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KEVIN MCBRIDE, M.D.
M.D.
Surgery Physician
NPI: 1265421002Individual
Specialties, Licenses & Credentials
Surgery PhysicianPrimary
Surgery
Code: 208600000X
44628(MA)
Research & Publications (20)
Linkage analysis of left ventricular outflow tract malformations (aortic valve stenosis, coarctation of the aorta, and hypoplastic left heart syndrome).
PMID 19142209·Eur J Hum Genet·2009
8-other
NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling.
PMID 18593716·Hum Mol Genet·2008
7-preclinical
Heritability of plasma amino acid levels in different nutritional states.
PMID 17005426·Mol Genet Metab·2007
8-other
Regulation of hypermutation by activation-induced cytidine deaminase phosphorylation.
PMID 16723391·Proc Natl Acad Sci U S A·2006
7-preclinical
Epidemiology of noncomplex left ventricular outflow tract obstruction malformations (aortic valve stenosis, coarctation of the aorta, hypoplastic left heart syndrome) in Texas, 1999-2001.
PMID 16007587·Birth Defects Res A Clin Mol Teratol·2005
8-other
Inheritance analysis of congenital left ventricular outflow tract obstruction malformations: Segregation, multiplex relative risk, and heritability.
PMID 15690347·Am J Med Genet A·2005
8-other
Developmental outcomes with early orthotopic liver transplantation for infants with neonatal-onset urea cycle defects and a female patient with late-onset ornithine transcarbamylase deficiency.
PMID 15466081·Pediatrics·2004
5-case
A family-based association study of congenital left-sided heart malformations and 5,10 methylenetetrahydrofolate reductase.
PMID 15390319·Birth Defects Res A Clin Mol Teratol·2004
8-other
Does intranasal application of zinc sulfate produce anosmia in the mouse? An olfactometric and anatomical study.
PMID 14627534·Chem Senses·2003
7-preclinical
Aortoesophageal fistula in a 13-yr-old girl: complication after nasogastric tube placement in the setting of right-sided aortic arch.
PMID 12780959·Pediatr Crit Care Med·2002
8-other
Hb Dartmouth [alpha66(E15)Leu-->Pro (alpha2) (CTG-->CCG)]: a novel alpha2-globin gene mutation associated with severe neonatal anemia when inherited in trans with Southeast Asian alpha-thalassemia-1.
PMID 11791870·Hemoglobin·2001
5-case
The effect of back reflections on the acoustic power delivered by physiotherapy ultrasound machines.
PMID 19679389·Ultrasound Med Biol·2009
8-other
Neuroprosthesis peroneal functional electrical stimulation in the acute inpatient rehabilitation setting: a case series.
PMID 19270044·Phys Ther·2009
5-case
Effects of dietary crude protein and supplemental urea levels on nitrogen and phosphorus utilization by feedlot cattle.
PMID 19028866·J Anim Sci·2009
7-preclinical
Acute dilated cardiomyopathy in a patient with deficiency of long-chain 3-hydroxyacyl-CoA dehydrogenase.
PMID 19083141·Pediatr Cardiol·2009
5-case
Formative design and evaluation of patient-delivered partner therapy informational materials and packaging.
PMID 19103640·Sex Transm Infect·2009
8-other
Lenalidomide oral monotherapy produces a high response rate in patients with relapsed or refractory mantle cell lymphoma.
PMID 19245430·Br J Haematol·2009
3-trial
The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly.
PMID 19265751·Genet Med·2009
8-other
The anti-neurodegeneration drug clioquinol inhibits the aging-associated protein CLK-1.
PMID 18927074·J Biol Chem·2009
7-preclinical
Microcoil embolisation of mycotic cystic artery pseudoaneurysm: a viable option in high-risk patients.
PMID 19449062·Cardiovasc Intervent Radiol·2009
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
- 1681 WASHINGTON ST
BRAINTREE, MA 02184 - Phone
- (617) 296-0242
Quick Facts
- NPI
- 1265421002
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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