Results 141 to 150 of about 398,944 (237)

Drugs for preventing red blood cell dehydration in people with sickle cell disease. [PDF]

, 2018
BACKGROUND: Sickle cell disease is an inherited disorder of hemoglobin, resulting in abnormal red blood cells. These are rigid and may block blood vessels leading to acute painful crises and other complications.
Ballas, Samir K., Nagalla, Srikanth
core   +1 more source

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

Student'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 , Dr . Charitha Sravanthi Battu, Dr . K Raja Kumar   +2 more
doaj   +1 more source

Mechanistic Consequences of Piezo1 Gain‐of‐Function Variants for Decreased Red Cell Survival in Hereditary Xerocytosis

American Journal of Hematology, Volume 101, Issue 3, Page 619-622, March 2026.
Asya Makhro, Rick Huisjes, Elena Seiler, Min Qiao, Marije Bartels, Inga Hegemann, Patrick Eppenberger, Nicole Bender, Isabel Dorn, Anna Bogdanova, Richard van Wijk, Lars Kaestner   +11 more
wiley   +1 more source

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

Journal 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  

Association of Sickle Cell Trait With Hemoglobin A1c in African Americans

Journal of the American Medical Association (JAMA), 2017
Mary E. Lacy, G. Wellenius, A. Sumner, A. Correa, M. Carnethon, R. Liem, James G. Wilson, D. Sacks, D. Jacobs, A. Carson, Xi Luo, A. Gjelsvik, A. Reiner, R. Naik, Simin Liu, S. Musani, C. Eaton, Wen‐Chih Wu   +17 more
semanticscholar   +1 more source

The spectrum of sickle hemoglobin-related nephropathy: from sickle cell disease to sickle trait

Expert Review of Hematology, 2017
R. Naik, V. Derebail
semanticscholar   +1 more source

Fetal hemoglobin in sickle cell anemia: The Arab‐Indian haplotype and new therapeutic agents

American journal of hematology/oncology, 2017
Alawi H. Habara, Elmutaz M. Shaikho, M. Steinberg   +2 more
semanticscholar   +1 more source

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

Gomal 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, Sara Arif, Sher Zamir, Mohammad Amin Jan Mahsud, Shah Jahan   +4 more
doaj  

Forced chromatin looping raises fetal hemoglobin in adult sickle cells to higher levels than pharmacologic inducers.

Blood, 2016
L. Breda, I. Motta, S. Lourenço, Chiara Gemmo, Wulan Deng, J. Rupon, O. Abdulmalik, D. Manwani, G. Blobel, S. Rivella   +9 more
semanticscholar   +1 more source

Hemoglobin Sickle-Beta-Thalassemia With an Acute Crisis. [PDF]

Cureus
Tokuno H, Ishizuka K, Seki T, Kosaka S.
europepmc   +1 more source