High incidence of α-Mannosidosis in ‘MPS-like’ phenotypes

2. September 2020

α-Mannosidosis is an inherited lysosomal storage disorder caused by genetic mutations leading to limited or no expression of a...

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Diagnostic Strategy for Females Suspected of Fabry Disease

18. August 2020

Fabry disease (FD) is a X-linked inherited disorder where deficiency of the α-Galactosidase A (α-Gal A) enzyme causes Globotriaosylceramide...

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Importance of including ASMD diagnostics in suspected Gaucher patients

4. August 2020

Acid Sphingomyelinase deficiency (ASMD), also known as Niemann-Pick Type A/B, is characterized by an enzyme deficiency that leads to...

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OPEN LETTER – We stay open for you and your patients – Please read

15. March 2020

We stay open for you and your patients! We used the last days to prepare us to continue our...

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Hemoglobinopathies and β-Thalassemia: Investigating High-Res Mass Spectrometry

18. February 2020

Early diagnosis of hemoglobin disorders and Thalassemias are become more important due to a high carrier frequency and ease...

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amedes and ARCHIMEDlife – a new strong international alliance

17. January 2020

ARCHIMEDlife is very proud to announce the strategic alliance with amedes Holding GmbH, a leading provider in interdisciplinary and...

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New cut-offs for lysosomal enzyme activities.

6. June 2019

We are happy to inform you that we have introduced a new diagnostic assay for the analysis of lysosomal...

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TDM für Psychopharmaka: (in German)

26. February 2019

Quantitative Bestimmung von Psychopharmaka in Blut, Serum oder Plasma Modernste Analysetechnik mittels Klinischer Massenspektrometrie (exakt, sensitiv, schnell) Kompetente fachärztliche Auskunft...

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First LEA assay launched

14. March 2018

LEA2 MPS Panel Our first LEA2 (Lysosomal Enzyme Activity) assay has now been started and with it several mucopolysaccharidoses...

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Awarded work: Hemoglobinopathies and Thalassemias

14. March 2018

Our awarded work (Poster Finalist at MSACL Europe, also see the PDF Poster Hemoglobinopathies_MSACL) on hemoglobinopathies and thalassemias is now...

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