Results 111 to 120 of about 34,389 (155)
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Sickle Cell Anemia

Annals of Internal Medicine, 1978
Excerpt To the editor: The "natural history" of sickle cell anemia in Saudi Arabs (Ann Intern Med88:1-6, 1978) is certainly different from the disease as we see it in the United States but not as d...
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Sickle Cell Anemia

2010
Sickle cell anemia (SCA or SS homozygous sickle cell disease) is an inherited blood disorder caused by single nucleotide substitution in the β-globin gene that renders their hemoglobin (HbS) much less soluble than normal hemoglobin (HbA) when deoxygenated. The polymerization of HbS upon deoxygenation is the basic pathophysiologic event leading
Connes Philippe   +3 more
openaire   +1 more source

Sickle Cell Anemia

Medical Clinics of North America, 1966
J F, Desforges, M Y, Wang
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Sickle Cell Anemia

2014
Sickle cell anemia is one of the first diseases understood at the molecular level. Valine substituted for glutamic acid in the beta globin subunit leads to decreased solubility in the de-oxygenated state. It may partially protect infants from cerebral falciparum malaria in the heterozygous state (sickle trait), and geographic distribution of the ...
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Sickle Cell Anemia

AJN, American Journal of Nursing, 1971
G A, Weiss, H J, Rosenblate
openaire   +4 more sources

“Pseudo-Sickle” Cell Anemia

The American Journal of the Medical Sciences, 2009
Rahil, Kasmani   +2 more
openaire   +2 more sources

Sickle cell anemia

Praxis, 2011
A, von Keudell   +4 more
openaire   +3 more sources

Biologic and Clinical Efficacy of LentiGlobin for Sickle Cell Disease

New England Journal of Medicine, 2022
Julie Kanter   +2 more
exaly  

Sickle Cell Anemia

Postgraduate Medicine, 1965
openaire   +2 more sources

Sickle Cell Anemia

American Journal of Nursing, 1999
openaire   +2 more sources

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