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

Cerebral cavernous malformations and unilateral moyamoya in a patient with a new mutation in the KRIT-1 /CCM1 gene.

Cerebrovascular diseases (Basel, Switzerland) - 1 Jan 2014

Melis Marta, Cau Milena, Corraine Simona, Secci Simona, Addis Maria, Melis Maurizio

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 Cerebral Angiography
Share to DNA Mutational Analysis
Share to Hemangioma, Cavernous, Central Nervous System

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to KRIT1 Protein

Share to Magnetic Resonance Angiography

Share to Microtubule-Associated Proteins

Share to Moyamoya Disease

Share to Proto-Oncogene Proteins

Source

Identifiers

PMID: 25413039
DOI: 10.1159/000368215

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Cerebral cavernous malformations and unilateral moyamoya in a patient with a new mutation in the KRIT-1 /CCM1 gene.PMID 25413039Read ↗

KRIT1 Gene in Patients with Cerebral Cavernous Malformations: Clinical Features and Molecular Characterization of Novel Variants.Semantic proximity Read ↗

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

Recent insights into cerebral cavernous malformations: the molecular genetics of CCM.Semantic proximity Read ↗

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

Molecular diagnosis in cerebral cavernous malformations.Semantic proximity Read ↗

Comprehensive analysis of Novel mutations in CCM1/KRIT1 and CCM2/MGC4607 and their clinical implications in Cerebral Cavernous malformations.Semantic proximity Read ↗

Description of Two Families with New Mutations in Familial Cerebral Cavernous Malformations Genes.Semantic proximity Read ↗

Novel KRIT1/CCM1 heterozygous nonsense mutation (c.715 C>T) associated with cerebral and cerebellar cavernous malformations in a paediatric patient.Semantic proximity Read ↗

Identification of eight novel 5'-exons in cerebral capillary malformation gene-1 (CCM1) encoding KRIT1.Semantic proximity Read ↗

[A novel Krit-1 mutation in Han family with cerebral cavernous malformation].Semantic proximity Read ↗

A novel deletion mutation in CCM1 gene (krit1) is detected in a Chinese family with cerebral cavernous malformations.Semantic proximity Read ↗

KRIT1 is mutated in hyperkeratotic cutaneous capillary-venous malformation associated with cerebral capillary malformation.Semantic proximity Read ↗

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