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

Clinical profile of motor neuron disease patients with lower urinary tract symptoms and neurogenic bladder.

Journal of the neurological sciences - 15 Jul 2017

Vázquez-Costa Juan Francisco, Arlandis Salvador, Hervas David, Martínez-Cuenca Esther, Cardona Fernando, Pérez-Tur Jordi, Broseta Enrique, Sevilla Teresa

Abstract excerpt

INTRODUCTION: Lower urinary tract symptoms (LUTS) are frequent in motor neuron disease (MND) patients, but clinical factors related to them are unknown. We describe differences in LUTS among MND phenotypes and their relationship with other clinical characteristics, including prognosis. METHODS: For this study, we collected clinical data of a previously published cohort of patients diagnosed with classical...

Read the complete abstract on PubMed

Topics

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

Share to Amyotrophic Lateral Sclerosis
Share to C9orf72 Protein

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cross-Sectional Studies

Share to Motor Neuron Disease

Share to Multivariate Analysis

Share to Muscular Atrophy, Spinal

Share to Sex Factors

Share to Survival Analysis

Source

Identifiers

PMID: 28566149
DOI: 10.1016/j.jns.2017.04.053

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical profile of motor neuron disease patients with lower urinary tract symptoms and neurogenic bladder.PMID 28566149Read ↗

Phenotypic and molecular analyses of primary lateral sclerosisSemantic proximity Read ↗

Biomarkers in Motor Neuron Disease: A State of the Art ReviewSemantic proximity Read ↗

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

Primary lateral sclerosis.Semantic proximity Read ↗

Natural History of "Pure" Primary Lateral Sclerosis.Semantic proximity Read ↗

Onset of bladder and motor symptoms in multiple system atrophy: differences according to phenotype.Semantic proximity Read ↗

Early pathogenesis of spinal and bulbar muscular atrophy uncovered by human iPSC-derived motor neurons highlights pathogenic neuropeptides as therapeutic targetsSemantic proximity Read ↗

Heterogeneous phenotype and cardiovascular comorbidities in Swedish patients with spinobulbar muscular atrophy.Semantic proximity Read ↗

Urinary and erectile dysfunction in multiple system atrophy (MSA).Semantic proximity Read ↗

[Clinical characteristics of urinary system symptoms in 11 patients with neuronal intranuclear inclusion disease].Semantic proximity Read ↗

Electrophysiological Characterization of C9ORF72-Associated Amyotrophic Lateral Sclerosis: A Retrospective Study.Semantic proximity Read ↗

Biomarkers of Spinal and Bulbar Muscle Atrophy (SBMA): A Comprehensive ReviewSemantic proximity Read ↗

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