Niemann-Pick B - RS - 5th infusion.
Por um escritor misterioso
Descrição
TAVI in Patient Suffering from Niemann–Pick Disease (Acid Sphingomyelinase Deficiency) with Concomitant Situs Inversus and Dextrocardia
Lysosomal storage diseases: Diagnostic confirmation and management of presymptomatic individuals
Frontiers Expert opinion on patient journey, diagnosis and clinical monitoring in acid sphingomyelinase deficiency in Turkey: a pediatric metabolic disease specialist's perspective
Necroptosis in Niemann–Pick disease, type C1: a potential therapeutic target
Experimental treatment for Niemann-Pick disease type C1 appears safe, effective
Interstitial lung disease in lysosomal storage disorders
Potential treatment for Niemann-Pick type C, a rare neurodegenerative disease
JCM, Free Full-Text
PDF) Novel first-dose adverse drug reactions during a phase I trial of olipudase alfa (recombinant human acid sphingomyelinase) in adults with Niemann–Pick disease type B (acid sphingomyelinase deficiency)
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