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Joint Bone Spine
|
July 7, 2024
Cluster analysis of clinical manifestations assigns systemic lupus erythematosus-phenotype subgroups: A multicentre study on 440 patients
Fanny Mariette, Véronique Le Guern, Yann Nguyen, et al.
Autoimmunity Reviews
|
July 15, 2018
Classification of primary antiphospholipid syndrome as systemic lupus erythematosus: Analysis of a cohort of 214 patients
Romain Paule, Nathalie Morel, Véronique Le Guern, et al.
Neuromuscular Disorders : NMD
|
October 29, 2000
Charcot-Marie-Tooth 2-like presentation of an Algerian family with giant axonal neuropathy
R Zemmouri, H Azzedine, S Assami, et al.
Lupus
|
April 29, 2018
Disease severity of proliferative lupus nephritis in Maghrebians
F Tamirou, N Costedoat-Chalumeau, G Medkouri, et al.
Annals of the Rheumatic Diseases
|
September 5, 2006
Tolerance and efficacy of rituximab and changes in serum B cell biomarkers in patients with systemic complications of primary Sjögren's syndrome
Raphaèle Seror, Christelle Sordet, Loic Guillevin, et al.
Human Genetics
|
January 1, 1996
Molecular genetic analysis of the 17p11.2 region in patients with hereditary neuropathy with liability to pressure palsies (HNPP)
V Timmerman, A Löfgren, E Le Guern, et al.
Clinical Reviews in Allergy & Immunology
|
February 13, 2015
A Critical Review of the Effects of Hydroxychloroquine and Chloroquine on the Eye
Nathalie Costedoat-Chalumeau, Bertrand Dunogué, Gaëlle Leroux, et al.
American Journal of Obstetrics and Gynecology
|
April 4, 2021
Is the presence of antiphospholipid antibodies a poor prognostic factor for patients with hemolysis, elevated liver enzymes, and low platelet count syndrome?
Mathilde Pécourt, Cécile Yelnik, Louise Ghesquiere, et al.
Archives of Neurology
|
April 23, 2003
Phenotypical features of a Moroccan family with autosomal recessive Charcot-Marie-Tooth disease associated with the S194X mutation in the GDAP1 gene
Nazha Birouk, Hamid Azzedine, Odile Dubourg, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
December 25, 2015
Parkinson disease male-to-female ratios increase with age: French nationwide study and meta-analysis
Frédéric Moisan, Sofiane Kab, Fatima Mohamed, et al.
Page
of 49
Search research articles
Search
Showing results (291-300 of 486) with videos related to
Sort By:
Page
of 49
Joint Bone Spine
|
July 7, 2024
Cluster analysis of clinical manifestations assigns systemic lupus erythematosus-phenotype subgroups: A multicentre study on 440 patients
Fanny Mariette, Véronique Le Guern, Yann Nguyen, et al.
Autoimmunity Reviews
|
July 15, 2018
Classification of primary antiphospholipid syndrome as systemic lupus erythematosus: Analysis of a cohort of 214 patients
Romain Paule, Nathalie Morel, Véronique Le Guern, et al.
Neuromuscular Disorders : NMD
|
October 29, 2000
Charcot-Marie-Tooth 2-like presentation of an Algerian family with giant axonal neuropathy
R Zemmouri, H Azzedine, S Assami, et al.
Lupus
|
April 29, 2018
Disease severity of proliferative lupus nephritis in Maghrebians
F Tamirou, N Costedoat-Chalumeau, G Medkouri, et al.
Annals of the Rheumatic Diseases
|
September 5, 2006
Tolerance and efficacy of rituximab and changes in serum B cell biomarkers in patients with systemic complications of primary Sjögren's syndrome
Raphaèle Seror, Christelle Sordet, Loic Guillevin, et al.
Human Genetics
|
January 1, 1996
Molecular genetic analysis of the 17p11.2 region in patients with hereditary neuropathy with liability to pressure palsies (HNPP)
V Timmerman, A Löfgren, E Le Guern, et al.
Clinical Reviews in Allergy & Immunology
|
February 13, 2015
A Critical Review of the Effects of Hydroxychloroquine and Chloroquine on the Eye
Nathalie Costedoat-Chalumeau, Bertrand Dunogué, Gaëlle Leroux, et al.
American Journal of Obstetrics and Gynecology
|
April 4, 2021
Is the presence of antiphospholipid antibodies a poor prognostic factor for patients with hemolysis, elevated liver enzymes, and low platelet count syndrome?
Mathilde Pécourt, Cécile Yelnik, Louise Ghesquiere, et al.
Archives of Neurology
|
April 23, 2003
Phenotypical features of a Moroccan family with autosomal recessive Charcot-Marie-Tooth disease associated with the S194X mutation in the GDAP1 gene
Nazha Birouk, Hamid Azzedine, Odile Dubourg, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
December 25, 2015
Parkinson disease male-to-female ratios increase with age: French nationwide study and meta-analysis
Frédéric Moisan, Sofiane Kab, Fatima Mohamed, et al.
Page
of 49