Pascale E Karam
7PUBLICATIONS
4CO-AUTHORS
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Publications (7)
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|Feb 27, 2026
Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report.Rima Hanna-Wakim, Pascale E Karam, Mazen Kurban
|Jan 27, 2026
Towards Next-Generation Sequencing as a First-Tier Diagnostic Test for Fructose-1,6-Bisphosphatase Deficiency.Nadine Yazbeck, Abir Barhoumi, Pascale E Karam
|Sep 08, 2025
Diagnostic Challenges and Outcome of Classical Phenylketonuria in a Resource-Constrained Middle Eastern Country.Nadine Yazbeck, Rudy N Zalzal, Fadi El Oueichek
|Aug 14, 2025
The Diagnostic Saga of a Rare Congenital Bile Acid Synthesis Disorder: A Case Report.Nadine Yazbeck, Rima Hanna-Wakim, Dolly Noun
|Jul 25, 2025
Riboflavin Transporter Deficiency Type 2: Expanding the Phenotype of the Lebanese Founder Mutation p.Gly306Arg in the SLC52A2 Gene.Jean-Marc T Jreissati, Leonard Lawandos, Julien T Jreissati
|Apr 24, 2025
Mitochondria and Peroxisome Crosstalk in Peroxisome Biogenesis Disorder 8A Caused by a Rare Variant in PEX16 Gene.Mohamad Wehbe, Rudy N Zalzal, Riyad El-Khoury
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