Zobrazeno 1 - 10
of 1 348
pro vyhledávání: '"Saxena Renu"'
Autor:
Verma I, Bijarnia Sunita, Saxena Renu, Kohli Sudha, Puri Ratna, Thomas Elizabeth, Chowdhary Debashish, Jha S, Grover A
Publikováno v:
Indian Journal of Ophthalmology, Vol 53, Iss 3, Pp 167-171 (2005)
PURPOSE: Leber′s hereditary optic neuropathy (LHON) presents in early adulthood with painless progressive blindness of one or both eyes. Usually there is a positive family history of similar disease on the maternal side. Definitive diagnosis can be
Externí odkaz:
https://doaj.org/article/716b72f9ec6a483dba2a2084e1fc8054
Autor:
Pandey Sanjay, Mishra Rahasya Mani, Pandey Sweta, Shah Vineet, Ahuja Rajesh Kumar, Saxena Renu
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 34, Iss 2, Pp 100-102 (2012)
BACKGROUND: Glutathione S-transferase gene deletions are known detoxification agents and cause oxidative damage. Due to the different pathophysiology of anemia in thalassemia and sickle cell disease, there are significant differences in the pathophys
Externí odkaz:
https://doaj.org/article/727f6463d9c1473f8e949f058bfaa2c3
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 52, Iss 3, Pp 360-362 (2009)
Hemoglobin color scale (HCS) is a commercially available test to screen anaemia in the absence of laboratory based hemoglobinometry. The present study was aimed at to compare the efficacy of HCS with Sahli′s method (SM) for haemoglobin estimation a
Externí odkaz:
https://doaj.org/article/3901ddc51d864aa59eb56ad624f11a67
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 52, Iss 2, Pp 257-259 (2009)
A new born with a mongoloid slant, brachycephaly and low-set ears presented at birth with a total leucocyte count of 57 x 10 3 /µL and the differential leucocyte count revealed 70% of these to be blasts. The morphology of the blasts was not characte
Externí odkaz:
https://doaj.org/article/4f977cefa30448468fe5e7d6f07a9566
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 51, Iss 3, Pp 437-439 (2008)
Acute promyelocytic leukemia (APML) is a well-characterized malignancy with typical clinico-hematological and molecular features. However, Indian data on this malignancy are limited. This study was conducted to determine the clinico-hematological pro
Externí odkaz:
https://doaj.org/article/4cfd0187f6ea49e8ad16d656072ed17c
Autor:
Rezende, Suely M., Neumann, Ignacio, Angchaisuksiri, Pantep, Awodu, Omolade, Boban, Ana, Cuker, Adam, Curtin, Julie A., Fijnvandraat, Karin, Gouw, Samantha C., Gualtierotti, Roberta, Makris, Michael, Nahuelhual, Paula, O’Connell, Niamh, Saxena, Renu, Shima, Midori, Wu, Runhui, Rosendaal, Frits R.
Publikováno v:
In Journal of Thrombosis and Haemostasis September 2024 22(9):2629-2652
Publikováno v:
In Hematology, Transfusion and Cell Therapy January-March 2024 46(1):22-29
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 52, Iss 2, Pp 255-256 (2009)
Pseudo Chediak-Higashi anomaly in acute leukemia is a rarely described entity. The significance of this intriguing morphological finding largely remains unknown, although some authors have predicted a poorer outcome in such cases because of a higher
Externí odkaz:
https://doaj.org/article/822c025c50104f309c17a650a34d3cb6
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 51, Iss 2, Pp 296-297 (2008)
We report an unusual observation of Cryptococcal neoformans profiles engulfed by neutrophils on a routine peripheral blood smear examination in an HIV-negative young female patient who presented with perforation of large bowel following a pregnancy t
Externí odkaz:
https://doaj.org/article/bd25a0152fff4c2fab90838422fc0b4e