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Arthritis and Rheumatism|January 11, 2003
Interstitial lung disease in polymyositis and dermatomyositisI Marie, E Hachulla, P Chérin, et al.
La Revue De Medecine Interne|July 28, 1999
[Macrophagic myofasciitis: description and etiopathogenic hypotheses. Study and Research Group on Acquired and Dysimmunity-related Muscular Diseases (GERMMAD) of the French Association against Myopathies (AFM)]P Chérin, P Laforet, R K Ghérardi, et al.
Presse Medicale (Paris, France : 1983)|March 8, 2000
[Macrophagic myofasciitis. Study and Research Group on Acquired and Dysimmunity-related muscular diseases (GERMMAD)]P Chérin, P Laforêt, R K Ghérardi, et al.
Neuromuscular Disorders : NMD|June 19, 2001
Macrophagic myofasciitis associated with inclusion body myositis: a report of three casesP Chérin, D Menard, P Mouton, et al.
Lancet (London, England)|August 26, 1998
Macrophagic myofasciitis: an emerging entity. Groupe d'Etudes et Recherche sur les Maladies Musculaires Acquises et Dysimmunitaires (GERMMAD) de l'Association Française contre les Myopathies (AFM)R K Gherardi, M Coquet, P Chérin, et al.
Clinical Genetics|June 1, 2011
Fabry disease 'The New Great Imposter': results of the French Observatoire in Internal Medicine Departments (FIMeD)O Lidove, P Kaminsky, E Hachulla, et al.
Rheumatology (Oxford, England)|September 29, 1999
Temporal 67gallium uptake is increased in temporal arteritisT Généreau, O Lortholary, L Guillevin, et al.
Journal of Immunology (Baltimore, Md. : 1950)|September 7, 2001
Severe perturbations of the blood T cell repertoire in polymyositis, but not dermatomyositis patientsO Benveniste, P Chérin, T Maisonobe, et al.
La Revue De Medecine Interne|September 11, 2019
[Diagnostic journey of type 1 Gaucher Disease patients: A survey including internists and hematologists]S Deriaz, C Serratrice, O Lidove, et al.
Journal of Inherited Metabolic Disease|June 10, 2010
The neurological manifestations of Gaucher disease type 1: the French Observatoire on Gaucher disease (FROG)P Chérin, C Rose, C de Roux-Serratrice, et al.
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