Lauren B. Flueckinger

Corticobasal syndrome in a man with Gaucher disease type 1: Expansion of the understanding of the neurological spectrum

Jeffrey W. Cooney, P. Kishnani, R. Alcalay, 2018, Molecular genetics and metabolism reports.

Bone manifestations in neuronopathic Gaucher disease while receiving high-dose enzyme replacement therapy.

D. Frush, P. Kishnani, Christine I. Ha, 2019, Molecular genetics and metabolism.

Multigenerational case examples of hypophosphatasia: Challenges in genetic counseling and disease management

P. Kishnani, C. Rockman‐Greenberg, Ricardo Ong, 2020, Molecular genetics and metabolism reports.