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CARLOS LAM, M.D.
M.D.
Internal Medicine Physician
NPI: 1366481590Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
4664(HI)
Research & Publications (20)
Cyclic ADP-ribose links metabolism to multiple fission in the dinoflagellate Crypthecodinium cohnii.
PMID 19201464·Cell Calcium·2009
7-preclinical
Diagnosis and spectrum of melamine-related renal disease: plausible mechanism of stone formation in humans.
PMID 19171128·Clin Chim Acta·2009
8-other
A genome-wide scan maps a novel high myopia locus to 5p15.
PMID 18421076·Invest Ophthalmol Vis Sci·2008
8-other
Apple polyphenols inhibit plasma CETP activity and reduce the ratio of non-HDL to HDL cholesterol.
PMID 18496813·Mol Nutr Food Res·2008
7-preclinical
A universal algorithm for de novo decrypting of heterozygous indel sequences: a tool for personalized medicine.
PMID 18078814·Clin Chim Acta·2008
8-other
Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: identification of 17 novel mutations and its genetic heterogeneity.
PMID 18034201·J Hum Genet·2008
8-other
What makes a good program? A case study of a school admitting high academic achievers.
PMID 18956120·ScientificWorldJournal·2008
8-other
Conjugated and non-conjugated octadecaenoic acids affect differently intestinal acyl coenzyme A: cholesterol acyltransferase activity.
PMID 18078940·Atherosclerosis·2008
7-preclinical
Towards a Chinese conception of adolescent development in a migration context.
PMID 17525817·ScientificWorldJournal·2007
8-other
The use of cyberpornography by young men in Hong Kong: some psychosocial correlates.
PMID 17186123·Arch Sex Behav·2007
8-other
Role of nitric oxide pathway in placental dysfunction following fetal bypass.
PMID 17720400·Ann Thorac Surg·2007
7-preclinical
DNA-based diagnosis of malignant osteopetrosis by whole-genome scan using a single-nucleotide polymorphism microarray: standardization of molecular investigations of genetic diseases due to consanguinity.
PMID 17033731·J Hum Genet·2007
8-other
A patient with novel ABCB11 gene mutations with phenotypic transition between BRIC2 and PFIC2.
PMID 16290310·J Hepatol·2006
5-case
An inter-crystal scatter correction method for DOI PET image reconstruction.
PMID 17344643·Igaku Butsuri·2006
8-other
A review of carbon nanotube toxicity and assessment of potential occupational and environmental health risks.
PMID 16686422·Crit Rev Toxicol·2006
6-review
Analysis of polymerase chain reaction products by denaturing high-performance liquid chromatography.
PMID 16916254·Methods Mol Biol·2006
8-other
Association of apolipoprotein E polymorphisms with normal tension glaucoma in a Chinese population.
PMID 16778644·J Glaucoma·2006
8-other
Neuroleptic malignant syndrome and aripiprazole.
PMID 16721313·J Am Acad Child Adolesc Psychiatry·2006
5-case
Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome.
PMID 16153625·Clin Chim Acta·2006
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1481 S KING ST, SUITE 410
HONOLULU, HI 96814 - Phone
- (808) 946-0225
Quick Facts
- NPI
- 1366481590
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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