Haya S. Alfaris
Toronto, ON, Canada
Last Updated: 09/26/2026
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Found 10 publications
GLUT1 Deficiency Syndrome with Coexistent Movement Disorder and Anemia.
Journal: Movement disorders clinical practice
Published: December 09, 2025
Phenotypic Clues in Infantile-Onset Parkinsonism-Dystonia-2: A Treatable Neurotransmitter Disorder.
Journal: Movement disorders clinical practice
Published: December 04, 2025
Reply: "Leigh Syndrome Due to the Variant c.1019T>C in COX15".
Journal: Movement disorders clinical practice
Published: September 15, 2025
Phenotypic Exploration in Patients with Heterozygous Variant in AFG3L2 Gene: A Case-Series and Literature Review.
Journal: Movement disorders clinical practice
Published: August 23, 2025
Novel ENPP1 Gene Mutation Causing Generalized Arterial Calcification of Infancy: A case report.
Journal: Neurosciences (Riyadh, Saudi Arabia)
Published: February 12, 2025
Clinical Phenotype and Neuroimaging Findings in Siblings with COX15 Deficiency: Case Report and Review of Previously Reported Cases.
Journal: Movement disorders clinical practice
Published: January 27, 2025
Co-existence of anti-glutamic acid decarboxylase-65 and anti-sry-like high-mobility group box receptor antibody-associated autoimmune encephalitis: A rare case report.
Journal: Epilepsy & behavior reports
Published: November 09, 2023
A Child with Progressive Hypertrophic Cardiomyopathy and Lactic Acidosis.
Journal: Clinical chemistry
Published: October 20, 2020
Beyond a routine blood gas, an easily picked but missed diagnosis of chronic Encephalopathy.
Journal: International journal of pediatrics & adolescent medicine
Published: October 29, 2019
Showing 1-10 of 10
Last Updated: 09/26/2026