Results 181 to 190 of about 25,718 (237)

Hemoglobin C Disease With Splenomegaly and With Factor II Mutation Gene Thrombophilia: A Case Report. [PDF]

Cureus
Vázquez-Folch SJ, Jiménez-Berríos GA, Izquierdo N, Vazquez VJ.   +3 more
europepmc   +1 more source

Lack of knowledge of thalassemia among non-medical university students in Saudi Arabia: a cross-sectional study. [PDF]

Front Public Health
Alhusseini N, Cahusac PMB, Alsouss YO, Kemahli S.   +3 more
europepmc   +1 more source

Understanding the Outcomes of Extracorporeal Membrane Oxygen Support in Patients With Sickle Cell Trait. [PDF]

Crit Care Explor
Willsey KM, Plazak ME, Belyayev L, Rabin J, Athale J, Kim N, Gladwin MT, Grazioli A.   +7 more
europepmc   +1 more source

Pubertal Assessment and Growth in Patients With Hemoglobinopathies: A Longitudinal Multicenter Study on the Association With Ferritin Levels. [PDF]

Eur J Haematol
Dülberg J, Sanchez C, Burckhardt MA, Alacán Friedrich L, Salow V, Radauer-Plank A, Borgmann-Staudt A, Cario H, Diepold M, Drexler B, Infanti L, Kroiss S, Dietliker N, Merki R, Njue L, Oevermann L, Rovó A, Scheinemann K, Schneider M, Balcerek M, Diesch-Furlanetto T.   +20 more
europepmc   +1 more source

A Novel Alpha1-Variant (HBA1:c.-35T>C) Complexed With the First Reported Hb M-Saskatoon in the Chinese Population. [PDF]

Mol Genet Genomic Med
Yang Y, Zhao Y, Luan L, Li G, Deng Q, Ge Y.   +5 more
europepmc   +1 more source

IFN-γ increases δ-globin gene expression through activation of the JAK/STAT pathway in erythroid cells.

Blood
Zhu J, Chin K, Zou J, Aerbajinai W, Lin WC, Li H, Rodgers GP.   +6 more
europepmc   +1 more source

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Hemoglobinopathies

2022
Hemoglobinopathies are a group of inherited blood disorders characterized by compromised hemoglobin function. Hemoglobin is a 64kDa protein, consisting of four globin polypeptides each containing one heme molecule; blood acquires its red color from this heme molecule.
Eugene Khandros, Janet L. Kwiatkowski
  +4 more sources

Hemoglobinopathies

Hematology, 2003
AbstractThe outlook for patients with sickle cell disease has improved steadily during the last two decades. In spite of these improvements, curative therapies are currently available only to a small minority of patients. The main theme of this chapter is to describe new therapeutic options that are at different stages of development that might result ...
George F, Atweh, Joseph, DeSimone, Yogen, Saunthararajah, Hassana, Fathallah, Rona S, Weinberg, Ronald L, Nagel, Mary E, Fabry, Robert J, Adams   +7 more
openaire   +2 more sources