Results 111 to 120 of about 135,809 (156)
Enzyme replacement therapy in infants and very young children with Gaucher disease using velaglucerase alfa: a single-center experience. [PDF]
Front PediatrGoker-Alpan O +3 more
europepmc +1 more source
Estudio prospectivo clínico y radiológico de la enfermedad de Pompe del adulto
, 2018 Enzyme replacement therapy has shown to be effective for late onset Pompe disease (LOPD). The discovery of biomarkers useful for monitoring disease progression is one of the priority research topics in Pompe disease. Muscle MRI could be one posible test but the correlation between muscle MRI and muscle strength and function has been only partially ...
openaire +1 more source
Caracterización clínica y funcional de los pacientes con enfermedad de Pompe en Colombia
, 2016 La enfermedad de Pompe es una patología neuromuscular hereditaria rara caracterizada por la deficiencia de la enzima alfa glucosidasa ácida lo que lleva a un depósito de glucógeno en numerosos tejidos principalmente en el tejido muscular. El propósito de este trabajo es caracterizar clínica y funcionalmente a los pacientes con enfermedad de Pompe en ...
openaire +1 more source
ESICM LIVES 2018 : Paris, France. 20-24 October 2018. [PDF]
Intensive Care Med Exp, 2018 europepmc +1 more source
Giorgia Marangon, "La poesía de Ugo Foscolo y su alter ego en francés" [PDF]
Mimmi, Franco
core +1 more source
World Congress on Osteoporosis, Osteoarthritis and Musculoskeletal Diseases (WCO-IOF-ESCEO 2025). [PDF]
Aging Clin Exp Reseuropepmc +1 more source