Brain Imaging Features in Knobloch Syndrome Type 1 due to COL18A1 Mutation (P2-6.017)

To reinforce brain abnormalities beyond encephalocele as features of Knobloch syndrome and expand on the heterogeneity of known neuroimaging findings.

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Publication Details

Journal
Neurology
Published
2025-04-07
DOI
https://doi.org/10.1212/wnl.0000000000208626
Citations
1
Primary Topic
Cell Adhesion Molecules Research
Type
article
Field-Weighted Citation Impact
1.62
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article

Brain Imaging Features in Knobloch Syndrome Type 1 due to COL18A1 Mutation (P2-6.017)

Arayamparambil C. Anilkumar, Sedat Gul, Rachel M Garn
1 citations
Neurology
Cell Adhesion Molecules Research
1.62
article

Brain Imaging Features in Knobloch Syndrome Type 1 due to COL18A1 Mutation (P2-6.017)

Arayamparambil C. Anilkumar, Sedat Gul, Rachel M Garn
article en
1 citations

Abstract

To reinforce brain abnormalities beyond encephalocele as features of Knobloch syndrome and expand on the heterogeneity of known neuroimaging findings.

NeurologyVol. 104(7_Supplement_1)
SUNY Upstate Medical University (US)
Openalex Percentile: Top 21%
Cell Adhesion Molecules Research
1.62
DOISourceOpenAlex
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Brain Imaging Features in Knobloch Syndrome Type 1 due to COL18A1 Mutation (P2-6.017) — Arayamparambil C. Anilkumar, Sedat Gul, et al. · Neurology (2025) | TGRS Research Map | TGRS