Filter your results
- 2
- 2
- 4
- 4
- 2
- 2
- 3
- 1
- 4
- 2
- 2
- 2
- 2
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 4
- 3
- 3
- 3
- 3
- 2
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
|
|
sorted by
|
Variable age of onset and clinical severity in transferrin receptor 2 related haemochromatosis: novel observationsBritish Journal of Haematology, 2013, 162 (2), pp.278-81. ⟨10.1111/bjh.12350⟩
Journal articles
inserm-00836894v1
|
|||
|
Hereditary hypotransferrinemia can lead to elevated transferrin saturation and, when associated to HFE or HAMP mutations, to iron overloadBlood Cells, Molecules and Diseases, 2015, 54 (2), pp.151-154. ⟨10.1016/j.bcmd.2014.11.020⟩
Journal articles
hal-01120455v1
|
||
|
Non-HFE hemochromatosis: Pathophysiological and diagnostic aspects.Clinics and Research in Hepatology and Gastroenterology, 2013, 38 (2), pp.143-154. ⟨10.1016/j.clinre.2013.11.003⟩
Journal articles
hal-00925741v1
|
||
Insuffisance ovarienne prématurée chez deux patientes présentant une délétion XqMorphologie, 2015, 20es Journées du Collège des Histologistes, Embryologistes et Cytogénéticiens - Paris 12-14 mars 2015, 99 (327), pp.168. ⟨10.1016/j.morpho.2015.09.043⟩
Journal articles
hal-01245011v1
|