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Brain Communications|April 8, 2024
1H and 31P magnetic resonance spectroscopy reveals potential pathogenic and biomarker metabolite alterations in Lafora diseaseKimberly L Chan, Aparna Panatpur, Souad Messahel, et al.
Pediatric Transplantation|January 23, 2026
Racial Disparities in Pediatric Patients With Cholestatic Liver Disease Undergoing Liver Transplant: A UNOS Database StudyAhmad Anouti, Hamza Dahshi, Elias D Rady, et al.
Orphanet Journal of Rare Diseases|December 20, 2024
Neuronal ceroid lipofuscinoses type 7 (CLN7): a case series reporting cross sectional and retrospective clinical data to evaluate validity of standardized tools to assess disease progression, quality of life, and adaptive skillsSaima Kayani, Veronica BordesEdgar, Andrea Lowden, et al.
Research Square|July 9, 2024
Neuronal Ceroid Lipofuscinoses Type 7 (CLN7)- A Case Series Reporting Cross Sectional and Retrospective Clinical Data to Evaluate Validity of Standardized Tools to Assess Disease Progression, Quality of Life, and Adaptive SkillsSaima Kayani, Veronica Bordes Edgar, Andrea Lowden, et al.
Ebiomedicine|November 28, 2025
First-in-human high dose AAV9 intrathecal gene therapy for paediatric CLN7 disease: a phase 1, open-label, single ascending dose, non-randomised clinical trialBenjamin M Greenberg, Berge Minassian, Souad Messahel, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|July 7, 2025
The current state of simultaneous heart-liver transplantation in the United StatesAhmad Anouti, Ali H Dakroub, Hussein Krayem, et al.
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