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

The Expanding Role of Genetics in Cerebral Palsy.

Physical medicine and rehabilitation clinics of North America - 1 Feb 2020

Emrick Lisa T, DiCarlo Shannon M

Abstract excerpt

Cerebral palsy is a clinical diagnosis of a nonprogressive developmental disorder of motor impairment. The scope of the diagnosis of cerebral palsy has been broadening significantly in recent years to include patients with genetic disorders. This article helps clinicians to determine which patients would benefit from a thorough genetic/metabolic evaluation and helps to delineate an approach for the work-up, with...

Read the complete abstract on PubMed

Topics

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

Share to Cerebral Palsy
Share to Exome Sequencing
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to Genomics

Share to Karyotyping

Share to Physical Examination

Source

Identifiers

PMID: 31760988
DOI: 10.1016/j.pmr.2019.09.006

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The Expanding Role of Genetics in Cerebral Palsy.PMID 31760988Read ↗

The emerging genetic landscape of cerebral palsy.Semantic proximity Read ↗

Genetics of Cerebral Palsy: Diagnosis, Differential Diagnosis, and BeyondSemantic proximity Read ↗

Genomics in Cerebral Palsy phenotype across the lifespan: Comparison of diagnostic yield between children and adult population.Semantic proximity Read ↗

Potential clinical applications of advanced genomic analysis in cerebral palsy.Semantic proximity Read ↗

[Advances in genetic research of cerebral palsy].Semantic proximity Read ↗

Cerebral palsy as a childhood-onset neurological disorder caused by both genetic and environmental factors.Semantic proximity Read ↗

Genetic and Genomic Insights Into Cerebral Palsy: Relevance for Precision Diagnosis and Personalised OutcomesSemantic proximity Read ↗

Insights From Genetic Studies of Cerebral PalsySemantic proximity Read ↗

Clinical Phenotype of Cerebral Palsy Depends on the Cause: Is It Really Cerebral Palsy? A Retrospective Study.Semantic proximity Read ↗

Systematic Review on Genetic Variants in Children With Cerebral Palsy.Semantic proximity Read ↗

Cerebral palsy and related neuromotor disorders: Overview of genetic and genomic studies.Semantic proximity Read ↗

Genetic testing in adults with neurologic disorders: indications, approach, and clinical impactsSemantic proximity Read ↗

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