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Type B Niemann-Pick disease: findings at chest radiography, thin-section CT, and pulmonary function testing.
Liver and skin histopathology in adults with acid sphingomyelinase deficiency (Niemann-Pick disease type B).
A prospective, cross-sectional survey study of the natural history of Niemann-Pick disease type B.
Niemann-Pick Disease, Type A
Niemann-Pick Disease, Type B
Lyso-sphingomyelin is elevated in dried blood spots of Niemann-Pick B patients.
Successful within-patient dose escalation of olipudase alfa in acid sphingomyelinase deficiency.
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).
Cause of death in patients with chronic visceral and chronic neurovisceral acid sphingomyelinase deficiency (Niemann-Pick disease type B and B variant): Literature review and report of new cases.
Clearance of Hepatic Sphingomyelin by Olipudase Alfa Is Associated With Improvement in Lipid Profiles in Acid Sphingomyelinase Deficiency.
Corrigendum to "Cause of death in patients with chronic visceral and chronic neurovisceral acid sphingomyelinase deficiency (Niemann-Pick disease type B and B variant): Literature review and report of new cases" [Mol. Genet. Metab. 118 (2016) 206-213].
Niemann Pick Diseases