Related Experiment Videos
Hematologically important mutations: band 3 and protein 4.2 variants in hereditary spherocytosis
1Department of Pediatrics, Yale University School of Medicine, 333 Cedar Street, New Haven, CT 06520-8064, USA. patrick_gallagher@qm.yale.edu
Blood Cells, Molecules & Diseases
|March 28, 1998
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Disorders of erythrocyte volume homeostasis.
International journal of laboratory hematology·2015
One size does not fit all: why universal decolonization strategies to prevent methicillin-resistant Staphylococcus aureus colonization and infection in adult intensive care units may be inappropriate for neonatal intensive care units.
Journal of perinatology : official journal of the California Perinatal Association·2014
Late-onset Leclercia adecarboxylata sepsis in a premature neonate.
Journal of perinatology : official journal of the California Perinatal Association·2013
Refinement of the hereditary xerocytosis locus on chromosome 16q in a large Canadian kindred.
Blood cells, molecules & diseases·2011
Erythropoietin mediates terminal granulocytic differentiation of committed myeloid cells with ectopic erythropoietin receptor expression.
European journal of haematology·2001
Hematologic manifestations of sitosterolemia: Phenotypic spectrum and long-term outcomes in seven genetically confirmed patients.
Blood cells, molecules & diseases·2026
Characterisation of clinical, hematological and molecular variability in individuals with sickle β-thalassemia.
Blood cells, molecules & diseases·2026
Metabolic dysregulation linked to sickling tendency in sickle cell anemia independent of HbF.
Blood cells, molecules & diseases·2026
Recurrent KCNN4 p.Ser314Pro variant in a child with Gardos channelopathy: a 6-year follow-up.
Blood cells, molecules & diseases·2026
Living with sickle cell disease in the Arab world: Quality of life beyond clinical severity.
Blood cells, molecules & diseases·2026
Compound heterozygous variants in F7 gene causing severe factor VII deficiency without bleeding: A genotypic and laboratory analysis.
Blood cells, molecules & diseases·2026
Treatment Adherence in Haemophilia: Methods of Assessment, Clinical Outcomes, and Real-World Evidence.
Haemophilia : the official journal of the World Federation of Hemophilia·2026
Thrombotic and ischemic event reporting with anticoagulant reversal agents: a multi-agent FAERS pharmacovigilance study.
Journal of thrombosis and thrombolysis·2026
Hand-powered micro-slit-gated microfluidics for concurrent blood typing and hematocrit estimation.
Biosensors & bioelectronics·2026