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MICHAEL HUIE, M.D., PH.D.
M.D., PH.D.
Dermatology Physician
NPI: 1457417172Individual
Specialties, Licenses & Credentials
Dermatology PhysicianPrimary
Dermatology
Code: 207N00000X
G81413(CA)
Research & Publications (13)
Phase II study of interferon-alpha and doxycycline for advanced renal cell carcinoma.
PMID 16205854·Invest New Drugs·2006
3-trial
Phase I study of piritrexim and gemcitabine in patients with advanced solid tumors.
PMID 16317274·Am J Clin Oncol·2005
3-trial
Homozygosity for multiple contiguous single-nucleotide polymorphisms as an indicator of large heterozygous deletions: identification of a novel heterozygous 8-kb intragenic deletion (IVS7-19 to IVS15-17) in a patient with glycogen storage disease type II.
PMID 11854868·Am J Hum Genet·2002
8-other
Antibodies to human fetal erythroid cells from a nonimmune phage antibody library.
PMID 11226299·Proc Natl Acad Sci U S A·2001
8-other
Chemokine IP-10: an adjunct marker for latent tuberculosis infection in children.
PMID 19460249·Int J Tuberc Lung Dis·2009
8-other
Vorinostat (NSC# 701852) in patients with relapsed non-small cell lung cancer: a Wisconsin Oncology Network phase II study.
PMID 19347984·J Thorac Oncol·2009
3-trial
Dose-escalation study of fixed-dose rate gemcitabine combined with capecitabine in advanced solid malignancies.
PMID 18841362·Cancer Chemother Pharmacol·2009
3-trial
Expression of CD70 and the TH17 transcription factor RORgammaT in human contact dermatitis.
PMID 19112760·J Drugs Dermatol·2008
8-other
Computer assisted cloning of human neutral alpha-glucosidase C (GANC): a new paralog in the glycosyl hydrolase gene family 31.
PMID 12370436·Proc Natl Acad Sci U S A·2002
8-other
Identification of six novel mutations in the acid alpha-glucosidase gene in three Spanish patients with infantile onset glycogen storage disease type II (Pompe disease).
PMID 11738358·Neuromuscul Disord·2002
5-case
SCID in Jack Russell terriers: a new animal model of DNA-PKcs deficiency.
PMID 11489998·J Immunol·2001
7-preclinical
Intercellular transfer of the virally derived precursor form of acid alpha-glucosidase corrects the enzyme deficiency in inherited cardioskeletal myopathy Pompe disease.
PMID 11268285·Hum Gene Ther·2001
7-preclinical
Frequent mutations in Japanese patients with acid maltase deficiency.
PMID 11053688·Neuromuscul Disord·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
- 585 KELLY AVE
HALF MOON BAY, CA 94019 - Phone
- (650) 712-1200
Quick Facts
- NPI
- 1457417172
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 13
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