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MITCHELL WARMAN, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1669275269Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2.
PMID 19118815·Am J Hum Genet·2009
8-other
FGFR3 promotes synchondrosis closure and fusion of ossification centers through the MAPK pathway.
PMID 18923003·Hum Mol Genet·2009
7-preclinical
Normal growth and development in mice over-expressing the CCN family member WISP3.
PMID 19401829·J Cell Commun Signal·2009
8-other
A mutation in the signal sequence of LRP5 in a family with an osteoporosis-pseudoglioma syndrome (OPPG)-like phenotype indicates a novel disease mechanism for trinucleotide repeats.
PMID 19177549·Hum Mutat·2009
8-other
Nasopharyngeal carcinoid tumor: successful therapy for a tumor in a unique location.
PMID 19248962·Otolaryngol Head Neck Surg·2009
5-case
The binding between sclerostin and LRP5 is altered by DKK1 and by high-bone mass LRP5 mutations.
PMID 18521528·Calcif Tissue Int·2008
7-preclinical
Radiology quiz case. Cervical sympathetic schwannoma.
PMID 18645132·Arch Otolaryngol Head Neck Surg·2008
5-case
Invasive tracheal aspergillosis treated successfully with voriconazole: clinical report and review of the literature.
PMID 17987775·Ann Otol Rhinol Laryngol·2007
5-case
[Varicella zoster virus infection involving the maxillary branch of the trigeminal nerve].
PMID 17352273·Harefuah·2007
8-other
The role of lubricin in the mechanical behavior of synovial fluid.
PMID 17404241·Proc Natl Acad Sci U S A·2007
4-observational
The CCN family member Wisp3, mutant in progressive pseudorheumatoid dysplasia, modulates BMP and Wnt signaling.
PMID 17823661·J Clin Invest·2007
7-preclinical
Association between friction and wear in diarthrodial joints lacking lubricin.
PMID 17968947·Arthritis Rheum·2007
7-preclinical
Somatic mosaicism in a male with an exon skipping mutation in PDHA1 of the pyruvate dehydrogenase complex results in a milder phenotype.
PMID 16412675·Mol Genet Metab·2006
5-case
Hip joint replacement surgery for idiopathic osteoarthritis aggregates in families.
PMID 16507126·Arthritis Res Ther·2006
8-other
Heterozygous mutations in natriuretic peptide receptor-B (NPR2) are associated with short stature.
PMID 16384845·J Clin Endocrinol Metab·2006
5-case
The Wnt co-receptor LRP5 is essential for skeletal mechanotransduction but not for the anabolic bone response to parathyroid hormone treatment.
PMID 16790443·J Biol Chem·2006
4-observational
Reduced affinity to and inhibition by DKK1 form a common mechanism by which high bone mass-associated missense mutations in LRP5 affect canonical Wnt signaling.
PMID 15923613·Mol Cell Biol·2005
7-preclinical
Association of articular cartilage degradation and loss of boundary-lubricating ability of synovial fluid following injury and inflammatory arthritis.
PMID 15934070·Arthritis Rheum·2005
7-preclinical
Consequences of disease-causing mutations on lubricin protein synthesis, secretion, and post-translational processing.
PMID 16000300·J Biol Chem·2005
7-preclinical
Lrp5-independent activation of Wnt signaling by lithium chloride increases bone formation and bone mass in mice.
PMID 16293698·Proc Natl Acad Sci U S A·2005
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 900 S LIMESTONE CTW 304
LEXINGTON, KY 40536 - Phone
- (859) 323-2834
Quick Facts
- NPI
- 1669275269
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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