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AnemoCheck-LRS: an optimized, color-based point-of-care test to identify severe anemia in limited-resource settings.
Published in:
2020
By:
- Perez-Plazola, Marina S.;
- Tyburski, Erika A.;
- Smart, Luke R.;
- Howard, Thad A.;
- Pfeiffer, Amanda;
- Ware, Russell E.;
- Lam, Wilbur A.;
- McGann, Patrick T.
Publication type:
journal article
Surveillance for sickle cell disease, United Republic of Tanzania.
Published in:
Bulletin of the World Health Organization, 2020, v. 98, n. 12, p. 859, doi. 10.2471/BLT.20.253583
By:
- Ambrose, Emmanuela E.;
- Smart, Luke R.;
- Charles, Mwesige;
- Hernandez, Arielle G.;
- Latham, Teresa;
- Hokororo, Adolfine;
- Beyanga, Medard;
- Howard, Thad A.;
- Kamugisha, Erasmus;
- McElhinney, Kathryn E.;
- Tebuka, Erius;
- Ware, Russell E.
Publication type:
Article
Whole Exome Sequencing Identifies Novel Genes for Fetal Hemoglobin Response to Hydroxyurea in Children with Sickle Cell Anemia.
Published in:
PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0110740
By:
- Sheehan, Vivien A.;
- Crosby, Jacy R.;
- Sabo, Aniko;
- Mortier, Nicole A.;
- Howard, Thad A.;
- Muzny, Donna M.;
- Dugan-Perez, Shannon;
- Aygun, Banu;
- Nottage, Kerri A.;
- Boerwinkle, Eric;
- Gibbs, Richard A.;
- Ware, Russell E.;
- Flanagan, Jonathan M.
Publication type:
Article
Trends in sickle cell trait and disease screening in the Republic of Uganda, 2014–2019.
Published in:
Tropical Medicine & International Health, 2021, v. 26, n. 1, p. 23, doi. 10.1111/tmi.13506
By:
- Hernandez, Arielle G.;
- Kiyaga, Charles;
- Howard, Thad A.;
- Ssewanyana, Isaac;
- Ndeezi, Grace;
- Aceng, Jane R.;
- Ware, Russell E.
Publication type:
Article
Lack of hydroxyurea‐associated mutagenesis in pediatric sickle cell disease patients.
Published in:
Environmental & Molecular Mutagenesis, 2023, v. 64, n. 3, p. 167, doi. 10.1002/em.22536
By:
- Torous, Dorothea K.;
- Avlasevich, Svetlana;
- Bemis, Jeffrey C.;
- Howard, Thad;
- Ware, Russell E.;
- Fung, Chunkit;
- Chen, Yuhchyau;
- Sahsrabudhe, Deepak;
- MacGregor, James T.;
- Dertinger, Stephen D.
Publication type:
Article
Effects of Combined UDP-Glucuronosyltransferase (UGT) 1A1*28 and 1A6*2 on Paracetamol Pharmacokinetics in β-Thalassemia/HbE.
Published in:
Pharmacology, 2007, v. 79, n. 2, p. 97, doi. 10.1159/000097908
By:
- Tankanitlert, Jeeranut;
- Morales, Noppawan Phumala;
- Howard, Thad A.;
- Fucharoen, Pranee;
- Ware, Russell E.;
- Fucharoen, Suthat;
- Chantharaksri, Udom
Publication type:
Article
Phenotypic and functional analysis of lymphocytes in paroxysmal nocturnal hemoglobinuria.
Published in:
American Journal of Hematology, 1995, v. 50, n. 4, p. 244, doi. 10.1002/ajh.2830500405
By:
- Tseng, Jennifer E.;
- Hall, Sharon E.;
- Howard, Thad A.;
- Ware, Russell E.
Publication type:
Article
A pharmacokinetic study of paracetamol in Thai β-thalassemia/HbE patients.
Published in:
European Journal of Clinical Pharmacology, 2006, v. 62, n. 9, p. 743, doi. 10.1007/s00228-006-0167-2
By:
- Tankanitlert, Jeeranut;
- Howard, Thad A.;
- Temsakulphong, Anusorn;
- Sirankapracha, Pornpan;
- Morales, Noppawan;
- Sanvarinda, Yupin;
- Fucharoen, Pranee;
- Ware, Russell E.;
- Fucharoen, Suthat;
- Chantharaksri, Udom
Publication type:
Article
Genetic Modifiers of White Blood Cell Count, Albuminuria and Glomerular Filtration Rate in Children with Sickle Cell Anemia.
Published in:
PLoS ONE, 2016, v. 11, n. 10, p. 1, doi. 10.1371/journal.pone.0164364
By:
- Schaefer, Beverly A.;
- Flanagan, Jonathan M.;
- Alvarez, Ofelia A.;
