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British Journal of Haematology|January 20, 2021
Sickle cell disease: progress towards combination drug therapyBetty S Pace, Athena Starlard-Davenport, Abdullah KutlarActa Haematologica|June 29, 2020
DIAPH1 Mutation as a Novel Cause of Autosomal Dominant Macrothrombocytopenia and Hearing LossNabin Raj Karki, Germame Ajebo, Natasha Savage, et al.Hemoglobin|January 8, 2015
A new Aγ-globin chain variant: Hb F-Sykesville MD [Aγ113(G15)Val → Ile; HBG1: c.340G>A] detected in a Caucasian babyNiren Patel, Jason Fixler, Yoram Unguru, et al.Acta Haematologica|November 24, 2021
Indolent T-Lymphoblastic Proliferation in Idiopathic Multicentric Castleman DiseaseNabin Raj Karki, Ahmed Samire Arfa, Natasha Savage, et al.International Journal of Medical Sciences|April 1, 2006
Hb J- Meerut [alpha 120 (H3) Ala ->Glu (alpha1)] in a Turkish maleGunçag Dinçol, Serkan Güvenç, Dedrey Elam, et al.Clinical Journal of Sport Medicine : Official Journal of the Canadian Academy of Sport Medicine|November 4, 2004
Erythrocyte sickling during exercise and thermal stressMichael F Bergeron, Joseph G Cannon, Elaina L Hall, et al.Clinical and Translational Science|June 4, 2014
CYP2C9 allelic variants and frequencies in a pediatric sickle cell disease cohort: implications for NSAIDs pharmacotherapyCheedy Jaja, Niren Patel, Stuart A Scott, et al.JMIR Research Protocols|March 26, 2026
Community Health Worker-Integrated Model for Sickle Cell Disease Management: Protocol for a Feasibility StudyTilicia Mayo-Gamble, Doreen Ugwu, Tobi Oloyede, et al.Genetic Testing and Molecular Biomarkers|August 24, 2016
Progressing Preemptive Genotyping of CYP2C19 Allelic Variants for Sickle Cell Disease PatientsCheedy Jaja, Nadine Barrett, Niren Patel, et al.Acta Haematologica|December 18, 2002
Interaction of sickle cell trait with hereditary spherocytosis: splenic infarcts and sequestrationCelatettin Ustun, Ferdane Kutlar, Leslie Holley, et al.Pageof 12