Maryam Nabavi Nouri

8PUBLICATIONS
9CO-AUTHORS
Developmental genetics (incl. sex determination)Infant and child healthAutoimmunityVenereologyNeurogenetics
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Publications (8)

|Jul 28, 2026
Expanding the Neuroimaging Spectrum of 17p13.3 Deletions: Lissencephaly with Cerebellar Hypoplasia as a Novel Phenotype.

|Jul 06, 2026
Ictal Asystole or Vasovagal Syncope? A Diagnostic Pitfall in Pediatric Drug-Resistant Epilepsy.

|Apr 02, 2026
Global disparities in the recognition, diagnosis, and management of seizures or epilepsy of autoimmune etiology.

Emily Guarasci, Robyn Whitney, Adrian Budhram

|Apr 05, 2025
Circumstances surrounding sudden unexpected death in epilepsy in children: A national case series.

Robyn Whitney, Anne Keller, Shelly-Anne Li

|Dec 28, 2024
Towards a histological diagnosis of childhood small vessel CNS vasculitis.

Maryam Nabavi Nouri, Anastasia Dropol, Pascal N Tyrrell

|Jul 27, 2024
From Alpha-Thalassemia Trait to NPRL3-Related Epilepsy: A Genomic Diagnostic Odyssey.

Maryam Nabavi Nouri, Lama Alandijani, Kalene van Engelen

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Frequent Collaborators

3 joint publications

Robyn Whitney

2 joint publications

Adrian Budhram

1 joint publications

Anne Keller

1 joint publications

Anita N Datta