- Nelson, Stephen C.;
- Aygun, Banu;
- Nottage, Kerri A.;
- George, Alex;
- Roberts, Carla W.;
- Piccone, Connie M.;
- Howard, Thad A.;
- Davis, Barry R.;
- Ware, Russell E.
Publication type:
Article
Sickle cell screening in Uganda: High burden, human immunodeficiency virus comorbidity, and genetic modifiers.
Published in:
2019
By:
- Kiyaga, Charles;
- Hernandez, Arielle G.;
- Ssewanyana, Isaac;
- Schaefer, Beverly A.;
- McElhinney, Kathryn E.;
- Ndeezi, Grace;
- Howard, Thad A.;
- Ndugwa, Christopher M.;
- Ware, Russell E.;
- Aceng, Jane R.
Publication type:
journal article
Robust clinical and laboratory response to hydroxyurea using pharmacokinetically guided dosing for young children with sickle cell anemia.
Published in:
American Journal of Hematology, 2019, v. 94, n. 8, p. 871, doi. 10.1002/ajh.25510
By:
- McGann, Patrick T.;
- Niss, Omar;
- Dong, Min;
- Marahatta, Anu;
- Howard, Thad A.;
- Mizuno, Tomoyuki;
- Lane, Adam;
- Kalfa, Theodosia A.;
- Malik, Punam;
- Quinn, Charles T.;
- Ware, Russell E.;
- Vinks, Alexander A.
Publication type:
Article
Realizing effectiveness across continents with hydroxyurea: Enrollment and baseline characteristics of the multicenter REACH study in Sub‐Saharan Africa.
Published in:
American Journal of Hematology, 2018, v. 93, n. 4, p. 537, doi. 10.1002/ajh.25034
By:
- McGann, Patrick T.;
- Williams, Thomas N.;
- Olupot‐Olupot, Peter;
- Tomlinson, George A.;
- Lane, Adam;
- Luís Reis da Fonseca, José;
- Kitenge, Robert;
- Mochamah, George;
- Wabwire, Ham;
- Stuber, Susan;
- Howard, Thad A.;
- McElhinney, Kathryn;
- Aygun, Banu;
- Latham, Teresa;
- Santos, Brígida;
- Tshilolo, Léon;
- Ware, Russell E.;
- for the REACH Investigators
Publication type:
Article
Characteristics of a rapid, point-of-care lateral flow immunoassay for the diagnosis of sickle cell disease.
Published in:
American Journal of Hematology, 2016, v. 91, n. 2, p. 205, doi. 10.1002/ajh.24232
By:
- McGann, Patrick T.;
- Schaefer, Beverly A.;
- Paniagua, Mary;
- Howard, Thad A.;
- Ware, Russell E.
Publication type:
Article
Genetic modifiers of sickle cell anemia in the BABY HUG cohort: influence on laboratory and clinical phenotypes.
Published in:
American Journal of Hematology, 2013, v. 88, n. 7, p. 571, doi. 10.1002/ajh.23457
By:
- Sheehan, Vivien A.;
- Luo, Zhaoyu;
- Flanagan, Jonathan M.;
- Howard, Thad A.;
- Thompson, Bruce W.;
- Wang, Winfred C.;
- Kutlar, Abdullah;
- Ware, Russell E.
Publication type:
Article
A novel laboratory technique demonstrating the influences of RHD zygosity and the RhCcEe phenotype on erythrocyte D antigen expression.
Published in:
American Journal of Hematology, 2012, v. 87, n. 3, p. 266, doi. 10.1002/ajh.22254
By:
- McGann, Patrick T.;
- Despotovic, Jenny M.;
- Howard, Thad A.;
- Ware, Russell E.
Publication type:
Article
Microarray analysis of liver gene expression in iron overloaded patients with sickle cell anemia and beta-thalassemia.
Published in:
American Journal of Hematology, 2009, v. 84, n. 6, p. 328, doi. 10.1002/ajh.21407
By:
- Flanagan, Jonathan M.;
- Steward, Shirley;
- Hankins, Jane S.;
- Howard, Thad M.;
- Neale, Geoffrey;
- Ware, Russell E.
Publication type:
Article
UGT1A1 promoter polymorphisms and the development of hyperbilirubinemia and gallbladder disease in children with sickle cell anemia.
Published in:
American Journal of Hematology, 2008, v. 83, n. 10, p. 800, doi. 10.1002/ajh.21264
By:
- Carpenter, Shannon L.;
- Lieff, Susan;
- Howard, Thad A.;
- Eggleston, Barry;
- Ware, Russell E.
Publication type:
Article
