Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Husain Alkhaldy"'
Publikováno v:
Hematology, Vol 29, Iss 1 (2024)
Background Inherited hemoglobin disorders are common in clinical practice. While qualitative (i.e. sickle cell disease) and quantitative (thalassemia) hemoglobinopathies are usually diagnosed clinically and confirmed through simple laboratory assessm
Externí odkaz:
https://doaj.org/article/bbe61b851c304898a3a88348dbfe0d0c
Autor:
Husain Alkhaldy, Mortadah Alsalman, Mariyyah Almuhaini, Renad Alshehri, Samar Almusaad, Wejdan Al-Qahtani, Tamer A Samih, Mohammed Makkawi
Publikováno v:
Journal of Applied Hematology, Vol 14, Iss 4, Pp 335-339 (2023)
Adult patients with sickle cell disease usually have atrophied spleens due to autosplenectomy, and only rarely have complications related to the spleen, such as splenic sequestration and infarctions. However, some sickle cell haplotypes/genotypes are
Externí odkaz:
https://doaj.org/article/52aabcb546044d1f98086fbd335978f5
Autor:
Husain Alkhaldy, Abdullah Algarni, Omayma Bakheet, Afaf Qahtani, Lama Alasiri, Mohammed Makkawi
Publikováno v:
Journal of Applied Hematology, Vol 14, Iss 4, Pp 331-334 (2023)
High oxygen affinity hemoglobin (HOAH) variants are rare hemoglobinopathies sometimes associated with congenital erythrocytosis. Patients with HOAH are usually asymptomatic and are incidentally discovered when unexplained erythrocytosis is observed i
Externí odkaz:
https://doaj.org/article/81ceaa039cf34464857497c6ea259b31