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BRUCE GELB, M.D.
M.D.
Transplant Surgery Physician
NPI: 1780861054IndividualAccepts Medicare
Specialties, Licenses & Credentials
Transplant Surgery PhysicianPrimary
Transplant Surgery
Code: 204F00000X
242945(NY)
CMS Specialties
PrimaryGENERAL SURGERY
Education
UNIVERSITY OF TEXAS MEDICAL SCHOOL AT SAN ANTONIO
Class of 2003
Research & Publications (20)
Noonan syndrome and related disorders: dysregulated RAS-mitogen activated protein kinase signal transduction.
PMID 16987887·Hum Mol Genet·2006
6-review
Genetic basis of syndromes associated with congenital heart disease.
PMID 11357015·Curr Opin Cardiol·2001
6-review
Recent advances in the understanding of genetic causes of congenital heart defects.
PMID 10704426·Front Biosci·2000
6-review
Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum.
PMID 19206169·Hum Mutat·2009
8-other
Phosphatase-defective LEOPARD syndrome mutations in PTPN11 gene have gain-of-function effects during Drosophila development.
PMID 18849586·Hum Mol Genet·2009
7-preclinical
PTPN11 analysis for the prenatal diagnosis of Noonan syndrome in fetuses with abnormal ultrasound findings.
PMID 18759865·Clin Genet·2009
8-other
Ablation of cathepsin k activity in the young mouse causes hypermineralization of long bone and growth plates.
PMID 19172215·Calcif Tissue Int·2009
7-preclinical
Diverse driving forces underlie the invariant occurrence of the T42A, E139D, I282V and T468M SHP2 amino acid substitutions causing Noonan and LEOPARD syndromes.
PMID 18372317·Hum Mol Genet·2008
8-other
Somatically acquired JAK1 mutations in adult acute lymphoblastic leukemia.
PMID 18362173·J Exp Med·2008
7-preclinical
Multiple thoracic aortic aneurysms after mediastinitis in an infant after repair of coarctation of the aorta.
PMID 18242288·J Thorac Cardiovasc Surg·2008
5-case
Transcription factor Ap2delta associates with Ash2l and ALR, a trithorax family histone methyltransferase, to activate Hoxc8 transcription.
PMID 18495928·Proc Natl Acad Sci U S A·2008
7-preclinical
Deficiency and inhibition of cathepsin K reduce body weight gain and increase glucose metabolism in mice.
PMID 18818416·Arterioscler Thromb Vasc Biol·2008
7-preclinical
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy.
PMID 17603483·Nat Genet·2007
7-preclinical
Diversity, parental germline origin, and phenotypic spectrum of de novo HRAS missense changes in Costello syndrome.
PMID 17054105·Hum Mutat·2007
8-other
Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome.
PMID 17143282·Nat Genet·2007
4-observational
Novel functional interaction between Na+/H+ exchanger 1 and tyrosine phosphatase SHP-2.
PMID 17289818·Am J Physiol Regul Integr Comp Physiol·2007
7-preclinical
The genetics of congenital heart disease: a review of recent developments.
PMID 17413276·Curr Opin Cardiol·2007
6-review
Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics.
PMID 17519398·Circulation·2007
6-review
Evaluation of pulmonary artery banding in the setting of ventricular septal defects and severely elevated pulmonary vascular resistance.
PMID 18377533·Congenit Heart Dis·2006
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
- 403 E 34TH ST, 3RD FLOOR
NEW YORK, NY 10016 - Phone
- (212) 263-8134
Quick Facts
- NPI
- 1780861054
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 23
- Publications
- 20
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