Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Respiratory alterations in patients with amyotrophic lateral sclerosis.

Medicina clinica - 1 May 2026

Riveiro Vanessa, Ferreiro Lucía, Abelleira Romina, Rodríguez-Núñez Nuria, Toubes María E, Ricoy Jorge, García-Sobrino Tania, Valdés Luis, Zamarrón Carlos

Abstract excerpt

INTRODUCTION: Amyotrophic lateral sclerosis (ALS) is a progressive and heterogeneous neurodegenerative disease that manifests itself in different phenotypes depending on the anatomical region affected. PATIENTS AND METHODS: Retrospective observational study of patients diagnosed with ALS in our healthcare area, classified by phenotypes to assess their relationship with functional respiratory variables, gas...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aged
Share to Amyotrophic Lateral Sclerosis

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Incidence

Share to Phenotype

Share to Prevalence

Share to Respiration Disorders

Share to Sleep Apnea, Obstructive

Share to Vital Capacity

Source

Identifiers

PMID: 41819726
DOI: 10.1016/j.medcli.2026.107365

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 23 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Respiratory alterations in patients with amyotrophic lateral sclerosis.PMID 41819726Read ↗

Longitudinal respiratory trajectories in motor neuron disease phenotypes: Multiparametric characterization and clinical management.Semantic proximity Read ↗

The Prognostic Role of Obstructive Sleep Apnea at the Onset of Amyotrophic Lateral Sclerosis.Semantic proximity Read ↗

Progressive speech impairment as the first manifestation of amyotrophic lateral sclerosis: Case report and literature reviewSemantic proximity Read ↗

Uncoupling of apnea-hypopnea index and oxygen desaturation in als: characterization and diagnostic implications of an "AHI-SpO₂ dissociation" phenotype.Semantic proximity Read ↗

Predicting Disease Progression and Survival in Amyotrophic Lateral Sclerosis.Semantic proximity Read ↗

Respiratory impairment in a mouse model of amyotrophic lateral sclerosis.Semantic proximity Read ↗

Sleep phenotypes and respiratory disturbances in spinal muscular atrophy: A systematic review of clinical evidence.Semantic proximity Read ↗

What is amyotrophic lateral sclerosis prevalence?Semantic proximity Read ↗

ALS motor phenotypes: a revised 'OPM' classification.Semantic proximity Read ↗

Evaluation and management of amyotrophic lateral sclerosis.Semantic proximity Read ↗

The management of amyotrophic lateral sclerosis.Semantic proximity Read ↗

Cardiovascular diseases may play a negative role in the prognosis of amyotrophic lateral sclerosis.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.