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MICHAEL WHYTE, MD
MD
Endocrinology, Diabetes & Metabolism Physician
NPI: 1235168071Individual
Specialties, Licenses & Credentials
Endocrinology, Diabetes & Metabolism PhysicianPrimary
Internal Medicine — Endocrinology, Diabetes & Metabolism
Code: 207RE0101X
R9422(MO)
Research & Publications (20)
Chronic recurrent multifocal osteomyelitis mimicked in childhood hypophosphatasia.
PMID 19335222·J Bone Miner Res·2009
5-case
Atypical femoral fractures, bisphosphonates, and adult hypophosphatasia.
PMID 19113923·J Bone Miner Res·2009
8-other
Bisphosphonate-induced osteopetrosis: novel bone modeling defects, metaphyseal osteopenia, and osteosclerosis fractures after drug exposure ceases.
PMID 18505375·J Bone Miner Res·2008
5-case
Juvenile Paget's disease: the second reported, oldest patient is homozygous for the TNFRSF11B "Balkan" mutation (966_969delTGACinsCTT), which elevates circulating immunoreactive osteoprotegerin levels.
PMID 17352649·J Bone Miner Res·2007
5-case
Paget's disease of bone and genetic disorders of RANKL/OPG/RANK/NF-kappaB signaling.
PMID 16831914·Ann N Y Acad Sci·2006
6-review
Homozygosity for TNSALP mutation 1348c>T (Arg433Cys) causes infantile hypophosphatasia manifesting transient disease correction and variably lethal outcome in a kindred of black ancestry.
PMID 16769381·J Pediatr·2006
6-review
Neuropsychological performance over time in people at high risk of developing schizophrenia and controls.
PMID 16388781·Biol Psychiatry·2006
4-observational
Declarative memory in unaffected adult relatives of patients with schizophrenia: a systematic review and meta-analysis.
PMID 16006102·Schizophr Res·2005
4-observational
Disseminated Scedosporium prolificans infection and survival of a child with acute lymphoblastic leukemia.
PMID 15818301·Pediatr Infect Dis J·2005
5-case
Misinterpretation of osteodensitometry with high bone density: BMD Z > or = + 2.5 is not "normal".
PMID 15722580·J Clin Densitom·2005
5-case
Heritable disorders of the RANKL/OPG/RANK signaling pathway.
PMID 15615493·J Musculoskelet Neuronal Interact·2004
6-review
Marrow cell transplantation for infantile hypophosphatasia.
PMID 12674323·J Bone Miner Res·2003
5-case
Familial expansile osteolysis (excessive RANK effect) in a 5-generation American kindred.
PMID 11889411·Medicine (Baltimore)·2002
6-review
Expansile skeletal hyperphosphatasia is caused by a 15-base pair tandem duplication in TNFRSF11A encoding RANK and is allelic to familial expansile osteolysis.
PMID 11771666·J Bone Miner Res·2002
8-other
Increased risk of fibrosing alveolitis associated with interleukin-1 receptor antagonist and tumor necrosis factor-alpha gene polymorphisms.
PMID 10934117·Am J Respir Crit Care Med·2000
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 4921 PARKVIEW PL, DIV IM BONE & MINERAL, STE 5C
SAINT LOUIS, MO 63110 - Phone
- (314) 454-7775
Quick Facts
- NPI
- 1235168071
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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