Identification of hemochromatosis gene polymorphisms in chronically transfused patients with sickle cell disease.
Published in:
American Journal of Hematology, 2003, v. 74, n. 4, p. 243, doi. 10.1002/ajh.10426
By:
- Michael R. Jeng;
- Patricia Adams-Graves;
- Thad A. Howard;
- Matthew R. Whorton;
- Chin-Shang Li;
- Russell E. Ware
Publication type:
Article
Operational analysis of the national sickle cell screening programme in the Republic of Uganda.
Published in:
African Journal of Laboratory Medicine, 2021, v. 10, n. 1, p. 1, doi. 10.4102/ajlm.v10i1.1303
By:
- Hernandez, Arielle G.;
- Kiyaga, Charles;
- Howard, Thad A.;
- Ssewanyana, Isaac;
- Ndeezi, Grace;
- Aceng, Jane R.;
- Ware, Russell E.
Publication type:
Article
Hydroxyurea Pharmacokinetics in Pediatric Patients After Total Pancreatectomy With Islet Autotransplantation.
Published in:
Journal of Clinical Pharmacology, 2021, v. 61, n. 4, p. 547, doi. 10.1002/jcph.1759
By:
- Boucher, Alexander A.;
- Dong, Min;
- Vinks, Alexander A.;
- Marahatta, Anu;
- Howard, Thad A.;
- Ware, Russell E.;
- Nathan, Jaimie D.;
- Abu‐El‐Haija, Maisam;
- Luchtman‐Jones, Lori
Publication type:
Article
Hydroxycarbamide alters erythroid gene expression in children with sickle cell anaemia.
Published in:
British Journal of Haematology, 2012, v. 157, n. 2, p. 240, doi. 10.1111/j.1365-2141.2012.09061.x
By:
- Flanagan, Jonathan M.;
- Steward, Shirley;
- Howard, Thad A.;
- Mortier, Nicole A.;
- Kimble, Amy C.;
- Aygun, Banu;
- Hankins, Jane S.;
- Neale, Geoffrey A.;
- Ware, Russell E.
Publication type:
Article
Chromosome damage and repair in children with sickle cell anaemia and long-term hydroxycarbamide exposure.
Published in:
British Journal of Haematology, 2011, v. 154, n. 1, p. 134, doi. 10.1111/j.1365-2141.2011.08698.x
By:
- McGann, Patrick T.;
- Howard, Thad A.;
- Flanagan, Jonathan M.;
- Lahti, Jill M.;
- Ware, Russell E.
Publication type:
Article
Genotoxicity associated with hydroxyurea exposure in infants with sickle cell anemia: Results from the BABY-HUG phase III clinical trial.
Published in:
Pediatric Blood & Cancer, 2012, v. 59, n. 2, p. 254, doi. 10.1002/pbc.23365
By:
- McGann, Patrick T.;
- Flanagan, Jonathan M.;
- Howard, Thad A.;
- Dertinger, Stephen D.;
- He, Jin;
- Kulharya, Anita S.;
- Thompson, Bruce W.;
- Ware, Russell E.
Publication type:
Article
A novel G6PD mutation leading to chronic hemolytic anemia.
Published in:
Pediatric Blood & Cancer, 2008, v. 51, n. 6, p. 816, doi. 10.1002/pbc.21715
By:
- McDade, Jenny;
- Abramova, Tatiana;
- Mortier, Nicole;
- Howard, Thad;
- Ware, Russell E.
Publication type:
Article
Stroke Prevention with Hydroxyurea Enabled through Research and Education: A Phase 2 Primary Stroke Prevention Trial in Sub-Saharan Africa.
Published in:
Acta Haematologica, 2023, v. 146, n. 2, p. 95, doi. 10.1159/000526322
By:
- Smart, Luke R.;
- Ambrose, Emmanuela E.;
- Balyorugulu, Georgina;
- Songoro, Primrose;
- Shabani, Idd;
- Komba, Protas;
- Charles, Mwesige;
- Howard, Thad A.;
- McElhinney, Kathryn E.;
- O'Hara, Sara M.;
- Odame, Jodie;
- Nakafeero, Maria;
- Adams, Janet;
- Stuber, Susan E.;
- Lane, Adam;
- Latham, Teresa S.;
- Makubi, Abel N.;
- Ware, Russell E.
Publication type:
Article
Identification and characterization of an inherited mutation of PIG-A in a patient with paroxysmal nocturnal haemoglobinuria.
Published in:
British Journal of Haematology, 1996, v. 93, n. 3, p. 590, doi. 10.1046/j.1365-2141.1996.d01-1701.x
By:
- Endo, Morito;
- Ware, Russell E.;
- Vreeke, Teresa M.;
- Howard, Thad A.;
- Parker, Charles J.
Publication type:
Article

