Willem De Ridder

Antwerpen, VLG, Belgium

Last Updated: 09/26/2026

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Found 36 publications

A 5' UTR CCG expansion in TBC1D7 causes oculopharyngodistal myopathy.

A 5' UTR CCG expansion in TBC1D7 causes oculopharyngodistal myopathy.

Journal: medRxiv : the preprint server for health sciences
Published: April 10, 2026

Brachio-cervical inflammatory myopathy: multilevel clinical, histopathological and multi-omic analyses of a syndrome variably associated with systemic sclerosis.

Brachio-cervical inflammatory myopathy: multilevel clinical, histopathological and multi-omic analyses of a syndrome variably associated with systemic sclerosis.

Journal: Acta neuropathologica
Published: November 18, 2025

Ageing-Associated Dysregulation of Myogenic Differentiation in Inclusion Body Myositis.

Ageing-Associated Dysregulation of Myogenic Differentiation in Inclusion Body Myositis.

Journal: Journal of cachexia, sarcopenia and muscle
Published: November 07, 2025

Gender differences in Myasthenia Gravis in a neuromuscular reference center in Belgium.

Gender differences in Myasthenia Gravis in a neuromuscular reference center in Belgium.

Journal: Acta neurologica Belgica
Published: April 03, 2025

Ageing Signatures and Disturbed Muscle Regeneration in Muscle Proteome of Inclusion Body Myositis.

Ageing Signatures and Disturbed Muscle Regeneration in Muscle Proteome of Inclusion Body Myositis.

Journal: Journal of cachexia, sarcopenia and muscle
Published: March 21, 2025

Chronic sarcoid myopathy mimicking facioscapulohumeral muscular dystrophy: a case report.

Chronic sarcoid myopathy mimicking facioscapulohumeral muscular dystrophy: a case report.

Journal: Neuromuscular disorders : NMD
Published: February 18, 2025

TBK1-associated motor neuron disease with concomitant vacuolar myopathy: a case resembling a multisystem proteinopathy.

TBK1-associated motor neuron disease with concomitant vacuolar myopathy: a case resembling a multisystem proteinopathy.

Journal: Neuromuscular disorders : NMD
Published: February 06, 2025

A heterozygous 9q34 deletion encompassing SPTAN1 as a cause of distal myopathy.

A heterozygous 9q34 deletion encompassing SPTAN1 as a cause of distal myopathy.

Journal: European journal of human genetics : EJHG
Published: December 17, 2024

Muscle Biopsy Findings in Valosin-Containing Protein Multisystem Proteinopathy.

Muscle Biopsy Findings in Valosin-Containing Protein Multisystem Proteinopathy.

Journal: Neurology. Genetics
Published: November 26, 2024

Heterozygous loss-of-function variants in SPTAN1 cause an early childhood onset distal myopathy.

Heterozygous loss-of-function variants in SPTAN1 cause an early childhood onset distal myopathy.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 15, 2024

Heterozygous loss-of-function variants in SPTAN1 cause a novel early childhood onset distal myopathy with chronic neurogenic features.

Heterozygous loss-of-function variants in SPTAN1 cause a novel early childhood onset distal myopathy with chronic neurogenic features.

Journal: medRxiv : the preprint server for health sciences
Published: October 07, 2024

TBP Repeat Expansion Analysis in Patients Carrying Heterozygous STUB1 Variants.

TBP Repeat Expansion Analysis in Patients Carrying Heterozygous STUB1 Variants.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: October 04, 2024
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Last Updated: 09/26/2026