Monica P. Panades

Barcelona, CT, Spain

Last Updated: 09/26/2026

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Found 11 publications

Evaluation of Digital Technologies for Home-Based Assessment in People With Amyotrophic Lateral Sclerosis.

Evaluation of Digital Technologies for Home-Based Assessment in People With Amyotrophic Lateral Sclerosis.

Journal: Annals of clinical and translational neurology
Published: December 23, 2025

Optimised machine learning for time-to-event prediction in healthcare applied to timing of gastrostomy in ALS: a multi-centre, retrospective model development and validation study.

Optimised machine learning for time-to-event prediction in healthcare applied to timing of gastrostomy in ALS: a multi-centre, retrospective model development and validation study.

Journal: EBioMedicine
Published: May 20, 2025

Dynamic modelling of the ALSFRS-R: leveraging population-based scores using neural networks.

Dynamic modelling of the ALSFRS-R: leveraging population-based scores using neural networks.

Journal: EBioMedicine
Published: May 13, 2025

Clinical trajectories of genetic variants in ALS: a European observational study within PRECISION-ALS.

Clinical trajectories of genetic variants in ALS: a European observational study within PRECISION-ALS.

Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: May 06, 2025

Sex-specific DNA methylation differences in Amyotrophic lateral sclerosis.

Sex-specific DNA methylation differences in Amyotrophic lateral sclerosis.

Journal: bioRxiv : the preprint server for biology
Published: December 09, 2024

Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence data.

Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence data.

Journal: Frontiers in cellular neuroscience
Published: September 21, 2022

Facial Onset Sensory and Motor Neuronopathy: New Cases, Cognitive Changes, and Pathophysiology.

Facial Onset Sensory and Motor Neuronopathy: New Cases, Cognitive Changes, and Pathophysiology.

Journal: Neurology. Clinical practice
Published: April 12, 2021

Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis.

Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis.

Journal: NPJ genomic medicine
Published: December 15, 2020

Mutations in the Glycosyltransferase Domain of GLT8D1 Are Associated with Familial Amyotrophic Lateral Sclerosis.

Mutations in the Glycosyltransferase Domain of GLT8D1 Are Associated with Familial Amyotrophic Lateral Sclerosis.

Journal: Cell reports
Published: August 24, 2018

Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohort.

Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohort.

Journal: Neurobiology of aging
Published: May 11, 2018

Reconsidering the causality of TIA1 mutations in ALS.

Reconsidering the causality of TIA1 mutations in ALS.

Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: December 14, 2017
Showing 1-11 of 11

Last Updated: 09/26/2026