Area of research
Oncology · Endocrinology, Diabetes and Metabolism
Research interest
Research interests include Bone health and treatments, Alkaline Phosphatase Research Studies, Parathyroid Disorders and Treatments, and Bone health and osteoporosis research.
Hypophosphatasia: who among us is a carrier?
Burosumab vs conventional therapy in children with X-linked hypophosphatemia: results of the open-label, phase 3 extension period
Pediatric hypophosphatasia: avoid diagnosis missteps!
LRP6 High Bone Mass Characterized in Two Generations Harboring a Unique Mutation of Low-Density Lipoprotein Receptor-Related Protein 6.
Effect of Burosumab Compared With Conventional Therapy on Younger vs Older Children With X-linked Hypophosphatemia
Dysosteosclerosis: Clinical and Radiological Evolution Reflecting Genetic Heterogeneity.
Sustained Efficacy and Safety of Burosumab, a Monoclonal Antibody to FGF23, in Children With X-Linked Hypophosphatemia
Patient-Reported Outcomes from a Randomized, Active-Controlled, Open-Label, Phase 3 Trial of Burosumab Versus Conventional Therapy in Children with X-Linked Hypophosphatemia
Patient-Reported Outcomes from a Randomized, Active-Controlled, Open-Label, Phase 3 Trial of Burosumab Versus Conventional Therapy in Children with X-Linked Hypophosphatemia.
Tumor-Induced Osteomalacia: Treatment Progress Using Burosumab, an Anti-FGF23 Monoclonal Antibody.
X-Linked Hypophosphatemia: Uniquely Mild Disease Associated With PHEX 3'-UTR Mutation c.*231A>G (A Retrospective Case-Control Study).
ZNF687 Mutations in an Extended Cohort of Neoplastic Transformations in Paget's Disease of Bone: Implications for Clinical Pathology.
Burosumab versus conventional therapy in children with X-linked hypophosphataemia: a randomised, active-controlled, open-label, phase 3 trial
Natural History of Perinatal and Infantile Hypophosphatasia: A Retrospective Study
Skeletal Fluorosis Due To Inhalation Abuse of a Difluoroethane-Containing Computer Cleaner
Factors influencing success of clinical genome sequencing across a broad spectrum of disorders
Periodontal Defects in the A116T Knock-in Murine Model of Odontohypophosphatasia
Whole-exome sequencing identifies mutations in the nucleoside transporter gene SLC29A3 in dysosteosclerosis, a form of osteopetrosis
Enzyme replacement prevents enamel defects in hypophosphatasia mice