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MYO MAW, MD
MD
Cardiovascular Disease Physician
NPI: 1871565242IndividualAccepts Medicare
Specialties, Licenses & Credentials
Cardiovascular Disease PhysicianPrimary
Internal Medicine — Cardiovascular Disease
Code: 207RC0000X
136246-1(NY)
CMS Specialties
PrimaryCARDIOVASCULAR DISEASE (CARDIOLOGY)
Education
OTHER
Class of 1969
Research & Publications (15)
Effects of presynaptic mutations on a postsynaptic Cacna1s calcium channel colocalized with mGluR6 at mouse photoreceptor ribbon synapses.
PMID 18952919·Invest Ophthalmol Vis Sci·2009
7-preclinical
Detection of vaccine-like infectious bursal disease (IBD) virus in IBD vaccine-free chickens in Japan.
PMID 18772560·J Vet Med Sci·2008
7-preclinical
A missense mutation in ALDH18A1, encoding Delta1-pyrroline-5-carboxylate synthase (P5CS), causes an autosomal recessive neurocutaneous syndrome.
PMID 18478038·Eur J Hum Genet·2008
5-case
Chicken B lymphoma DT40 cells as a useful tool for in vitro analysis of pathogenic infectious bursal disease virus.
PMID 18460838·J Vet Med Sci·2008
7-preclinical
Expression of the inhibitor of DNA-binding (ID)-1 protein as an angiogenic mediator in tumour advancement of uterine cervical cancers.
PMID 19002177·Br J Cancer·2008
8-other
Nucleotide sequence analysis of VP2 hypervariable domain of infectious bursal disease virus detected in Japan from 1993 to 2004.
PMID 17675805·J Vet Med Sci·2007
7-preclinical
A practical tissue sampling method using ordinary paper for molecular detection of infectious bursal disease virus RNA by RT-PCR.
PMID 17274294·Avian Dis·2006
7-preclinical
Acute coronary syndrome critical pathway: chest PAIN caremap: a qualitative research study--provider-level intervention.
PMID 18340201·Crit Pathw Cardiol·2005
8-other
Structural determinants of L-type channel activation in segment IIS6 revealed by a retinal disorder.
PMID 16157588·J Biol Chem·2005
8-other
A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation.
PMID 15897456·Proc Natl Acad Sci U S A·2005
4-observational
Clinical manifestations of a unique X-linked retinal disorder in a large New Zealand family with a novel mutation in CACNA1F, the gene responsible for CSNB2.
PMID 15807819·Clin Exp Ophthalmol·2005
8-other
Screen for usher syndrome 1B mutations in the ovine myosin VIIa gene.
PMID 15180259·Adv Exp Med Biol·2003
7-preclinical
Identification of a new TWIST mutation (7p21) with variable eyelid manifestations supports locus homogeneity of BPES at 3q22.
PMID 11474656·J Med Genet·2001
8-other
A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration.
PMID 10587575·Hum Mol Genet·2000
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 3180 41ST ST
ASTORIA, NY 11103 - Phone
- (718) 278-5100
Quick Facts
- NPI
- 1871565242
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 57
- Publications
- 15
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