Search Results - "Glaros, Alexander K"

A systematic literature review of frequency of vaso-occlusive crises in sickle cell disease by Zaidi, Ahmar U, Glaros, Alexander K, Lee, Soyon, Wang, Taiji, Bhojwani, Rhea, Morris, Eric, Donohue, Breanne, Paulose, Jincy, Iorga, Åerban R, Nellesen, Dave

“…Abstract Background and purpose Sickle cell disease (SCD) is a collection of rare inherited blood disorders affecting approximately 100,000 people in the U.S…”
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Voxelotor: alteration of sickle cell disease pathophysiology by a first-in-class polymerization inhibitor by Glaros, Alexander K., Razvi, Reza, Shah, Nirmish, Zaidi, Ahmar U.

“…Sickle cell disease, despite its recognition as a severely debilitating genetic condition affecting hundreds of thousands of neonates throughout the world each…”
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Targeting TRPV1 activity via high‐dose capsaicin in patients with sickle cell disease by Glaros, Alexander K., Callaghan, Michael U., Smith, Wally R., Zaidi, Ahmar U.

“…Evidence suggests neuropathic pain (NP) develops over time in sickle cell disease (SCD), contributing to a complex, difficult‐to‐treat phenotype, with…”
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Voxelotor (GBT440) in pediatric sickle cell disease: A review by Jamalapur, Sri Lakshmi, Glaros, Alexander K., Ravindranath, Yaddanapudi

“…Sickle cell disease (SCD) was first described in 1910 in African Americans, and the mutant hemoglobin S (HbS) was identified by electrophoresis in 1948. Sickle…”
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Prophylactic Hydroxyurea Treatment Is Associated with Improved Cerebral Hemodynamics as a Surrogate Marker of Stroke Risk in Sickle Cell Disease: A Retrospective Comparative Analysis by Peine, Brian R., Callaghan, Michael U., Callaghan, Joseph H., Glaros, Alexander K.

“…Sickle cell disease (SCD) increases the incidence of childhood stroke eighty-fold. Stroke risk can be estimated by measurement of the blood velocity through…”
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Navigating a new terrain: how Twitter is changing hematologists by Zaidi, Ahmar U., Glaros, Alexander K., Weyand, Angela C.

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My Two Teachers by Glaros, Alexander K

“…He was a Warrior. Every breath was his battlefield…”
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Burden of Illness of Alpha- and Beta-Thalassemia: A Qualitative Study by Sheth, Sujit, Glaros, Alexander K, Martin, Mona, Abel, Cristina, Lenderking, William R, Morris, Susan, Gilroy, Keely S, Kuo, Kevin H.M.

“…Alpha (α)- and beta (β)-thalassemia are inherited red blood cell disorders with a wide spectrum of symptoms, functional manifestations, and disease burden. The…”
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Smaart Criz: Sickle Cell Mechanisms of Activation, Adhesion, Rheology, and Thrombosis (SMAART) in Response to P-Selectin Inhibition by Guzzardo, Gianna G., Chitlur, Meera, Hines, Patrick C., Zaidi, Aliya U., Borhan, Rasa, Cinciarelli, Kelsey, Glaros, Alexander K

“…Sickle cell disease (SCD) pathophysiology involves uncontrolled inflammation, dysregulated coagulation, and adherence of erythrocytes, leukocytes, and…”
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A Phase 2/3, Double-Blind, Randomized, Placebo-Controlled, Multicenter Study of Mitapivat in Patients with Sickle Cell Disease: RISE UP Phase 2 Results by Idowu, Modupe, Otieno, Lucas, Dumitriu, Bogdan, Lobo, Clarisse LC, Thein, Swee Lay, Andemariam, Biree, Nnodu, Obiageli E, Inati, Adlette, Glaros, Alexander K, Saad, Sara Teresinha Olalla, Bartolucci, Pablo, Colombatti, Raffaella, Taher, Ali T, Abboud, Miguel R, Oluyadi, Abdulafeez, Iyer, Varsha, Yin, Ophelia, Morris, Susan, Yates, Amber M, Shao, Hui, Patil, Spurthi, Urbstonaitis, Rolandas, Zaidi, Ahmar U, Smith, Wally R

“…Background: Sickle cell disease (SCD) is characterized by the presence of hemoglobin S (HbS), a structural variant caused by a mutation in the HBB gene…”
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