Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Arun Kumar Harith"'
Autor:
Geet Aggarwal, Aseem Kumar Tiwari, Swati Pabbi, Gunajn Bhardwaj, Ganesh Rawat, Nandram, Arun Kumar Harith, Kamini Vinayak
Publikováno v:
Global Journal of Transfusion Medicine, Vol 7, Iss 1, Pp 12-17 (2022)
Background and Objectives: Indian studies on evaluation of storage lesions in red blood cells (RBCs) are either limited to 21 or 28 days or have evaluated limited parameters for 42 days. Moreover, issue of transfusion of “fresh” versus “old”
Externí odkaz:
https://doaj.org/article/6db2d22636ea48c3bea5c1e88ac07ef8
Autor:
Reeta Choudhary, Charu Yadav, Pallavi Jain, Shyam Bihari Bansal, Beena Bansal, Arun Kumar Harith
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 14, Iss 8, Pp 01-05 (2020)
Introduction: Chronic Kidney Disease (CKD), a condition characterised by a gradual loss of renal function over the time, has emerged as a major public health concern with 17% prevalence in Indian population. Decrease in renal function in CKD lead
Externí odkaz:
https://doaj.org/article/93c3eff3a8804cce8d5f3e34e20bbe61
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 17, Iss 1, Pp 1-6 (2016)
Congenital Erythropoietic Porphyria (CEP) is a rare inborn error of metabolism charectorised by a deficiency of UROS III enzyme, an important enzyme in the heme biosythetic pathway. It is an autosomal recessive disease and only around 200 cases have
Externí odkaz:
https://doaj.org/article/ac11d45f567d499a86210e482b58c340
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 11, Iss 2, Pp BC26-BC29 (2017)
Introduction: Laboratory investigations account for significant percentage of healthcare expenses. Every hospital and laboratory especially in the government sector wants to cut down the expenses on reports and offer inferior printouts of reports.
Externí odkaz:
https://doaj.org/article/62071c04152847a59b8718a52be28521
Publikováno v:
Indian Journal of Dermatology, Vol 61, Iss 4, Pp 467-467 (2016)
Hereditary porphyrias are a group of metabolic disorders of heme biosynthesis pathway that are characterized by acute neurovisceral symptoms, skin lesions, or both. Congenital erythropoietic porphyria (CEP) is an extremely rare disease with a mutatio
Externí odkaz:
https://doaj.org/article/bf643b97308f48a59933af34ff1e7d05
Publikováno v:
Journal of Advances in Medicine and Medical Research. :91-99
Background: A short Turn Around Time (TAT) is unanimously desired and equated to efficiency of a hospital laboratory. Despite automation, laboratories often find it difficult to meet the TAT demands. The major lacuna noticed was that our technicians
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b5bf79d4ee96fc90cdb8055caf33faa
https://doi.org/10.9734/jammr/2022/v34i2231582
https://doi.org/10.9734/jammr/2022/v34i2231582
Autor:
Arun Kumar Harith, Charu Yadav, Reeta Choudhary, Shyam Bihari Bansal, Pallavi Jain, Beena Bansal
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 14, Iss 8, Pp 01-05 (2020)
Introduction: Chronic Kidney Disease (CKD), a condition characterised by a gradual loss of renal function over the time, has emerged as a major public health concern with 17% prevalence in Indian population. Decrease in renal function in CKD leads to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4460828275b0a4db1f215627269b38f8
Publikováno v:
Indian J Clin Biochem
Multiple myeloma is characterized by the presence of M-protein (monoclonal) in blood or urine. These proteins are immunoglobulins which are produced by a clone of abnormally proliferating B-lymphocytes and/or plasma cells. To evaluate M-protein, seru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::573702a0fbcc4a163eb83e72852ccd86
https://doi.org/10.1007/s12291-020-00929-y
https://doi.org/10.1007/s12291-020-00929-y
Publikováno v:
Journal of Case Reports. :113-115
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::457e720805b7c5428e9b9a9dbaaf0297
https://doi.org/10.17659/01.2020.0030
https://doi.org/10.17659/01.2020.0030
Publikováno v:
Medical Journal Armed Forces India. 74:300-303
A 60-year-old female presented with a 20-year history of progressive dark bluish discoloration of skin and passage of dark colored urine, painful arthritis and a recent history of invasive ductal carcinoma of right breast. Skin biopsy revealed hyalin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8af62fdfe80160af9f15abad73025d25
https://doi.org/10.1016/j.mjafi.2017.06.009
https://doi.org/10.1016/j.mjafi.2017.06.009