Zobrazeno 1 - 10 of 14 pro vyhledávání: '"Husain Alkhaldy"'
1
Akademický článek
Hemoglobin J-Auckland: a clinically silent low oxygen affinity variant presenting with persistent asymptomatic hypoxemia at high altitude
Autor: Ali Alsuheel Asseri, Ibrahim Tawhari, Afaf Haif Qahtani, Ibrahim A. Asiri, 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
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2
Akademický článek
Splenic sequestration and infarction upon exposure to high altitude in adult patients with sickle cell anemia
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
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3
Akademický článek
First observation of hemoglobin ypsilanti in Saudi Arabia: A high oxygen affinity hemoglobin presenting with extreme erythrocytosis
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
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4
Akademický článek
Hemoglobin J-Auckland: a clinically silent low oxygen affinity variant presenting with persistent asymptomatic hypoxemia at high altitude.
Autor: Asseri, Ali Alsuheel1 (AUTHOR) Alsoheel11@kku.edu.sa, Tawhari, Ibrahim2 (AUTHOR), Qahtani, Afaf Haif3 (AUTHOR), Asiri, Ibrahim A.4 (AUTHOR), Alkhaldy, Husain2 (AUTHOR)
Publikováno v: Hematology. Dec2024, Vol. 29 Issue 1, p1-7. 7p.
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8
Akademický článek
The pattern of health care provision and utilization among adult patients with sickle cell disease in Southern Saudi Arabia.
Autor: Alkhaldy, Husain1 (AUTHOR), Asiri, Bandar2 (AUTHOR), Ahmed, Meteb2 (AUTHOR), Khozam, Sabah3 (AUTHOR), Alzahrani, Abdulbari2 (AUTHOR), Alqahtani, Yahya2 (AUTHOR), Alshamrani, Nouf3 (AUTHOR), Bakheet, Omayma4 (AUTHOR)
Publikováno v: Saudi Journal for Health Sciences. Jan-Apr2021, Vol. 10 Issue 1, p38-42. 5p.
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9
Akademický článek
The pattern of iron deficiency with and without anemia among medical college girl students in high altitude southern Saudi Arabia.
Autor: Alkhaldy, Husain1 (AUTHOR), Hadi, Rawan1 (AUTHOR), Alghamdi, Khalid1 (AUTHOR), Alqahtani, Saleh2 (AUTHOR), Al Jabbar, Ibraheem2 (AUTHOR), Al Ghamdi, Ibrahim2 (AUTHOR), Bakheet, Omayma2 (AUTHOR), Saleh, Rayyh3 (AUTHOR), Shehata, Shehata4 (AUTHOR), Aziz, Shahid1 (AUTHOR)
Publikováno v: Journal of Family Medicine & Primary Care. Sep2020, Vol. 9 Issue 9, p5018-5025. 8p.
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