Back to Search
CHRISTINA LAM, M.D.
M.D.
Medical Biochemical Genetics
NPI: 1558560169Individual
Specialties, Licenses & Credentials
Medical Biochemical GeneticsPrimary
Medical Genetics — Medical Biochemical Genetics
Code: 207SG0207X
60643815(WA)
Clinical Genetics (M.D.) Physician
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
60643815(WA)
Pediatrics Physician
Pediatrics
Code: 208000000X
60643815(WA)
Research & Publications (20)
Diagnosis and spectrum of melamine-related renal disease: plausible mechanism of stone formation in humans.
PMID 19171128·Clin Chim Acta·2009
8-other
Cyclic ADP-ribose links metabolism to multiple fission in the dinoflagellate Crypthecodinium cohnii.
PMID 19201464·Cell Calcium·2009
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
Prolonged use of high-dose morphine impairs angiogenesis and mobilization of endothelial progenitor cells in mice.
PMID 18633053·Anesth Analg·2008
7-preclinical
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
Autologous transplantation of endothelial progenitor cells attenuates acute lung injury in rabbits.
PMID 18292677·Anesthesiology·2008
4-observational
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
Comparison of the expectations of residents and rescue providers of community emergency medical response after mudslide disasters.
PMID 18028161·Disasters·2007
4-observational
High-dose morphine impairs vascular endothelial function by increased production of superoxide anions.
PMID 17325512·Anesthesiology·2007
7-preclinical
A patient with novel ABCB11 gene mutations with phenotypic transition between BRIC2 and PFIC2.
PMID 16290310·J Hepatol·2006
5-case
Allele dropout in PCR-based diagnosis of Wilson disease: mechanisms and solutions.
PMID 16510432·Clin Chem·2006
8-other
Genome-wide detection of allelic imbalance in renal cell carcinoma using high-density single-nucleotide polymorphism microarrays.
PMID 16513104·Clin Biochem·2006
8-other
Analysis of polymerase chain reaction products by denaturing high-performance liquid chromatography.
PMID 16916254·Methods Mol Biol·2006
8-other
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
Novel missense mutation in the CASR gene in a Chinese family with familial hypocalciuric hypercalcemia.
PMID 15963484·Clin Chim Acta·2005
5-case
DNA-based diagnosis of xeroderma pigmentosum group C by Whole-genome scan using single-nucleotide polymorphism microarray.
PMID 15654957·J Invest Dermatol·2005
8-other
Monitoring cytosolic calcium in the dinoflagellate Crypthecodinium cohnii with calcium orange-AM.
PMID 15829511·Plant Cell Physiol·2005
7-preclinical
DNA-based diagnosis of thyroid hormone resistance syndrome: a novel THRB mutation associated with mild resistance to thyroid hormone.
PMID 15913586·Clin Chim Acta·2005
5-case
A novel mutation, Y255X, of the ARSB gene in a Chinese family with mucopolysaccharidosis type VI.
PMID 15603718·Chin Med J (Engl)·2004
8-other
Severe acute respiratory syndrome: clinical and laboratory manifestations.
PMID 18458712·Clin Biochem Rev·2004
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
- 4800 SAND POINT WAY NE, M/S MB.8.632
SEATTLE, WA 98105 - Phone
- (206) 987-5230
Quick Facts
- NPI
- 1558560169
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 3
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile