Zobrazeno 1 - 10
of 454
pro vyhledávání: '"I.C Verma"'
Autor:
Vyom Mori, J.P.S. Sawhney, I.C. Verma, Ashwani Mehta, Renu Saxena, Rajiv Passey, Arun Mohanty, Bhuwanesh Kandpal, B.S. Vivek, Manish Sharma, Ashish Kumar Jain, Dipak Katare
Publikováno v:
International Journal of Cardiology: Heart & Vasculature, Vol 40, Iss , Pp 101023- (2022)
Aim: To study genetic variants in patients of familial dilated cardiomyopathy. Methodology: Patients with reduced ejection fraction of less than 45% and dilated left ventricle are considered to have dilated cardiomyopathy. Clinical history was taken
Externí odkaz:
https://doaj.org/article/45322e8d7fa7405b8553eefb7352aad4
Autor:
J.P.S. Sawhney, Shashi Ranjan Prasad, Manish Sharma, Kushal Madan, A. Mohanty, Rajiv Passey, Ashwani Mehta, B. Kandpal, Aman Makhija, Rajneesh Jain, R.R. Mantri, Bhola Shankar Vivek, S.C. Manchanda, I.C. Verma
Publikováno v:
Indian Heart Journal, Vol 71, Iss 2, Pp 118-122 (2019)
Aims: The prevalence of premature coronary artery disease (CAD) in India is two to three times more than other ethnic groups. Untreated heterozygous familial hypercholesterolemia (FH) is one of the important causes for premature CAD. As the age advan
Externí odkaz:
https://doaj.org/article/cd62a3cea114481baa6efd196f580d30
Akademický článek
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Publikováno v:
Journal of Pediatric Genetics.
Beckwith-Wiedemann syndrome (BWS; MIM# 130650) is a well-characterized pediatric overgrowth disorder. In approximately 5% of the cases, it is caused by pathogenic variants in the CDKN1C (cyclin-dependent kinase inhibitor 1C). CDKN1C gene encodes for
Autor:
S.R. Prasad, J.P.S. Sawhney, I.C. Verma, S.C. Manchanda, A. Mehta, A. Mohanty, B. Kandpal, M. Sharma
Publikováno v:
Indian Heart Journal, Vol 69, Iss S2, p S91 (2017)
Externí odkaz:
https://doaj.org/article/db9462b77d7b42c4bc33cc154cbaf4a4
Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Autor:
Ishpreet K. Biji, Siddharth Yadav, Samarth Kulshrestha, Renu Saxena, Sudha Kohli, I.C. Verma, Benu Kumar, Ratna Dua Puri
Publikováno v:
SSRN Electronic Journal.
Pathogenic variants in the transmembrane sulfate transporter protein SLC26A2 are associated with different phenotypes of inherited chondrodysplasias. As limited data is published from India, in this study we sought to elucidate the molecular basis of
Autor:
Vyom Mori, J.P.S. Sawhney, I.C. Verma, Ashwani Mehta, Renu Saxena, Rajiv Passey, Arun Mohanty, Bhuwanesh Kandpal, B.S. Vivek, Manish Sharma, Ashish Kumar Jain, Dipak Katare
Publikováno v:
International journal of cardiology. Heartvasculature. 40
To study genetic variants in patients of familial dilated cardiomyopathy.Patients with reduced ejection fraction of less than 45% and dilated left ventricle are considered to have dilated cardiomyopathy. Clinical history was taken and possible second
Autor:
I.C. Verma, Rajneesh Jain, Bhuwanesh Kandpal, R.R. Mantri, Rajiv Passey, S.R. Prasad, Arun Mohanty, Aman Makhija, Ashwani Mehta, Kushal Madan, Bhola Shankar Vivek, J.P.S. Sawhney, Manish Sharma, Subhash C. Manchanda
Publikováno v:
Indian Heart Journal
Indian Heart Journal, Vol 71, Iss 2, Pp 118-122 (2019)
Indian Heart Journal, Vol 71, Iss 2, Pp 118-122 (2019)
Aims: The prevalence of premature coronary artery disease (CAD) in India is two to three times more than other ethnic groups. Untreated heterozygous familial hypercholesterolemia (FH) is one of the important causes for premature CAD. As the age advan