Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Balasundaram Krishnamurthy"'
Autor:
Manish Jain, Balasundaram Krishnamurthy, Jagadish Deshpande, Harish Verma, Mohammad Ahmad, Raman Sethi, Ashish Bavdekar, Lalitendu Mohanty, Abhishek Kunwar, Niranjana S Mahantashetti, Deepa Sharma, Jayaseelan Visalakshi, Sunil Bahl, Shailesh D. Pawar, Mannancheril A Mathew, Pradeep Haldar, Roland W. Sutter
Publikováno v:
Journal of the Pediatric Infectious Diseases Society. 11:60-68
Introduction Following the withdrawal of Sabin type 2 from trivalent oral poliovirus vaccine (tOPV) in 2016, the introduction of ≥1 dose of inactivated poliovirus vaccine (IPV) in routine immunization was recommended, either as 1 full dose (0.5mL,
Autor:
Balasundaram Krishnamurthy, Mysore R. Savitha, Sosalagere M. Dinesh, Doddaiah Narayanappa, Nallur B. Ramachandra, Kusuma Lingaiah
Publikováno v:
Genetic Testing and Molecular Biomarkers. 15:715-720
Congenital heart disease (CHD) is the most common type of birth defect, affecting 1% of all live births. The recent exponential increase in the knowledge of medical genetics has revolutionized the understanding of CHDs during the past few decades. GA
Autor:
Sosalagere M. Dinesh, L. Kusuma, Balasundaram Krishnamurthy, Doddaiah Narayanappa, Nallur B. Ramachandra, Mysore R. Savitha, R. Smitha
Publikováno v:
Genetic Testing and Molecular Biomarkers. 14:873-879
Congenital heart disease (CHD) is a common congenital birth defect, affecting nearly 1% of all live births, and is the most common cause of infant death. NKX2.5 is an important transcription factor expressed during vertebrate heart development and in
Autor:
Abbas Hyderi, Sameul C. Karat, Narayanappa Doddaiah, Zareen M. Patel, Nallur B. Ramachandra, Smitha Rame Gowda, Mysore R. Savitha, Harshavardhan M. Gawde, Balasundaram Krishnamurthy
Publikováno v:
International Journal of Human Genetics. 10:131-139
Congenital heart disease (CHD) is the most common form of human birth defects accounting for about 30% of the total anomalies. The prevalence of CHD worldwide is found to range between 1.0 - 150/ 1000 live births. The causes for CHD can be categorize
Publikováno v:
International Journal of Human Genetics. 7:289-296
KEYWORDS Turner syndrome; Klinefelter syndrome; young mother; nondisjunction; maternal grandmother age ABSTRACT Majority of the chromosomal abnormalities are incompatible with embryonic or fetal survival but trisomy 21 and sex chromosomal trisomies h
Autor:
Narayanappa Doddaiah, Balasundaram Krishnamurthy, Mysore R. Savitha, Smitha Ramegowda, Subramanyam N. Prasanth, Nallur B. Ramachandra
Publikováno v:
International Journal of Human Genetics. 7:241-248
Congenital heart disease (CHD) is the leading cause of mortality in the first year of life. Prevalence of CHD worldwide is found to range from 1.0 to 50.89 per 1000 livebirths including India. The ...
Autor:
Balasundaram Krishnamurthy, Kusuma Lingaiah, Bharath A Parshwanath, Nallur B. Ramachandra, Savitha R Mysore
Publikováno v:
Indian Journal of Human Genetics
Birth defects have become the important cause of mortality and morbidity in the perinatal period. Congenital heart disease (CHD) is the most common birth defect which includes the varying forms of cardiac abnormalities and occurs with an incidence of
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Autor:
Balasundaram Krishnamurthy, Doddaiah Narayanappa, Ramachandra B Nallur, Dinesh M Sosalagere, Savitha R Mysore, Kusuma Lingaiah
Publikováno v:
The Indian Journal of Medical Research
Background & objectives: Cardiac malformations in the young constitute a major portion of clinically significant birth defects. Congenital heart disease (CHD) is a common congenital cardiac birth defect, affecting nearly 1 per cent of all live births
Autor:
Nallur B. Ramachandra, Mysore R. Savitha, Sosalagere M. Dinesh, Doddaiah Narayanappa, Balasundaram Krishnamurthy, Lingaiah Kusuma
Publikováno v:
Genetic testing and molecular biomarkers. 15(7-8)
Cardiac malformations contribute greatly to cardiovascular disease in the young, constituting a major portion of clinically significant birth defects. Congenital heart disease (CHD) is a common congenital cardiac birth defect, affecting nearly 1% of