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MANPREET BASSI, MD
MD
Emergency Medicine Physician
NPI: 1457892622IndividualAccepts Medicare
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
A182651(CA)
CMS Specialties
PrimaryMEDICAL TOXICOLOGY
Education
UNIVERSITY OF CALIFORNIA, DAVIS SCHOOL OF MEDICINE
Class of 2019
Research & Publications (20)
An in vitro study on the effects of freezing, spine segment, repeat measurement, and individual cord properties on cord interstitial pressure.
PMID 19214093·Spine (Phila Pa 1976)·2009
4-observational
Identification and characterisation of human xCT that co-expresses, with 4F2 heavy chain, the amino acid transport activity system xc-.
PMID 11417227·Pflugers Arch·2001
7-preclinical
Characterization of two novel SETX mutations in AOA2 patients reveals aspects of the pathophysiological role of senataxin.
PMID 19593598·Neurogenetics·2010
5-case
Endoclip-assisted resection of large pedunculated colorectal polyps: technical aspects and outcome.
PMID 19657735·Dig Dis Sci·2010
8-other
A randomised study comparing the antiplatelet and antiinflammatory effect of clopidogrel 150 mg/day versus 75 mg/day in patients with ST-segment elevation acute myocardial infarction and poor responsiveness to clopidogrel: results from the DOUBLE study.
PMID 19604542·Thromb Res·2010
4-observational
Defective ciliogenesis, embryonic lethality and severe impairment of the Sonic Hedgehog pathway caused by inactivation of the mouse complex A intraflagellar transport gene Ift122/Wdr10, partially overlapping with the DNA repair gene Med1/Mbd4.
PMID 19000668·Dev Biol·2009
7-preclinical
Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum.
PMID 19196735·J Med Genet·2009
8-other
Aberrant splicing due to a silent nucleotide change in CCM2 gene in a family with cerebral cavernous malformation.
PMID 19475721·Clin Genet·2009
8-other
Clinical and genetic familial study of a large cohort of Italian children with idiopathic epilepsy.
PMID 19200853·Brain Res Bull·2009
8-other
Dispersed phantom scatterer technique reveals subtle differences in substrate recognition by phospholipase D inactive mutants.
PMID 19241409·Chembiochem·2009
7-preclinical
Charcot-Marie-Tooth type 1a in a child with Long QT syndrome.
PMID 18799333·Eur J Paediatr Neurol·2009
5-case
Pleiotropic effects of spastin on neurite growth depending on expression levels.
PMID 19141076·J Neurochem·2009
7-preclinical
The low-affinity receptor for neurotrophins p75NTR plays a key role for satellite cell function in muscle repair acting via RhoA.
PMID 19553472·Mol Biol Cell·2009
7-preclinical
Cornelia de Lange syndrome mutations in SMC1A or SMC3 affect binding to DNA.
PMID 18996922·Hum Mol Genet·2009
8-other
A study of pancreatic function among subjects over ninety years of age.
PMID 19407477·Pancreatology·2009
8-other
A novel CLN8 mutation in late-infantile-onset neuronal ceroid lipofuscinosis (LINCL) reveals aspects of CLN8 neurobiological function.
PMID 19431184·Hum Mutat·2009
5-case
Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunction.
PMID 18946002·Neurology·2008
5-case
A novel de novo nonsense mutation in ATP1A2 associated with sporadic hemiplegic migraine and epileptic seizures.
PMID 18644608·J Neurol Sci·2008
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
- 2823 FRESNO ST
FRESNO, CA 93721 - Phone
- (559) 443-2682
Quick Facts
- NPI
- 1457892622
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 7
- Publications
- 20
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