Xing-chang Wei

Calgary, AB, Canada

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 44 publications

CAR/CanSPR Practice Guidelines: FAST MRI for Pediatric Neuroimaging.

CAR/CanSPR Practice Guidelines: FAST MRI for Pediatric Neuroimaging.

Journal: Canadian Association of Radiologists journal = Journal l'Association canadienne des radiologistes

Published: June 12, 2026

Imaging Methods for New-Onset Seizures at Canadian Pediatric Hospitals.

Imaging Methods for New-Onset Seizures at Canadian Pediatric Hospitals.

Journal: Canadian Association of Radiologists journal = Journal l'Association canadienne des radiologistes

Published: December 16, 2025

Successful Treatment of Pediatric Neurosarcoidosis With Corticosteroids, Infliximab, and Methotrexate.

Successful Treatment of Pediatric Neurosarcoidosis With Corticosteroids, Infliximab, and Methotrexate.

Journal: Pediatric neurology

Published: March 31, 2025

Superior lesion detection on 3D FSE T1WI with magnetization transfer and CHESS preparation pulses in children with focal epilepsy: Preliminary results.

Superior lesion detection on 3D FSE T1WI with magnetization transfer and CHESS preparation pulses in children with focal epilepsy: Preliminary results.

Journal: Epileptic disorders : international epilepsy journal with videotape

Published: July 03, 2024

Chronic recurrent multifocal osteomyelitis with a comprehensive approach to differential diagnosis of paediatric skull pain.

Chronic recurrent multifocal osteomyelitis with a comprehensive approach to differential diagnosis of paediatric skull pain.

Journal: BMJ case reports

Published: January 04, 2023

Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders.

Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders.

Journal: American journal of human genetics

Published: November 05, 2021

Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders.

Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders.

Journal: American journal of human genetics

Published: April 06, 2021

Nucleocytoplasmic transport of the RNA-binding protein CELF2 regulates neural stem cell fates.

Nucleocytoplasmic transport of the RNA-binding protein CELF2 regulates neural stem cell fates.

Journal: Cell reports

Published: November 16, 2020

MITO-FIND: A study in 390 patients to determine a diagnostic strategy for mitochondrial disease.

MITO-FIND: A study in 390 patients to determine a diagnostic strategy for mitochondrial disease.

Journal: Molecular genetics and metabolism

Published: June 08, 2020

Diffuse Intracerebral Hemorrhage in an Infant With a Novel Homozygous Variant Leading to Severe Protein C Deficiency.

Diffuse Intracerebral Hemorrhage in an Infant With a Novel Homozygous Variant Leading to Severe Protein C Deficiency.

Journal: Journal of pediatric hematology/oncology

Published: April 18, 2020

Considering immunologic and genetic evaluation for HLH in neuroinflammation: A case of Griscelli syndrome type 2 with neurological symptoms and a lack of albinism.

Considering immunologic and genetic evaluation for HLH in neuroinflammation: A case of Griscelli syndrome type 2 with neurological symptoms and a lack of albinism.

Journal: Pediatric blood & cancer

Published: January 02, 2020

Transiently elevated plasma methionine, S-adenosylmethionine and S-adenosylhomocysteine: Unreported laboratory findings in a patient with NGLY1 deficiency, a congenital disorder of deglycosylation.

Transiently elevated plasma methionine, S-adenosylmethionine and S-adenosylhomocysteine: Unreported laboratory findings in a patient with NGLY1 deficiency, a congenital disorder of deglycosylation.

Journal: JIMD reports

Published: February 26, 2019

Showing 1-12 of 44

Last Updated: 09/26/2026