Moyamoya Disease in the Pacific - A Novel Cohort (P2-2.012)

We aim to phenotype and genotype a cohort of newly described patients with Moyamoya disease who are of Polynesian or Māori (indigenous peoples of New Zealand) ancestry.

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Publication Details

Journal
Neurology
Published
2025-04-07
DOI
https://doi.org/10.1212/wnl.0000000000211105
Primary Topic
Moyamoya disease diagnosis and treatment
Type
article
Field-Weighted Citation Impact
0.00
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article

Moyamoya Disease in the Pacific - A Novel Cohort (P2-2.012)

Richard H Roxburgh, Chirag Patel, Miriam Rodrigues, P. Alan Barber et al.
Neurology
Moyamoya disease diagnosis and treatment
article

Moyamoya Disease in the Pacific - A Novel Cohort (P2-2.012)

Richard H Roxburgh, Chirag Patel, Miriam Rodrigues, P. Alan Barber, Joseph E. Donnelly, Zofia E Karasinska-Stanley
article en

Abstract

We aim to phenotype and genotype a cohort of newly described patients with Moyamoya disease who are of Polynesian or Māori (indigenous peoples of New Zealand) ancestry.

NeurologyVol. 104(7_Supplement_1)
University of Auckland (NZ), Auckland City Hospital (NZ)
Life below water
Openalex Percentile: Top 89%
Moyamoya disease diagnosis and treatment
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Moyamoya Disease in the Pacific - A Novel Cohort (P2-2.012) — Richard H Roxburgh, Chirag Patel, et al. · Neurology (2025) | TGRS Research Map | TGRS