K Issa, Q Naziri, AV Maheshwari, VJ Rasquinha… - The Journal of …, 2013 - Elsevier
The purpose of this study was to compare the outcomes of cementless primary total hip arthroplasty (THA) in sickle cell patients compared to the remaining cohort of osteonecrosis …
Phthalimide derivatives containing furoxanyl subunits as nitric oxide (NO)-donors (3a–g) were designed, synthesized, and evaluated in vitro and in vivo for their potential uses in the …
A novel series of thalidomide derivatives (4a–f) designed by molecular hybridization were synthesized and evaluated in vitro and in vivo for their potential use in the oral treatment of …
Sickle Cell Disease (SCD) is one of the most prevalent hematological diseases in the world. SCD is a genetic disease characterized by punctual mutation that basis on the exchange of …
Resumo Sickle Cell Disease (SCD) is a disease characterized by a punctual mutation (GTG- GAG) in the sixth codon of the gamma globin gene leading to a substitution of glutamic acid …
Fetal hemoglobin (HbF) induction constitutes a valuable and validated approach to treat the symptoms of sickle cell disease (SCD). Here, we synthesized pomalidomide–nitric oxide …
TRF de Melo, C Kumkhaek… - European journal of …, 2018 - Elsevier
Abstract N-oxide derivatives 5 (a–b), 8 (a–b), and 11 (a–c) were designed, synthesized and evaluated in vitro and in vivo as potential drugs that are able to ameliorate sickle cell …
RC Chelucci, IJ de Oliveira, KP Barbieri… - Medicinal Chemistry …, 2019 - Springer
Abstract Sickle Cell Anemia (SCA) is one of the most prevalent hereditary hematological diseases worldwide. The disease is characterized by chronic inflammation, hypercoagulable …
TR Ferreira de Melo, CM Chin… - Future Medicinal …, 2014 - Taylor & Francis
Editorial de Melo, Chin & dos Santos approved by the US FDA to treat SCD. In vivo, HU is metabolized to NO, which induces the expression of the γ-globin gene (HbG1 and HbG2) …