Pascale E. Karam
Beirut, BA, Lebanon
Last Updated: 09/26/2026
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Found 25 publications
Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report.
Journal: Genes
Published: January 08, 2026
Mitochondrial dysfunction in hyperkalemic periodic paralysis: A case report and literature review.
Journal: BMC pediatrics
Published: January 06, 2026
Riboflavin Transporter Deficiency Type 2: Expanding the Phenotype of the Lebanese Founder Mutation p.Gly306Arg in the SLC52A2 Gene.
Journal: Metabolites
Published: May 30, 2025
Seizure control in glycine encephalopathy using the Ketamine-Dextromethorphan-Sodium benzoate triple therapy.
Journal: Epilepsy & behavior reports
Published: April 29, 2025
The Diagnostic Saga of a Rare Congenital Bile Acid Synthesis Disorder: A Case Report.
Journal: Clinical medicine insights. Pediatrics
Published: January 28, 2025
Diagnostic Challenges and Outcome of Classical Phenylketonuria in a Resource-Constrained Middle Eastern Country.
Journal: International journal of pediatrics
Published: January 17, 2025
Hyperornithinemia-hyperammonemia-homocitrullinuria: a rare neurometabolic disorder in two siblings.
Journal: Metabolic brain disease
Published: April 05, 2024
Diagnostic challenges and outcome of fatty acid oxidation defects in a tertiary care center in Lebanon.
Journal: Orphanet journal of rare diseases
Published: January 30, 2024
Genetic literacy among primary care physicians in a resource-constrained setting.
Journal: BMC medical education
Published: August 01, 2023
Mitochondrial depletion syndrome type 3: the Lebanese variant.
Journal: Frontiers in genetics
Published: May 01, 2023
Last Updated: 09/26/2026