Michael Whyte

9PUBLICATIONS
22CO-AUTHORS
Paediatrics not elsewhere classifiedPredictive and prognostic markersDevelopmental genetics (incl. sex determination)Infant and child healthCell physiology
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Publications (9)

|Jun 21, 2024
Pediatric hypophosphatasia: avoid diagnosis missteps!

Michael P Whyte, William H McAlister, Karen E Mack

|Apr 17, 2023
LRP6 High Bone Mass Characterized in Two Generations Harboring a Unique Mutation of Low-Density Lipoprotein Receptor-Related Protein 6.

Michael P Whyte, Steven Mumm, Jonathan C Baker

|Aug 22, 2022
Dysosteosclerosis: Clinical and Radiological Evolution Reflecting Genetic Heterogeneity.

Serap Turan, Steven Mumm, Ceren Alavanda

|Jan 23, 2021
Patient-Reported Outcomes from a Randomized, Active-Controlled, Open-Label, Phase 3 Trial of Burosumab Versus Conventional Therapy in Children with X-Linked Hypophosphatemia.

Raja Padidela, Michael P Whyte, Francis H Glorieux

|Feb 28, 2020
ZNF687 Mutations in an Extended Cohort of Neoplastic Transformations in Paget's Disease of Bone: Implications for Clinical Pathology.

Federica Scotto di Carlo, Laura Pazzaglia, Steven Mumm

|Jan 08, 2020
X-Linked Hypophosphatemia: Uniquely Mild Disease Associated With PHEX 3'-UTR Mutation c.*231A>G (A Retrospective Case-Control Study).

Pamela S Smith, Gary S Gottesman, Fan Zhang

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Frequent Collaborators

2 joint publications

Steven Mumm

1 joint publications

Fernando Gianfrancesco

1 joint publications

Raja Padidela

1 joint publications

Francis H Glorieux