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W WILCOX, M.D.
M.D.
Family Medicine Physician
NPI: 1275538761Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
05864(MS)
Research & Publications (20)
Fabry disease: progression of nephropathy, and prevalence of cardiac and cerebrovascular events before enzyme replacement therapy.
PMID 19218538·Nephrol Dial Transplant·2009
8-other
Lysosomal Disease Network's "WORLD Symposium 2009". Introduction.
PMID 19083251·Mol Genet Metab·2009
8-other
A novel interaction between fibroblast growth factor receptor 3 and the p85 subunit of phosphoinositide 3-kinase: activation-dependent regulation of ERK by p85 in multiple myeloma cells.
PMID 19286672·Hum Mol Genet·2009
8-other
AORN Interviews . . . William H. Wilcox: part one of two-part Interview. Interview by Patricia C. Seifert.
PMID 19499630·AORN J·2009
8-other
Experimental comparison of tracking algorithms in the presence of aircraft boundary-layer distortions for emulated free-space laser communication links.
PMID 19107161·Appl Opt·2009
8-other
Emulation of dynamic wavefront disturbances using a deformable mirror.
PMID 19259183·Opt Express·2009
8-other
FGFR3 promotes synchondrosis closure and fusion of ossification centers through the MAPK pathway.
PMID 18923003·Hum Mol Genet·2009
7-preclinical
High molecular weight FGF2: the biology of a nuclear growth factor.
PMID 18850066·Cell Mol Life Sci·2009
6-review
AORN interviews...William H Wilcox. Interview by Patricia C Seifert.
PMID 19606573·AORN J·2009
8-other
Fibroblast growth factor inhibits interferon gamma-STAT1 and interleukin 6-STAT3 signaling in chondrocytes.
PMID 18950705·Cell Signal·2009
7-preclinical
Evaluation of prenatal-onset osteochondrodysplasias by ultrasonography: a retrospective and prospective analysis.
PMID 18627037·Am J Med Genet A·2008
8-other
Analysis of STAT1 activation by six FGFR3 mutants associated with skeletal dysplasia undermines dominant role of STAT1 in FGFR3 signaling in cartilage.
PMID 19088846·PLoS One·2008
7-preclinical
Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia.
PMID 18587396·Nat Genet·2008
8-other
Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golgin.
PMID 18997784·Nat Genet·2008
8-other
Living and loving "decent": religion and relationship quality among urban parents.
PMID 18784851·Soc Sci Res·2008
8-other
Enzyme replacement therapy stabilizes obstructive pulmonary Fabry disease associated with respiratory globotriaosylceramide storage.
PMID 18937048·J Inherit Metab Dis·2008
5-case
WITHDRAWN: Familial Degenerative Encephalopathy with Intracranial Calcification and Metaphyseal Dysplasia.
PMID 19016590·J Bone Miner Res·2008
8-other
Characterization of Fabry disease in 352 pediatric patients in the Fabry Registry.
PMID 18596579·Pediatr Res·2008
8-other
Reversible leukoencephalopathy with acute neurological deterioration and permanent residua in classical homocystinuria: A case report.
PMID 18210212·J Inherit Metab Dis·2008
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
- 2024 15TH ST FL 2
MERIDIAN, MS 39301 - Phone
- (601) 553-2000
Quick Facts
- NPI
- 1275538761
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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