How I use hydroxyurea to treat young patients with sickle cell anemia

Por Ware, Russell E.
Publicado em 2010

Is Sickle Cell Anemia a Neglected Tropical Disease?

Por Ware, Russell E.
Publicado em 2013

Hydroxycarbamide: Clinical Aspects

Por Ware, Russell E.
Publicado no C R Biol (2012)

Hydroxyurea for sickle cell anemia: What have we learned and what questions still remain?

Por McGann, Patrick T., Ware, Russell E.
Publicado em 2011

Stroke With Transfusions Changing to Hydroxyurea (SWiTCH)

Por Ware, Russell E., Helms, Ronald W.
Publicado em 2012

Hydroxyurea for Children with Sickle Cell Disease

Por Heeney, Matthew M., Ware, Russell E.
Publicado no Hematol Oncol Clin North Am (2010)

Hydroxyurea therapy for sickle cell anemia

Por McGann, Patrick T, Ware, Russell E
Publicado no Expert Opin Drug Saf (2015)

Red blood cell alloimmunization in sickle cell disease: pathophysiology, risk factors, and transfusion management

Por Yazdanbakhsh, Karina, Ware, Russell E., Noizat-Pirenne, France
Publicado em 2012

Brown recluse spider (Loxosceles reclusa) envenomation leading to acute hemolytic anemia in six adolescents

Por McDade, Jenny, Aygun, Banu, Ware, Russell E
Publicado no J Pediatr (2010)

Current Management of Sickle Cell Anemia

Por McGann, Patrick T., Nero, Alecia C., Ware, Russell E.
Publicado em 2013

Sickle cell anemia in sub-Saharan Africa: advancing the clinical paradigm through partnerships and research

Por McGann, Patrick T., Hernandez, Arielle G., Ware, Russell E.
Publicado no Blood (2017)

Transcellular movement of hydroxyurea is mediated by specific solute carrier transporters

Por Walker, Aisha L., Franke, Ryan M., Sparreboom, Alex, Ware, Russell E.
Publicado no Exp Hematol (2011)

Original Research: Sickle cell anemia and pediatric strokes: Computational fluid dynamics analysis in the middle cerebral artery

Por Rivera, Christian P, Veneziani, Alessandro, Ware, Russell E, Platt, Manu O
Publicado no Exp Biol Med (Maywood) (2016)

Reply to iManage: A Novel Self-management App for Sickle Cell Disease

Por Crosby, Lori E., Ware, Russell E., Joffe, Naomi E., Britto, Maria T.
Publicado no Pediatr Blood Cancer (2016)

Brief Report: A Novel G6PD Mutation Leading to Chronic Hemolytic Anemia

Por McDade, Jenny, Abramova, Tatiana, Mortier, Nicole, Howard, Thad, Ware, Russell E.
Publicado em 2008

Organic anion transporting polypeptide 1B transporters modulate hydroxyurea pharmacokinetics

Por Walker, Aisha L., Lancaster, Cynthia S., Finkelstein, David, Ware, Russell E., Sparreboom, Alex
Publicado em 2013

A novel laboratory technique demonstrating the influences of RHD zygosity and the RhCcEe phenotype on erythrocyte D antigen expression

Por McGann, Patrick T., Despotovic, Jenny M., Howard, Thad A., Ware, Russell E.
Publicado no Am J Hematol (2011)

Shared Decision Making for Hydroxyurea Treatment Initiation in Children with Sickle Cell Anemia

Por Crosby, Lori E., Shook, Lisa M., Ware, Russell E., Brinkman, William B.
Publicado no Pediatr Blood Cancer (2014)

Glomerular Hyperfiltration and Albuminuria in Children with Sickle Cell Anemia

Por Aygun, Banu, Mortier, Nicole A., Smeltzer, Matthew P., Hankins, Jane S., Ware, Russell E.
Publicado em 2011

The Diagnostic Dilemma of Congenital Unstable Hemoglobinopathies

Por Yates, Amber Mayfield, Mortier, Nicole A., Hyde, Kristina S., Hankins, Jane S., Ware, Russell E.
Publicado no Pediatr Blood Cancer (2010)