Temat: "Sickle cell trait" - OpacWWW

Skocz do pozycji: 1.

Tytuł:: α-Thalassemia does not seem to influence erythrocyte deformability in sickle cell trait carriers.
Autorzy:: Vayá A; Haemorheology and Haemostasis Unit, Service of Clinical Pathology, La Fe University Hospital , Valencia , Spain .
Collado S
Alis R
Vera B
Romagnoli M
Barragán E; Pokaż więcej
Źródło:: Hemoglobin [Hemoglobin] 2014; Vol. 38 (3), pp. 165-8. Date of Electronic Publication: 2014 Mar 07.
Typ publikacji:: Clinical Trial; Comparative Study; Journal Article
MeSH Terms:: Erythrocyte Deformability*
Erythrocytes/*metabolism
Sickle Cell Trait/*metabolism
alpha-Thalassemia/*metabolism
Adult ; Amino Acid Substitution ; Erythrocyte Indices ; Erythrocytes/pathology ; Female ; Hemoglobin, Sickle/genetics ; Hemoglobin, Sickle/metabolism ; Humans ; Male ; Middle Aged ; Mutation, Missense ; Sickle Cell Trait/genetics ; Sickle Cell Trait/pathology ; alpha-Thalassemia/genetics ; alpha-Thalassemia/pathology

Czasopismo naukowe

Skocz do pozycji: 2.

Tytuł:: Effects of a single sickling event on the mechanical fragility of sickle cell trait erythrocytes.
Autorzy:: Presley TD; Department of Physics, Wake Forest University, Winston-Salem, North Carolina 27109, USA.
Perlegas AS
Bain LE
Ballas SK
Nichols JS
Sabio H
Gladwin MT
Kato GJ
Kim-Shapiro DB; Pokaż więcej
Źródło:: Hemoglobin [Hemoglobin] 2010; Vol. 34 (1), pp. 24-36.
Typ publikacji:: Journal Article; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural
MeSH Terms:: Erythrocytes/*pathology
Sickle Cell Trait/*blood
Sickle Cell Trait/*pathology
Hemoglobin, Sickle/analysis ; Hemoglobin, Sickle/metabolism ; Hemolysis ; Humans