Found: 26

AnemoCheck-LRS: an optimized, color-based point-of-care test to identify severe anemia in limited-resource settings.

Surveillance for sickle cell disease, United Republic of Tanzania.

Whole Exome Sequencing Identifies Novel Genes for Fetal Hemoglobin Response to Hydroxyurea in Children with Sickle Cell Anemia.

Trends in sickle cell trait and disease screening in the Republic of Uganda, 2014–2019.

Lack of hydroxyurea‐associated mutagenesis in pediatric sickle cell disease patients.

Effects of Combined UDP-Glucuronosyltransferase (UGT) 1A128 and 1A62 on Paracetamol Pharmacokinetics in β-Thalassemia/HbE.

Phenotypic and functional analysis of lymphocytes in paroxysmal nocturnal hemoglobinuria.

A pharmacokinetic study of paracetamol in Thai β-thalassemia/HbE patients.

Genetic Modifiers of White Blood Cell Count, Albuminuria and Glomerular Filtration Rate in Children with Sickle Cell Anemia.

Sickle cell screening in Uganda: High burden, human immunodeficiency virus comorbidity, and genetic modifiers.

Robust clinical and laboratory response to hydroxyurea using pharmacokinetically guided dosing for young children with sickle cell anemia.

Realizing effectiveness across continents with hydroxyurea: Enrollment and baseline characteristics of the multicenter REACH study in Sub‐Saharan Africa.

Characteristics of a rapid, point-of-care lateral flow immunoassay for the diagnosis of sickle cell disease.

Genetic modifiers of sickle cell anemia in the BABY HUG cohort: influence on laboratory and clinical phenotypes.

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

Microarray analysis of liver gene expression in iron overloaded patients with sickle cell anemia and beta-thalassemia.

UGT1A1 promoter polymorphisms and the development of hyperbilirubinemia and gallbladder disease in children with sickle cell anemia.

Identification of hemochromatosis gene polymorphisms in chronically transfused patients with sickle cell disease.

Operational analysis of the national sickle cell screening programme in the Republic of Uganda.

Hydroxyurea Pharmacokinetics in Pediatric Patients After Total Pancreatectomy With Islet Autotransplantation.

Hydroxycarbamide alters erythroid gene expression in children with sickle cell anaemia.

Chromosome damage and repair in children with sickle cell anaemia and long-term hydroxycarbamide exposure.

Genotoxicity associated with hydroxyurea exposure in infants with sickle cell anemia: Results from the BABY-HUG phase III clinical trial.

A novel G6PD mutation leading to chronic hemolytic anemia.

Stroke Prevention with Hydroxyurea Enabled through Research and Education: A Phase 2 Primary Stroke Prevention Trial in Sub-Saharan Africa.

Identification and characterization of an inherited mutation of PIG-A in a patient with paroxysmal nocturnal haemoglobinuria.