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Haya S AlFaris

Showing results (1-10 of 8) with videos related to

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International Journal of Pediatrics & Adolescent Medicine|March 15, 2021
Beyond a routine blood gas, an easily picked but missed diagnosis of chronic EncephalopathyHaya S AlFaris, Ghasan Elhissi, Aziza Chedrawi, et al.
Neurosciences (Riyadh, Saudi Arabia)|June 4, 2026
Novel <i>ENPP</i>1 Gene Mutation Causing Generalized Arterial Calcification of Infancy: A case reportHaifa M AlTurki, Haya S AlFaris, Mohammed A Al-Owain, et al.
Clinical Chemistry|March 10, 2022
A Child with Progressive Hypertrophic Cardiomyopathy and Lactic AcidosisHaya S AlFaris, Zuhair A Rahbeeni, Roy W A Peake, et al.
Movement Disorders Clinical Practice|September 27, 2025
Reply: "Leigh Syndrome Due to the Variant c.1019T>C in COX15"Haya S AlFaris, Sangeetha Yoganathan, Marcus N Callister, et al.
Movement Disorders Clinical Practice|May 29, 2025
Clinical Phenotype and Neuroimaging Findings in Siblings with COX15 Deficiency: Case Report and Review of Previously Reported CasesHaya S AlFaris, Sangeetha Yoganathan, Marcus N Callister, et al.
Movement Disorders Clinical Practice|April 6, 2026
Phenotypic Clues in Infantile-Onset Parkinsonism-Dystonia-2: A Treatable Neurotransmitter DisorderSangeetha Yoganathan, Haya S AlFaris, Lindsey Vogt, et al.
Movement Disorders Clinical Practice|May 11, 2026
GLUT1 Deficiency Syndrome with Coexistent Movement Disorder and AnemiaSangeetha Yoganathan, Haya S AlFaris, Anika Menetrey, et al.
Movement Disorders Clinical Practice|May 12, 2026
Phenotypic Exploration in Patients with Heterozygous Variant in AFG3L2 Gene: A Case-Series and Literature ReviewSangeetha Yoganathan, Laura Tochen, Jacky Ganguly, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
International Journal of Pediatrics & Adolescent Medicine|March 15, 2021
Beyond a routine blood gas, an easily picked but missed diagnosis of chronic EncephalopathyHaya S AlFaris, Ghasan Elhissi, Aziza Chedrawi, et al.
Neurosciences (Riyadh, Saudi Arabia)|June 4, 2026
Novel <i>ENPP</i>1 Gene Mutation Causing Generalized Arterial Calcification of Infancy: A case reportHaifa M AlTurki, Haya S AlFaris, Mohammed A Al-Owain, et al.
Clinical Chemistry|March 10, 2022
A Child with Progressive Hypertrophic Cardiomyopathy and Lactic AcidosisHaya S AlFaris, Zuhair A Rahbeeni, Roy W A Peake, et al.
Movement Disorders Clinical Practice|September 27, 2025
Reply: "Leigh Syndrome Due to the Variant c.1019T>C in COX15"Haya S AlFaris, Sangeetha Yoganathan, Marcus N Callister, et al.
Movement Disorders Clinical Practice|May 29, 2025
Clinical Phenotype and Neuroimaging Findings in Siblings with COX15 Deficiency: Case Report and Review of Previously Reported CasesHaya S AlFaris, Sangeetha Yoganathan, Marcus N Callister, et al.
Movement Disorders Clinical Practice|April 6, 2026
Phenotypic Clues in Infantile-Onset Parkinsonism-Dystonia-2: A Treatable Neurotransmitter DisorderSangeetha Yoganathan, Haya S AlFaris, Lindsey Vogt, et al.
Movement Disorders Clinical Practice|May 11, 2026
GLUT1 Deficiency Syndrome with Coexistent Movement Disorder and AnemiaSangeetha Yoganathan, Haya S AlFaris, Anika Menetrey, et al.
Movement Disorders Clinical Practice|May 12, 2026
Phenotypic Exploration in Patients with Heterozygous Variant in AFG3L2 Gene: A Case-Series and Literature ReviewSangeetha Yoganathan, Laura Tochen, Jacky Ganguly, et al.
Pageof 1