Results 151 to 160 of about 429,758 (251)

Sickle hemoglobin disturbs normal coupling among erythrocyte O2 content, glycolysis, and antioxidant capacity.

Blood, 2013
S. Rogers, Jerlinda G. C. Ross, A. d'Avignon, Lindsey B. Gibbons, V. Gazit, Mojibade N Hassan, Dylan T. McLaughlin, Sherraine Griffin, Tara Neumayr, M. DeBaun, M. Debaun, Allan Doctor   +11 more
semanticscholar   +1 more source

When Pain Crisis Turns Lethal: A Case Report of Fat Embolism Syndrome in Sickle Cell Disease. [PDF]

J Clin Med
Alwaheed AJ.
europepmc   +1 more source

Mortality in sickle cell disease. Life expectancy and risk factors for early death.

New England Journal of Medicine, 1994
O. Platt, D. Brambilla, W. Rosse, P. Milner, O. Castro, M. Steinberg, P. Klug   +6 more
semanticscholar   +1 more source

Impact of Sickle Cell Hemoglobin Genotypes on Clinical Outcomes Among <i>Plasmodium falciparum</i> Malaria Patients in Luanda, Angola. [PDF]

Health Sci Rep
Sebastião CS, Ekundi-Valentim E, Cassinela E, Sacomboio E.   +3 more
europepmc   +1 more source

The LSD1 inhibitor RN-1 induces fetal hemoglobin synthesis and reduces disease pathology in sickle cell mice.

Blood, 2015
Shuaiying Cui, K. Lim, Lihong Shi, Mary P. Lee, Natee Jearawiriyapaisarn, Greggory Myers, A. Campbell, David Harro, Shigeki Iwase, R. Trievel, A. Rivers, J. Desimone, D. Lavelle, Y. Saunthararajah, J. D. Engel   +14 more
semanticscholar   +1 more source

Sickle cell disease and fetal hemoglobin

Saudi Journal of Medicine and Medical Sciences, 2018
openaire   +3 more sources

Dissecting the energies that stabilize sickle hemoglobin polymers.

Biophysical Journal, 2013
Yi-Hua H. Wang, F. Ferrone
semanticscholar   +1 more source

Inherited Anemia: A Contemporary Clinical and Lab Review. [PDF]

Healthcare (Basel)
Qadah T.
europepmc   +1 more source

Splenic Sequestration and Suspected Transient Aplastic Crisis in Sickle-Cell SC/Hemoglobin-G Disease in an Adult: A Case Report. [PDF]

Clin Med Insights Case Rep
Patel E, Gunter S, Hartner L.
europepmc   +1 more source

The Effect of Packed Red Blood Cell Transfusion on Complete Blood Count and Hemoglobin Fractions in Adult Patients with Sickle Cell Disease: A Prospective Single-Center Cohort Study in Saudi Arabia. [PDF]

Med Sci (Basel)
Al-Ansari RY, Al Ayidh FS, Aljurbua RM, AlJamily MI, Alsubaie YA, Almugahwi AA, Fadoul T, Halawi AH, Arulanantham ZJ, Woodman A.   +9 more
europepmc   +1 more source