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MARTA WHYTE, MD
MD
Surgical Critical Care Physician
NPI: 1639907694Individual
Specialties, Licenses & Credentials
Surgical Critical Care PhysicianPrimary
Surgery — Surgical Critical Care
Code: 2086S0102X
125.083548(IL)
Research & Publications (20)
Atypical femoral fractures, bisphosphonates, and adult hypophosphatasia.
PMID 19113923·J Bone Miner Res·2009
8-other
Chronic recurrent multifocal osteomyelitis mimicked in childhood hypophosphatasia.
PMID 19335222·J Bone Miner Res·2009
5-case
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
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
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
Disseminated Scedosporium prolificans infection and survival of a child with acute lymphoblastic leukemia.
PMID 15818301·Pediatr Infect Dis J·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
Expansile skeletal hyperphosphatasia: a new familial metabolic bone disease.
PMID 11127198·J Bone Miner Res·2000
5-case
The rise and rise of Staphylococcus aureus: laughing in the face of granulocytes.
PMID 19604261·Clin Exp Immunol·2009
6-review
Gelsolin in idiopathic pulmonary fibrosis: a new target supports a central role for epithelial injury in disease pathogenesis.
PMID 19478115·Thorax·2009
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2160 S 1ST AVE
MAYWOOD, IL 60153 - Phone
- (888) 584-7888
Quick Facts
- NPI
- 1639907694
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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