Dr. Pankaj B. Agrawal MD
Doctor
300 Longwood Ave Boston MA, 02115About
Dr. Pankaj B. Agrawal MD is a top Doctor in Boston, MA. With a passion for the field and an unwavering commitment to their specialty, Dr. Pankaj B. Agrawal MD is an expert in changing the lives of their patients for the better. Through their designated cause and expertise in the field, Dr. Pankaj B. Agrawal MD is a prime example of a true leader in health care. As a leader and expert in their field, Dr. Pankaj B. Agrawal MD is passionate about enhancing patient quality of life. They embody the values of communication, safety, and trust when dealing directly with patients. In Boston, MA, Dr. Pankaj B. Agrawal MD is a true asset to their field and dedicated to the profession of medicine.
Education and Training
Agartala Government Medical College 1991
Medical College Baroda 1990
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Fluconazole.
- Myofiber size correlates with MTM1 mutation type and outcome in X-linked myotubular myopathy.
- Novel CHD7 and FBN1 mutations in an infant with multiple congenital anamolies.
- Normal myofibrillar development followed by progressive sarcomeric disruption with actin accumulations in a mouse Cfl2 knockout demonstrates requirement of cofilin-2 for muscle maintenance.
- Congenital myopathy caused by a novel missense mutation in the CFL2 gene.
- A de novo T73I mutation in PTPN11 in a neonate with severe and prolonged congenital thrombocytopenia and Noonan syndrome.
- Whole genome sequencing identifies SCN2A mutation in monozygotic twins with Ohtahara syndrome and unique neuropathologic findings.
- Health care failure mode and effect analysis to reduce NICU line-associated bloodstream infections.
- Stimulating erythropoiesis in neonates.
- Mutation of KCNJ8 in a patient with Cantú syndrome with unique vascular abnormalities - support for the role of K(ATP) channels in this condition.
- Rare complete loss of function provides insight into a pleiotropic genome-wide association study locus.
- A compound heterozygous mutation in GPD1 causes hepatomegaly, steatohepatitis, and hypertriglyceridemia.
- NPHP3 mutations are associated with neonatal onset multiorgan polycystic disease in two siblings.
- Whole exome sequencing identifies RAI1 mutation in a morbidly obese child diagnosed with ROHHAD syndrome.
- Cofilin-2 phosphorylation and sequestration in myocardial aggregates: novel pathogenetic mechanisms for idiopathic dilated cardiomyopathy.
Treatments
- Birth Defects
Dr. Pankaj B. Agrawal MD's Practice location
Boston, MA 02115Get Direction
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