A Rare MYH11 Gene Missense Variant in a Patient with Intracerebral Vascular and Ascending Aortic Disease and Clinical Strokes (P3-14.004)

•To report a patient with complex brain and arterial pathology associated with a MYH11 gene missense variant.

Authors

Institutions

Publication Details

Journal
Neurology
Published
2025-04-07
DOI
https://doi.org/10.1212/wnl.0000000000212275
Citations
1
Primary Topic
Cerebrovascular and genetic disorders
Type
article
Field-Weighted Citation Impact
1.39
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A Rare MYH11 Gene Missense Variant in a Patient with Intracerebral Vascular and Ascending Aortic Disease and Clinical Strokes (P3-14.004)

Rodica E. Petrea, Viken L. Babikian, Natasha Y. Frank, Haley Huggins et al.
1 citations
Neurology
Cerebrovascular and genetic disorders
1.39
article

A Rare MYH11 Gene Missense Variant in a Patient with Intracerebral Vascular and Ascending Aortic Disease and Clinical Strokes (P3-14.004)

Rodica E. Petrea, Viken L. Babikian, Natasha Y. Frank, Haley Huggins, Cory D. Siegel, Oleksandr Olifir
article en
1 citations

Abstract

•To report a patient with complex brain and arterial pathology associated with a MYH11 gene missense variant.

NeurologyVol. 104(7_Supplement_1)
Brigham and Women's Hospital (US), Boston Medical Center (US), VA Boston Healthcare System (US)
Good health and well-being
Openalex Percentile: Top 22%
Cerebrovascular and genetic disorders
1.39
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.