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

Case of paediatric neuromuscular disease with a surprising clinical outcome: time to challenge the dogma?

Thorax - 1 Aug 2018

Wright Marie, Manzur Adnan, Bush Andy

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Diagnosis, Differential
Share to Infant
Share to Muscular Atrophy, Spinal
Share to Phenotype

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Prognosis

Share to Respiratory Distress Syndrome, Newborn

Source

Identifiers

PMID: 29382800
DOI: 10.1136/thoraxjnl-2017-211058

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Case of paediatric neuromuscular disease with a surprising clinical outcome: time to challenge the dogma?PMID 29382800Read ↗

Neuromuscular Pathology Case.Semantic proximity Read ↗

EMG disease in a pediatric patient.Semantic proximity Read ↗

Introduction: recent advances in hereditary neuromuscular diseases of childhood.Semantic proximity Read ↗

Intellectual disability in paediatric patients with genetic muscle diseases.Semantic proximity Read ↗

The dilemma of the short child without a clear diagnosis.Semantic proximity Read ↗

Persistent CNS dysfunction in a boy with CMT1XSemantic proximity Read ↗

Anaesthesia and orphan disease: a child with neuronal ceroid lipofuscinosis.Semantic proximity Read ↗

Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements.Semantic proximity Read ↗

Childhood onset of acquired neuromyotonia: association with a ganglioneuroma.Semantic proximity Read ↗

Unique presentation of rapidly fluctuating symptoms in a child with congenital myasthenic syndrome due to RAPSN mutation.Semantic proximity Read ↗

A novel presentation of DYT 16: acute onset in infancy and association with MRI abnormalities.Semantic proximity Read ↗

Respiratory insufficiency as a presenting symptom of congenital myasthenic syndromes.Semantic proximity Read ↗

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