Centre Hospitalier Universitaire Ibn Rochd

Mutations in CGI-58, the Gene Encoding a New Protein of the Esterase/Lipase/Thioesterase Subfamily, in Chanarin-Dorfman Syndrome

Caroline Lefèvre, Florence Jobard, F. Caux et al. · The American Journal of Human Genetics · 2001 · 460 citations · Full text

Mendelian Disorder, Biochemistry, Genetic Disorder +10

Revisiting Human IL-12Rβ1 Deficiency

Ludovic de Beaucoudrey, Arina Samarina, Jacinta Bustamante et al. · Medicine · 2010 · 379 citations · Full text

Algorithm for the management of patients at low, high and very high risk of osteoporotic fractures

John А. Kanis, Nicholas C. Harvey, Eugène McCloskey et al. · Osteoporosis International · 2019 · 354 citations · Full text

Early Tracheostomy versus Prolonged Endotracheal Intubation in Severe Head Injury

M. A. Bouderka, Bouchra Fakhir, Abderrahmane Bouaggad et al. · The Journal of Trauma: Injury, Infection, and Critical Care · 2004 · 283 citations

Prevalence of symptoms of asthma, rhinitis and eczema in 13‐ to 14‐year‐old children in Africa: the International Study of Asthma and Allergies in Childhood Phase III

N Aït-Khaled, Joseph Odhiambo, Neil Pearce et al. · Allergy · 2007 · 247 citations

Asthma, Environmental Allergy, Allergy Medicine +21