Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Sunidhi Rohatgi"'
Publikováno v:
Clinical Case Reports, Vol 12, Iss 4, Pp n/a-n/a (2024)
Key Clinical Message Fanconi anemia with Mitomycin C sensitivity is a rare, complex hematological condition. Our case study emphasizes the significance of early diagnosis, appropriate genetic testing, and cautious use of chemotherapeutic agents. Abst
Externí odkaz:
https://doaj.org/article/5723a393acd04b0aabd0c4971f2f6d29
Publikováno v:
International Journal of Research in Medical Sciences. 11:378
Hurler syndrome also known as mucopolysaccharidosis type 1H (MPS-1H) or gargoylism is an autosomal recessive disorder due to defective gene which encodes for enzyme alpha L-iduronidase (IUDA) located on chromosome 4p16.3 (gene encoding protein iduron
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b98639ca57c305d72f2dc86bf016556c
https://doi.org/10.18203/2320-6012.ijrms20223668
https://doi.org/10.18203/2320-6012.ijrms20223668
Autor:
Sunidhi Rohatgi, Nupur Rastogi
Publikováno v:
International Journal of Research in Medical Sciences. 9:3464
Follicular dendritic cell sarcoma (FDCS) most commonly involves lymph nodes but also affects extranodal sites like liver, spleen, pancreas less commonly. It is a low to intermediate grade malignancy. Unusual presentation, morphology or immunophenotyp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d16077ce71d67963274e3554a84d81c9
https://doi.org/10.18203/2320-6012.ijrms20214431
https://doi.org/10.18203/2320-6012.ijrms20214431