Results 81 to 90 of about 694,655 (127)
Racial disparities in anaemia associated with paediatric chronic kidney disease
British Journal of Haematology, EarlyView.
Manya Raina +3 more
wiley +1 more source
The Journal of Physiology, EarlyView.Abstract figure legend Downregulation of mitotically associated long non‐coding RNA (MANCR) disturbs transcriptome and proteome in endothelial cells, possibly leading to endothelial and vascular dysfunction in preeclampsia. Abstract Preeclampsia (PE) is a hypertensive disorder during pregnancy, which is characterized by a wide spectrum of endothelial ...
Si‐Yan Zhang, Chi Zhou, Jing Zheng
wiley +1 more source
Thalassemia minor presenting with vitamin B12 deficiency, paraparesis, and microcytosis
, 2018 Arwa Lardhi,1 Rania Alhaj Ali,1 Rola Ali,2 Tarek Mohammed1 1Internal Medicine Department, Doctor Soliman Fakeeh Hospital, Jeddah, Saudi Arabia; 2Umm al-Qura University, Mecca, Saudi Arabia Abstract: Vitamin B12 is essential for proper neurological ...
Alhaj Ali R, Ali R, Mohammed T, Lardhi A
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The Prevalence of Thalassemia Minor in The Aliabad Katool
Medical Laboratory Journal, 2007 Background & Objectives: Thalassemia syndromes isone of the inherited disorders in which one or more globulin chains are affected. On the basis of clinical symptoms, thalassemias are categorized as minor, intermediate, and major.
F Niknezhad +3 more
doaj
Armaghane Danesh Bimonthly Journal, 2022 Background & aim: Beta thalassemia is one of the most common hereditary diseases in Iran. The birth of a child with thalassemia causes many social and economic problems for parents and the health care system.
E Shams +3 more
doaj
Impact of Heat Block Drying on Morphologic Preservation and Staining of Peripheral Blood Smears
International Journal of Laboratory Hematology, Volume 48, Issue 6, Page 1341-1347, December 2026.ABSTRACT Introduction Morphologic evaluation of the peripheral blood smear is critical for diagnosis and ruling out certain hematologic disorders. While air‐drying is standard, some laboratories may use heat blocks to expedite drying. Excessive heat may induce morphologic artifacts, but there is a lack of systematic literature on this practice ...
Ryan C. Shean +4 more
wiley +1 more source
, 2009 Background: Hereditary hemochromatosis (HH) is an autosomal recessive disorder of iron metabolism caused by mutations in the HFE gene. Objectives: The aim of this study was to determine the occurrence of C282Y and H63D mutations among β–thalassemia ...
Abed, Abdalla +2 more
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American Journal of Hematology, Volume 101, Issue 11, Page 2799-2811, November 2026.ABSTRACT Children with SCD have elevated stroke risk, correlated with cerebral blood flow velocity (CBFV). HOPE Kids 2 was a phase 3, multicenter, double‐blind, placebo‐controlled trial evaluating the effect of voxelotor on CBFV. Participants aged 2 to < 15 years with SCD (HbSS/HbSβ0) and conditional CBFV (170 to < 200 cm/s) were randomized 1:1 to ...
Halima Bello‐Manga +58 more
wiley +1 more source
Adipocytokine concentrations in children with different types of beta-thalassemia
, 2014 Background. Beta-thalassemia is an inherited blood disorder. It results from the impaired production of ß-globin chains, leading to a relative excess of alpha-globin chains.
Polat, A. +4 more
core +1 more source
Expanding the Utility of Exome Sequencing in Preventive and Population Genetics
American Journal of Medical Genetics Part A, Volume 200, Issue 11, Page 2433-2442, November 2026.ABSTRACT Carrier screening is a long‐standing genetic testing process offered to at‐risk couples, with or without a family history, who might have pregnancies affected by an autosomal recessive (AR) or X‐linked (XL) disorder. A total of 276 unrelated individuals, initially referred for rare disorder screening by clinicians, were enrolled in this study ...
Charilaos Kostoulas +6 more
wiley +1 more source