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CHRISTIAN SHAW, M.D., PH.D
M.D., PH.D
Occupational Medicine Physician
NPI: 1205114816Individual
Specialties, Licenses & Credentials
Addiction Medicine (Preventive Medicine) Physician
Preventive Medicine — Addiction Medicine
Code: 2083A0300X
MD20130858(NM)
Occupational Medicine PhysicianPrimary
Preventive Medicine — Occupational Medicine
Code: 2083X0100X
49232(AZ)
Research & Publications (20)
Non-recurrent 17p11.2 deletions are generated by homologous and non-homologous mechanisms.
PMID 15526218·Hum Genet·2005
8-other
Small marker chromosomes in two patients with segmental aneusomy for proximal 17p.
PMID 15098121·Hum Genet·2004
5-case
Concealed antegrade penetration of the atrio-ventricular node.
PMID 19608289·Int J Cardiol·2011
5-case
Symptomatic intra-cardiac metastasis complicating non-small cell lung cancer: imaging findings and clinical course.
PMID 18956220·Ir J Med Sci·2011
5-case
No association of DPP6 with amyotrophic lateral sclerosis in an Italian population.
PMID 19525032·Neurobiol Aging·2011
8-other
Assay reproducibility and within-person variation of Müllerian inhibiting substance.
PMID 19409547·Fertil Steril·2010
4-observational
Direct impairment of vascular function by diesel exhaust particulate through reduced bioavailability of endothelium-derived nitric oxide induced by superoxide free radicals.
PMID 19440501·Environ Health Perspect·2009
7-preclinical
TDP-43 is consistently co-localized with ubiquitinated inclusions in sporadic and Guam amyotrophic lateral sclerosis but not in familial amyotrophic lateral sclerosis with and without SOD1 mutations.
PMID 19496940·Neuropathology·2009
8-other
Compound mutations in human anion exchanger 1 are associated with complete distal renal tubular acidosis and hereditary spherocytosis.
PMID 19625994·Kidney Int·2009
7-preclinical
Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotype.
PMID 19459885·Clin Genet·2009
5-case
Application of dual-genome oligonucleotide array-based comparative genomic hybridization to the molecular diagnosis of mitochondrial DNA deletion and depletion syndromes.
PMID 19546809·Genet Med·2009
8-other
A family of kassinatuerin-2 related peptides from the skin secretion of the African hyperoliid frog, Kassina maculata.
PMID 19427345·Peptides·2009
7-preclinical
Overexpression of the lily p70(s6k) gene in Arabidopsis affects elongation of flower organs and indicates TOR-dependent regulation of AP3, PI and SUP translation.
PMID 19651701·Plant Cell Physiol·2009
8-other
Amolopkinins W1 and W2--novel bradykinin-related peptides (BRPs) from the skin of the Chinese torrent frog, Amolops wuyiensis: antagonists of bradykinin-induced smooth muscle contraction of the rat ileum.
PMID 19428766·Peptides·2009
7-preclinical
Antibody affinity maturation and respiratory syncytial virus disease.
PMID 19584854·Nat Med·2009
7-preclinical
PdT-2: a novel myotropic type-2 tryptophyllin from the skin secretion of the Mexican giant leaf frog, Pachymedusa dacnicolor.
PMID 19427344·Peptides·2009
7-preclinical
Cyclic GMP protects human macrophages against peroxynitrite-induced apoptosis.
PMID 19422695·J Inflamm (Lond)·2009
8-other
The primary locus of motor neuron death in an ALS-PDC mouse model.
PMID 19633581·Neuroreport·2009
7-preclinical
PEGylation modulates the interfacial kinetics of proteases on peptide-capped gold nanoparticles.
PMID 19668832·Chem Commun (Camb)·2009
8-other
(Mis)classification of ethnicity on the New Zealand Cancer Registry: 1981-2004.
PMID 19465958·N Z Med J·2009
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
- 3014 E CAMELBACK RD STE 741
PHOENIX, AZ 85016 - Phone
- (480) 455-0462
Quick Facts
- NPI
- 1205114816
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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