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MICHAEL NEEDHAM, M.D.
M.D.
Family Medicine Physician
NPI: 1487942744Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
0101253135(VA)
Research & Publications (20)
Ligands for retinoic acid receptors are elevated in osteoarthritis and may contribute to pathologic processes in the osteoarthritic joint.
PMID 19479829·Arthritis Rheum·2009
8-other
Ca2+-activated Cl- current in retinal arteriolar smooth muscle.
PMID 18775864·Invest Ophthalmol Vis Sci·2009
7-preclinical
Mitogen-activated protein kinase-activated protein kinase 2 (MK2) modulates key biological pathways associated with OA disease pathology.
PMID 18562219·Osteoarthritis Cartilage·2009
8-other
Biogenic synthesis, purification, and chemical characterization of anti-inflammatory resolvins derived from docosapentaenoic acid (DPAn-6).
PMID 19324874·J Biol Chem·2009
7-preclinical
The identification of differentially expressed microRNA in osteoarthritic tissue that modulate the production of TNF-alpha and MMP13.
PMID 19008124·Osteoarthritis Cartilage·2009
8-other
Haploinsufficiency of the nerve growth factor beta gene in a 1p13 deleted female child with an insensitivity to pain.
PMID 19183217·Dev Med Child Neurol·2009
5-case
Phenotypic differences in alpha 1 antitrypsin-deficient sibling pairs may relate to genetic variation.
PMID 19353349·COPD·2008
8-other
Apolipoprotein epsilon alleles in sporadic inclusion body myositis: a reappraisal.
PMID 18060780·Neuromuscul Disord·2008
5-case
Attendance rates in a workplace predict subsequent outcome of employment-based reinforcement of cocaine abstinence in methadone patients.
PMID 19192855·J Appl Behav Anal·2008
2-rct
Array comparative genomic hybridisation-based identification of two imbalances of chromosome 1p in a 9-year-old girl with a monosomy 1p36 related phenotype and a family history of learning difficulties: a case report.
PMID 19019217·J Med Case Rep·2008
8-other
Prevalence of sporadic inclusion body myositis and factors contributing to delayed diagnosis.
PMID 18815046·J Clin Neurosci·2008
8-other
Sporadic inclusion body myositis: phenotypic variability and influence of HLA-DR3 in a cohort of 57 Australian cases.
PMID 18258695·J Neurol Neurosurg Psychiatry·2008
8-other
Novel prion protein gene mutation presenting with subacute PSP-like syndrome.
PMID 17353478·Neurology·2007
5-case
A randomized trial of employment-based reinforcement of cocaine abstinence in injection drug users.
PMID 17970256·J Appl Behav Anal·2007
2-rct
A mechanism of polarized light sensitivity in cone photoreceptors of the goldfish Carassius auratus.
PMID 17938422·Biophys J·2007
7-preclinical
Professional demeanor of chronically unemployed cocaine-dependent methadone patients in a therapeutic workplace.
PMID 17668330·Subst Use Misuse·2007
8-other
Executive functioning in children and adolescents with phenylketonuria.
PMID 17594394·Clin Genet·2007
8-other
Inclusion body myositis: current pathogenetic concepts and diagnostic and therapeutic approaches.
PMID 17582362·Lancet Neurol·2007
6-review
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1665 COCHRANE CIR BLDG 7494
FORT CARSON, CO 80913 - Phone
- (719) 524-2361
Quick Facts
- NPI
- 1487942744
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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