Zobrazeno 1 - 9
of 9
pro vyhledávání: '"A M Shanthala Devi"'
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 20, Iss 2, Pp 163-165 (2019)
Dorfman-Chanarin syndrome is a rare autosomal recessive neutral lipid storage disorder with congenital ichthyosis characterized by triglyceride deposition in multiple organs. The usual clinical presentation has been reported to correspond to that of
Externí odkaz:
https://doaj.org/article/e8ae0c60c1b84b528f5cd24a94032274
Autor:
A M Shanthala Devi, K G Gaikhonlungpou
Publikováno v:
Journal of Applied Hematology, Vol 5, Iss 1, Pp 29-31 (2014)
Background and Objectives: Multi-transfused thalassemic patients are prone to transfusions related complications. Study of these reactions and correlating them with the leukodepletion of the transfused packed red blood cells (PRBCs) reduces transfusi
Externí odkaz:
https://doaj.org/article/ca919142010a4fc1ba1455a2f5c06275
Publikováno v:
Journal of Laboratory Physicians. Jan-Jun2010, Vol. 2 Issue 1, p17-20. 4p.
Publikováno v:
Journal of Laboratory Physicians
Journal of Laboratory Physicians, Vol 2, Iss 01, Pp 017-020 (2010)
Journal of Laboratory Physicians, Vol 2, Iss 01, Pp 017-020 (2010)
Background: Autoimmune hemolytic anemia (AIHA) results from red cell destruction due to circulating autoantibodies against red cell membrane antigens. They are classified etiologically into primary and secondary AIHAs. A positive direct antiglobulin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81f456efe76d1db0455c5cf80329d627
http://europepmc.org/articles/PMC3147080
http://europepmc.org/articles/PMC3147080
Publikováno v:
Mapana - Journal of Sciences. 2:116-119
BbOd transfusion has developed os a clinical nique. Its development has progressed from ignorance to science and from cruelty to civilization over hundreds Of years. Transfusion has mode great contribution {or saving lives ond expanding operation cov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c8508dcd8301ef5f86504445a0fb266
https://doi.org/10.12723/mjs.4.15
https://doi.org/10.12723/mjs.4.15
Publikováno v:
Indian journal of hematologyblood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion. 32(Suppl 1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14013dd12105b7842d8aa91055c16bf6
https://pubmed.ncbi.nlm.nih.gov/27408416
https://pubmed.ncbi.nlm.nih.gov/27408416
Publikováno v:
Indian journal of hematologyblood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion. 28(1)
A positive direct Coombs test (DCT) is the hallmark of diagnosis of immune hemolytic anemias. The reagent used for the test is the Antihuman globulin (AHG), which may be either ‘Polyspecific’ or ‘Monospecific’. The advent of the Gel card syst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86623a245e6f67e64e220431a61b2da5
https://pubmed.ncbi.nlm.nih.gov/23449541
https://pubmed.ncbi.nlm.nih.gov/23449541
Publikováno v:
Indian journal of hematologyblood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion. 26(3)
Dear Editor, Glucose-6-phosphate dehydrogenase deficiency is the most common enzyme deficiency worldwide. Approximately 400 million people are said to be affected worldwide. According to world health organization 7.5% of world population are carriers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d05a730dab5571fe2f4abb3d941b0ba
https://pubmed.ncbi.nlm.nih.gov/21886401
https://pubmed.ncbi.nlm.nih.gov/21886401
Publikováno v:
Indian journal of pathologymicrobiology. 44(3)
Bleeding is a common manifestation of inherited and acquired disorders of haemostasis. Acquired disorders of haemostasis can be of varied etiology like liver disease, DIC, haemorrhagic disease of newborn and inhibitors to coagulation factors. Inhibit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9612840f4e2bd7745c73c1b637370f7d
https://pubmed.ncbi.nlm.nih.gov/12024937
https://pubmed.ncbi.nlm.nih.gov/12024937