Cheryl R. Greenberg-Rockman
Winnipeg, MB, Canada
Last Updated: 09/26/2026
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Found 73 publications
Attitudes of people with lived experience of hypophosphatasia (HPP) toward in-utero enzyme replacement therapy (IU-ERT) for life-threatening HPP.
Journal: Molecular genetics and metabolism
Published: June 17, 2026
iPSC generation from PBMCs of a MELAS patient for mitochondrial dysfunction studies.
Journal: Stem cell research
Published: March 09, 2026
Correspondence on "Mainstreaming of clinical genetic testing: a conceptual framework" by Mackley et al.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: July 25, 2025
The Global Hypophosphatasia Registry: lessons learned from a decade of real-world data.
Journal: Orphanet journal of rare diseases
Published: July 15, 2025
Metabolic Control and Frequency of Clinical Monitoring Among Canadian Children With Phenylalanine Hydroxylase Deficiency: A Retrospective Cohort Study.
Journal: JIMD reports
Published: June 09, 2025
Cognitive decline in an adult with ATR-16 syndrome due to an unbalanced translocation between 11p15.5 and 16p13.3: a case report.
Journal: Frontiers in genetics
Published: March 17, 2025
Biochemical phenotype of hypophosphatasia in asymptomatic individuals carrying ALPL variants.
Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: March 15, 2025
The ALPL gene variant project: results of the first 100 reclassified variants.
Journal: JBMR plus
Published: January 12, 2025
Generation of a new human iPSC cell line (UOMi010-A) from a patient with hypophosphatasia.
Journal: Stem cell research
Published: December 06, 2024
Lucerastat, an oral therapy for Fabry disease: results from a pivotal randomized phase 3 study and its open-label extension.
Journal: Nature communications
Published: July 24, 2024
Last Updated: 09/26/2026