Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Pradeep Rudramurthy"'
Publikováno v:
National Journal of Laboratory Medicine, Vol 11, Iss 3, Pp 17-20 (2022)
Introduction: Thalassaemia and other structural haemoglobinopathies are the major genetic disorders that cause significant morbidity in children. Haemoglobinopathies need to be diagnosed at the earliest in order to offer suitable treatment, carri
Externí odkaz:
https://doaj.org/article/4d63d2efe4084c32b7796a70942ad660
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 2, Pp EC09-EC11 (2016)
Introduction: Sickle cell disease is a monogenic disorder with considerable clinical diversity and Sickle haemoglobin is responsible for wide spectrum of disorders which vary with respect to severity of anaemia, frequency of crises and duration o
Externí odkaz:
https://doaj.org/article/08d900b4eeef4f848996b34785644ef7
Publikováno v:
Journal of Evolution of Medical and Dental Sciences. 8:919-923
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5300201daa46d9cf2681adb32a6cc7f
https://doi.org/10.14260/jemds/2019/204
https://doi.org/10.14260/jemds/2019/204
Autor:
Hemalata Lokanatha, Mahantesh Sangappa, Supriya Siddavatam, Pradeep Rudramurthy, Asha D Benakappa
Publikováno v:
Tropical Journal of Pathology and Microbiology. 3:181-187
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6005752cebf4dccae2fc0a6a79294ce
https://doi.org/10.17511/jopm.2017.i02.19
https://doi.org/10.17511/jopm.2017.i02.19
Autor:
Anand Prahlad Rao, Sanjay Kantharajpura Shivappa, Pradeep Rudramurthy, Jessica Laltlansangi Hlawndo, Jyothi Raghuram
Publikováno v:
International Journal of Contemporary Pediatrics. 7:696
Background: Polyarteritis nodosa (PAN) is a primary systemic necrotizing vasculitis predominantly targeting medium-sized arteries defined as the main visceral arteries and their branches. The objective of this study was to analyze the epidemiology, c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0e450f13b45f2e942f4065e679e16aa
https://doi.org/10.18203/2349-3291.ijcp20200702
https://doi.org/10.18203/2349-3291.ijcp20200702
Publikováno v:
Indian Journal of Dermatology
Chediak-Higashi syndrome (CHS) is a rare autosomal recessive disease, characterized by partial oculocutaneous albinism, frequent pyogenic infections, and the presence of abnormal large granules in leukocytes and other granulecontaining cells. The abn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac596eda23cc846f82d1a9b9a5da041a
https://doi.org/10.4103/0019-5154.159662
https://doi.org/10.4103/0019-5154.159662
Autor:
Premalata, Chennagiri Srinivasamurthy, Madhumathi, Davanam Satyanarayana, Lakshmidevi, Visweswraiah, Pradeep, Rudramurthy, Appaji, Lingappa, Mukherjee, Geetashree
Publikováno v:
Turkish Journal of Hematology; Dec2008, Vol. 25 Issue 4, p201-204, 4p, 3 Color Photographs
Akademický článek
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Autor:
Aditi R; Department of Pathology, M S Ramaiah Medical College, M S R Nagar, Bangalore, Karnataka 560054 India., Aarathi R; Department of Pathology, M S Ramaiah Medical College, M S R Nagar, Bangalore, Karnataka 560054 India., Pradeep R; Department of Pathology, Indira Gandhi Institute of Child Health, Bangalore, India., Hemalatha L; Department of Pathology, Indira Gandhi Institute of Child Health, Bangalore, India., Akshatha C; Department of Pathology, Dhanalakshmi Srinivasan Medical College, Perambular, India., Amar K; Department of Pathology, M S Ramaiah Medical College, M S R Nagar, Bangalore, Karnataka 560054 India.
Publikováno v:
Indian journal of surgical oncology [Indian J Surg Oncol] 2016 Mar; Vol. 7 (1), pp. 18-24. Date of Electronic Publication: 2015 Jul 04.