Mahesh Kappanayil

Summary

Country: India

Publications

  1. pmc Understanding the physiology of complex congenital heart disease using cardiac magnetic resonance imaging
    Mahesh Kappanayil
    Department of Pediatric Cardiology, Amrita Institute of Medical Sciences, Cochin, Kerala, India
    Ann Pediatr Cardiol 4:177-82. 2011
  2. pmc Characterization of a distinct lethal arteriopathy syndrome in twenty-two infants associated with an identical, novel mutation in FBLN4 gene, confirms fibulin-4 as a critical determinant of human vascular elastogenesis
    Mahesh Kappanayil
    Departments of Pediatric Cardiology, Amrita Institute of Medical Sciences and Research Centre, Kochi, India
    Orphanet J Rare Dis 7:61. 2012
  3. ncbi request reprint Anomalous left coronary artery from nonfacing pulmonary sinus: direct aortic reimplantation
    Gopalraj S Sunil
    Department of Cardiovascular and Thoracic Surgery, Amrita Institute of Medical Sciences and Research Centre, Kochi, Kerala, India
    Ann Thorac Surg 97:1819-21. 2014
  4. ncbi request reprint Imaging findings in a distinct lethal inherited arteriopathy syndrome associated with a novel mutation in the FBLN4 gene
    Ramiah Rajeshkannan
    Department of Radiology, Amrita Institute of Medical Sciences, AIMS PO, Ernakulam, India, 682041
    Eur Radiol 24:1742-8. 2014
  5. ncbi request reprint Sly Disease: Mucopolysaccharidosis Type VII
    Sheela Nampoothiri
    Department of Pediatric Genetics, Pediatric Cardiology, and Pathology, Amrita Institute of Medical Sciences and Research Center, Elamakkara PO, Cochin 682 026, Kerala, India
    Indian Pediatr 45:859-61. 2008
  6. pmc Two-ventricle repair for complex congenital heart defects palliated towards single-ventricle repair
    Brijesh P Kottayil
    Department of Cardiovascular and Thoracic Surgery, Amrita Institute of Medical Sciences and Research Centre, Kochi, Kerala, India
    Interact Cardiovasc Thorac Surg 18:266-71. 2014
  7. doi request reprint Images in cardiovascular medicine. Arterial tortuosity syndrome: phenotypic features and cardiovascular manifestations
    Gayathri Satish
    Department of Pediatric Cardiology, Amrita Institute of Medical Sciences and Research Centre, Amrita Lane, Elamakkara PO, Kochi, Kerala, India
    Circulation 117:e477-8. 2008

Collaborators

Detail Information

Publications7

  1. pmc Understanding the physiology of complex congenital heart disease using cardiac magnetic resonance imaging
    Mahesh Kappanayil
    Department of Pediatric Cardiology, Amrita Institute of Medical Sciences, Cochin, Kerala, India
    Ann Pediatr Cardiol 4:177-82. 2011
    ..This article introduces the reader to cardiac MRI and its utility through the clinical example of a child with a complex congenital cyanotic heart disease...
  2. pmc Characterization of a distinct lethal arteriopathy syndrome in twenty-two infants associated with an identical, novel mutation in FBLN4 gene, confirms fibulin-4 as a critical determinant of human vascular elastogenesis
    Mahesh Kappanayil
    Departments of Pediatric Cardiology, Amrita Institute of Medical Sciences and Research Centre, Kochi, India
    Orphanet J Rare Dis 7:61. 2012
    ..We describe a syndrome of lethal arteriopathy associated with a novel, identical mutation in the fibulin 4 gene (FBLN4) in a unique cohort of infants from South India...
  3. ncbi request reprint Anomalous left coronary artery from nonfacing pulmonary sinus: direct aortic reimplantation
    Gopalraj S Sunil
    Department of Cardiovascular and Thoracic Surgery, Amrita Institute of Medical Sciences and Research Centre, Kochi, Kerala, India
    Ann Thorac Surg 97:1819-21. 2014
    ..This easily reproducible technique was successfully used in 2 patients. It achieves a dual coronary repair without the use of complex aortic or pulmonary arterial flaps and without causing any distortion to the great vessels. ..
  4. ncbi request reprint Imaging findings in a distinct lethal inherited arteriopathy syndrome associated with a novel mutation in the FBLN4 gene
    Ramiah Rajeshkannan
    Department of Radiology, Amrita Institute of Medical Sciences, AIMS PO, Ernakulam, India, 682041
    Eur Radiol 24:1742-8. 2014
    ..We present the imaging findings of a newly identified lethal arteriopathy associated with a novel mutation in the gene encoding fibulin-4, occurring in a distinct community from southern India...
  5. ncbi request reprint Sly Disease: Mucopolysaccharidosis Type VII
    Sheela Nampoothiri
    Department of Pediatric Genetics, Pediatric Cardiology, and Pathology, Amrita Institute of Medical Sciences and Research Center, Elamakkara PO, Cochin 682 026, Kerala, India
    Indian Pediatr 45:859-61. 2008
    ..Extremely low levels of beta glucuronidase confirmed the diagnosis of Sly disease (Mucopolysaccharidosis VII). This is the first case of MPS VII reported from India...
  6. pmc Two-ventricle repair for complex congenital heart defects palliated towards single-ventricle repair
    Brijesh P Kottayil
    Department of Cardiovascular and Thoracic Surgery, Amrita Institute of Medical Sciences and Research Centre, Kochi, Kerala, India
    Interact Cardiovasc Thorac Surg 18:266-71. 2014
    ..Given the long-term functional and survival advantage, we have been consciously exploring the feasibility of a biventricular repair in these patients when they present later for Fontan completion...
  7. doi request reprint Images in cardiovascular medicine. Arterial tortuosity syndrome: phenotypic features and cardiovascular manifestations
    Gayathri Satish
    Department of Pediatric Cardiology, Amrita Institute of Medical Sciences and Research Centre, Amrita Lane, Elamakkara PO, Kochi, Kerala, India
    Circulation 117:e477-8. 2008