, et al.
Journal of Neuroradiology = Journal De Neuroradiologie
|
September 1, 1996
[Cerebral vascular accidents due to hydatid embolisms. Apropos of 2 cases]
A el Quessar, M Benabdejlil, A Mansouri, et al.
Human Genetics
|
February 1, 1997
Refinement of the locus for autosomal dominant cerebellar ataxia type II to chromosome 3p21.1-14.1
L Krols, J J Martin, G David, et al.
La Revue De Medecine Interne
|
January 1, 1997
[Cerebral infarction, pseudolupic syndrome and myxoma of the left atrium]
K Benbouazza, M el Alaoui Faris, A Benomar, et al.
Page
of 8