Transthyretin Amyloidosis (ATTRv): Advancing Early Diagnosis Through Genetic Testing
November 12, 2025
Transthyretin amyloidosis (ATTRv) is a progressive, life-threatening, and often underdiagnosed disease caused by the deposition of toxic transthyretin (TTR) amyloid… Read More
Press Release. ARCHIMEDlife achieves ISO 27001 Certification for Information Security Management
September 3, 2025
Vienna, Austria – [03.09.2025] — ARCHIMEDlife, international disease-focused Medical Laboratories* in Precision Medicine for Rare Disease and Specialty Diagnostics, is proud to… Read More
Award for Outstanding Achievements on Rare Diseases
April 17, 2025
We are very happy to share that our CEO, Dr. David C. Kasper, has been selected as the winner of… Read More
WORLDSymposium 2025 Poster Presentations – Updates on important diagnostic services
February 21, 2025
The WORLDSymposium for Lysosomal Storage Disorders convened in San Diego, CA, USA earlier this month. This important meeting brings together… Read More
Newborn Screening and Presymptomatic Treatment of Metachromatic Leukodystrophy
January 23, 2025
Metachromatic leukodystrophy (MLD) is a lysosomal storage disorder characterized by progressive neurodegeneration due to a deficiency in the enzyme arylsulfatase-A… Read More
MedLab Dubai. New directors appointed.
October 23, 2023
New directors appointed: @Gröning, MD, as Medical Director, Dr. med. Thomas Winkler , MD and David C. Kasper (also as Manager). Our mission together… Read More
Importance to include differential diagnostics for acid sphingomyelinase deficiency (ASMD) in patients suspected to have to Gaucher disease
June 1, 2023
Acid sphingomyelinase deficiency (ASMD), commonly called Niemann-Pick A/B disease, is an autosomal recessively inherited lysosomal storage disorder resulting from a… Read More
In-person Conferences once again!
January 17, 2022
With the start of 2022, ARCHIMEDlife is pleased to announce that we will be once again attending in-person conferences! The… Read More
Molecular basis of mucopolysaccharidosis IVA (Morquio A syndrome): A review and classification of GALNS gene variants and reporting of 68 novel variants
August 13, 2021
Mucopolysaccharidosis IVA (MPS IVA, Morquio A syndrome) is a rare autosomal recessive lysosomal storage disorder caused by mutations in the… Read More
