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

Teaching NeuroImage: Familial Cerebral Cavernous Malformation in PDCD10 Genotype.

Neurology - 24 Sept 2024

McKenna Mary Clare, Kleinerova Jana, Tacheva Asya, Redmond Janice, Bede Peter

Abstract excerpt

No abstract is available from the source.

Topics

Adult
Humans
Apoptosis Regulatory Proteins
Genotype
Hemangioma, Cavernous, Central Nervous System
Magnetic Resonance Imaging
Membrane Proteins
Proto-Oncogene Proteins

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 39173099
DOI: 10.1212/WNL.0000000000209799

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Teaching NeuroImage: Familial Cerebral Cavernous Malformation in PDCD10 Genotype.PMID 39173099Read ↗

Teaching NeuroImage: Primary Familial Brain Calcification in SLC20A2 Genotype.Semantic proximity Read ↗

Genetic and cellular basis of cerebral cavernous malformations: implications for clinical management.Semantic proximity Read ↗

Cerebral cavernous malformation: new molecular and clinical insightsSemantic proximity Read ↗

Teaching Video NeuroImage: New STUB1 Variant Causes Chorea, Tremor, Dystonia, Myoclonus, Ataxia, Depression, Cognitive Impairment, Epilepsy, and Superficial Siderosis.Semantic proximity Read ↗

Comprehensive CCM3 Mutational Analysis in Patients with Syndromic Cerebral Cavernous MalformationSemantic proximity Read ↗

Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations.Semantic proximity Read ↗

Review of familial cerebral cavernous malformations and report of seven additional families.Semantic proximity Read ↗

Gene symbol: CCM2. Disease: Cerebral Cavernous Malformations.Semantic proximity Read ↗

Comprehensive CCM3 Mutational Analysis in Two Patients with Syndromic Cerebral Cavernous Malformation.Semantic proximity Read ↗

Teaching NeuroImage: IBA57 Mutation-Associated Infantile Cavitating Leukoencephalopathy.Semantic proximity Read ↗

Clinical, neuroradiological and genetic findings in a cohort of patients with multiple Cerebral Cavernous Malformations.Semantic proximity Read ↗

Teaching NeuroImage: ROBO3 Mutation Causing Horizontal Gaze Palsy and Brainstem Malformation.Semantic proximity Read ↗

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