Dr. Michael Peter Whyte MD
Endocrinology-Diabetes | Endocrinology, Diabetes & Metabolism
4921 Parkview Pl 5th Floor Saint Louis MO, 63110About
Dr. Whyte focuses his practice on patients with advanced bone and mineral disease. You must have a referral from your primary care physician when you make your appointment with Dr. Whyte. Dr. Whyte is ...
Education and Training
Suny-Hlth Sci Ctr At Brooklyn, Coll of Med, Brooklyn Ny 1972
State University of New York Downstate Medical Center College of Medicine 1972
Board Certification
Internal MedicineAmerican Board of Internal MedicineABIM
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Transcription map of Xq27: candidates for several X-linked diseases.
- Angiokeratoma serpiginosum.
- Angiokeratoma serpiginosum.
- Mild autosomal dominant hypophosphatasia: in utero presentation in two families.
- Mild hypophosphatasia mimicking severe osteogenesis imperfecta in utero: bent but not broken.
- Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysis.
- Alkaline phosphatase knock-out mice recapitulate the metabolic and skeletal defects of infantile hypophosphatasia.
- Increased urine heparan and chondroitin sulphate excretion in patients with osteopetrosis.
- A five-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a six-generation Arkansas kindred.
- Deficiency of the alpha-subunit of the stimulatory G protein and severe extraskeletal ossification.
- Management and prevention of vitamin D deficiency rickets in captive-born juvenile chimpanzees (Pan troglodytes).
- X-linked hypophosphatemia attributable to pseudoexons of the PHEX gene.
- Hypophosphatasia: molecular diagnosis of Rathbun's original case.
- The sedlin gene for spondyloepiphyseal dysplasia tarda escapes X-inactivation and contains a non-canonical splice site.
- Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene.
Awards
- 2005-2013 Listed in Best Doctors in America (Best Doctors, Inc.)
- 1996 Distinguished Medical Service Award: The Magic Foundation for Childre
Treatments
- Endocrinology, Bone Problems
Fellowships
- Bone and Mineral Metabolism, Washington University School of Medicine, St. Louis, Missouri 1979
Dr. Michael Peter Whyte MD's Practice location
Practice At 4921 Parkview Pl 5th Floor
4921 Parkview Pl 5th Floor -Saint Louis, MO 63110Get Direction
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Nearest Hospitals
ST LOUIS CHILDRENS HOSPITALl
ONE CHILDRENS PLACE SAINT LOUIS MO 63110SHRINERS HOSPITALS FOR CHILDRENl
4400 CLAYTON AVE SAINT LOUIS MO 63110