Saskia Lassche

Heerlen, LI, Netherlands

Last Updated: 09/26/2026

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Found 24 publications

KBTBD13 is an actin-binding protein that modulates muscle kinetics.

KBTBD13 is an actin-binding protein that modulates muscle kinetics.

Journal: The Journal of clinical investigation

Published: February 01, 2024

An up-to-date myopathologic characterisation of facioscapulohumeral muscular dystrophy type 1 muscle biopsies shows sarcolemmal complement membrane attack complex deposits and increased skeletal muscle regeneration.

An up-to-date myopathologic characterisation of facioscapulohumeral muscular dystrophy type 1 muscle biopsies shows sarcolemmal complement membrane attack complex deposits and increased skeletal muscle regeneration.

Journal: Neuromuscular disorders : NMD

Published: October 25, 2023

Assessment of PABPN1 nuclear inclusions on a large cohort of patients and in a human xenograft model of oculopharyngeal muscular dystrophy.

Assessment of PABPN1 nuclear inclusions on a large cohort of patients and in a human xenograft model of oculopharyngeal muscular dystrophy.

Journal: Acta neuropathologica

Published: June 15, 2022

The double homeodomain protein DUX4c is associated with regenerating muscle fibers and RNA-binding proteins.

The double homeodomain protein DUX4c is associated with regenerating muscle fibers and RNA-binding proteins.

Journal: Skeletal muscle

Published: July 20, 2021

Facioscapulohumeral muscular dystrophy-Reproductive counseling, pregnancy, and delivery in a complex multigenetic disease.

Facioscapulohumeral muscular dystrophy-Reproductive counseling, pregnancy, and delivery in a complex multigenetic disease.

Journal: Clinical genetics

Published: May 12, 2021

Facioscapulohumeral dystrophy transcriptome signatures correlate with different stages of disease and are marked by different MRI biomarkers.

Facioscapulohumeral dystrophy transcriptome signatures correlate with different stages of disease and are marked by different MRI biomarkers.

Journal: Scientific reports

Published: March 09, 2021

Correlation Between Quantitative MRI and Muscle Histopathology in Muscle Biopsies from Healthy Controls and Patients with IBM, FSHD and OPMD.

Correlation Between Quantitative MRI and Muscle Histopathology in Muscle Biopsies from Healthy Controls and Patients with IBM, FSHD and OPMD.

Journal: Journal of neuromuscular diseases

Published: September 14, 2020

Age-Associated Salivary MicroRNA Biomarkers for Oculopharyngeal Muscular Dystrophy.

Age-Associated Salivary MicroRNA Biomarkers for Oculopharyngeal Muscular Dystrophy.

Journal: International journal of molecular sciences

Published: July 12, 2020

An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy.

An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy.

Journal: Brain : a journal of neurology

Published: June 18, 2020

Reduced specific force in patients with mild and severe facioscapulohumeral muscular dystrophy.

Reduced specific force in patients with mild and severe facioscapulohumeral muscular dystrophy.

Journal: Muscle & nerve

Published: April 14, 2020

Nerve ultrasound for distinguishing inflammatory neuropathy from amyotrophic lateral sclerosis: Not black and white.

Nerve ultrasound for distinguishing inflammatory neuropathy from amyotrophic lateral sclerosis: Not black and white.

Journal: Muscle & nerve

Published: August 16, 2019

Preserved single muscle fiber specific force in facioscapulohumeral muscular dystrophy.

Preserved single muscle fiber specific force in facioscapulohumeral muscular dystrophy.

Journal: Neurology

Published: June 16, 2019

Showing 1-12 of 24

Last Updated: 09/26/2026