Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Alok Hemal"'
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 9, Iss 4, Pp S36- (2024)
Externí odkaz:
https://doaj.org/article/697bb226e20c4300a43ce81c5a0213cc
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 9, Iss 4, Pp S66- (2024)
Externí odkaz:
https://doaj.org/article/41760483080f4958a17124fc23252ff8
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 9, Iss 4, Pp S66- (2024)
Externí odkaz:
https://doaj.org/article/5f5da960ac9d4999a25bed372b4f445b
Publikováno v:
Indian Pediatrics Case Reports, Vol 3, Iss 3, Pp 146-149 (2023)
Background: Acute lymphoblastic leukemia (ALL) is a common pediatric malignancy, typically manifesting with symptoms of bone marrow and hematolymphoid organ infiltration. Although hepatic involvement in the form of hepatosplenomegaly is seen in nearl
Externí odkaz:
https://doaj.org/article/d737d9ba2a7f478a9f96be37ec23c679
Publikováno v:
MAMC Journal of Medical Sciences, Vol 7, Iss 1, Pp 72-76 (2021)
Purpose: The aim of this study was to compare the levels of serum vitamin B12 of transfusion-dependent thalassemic (TDT) children with that of healthy controls. The other objectives were to compare the occurrence of vitamin B12 deficiency in cases an
Externí odkaz:
https://doaj.org/article/eb05c62d2b734383aa3a3aa36b934fa9
Autor:
Rupamon Nongbet, ALOK HEMAL
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 7, Iss 4, Pp S22- (2022)
Externí odkaz:
https://doaj.org/article/7c396e9ecf92448c9f6ed38bf0c28261
Publikováno v:
AIDS Research and Treatment, Vol 2018 (2018)
Background. With improving standards of care of children living with HIV (CLHIV), pediatric HIV related mortality rates are declining. New challenges like HIV status disclosure are emerging which need to be addressed to ensure their smooth transition
Externí odkaz:
https://doaj.org/article/5f1551cf434b44f6939850c70139043e
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 1, Iss 2, Pp 41-43 (2016)
Thalassemia is associated with several challenging comorbidities. Here we report a 20 year old thalassemic who presented with cauda equina syndrome due to paraspinal extra medullary hematopoiesis (EMH) and was treated with hydroxyurea, repeated blood
Externí odkaz:
https://doaj.org/article/e2d43fbb4a434e909513f9921ab2f3b0
Publikováno v:
Advances in Hematology, Vol 2015 (2015)
Chronic hemoglobinopathies like thalassemia are associated with many osteopathies like osteoporosis. Methods. This observational study was carried out to compare the bone mineral density (BMD) in transfusion dependent thalassemics with that of health
Externí odkaz:
https://doaj.org/article/7ec4b455e9bc4a09b4a6ea1f84a098c5
Publikováno v:
Indian Journal of Child Health. :8-11
Background: Vitamin D deficiency (VDD) is highly prevalent in healthy individuals. Studies suggest that Vitamin D plays an important role in immune system. Objective: The objective of this study was to assess the frequency of VDD in Indian children l