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

Late diagnosis of Duchenne's muscular dystrophy presenting as global developmental delay

7 Jul 2001

Abstract excerpt

<i>Many boys with Duchenne9s muscular dystrophy present with global developmental delay before specific motor disabilities are noticed</i>

Read the complete abstract on PubMed

Topics

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

Share to Cardiomyopathy and Myosin Studies
Share to Genetic Neurodegenerative Diseases
Share to Muscle Physiology and Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 11440945
DOI: 10.1136/bmj.323.7303.37

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Late diagnosis of Duchenne's muscular dystrophy presenting as global developmental delayPMID 11440945Read ↗

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

Failure of early diagnosis in symptomatic Duchenne muscular dystrophySemantic proximity Read ↗

The Infantile Neuroaxonal Dystrophy Rating Scale (INAD-RS)Semantic proximity Read ↗

[Duchenne muscular dystrophy: Case of atypical presentation and early diagnosis].Semantic proximity Read ↗

Practice parameter: Evaluation of the child with global developmental delay [RETIRED]Semantic proximity Read ↗

A clinical approach to developmental delay and intellectual disability.Semantic proximity Read ↗

Delayed diagnosis of Duchenne muscular dystrophy.Semantic proximity Read ↗

Phenotype of combined Duchenne and facioscapulohumeral muscular dystrophy.Semantic proximity Read ↗

'Double trouble': diagnostic challenges in Duchenne muscular dystrophy in patients with an additional hereditary skeletal dysplasia.Semantic proximity Read ↗

Atypical onset in a series of 122 cases with FacioScapuloHumeral Muscular DystrophySemantic proximity Read ↗

Myotonic dystrophy type I in childhood Long-term evolution in patients surviving the neonatal period.Semantic proximity Read ↗

Recognizing vascular Ehlers-Danlos syndrome (type IV) in the newborn.Semantic proximity Read ↗

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