Results 141 to 150 of about 46,454 (250)

Diagnostic patterns of haemoglobinopathies: A prospective observational study using high-performance liquid chromatography in a remote tertiary care center of Telangana.

open access: yesStudent's Journal of Health Research Africa
Background Haemoglobinopathies, including sickle cell disorders and thalassemias, are significant genetic conditions that alter hemoglobin structure and function.
Dr. Sumayya   +2 more
doaj   +1 more source

Multinational transfusion practices and outcomes in haematology patients admitted to the intensive care unit

open access: yesVox Sanguinis, Volume 121, Issue 2, Page 169-179, February 2026.
Abstract Background and Objectives The number of critically ill patients with haematological conditions is increasing, yet transfusion practices in this population remain poorly defined. This study aimed to compare transfusion strategies in critically ill patients with versus without haematological conditions.
Caroline M. Schaap   +288 more
wiley   +1 more source

Health Care Challenges of Hereditary Common Hematological Disorders in Odisha, India [PDF]

open access: yes, 2012
Medical Genetics over the past few decades have emerged as an important and powerful medical specialty with increasing appreciation of its role and function in the biomedical sciences.
Balgir, RS
core   +1 more source

βT87Q-Globin Gene Therapy Reduces Sickle Hemoglobin Production, Allowing for Ex Vivo Anti-sickling Activity in Human Erythroid Cells. [PDF]

open access: yesMol Ther Methods Clin Dev, 2020
Demirci S   +10 more
europepmc   +1 more source

Dental considerations in the management of children suffering from sickle cell disease: A case report

open access: yesJournal of Indian Society of Pedodontics and Preventive Dentistry, 2007
Sickle cell disease (SCD) is a genetically derived disorder characterized by the presence of an abnormal hemoglobin molecule, designated as hemoglobin S (HbS).
Ramakrishna Y
doaj  

Molecular insights into the irreversible mechanical behavior of sickle hemoglobin. [PDF]

open access: yesJ Biomol Struct Dyn, 2019
Yesudasan S   +4 more
europepmc   +1 more source

Detection of the sickle hemoglobin allele using a surface plasmon resonance based biosensor. [PDF]

open access: yesSens Actuators B Chem, 2019
Breveglieri G   +7 more
europepmc   +1 more source

PATTERN OF THALASSEMIAS AND OTHER HEMOGLOBINOPATHIES: A STUDY IN DISTRICT DERA ISMAIL KHAN, PAKISTAN

open access: yesGomal Journal of Medical Sciences, 2014
Background: Thalassemia is used to describe disorders with a significant decrease in the rate of synthesis of a globin chain. The term hemoglobinopathy is used to indicate those disorders with structurally abnormal hemoglobin.
Javaid Hussain   +4 more
doaj  

Rational modification of vanillin derivatives to stereospecifically destabilize sickle hemoglobin polymer formation. [PDF]

open access: yesActa Crystallogr D Struct Biol, 2018
Deshpande TM   +8 more
europepmc   +1 more source

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