• A computational model to understand mouse iron physiology and disease
• A new case of congenital atransferrinemia with a novel splice site mutation: c.293-63del
• Addition of oral iron to plasma transfusion in human congenital hypotransferrinemia: A 10-year observational follow-up with the effects on hematological parameters and growth
• Congenital Hypotransferrinemia, an Unusual Cause of Iron Deficiency Anemia: Report of Two Cases
• Hepatocyte divalent metal-ion transporter-1 is dispensable for hepatic iron accumulation and non-transferrin-bound iron uptake in mice
• Hereditary hypotransferrinemia can lead to elevated transferrin saturation and, when associated to HFE or HAMP mutations, to iron overload
• Inherited Disorders of Iron Overload
• Inherited iron overload disorders
• Inherited microcytic anemias
• Known and potential roles of transferrin in iron biology
• Label-free and ultrasensitive electrochemical transferrin detection biosensor based on a glassy carbon electrode and gold nanoparticles
• Molecular analysis of a novel case of congenital atransferrinemia
• Non-HFE hepatic iron overload
• Rare anemias due to genetic iron metabolism defects
• Recommendations for diagnosis, treatment, and prevention of iron deficiency and iron deficiency anemia
• Reversible atransferrinemia in a patient with chronic enteropathy: is transferrin mandatory for iron transport?
• Transferrin and transferrin receptors update