Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Ankita Dhanuka"'
Autor:
Bidyut Krishna Goswami, Rajashri Chakrabarty, Subrata Bhattacharjee, Ankita Dhanuka, Sarama Banerjee Goswami, Sudipta Chakrabarti
Publikováno v:
Biomedical and Biotechnology Research Journal, Vol 4, Iss 4, Pp 342-345 (2020)
Background: Inherited disorders of blood include thalassemias and hemoglobinopathies which are one of the major public problems in India. In sickle hemoglobin (HbS) hemoglobinopathies, production of abnormal sickle-shaped red cells results in variabl
Externí odkaz:
https://doaj.org/article/937afd3d2c66483abf17a6aaf2a107d7
Publikováno v:
Archives of Medicine and Health Sciences, Vol 7, Iss 2, Pp 201-205 (2019)
Background and Objective: Nutritional anemia is the most common and easily preventable cause of anemia. No comprehensive data regarding the magnitude of this problem are available in the literature in northern regions of West Bengal where a significa
Externí odkaz:
https://doaj.org/article/9ae0dac5fd4140758c06629ee5d5e80b
Publikováno v:
Archives of Medicine and Health Sciences, Vol 7, Iss 2, Pp 201-205 (2019)
Background and Objective: Nutritional anemia is the most common and easily preventable cause of anemia. No comprehensive data regarding the magnitude of this problem are available in the literature in northern regions of West Bengal where a significa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f9c79e20ae298d660e5cbd5643ae7c8
https://doi.org/10.4103/amhs.amhs_45_19
https://doi.org/10.4103/amhs.amhs_45_19
Publikováno v:
Kasr Al Ainy Medical Journal. 24:149
Mayer–Rokitansky–Kuster–Hauser syndrome is a rare disorder affecting 1 in 5000 women. It is characterized by congenital absence of the uterus and the vagina in a phenotypically and karyotypically normal female. Here, we report a case of atypica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c40b89b3a801e2c3ff39377843c82fca
https://doi.org/10.4103/kamj.kamj_11_18
https://doi.org/10.4103/kamj.kamj_11_18