Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Krishna Prasad Adiraju"'
Autor:
Mallikarjuna Shetty, Swaroopa Deme, KNKJ Mohan, Krishna Prasad Adiraju, Nageswar Rao Modugu, Naval Chandra, AMVR Narendra, Sathyanarayana Raju Yadati
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 10, Pp OC22-OC25 (2016)
Introduction: Splenic abscess is a rare entity with potentially life threatening complications. Sparse recent published data are available documenting the aetiological profile and management of patients with splenic abscess from India. Aim: To st
Externí odkaz:
https://doaj.org/article/ca804f5c34684e6b9fd27960687f61c5
Autor:
Penta Bhavanadhar, Vangipuram Rangacharyulu Srinivasan, Sai Satish Oruganti, Krishna Prasad Adiraju
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 7, Pp OC01-OC05 (2016)
Introduction: Anaemia is a contributor for adverse prognosis in Acute Coronary Syndrome (ACS), but the epidemiology and causes of anaemia in such patients is not defined. Aim: To study the prevalence and aetiology of anaemia in hospitalized patie
Externí odkaz:
https://doaj.org/article/8cee7a4f124f4aa5a1a7d2665bad61a5
Autor:
Mallikarjuna Shetty, Anukonda Moti Venkata Raja Narendra, Krishna Prasad Adiraju, Nageshwar Rao Modugu
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 6, Pp OC15-OC18 (2016)
Introduction: Aplastic Anaemia (AA) is a syndrome characterized by peripheral pancytopenia with hypo-cellular marrow. Acquired idiopathic AA is the most common variety, probably of an autoimmune aetiology. Bone Marrow Transplantation (BMT) is the
Externí odkaz:
https://doaj.org/article/ac514807ba124f51bd2eea8aa0e2b385
Autor:
M. Shetty, Krishna Prasad Adiraju, Uday Kumar Karnati, Saisubrahmanyam Pappu, Naval Chandra, Nageswara Rao Modugu, Sai Shivani Ranga, Sneha Sala
Publikováno v:
Journal of Evidence Based Medicine and Healthcare. 8:3435-3440
BACKGROUND Sickle delta beta thalassemia is a rare genetic disorder, with varied symptoms, signs, requiring careful monitoring for potential complications. It is due to sickle mutation and thalassemia mutation occurring together, with sparse data ava
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a8b89b84409892a50757f0a45bd3189
https://doi.org/10.18410/jebmh/2021/623
https://doi.org/10.18410/jebmh/2021/623
Publikováno v:
The Journal of the Association of Physicians of India. 68(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::105f409e5849c5fe0a2637722632c726
https://pubmed.ncbi.nlm.nih.gov/31979923
https://pubmed.ncbi.nlm.nih.gov/31979923
Autor:
Mohan K, N.R. Modugu, Yadati, Krishna Prasad Adiraju, M. Shetty, S. Deme, Naval Chandra, A. Narendra
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 10, Pp OC22-OC25 (2016)
Introduction Splenic abscess is a rare entity with potentially life threatening complications. Sparse recent published data are available documenting the aetiological profile and management of patients with splenic abscess from India. Aim To study th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fed6be0beeec4608a7f8846f925ecde
https://europepmc.org/articles/PMC5121710/
https://europepmc.org/articles/PMC5121710/
Autor:
Sai Satish Oruganti, Vangipuram Rangacharyulu Srinivasan, Penta Bhavanadhar, Krishna Prasad Adiraju
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 7, Pp OC01-OC05 (2016)
Introduction: Anaemia is a contributor for adverse prognosis in Acute Coronary Syndrome (ACS), but the epidemiology and causes of anaemia in such patients is not defined. Aim: To study the prevalence and aetiology of anaemia in hospitalized patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::266f1ef961a02c07e677497bfdc71848
https://europepmc.org/articles/PMC5020290/
https://europepmc.org/articles/PMC5020290/
Autor:
Satyanarayana Raju Yadati, Subbalaxmi V. S. Malladi, L. Vemu, N.R. Modugu, Krishna Prasad Adiraju, Naval Chandra, M. Shetty
Publikováno v:
International Journal of Infectious Diseases. 45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::845eee65e19ddc897a3d3b931859fc61
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 6, Pp OC15-OC18 (2016)
INTRODUCTION Aplastic Anaemia (AA) is a syndrome characterized by peripheral pancytopenia with hypo-cellular marrow. Acquired idiopathic AA is the most common variety, probably of an autoimmune aetiology. Bone Marrow Transplantation (BMT) is the trea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f674b11dd47792172ee69250266b75c
https://pubmed.ncbi.nlm.nih.gov/27504327
https://pubmed.ncbi.nlm.nih.gov/27504327
Autor:
Rapur Ram, Krishna Prasad Adiraju, Gudithi Swarnalatha, Chandanavalli Shyam Sunder Rao, Kaligotla Venkata Dakshinamurty
Publikováno v:
International Urology and Nephrology. 46:849-851
Defining anaemia as haemoglobin level less than 13 g/dL for men and less than 12 g/dL for women, the investigators of The Transplant European Study on Anemia Management (TRESAM) reported the prevalence of anaemia in renal transplant recipients as 38.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8cff79ed6803a4c873ddabf0f5cd9af8
https://doi.org/10.1007/s11255-013-0516-x
https://doi.org/10.1007/s11255-013-0516-x