Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Rekha Nirwan"'
Publikováno v:
Global Journal of Transfusion Medicine, Vol 8, Iss 1, Pp 92-95 (2023)
Thalassemia syndromes represent a group of inherited disorders characterized by decreased synthesis of one or more of the four globin chains in hemoglobin. The clinical spectrum ranges from asymptomatic carrier state to transfusion-dependent severe d
Externí odkaz:
https://doaj.org/article/ce13a2e42ce54613884fc30e9e271e75
Publikováno v:
Indian Journal of Pathology and Oncology. 9:360-363
Sarcomatoid carcinoma presenting as bone marrow metastasis with unknown primary is a rare entity. Usually patients present with widespread symptoms of extensive disease process. In the present case patient was evaluated for anemia and a subsequent bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e444f1f45e6a313f6985bb80ac85efa6
https://doi.org/10.18231/j.ijpo.2022.087
https://doi.org/10.18231/j.ijpo.2022.087
Publikováno v:
International Journal of Students� Research. 3:45
Osteopetrosis is a group of rare genetic diseases, consequent on absent or defective osteoclasts. A large number of genes have been found to be associated with the defect, each of which results in a clinically variable phenotype with regards to age a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28bc365da5aeadba0b44e0bcfd30d9c2
https://doi.org/10.4103/2230-7095.136496
https://doi.org/10.4103/2230-7095.136496
Publikováno v:
Global Journal of Transfusion Medicine. Jan-Jun2023, Vol. 8 Issue 1, p92-95. 4p.