Michael A. Van Es

Utrecht, UT, Netherlands

Last Updated: 09/26/2026

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Found 116 publications

Diagnostic Revision From Primary Lateral Sclerosis to Amyotrophic Lateral Sclerosis: A Cohort Study.

Diagnostic Revision From Primary Lateral Sclerosis to Amyotrophic Lateral Sclerosis: A Cohort Study.

Journal: Neurology

Published: May 29, 2026

Tofersen treatment in respiratory onset amyotrophic lateral sclerosis and a variant of uncertain significance in SOD1; a case report.

Tofersen treatment in respiratory onset amyotrophic lateral sclerosis and a variant of uncertain significance in SOD1; a case report.

Journal: European journal of human genetics : EJHG

Published: April 28, 2026

Fast and controlled access to tofersen for SOD1-related amyotrophic lateral sclerosis in The Netherlands; experiences using the orphan drug access protocol.

Fast and controlled access to tofersen for SOD1-related amyotrophic lateral sclerosis in The Netherlands; experiences using the orphan drug access protocol.

Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration

Published: April 13, 2026

Associations of cognitive and behavioural impairment in ALS with brain pathology: pTDP-43 versus microglial activation.

Associations of cognitive and behavioural impairment in ALS with brain pathology: pTDP-43 versus microglial activation.

Journal: Journal of neurology

Published: March 06, 2026

Bi-allelic intermediate ATXN2 repeat expansions are associated with slow progressing, leg-onset familial ALS.

Bi-allelic intermediate ATXN2 repeat expansions are associated with slow progressing, leg-onset familial ALS.

Journal: BMJ neurology open

Published: November 11, 2025

Serum small non-coding RNA define molecular subtypes in amyotrophic lateral sclerosis.

Serum small non-coding RNA define molecular subtypes in amyotrophic lateral sclerosis.

Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration

Published: November 01, 2025

Prodromal symptoms in amyotrophic lateral sclerosis from the perspective of the patient and of the caregiver.

Prodromal symptoms in amyotrophic lateral sclerosis from the perspective of the patient and of the caregiver.

Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration

Published: October 25, 2025

Reader Response: Genetic Associations With an Amyotrophic Lateral Sclerosis Reversal Phenotype.

Reader Response: Genetic Associations With an Amyotrophic Lateral Sclerosis Reversal Phenotype.

Journal: Neurology

Published: October 03, 2025

A VAPB (P56S) mutation in a Dutch patient with familial motor neuron disease: a case report.

A VAPB (P56S) mutation in a Dutch patient with familial motor neuron disease: a case report.

Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration

Published: September 04, 2025

Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis.

Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis.

Journal: Nature genetics

Published: August 15, 2025

Small RNA sequencing identifies serum tDR-1:34-Gly-GCC tiRNA levels as a biomarker for survival in amyotrophic lateral sclerosis.

Small RNA sequencing identifies serum tDR-1:34-Gly-GCC tiRNA levels as a biomarker for survival in amyotrophic lateral sclerosis.

Journal: iScience

Published: August 15, 2025

Primary Lateral Sclerosis: Implications for Diagnostic Criteria From a Natural History Study in the Netherlands.

Primary Lateral Sclerosis: Implications for Diagnostic Criteria From a Natural History Study in the Netherlands.

Journal: Neurology

Published: May 19, 2025

Showing 1-12 of 116

Last Updated: 09/26/2026