ASMD (acid sphingomyelinase deficiency), formerly Morbus Niemann-Pick type A/B: four adult cases with idiopathic hepatosplenomegaly and first results from enzyme replacement therapy (ERT) with olipudase alfa

Authors

Jan Koehler

Published

January 1, 2025

Abstract

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Journal

Zeitschrift für Gastroenterologie

Topics

DOI

10.1055/s-0044-1801115

ASMD (acid sphingomyelinase deficiency), formerly Morbus Niemann-Pick type A/B: four adult cases with idiopathic hepatosplenomegaly and first results from enzyme replacement therapy (ERT) with olipudase alfa

Authors

Jan Koehler

Published

January 1, 2025

Abstract

Supporters

Support the authors with ResearchCoin

Journal

Zeitschrift für Gastroenterologie

Topics

DOI

10.1055/s-0044-1801115

Paper

Paper

Paper

Paper

ASMD (acid sphingomyelinase deficiency), formerly Morbus Niemann-Pick type A/B: four adult cases with idiopathic hepatosplenomegaly and first results from enzyme replacement therapy (ERT) with olipudase alfa

Abstract

Supporters

Journal

Topics

DOI

ASMD (acid sphingomyelinase deficiency), formerly Morbus Niemann-Pick type A/B: four adult cases with idiopathic hepatosplenomegaly and first results from enzyme replacement therapy (ERT) with olipudase alfa

Abstract

Supporters

Journal

Topics

DOI