Cargando…
Genetic polymorphism of vitamin D receptors and plasminogen activator inhibitor‐1 and osteonecrosis risk in childhood acute lymphoblastic leukemia
BACKGROUND: Osteonecrosis (ON) is one of the major therapy‐related complications in childhood acute lymphoblastic leukemia (ALL). The purpose of the current study is to assess the frequency of ON in children with ALL and to detect whether polymorphisms in vitamin D receptor gene (VDR) and plasminoge...
Autores principales: | Sherief, Laila M., Beshir, Mohamed, Raafat, Nermin, Abdelkhalek, Elhamy R., Mokhtar, Wesam A., Elgerby, Khaled M., Soliman, Basma K., Salah, Hosam E., Mokhtar, Ghada A., Kamal, Naglaa M., ELsayed, Heba, Zakaria, Marwa |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8372120/ https://www.ncbi.nlm.nih.gov/pubmed/34042331 http://dx.doi.org/10.1002/mgg3.1700 |
Ejemplares similares
-
Serum endocan and endothelial dysfunction in childhood acute
lymphoblastic leukemia survivors: a tertiary center experience
por: Sherief, Laila M., et al.
Publicado: (2021) -
Hodgkin Lymphoma in Childhood: Clinicopathological features and therapy outcome at 2 Centers From a Developing Country
por: Sherief, Laila M., et al.
Publicado: (2015) -
Cerebral sinuses thrombosis prior to the diagnosis of acute lymphoblastic
leukemia in a child: A case report
por: Sherief, Laila M, et al.
Publicado: (2022) -
A Cross-sectional Study of Two Chemotherapy Protocols on Long Term Neurocognitive Functions in Egyptian Children Surviving Acute
Lymphoblastic Leukemia
por: Sherief, Laila M., et al.
Publicado: (2018) -
FcγRIIa and FcγRIIIa genes polymorphism in Egyptian children with primary immune thrombocytopenia
por: Zakaria, Marwa, et al.
Publicado: (2023)