Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Advithi, Rangaraju"'
Autor:
Advithi Rangaraju, Ashwin Dalal
Publikováno v:
Journal of Indian College of Cardiology, Vol 11, Iss 1, Pp 5-12 (2021)
Inherited cardiac disorders are clinically and genetically heterogeneous group of disorders where sudden cardiac death is mostly the first clinical presentation. The available clinical markers are insufficient to make an accurate diagnosis, and there
Externí odkaz:
https://doaj.org/article/a00f61f380f44834b2ac56571a2ee950
Autor:
Advithi Rangaraju, Shuba Krishnan, G. Aparna, Satish Sankaran, Ashraf U. Mannan, B. Hygriv Rao
Publikováno v:
Indian Pacing and Electrophysiology Journal, Vol 18, Iss 3, Pp 91-94 (2018)
Electrical storm (ES) is a life threatening clinical situation. Though a few clinical pointers exist, the occurrence of ES in a patient with remote myocardial infarction (MI) is generally unpredictable. Genetic markers for this entity have not been s
Externí odkaz:
https://doaj.org/article/b289b83843e347fcb699cb257cfcd9ce
Autor:
Mittanamalli S Sridhar, Advithi Rangaraju, Kavitha Anbarasu, Sharat Putta Reddy, Sachin Daga, Sita Jayalakshmi, Bajibhi Shaik
Publikováno v:
Indian Journal of Ophthalmology, Vol 65, Iss 5, Pp 354-357 (2017)
Purpose: The purpose of the study is to present anterior segment optical coherence tomography (AS-OCT) as an alternative method of evaluating Kayser–Fleischer (KF) ring in Wilson disease (WD) not only by ophthalmologists but also by other clinician
Externí odkaz:
https://doaj.org/article/4e0b129a50db4104b0258cb0d739dfe8
Publikováno v:
Journal of Medical and Scientific Research, Vol 3, Iss 4, Pp 192-197 (2015)
Wilson disease (WD) is an inborn error of copper metabolism leading to its accumulation in liver, kidney and cornea. It is caused by a defective ATPase protein which is coded by ATP7B gene. It follows an autosomal recessive mode of inheritance with a
Externí odkaz:
https://doaj.org/article/1ec34647069749cd88543549b3758e9a
Autor:
Lova Satyanarayana Matsa, Advithi Rangaraju, Viswamitra Vengaldas, Mona Latifi, Hossein Mehraban Jahromi, Venkateshwari Ananthapur, Pratibha Nallari
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e70523 (2013)
Dilated Cardiomyopathy (DCM) is characterized by systolic dysfunction, followed by heart failure necessitating cardiac transplantation. The genetic basis is well established by the identification of mutations in sarcomere and cytoskeleton gene/s. Mod
Externí odkaz:
https://doaj.org/article/a68a723b80a24037bf7fc1035198b1fe
Autor:
Shuba Krishnan, G. Aparna, Advithi Rangaraju, Satish Sankaran, Ashraf U Mannan, B. Hygriv Rao
Publikováno v:
Indian Pacing and Electrophysiology Journal
Indian Pacing and Electrophysiology Journal, Vol 18, Iss 3, Pp 91-94 (2018)
Indian Pacing and Electrophysiology Journal, Vol 18, Iss 3, Pp 91-94 (2018)
Electrical storm (ES) is a life threatening clinical situation. Though a few clinical pointers exist, the occurrence of ES in a patient with remote myocardial infarction (MI) is generally unpredictable. Genetic markers for this entity have not been s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1a84dc2705d233d383365abe59bfdf1
https://doi.org/10.1016/j.ipej.2018.01.003
https://doi.org/10.1016/j.ipej.2018.01.003
Publikováno v:
Meta Gene. 14:114-118
Wilson Disease is an autosomal recessive inherited disorder caused by abnormal copper metabolism. Mutations in P-type adenosine triphosphatase -ATP7B gene are known to result in excessive copper deposition in liver, brain and cornea leading to hepati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d09148686e34c7af85e8cd96aab68fa
https://doi.org/10.1016/j.mgene.2017.08.010
https://doi.org/10.1016/j.mgene.2017.08.010
Publikováno v:
Gene Reports. 8:94-99
Hypertrophic cardiomyopathy is a multifactorial disorder, with mutations implicated in 12 sarcomeric and cytoskeletal genes accounting for genotypic and phenotypic heterogeneity, making genetic and clinical diagnosis much more challenging. The geneti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4264e101fdc4850304f2bb39c9f1117e
https://doi.org/10.1016/j.genrep.2017.06.004
https://doi.org/10.1016/j.genrep.2017.06.004
Publikováno v:
Journal of Medical and Scientific Research, Vol 3, Iss 4, Pp 192-197 (2015)
Wilson disease (WD) is an inborn error of copper metabolism leading to its accumulation in liver, kidney and cornea. It is caused by a defective ATPase protein which is coded by ATP7B gene. It follows an autosomal recessive mode of inheritance with a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b24b4a189f1c9516dad95ab254de8fe7
http://jmsronline.com/article.aspx?ID=Clinical-and-genetic-heterogeneity-in-Wilson-disease
http://jmsronline.com/article.aspx?ID=Clinical-and-genetic-heterogeneity-in-Wilson-disease
Autor:
Risha Nahar L, Advithi Rangaraju, Vyjayanthi Srinivasan, Varalakshmi Mallidi, Kanaka Bhushanam GVVS
Publikováno v:
Journal of Medical and Scientific Research, Vol 3, Iss 1, Pp 22-26 (2015)
Infertility is defined as the inability of women to ever bear a child or become pregnant after one year unprotected sexual intercourse or carry a pregnancy to a live birth. Genetic counseling can increase a couple's chance of having a healthy baby. S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5172256fc6f048594bc894178b2ac75
http://jmsronline.com/article.aspx?ID=Genetic-evaluation-in-infertility
http://jmsronline.com/article.aspx?ID=Genetic-evaluation-in-infertility