A. Rideau

Molecular mechanism of hepcidin deficiency in a patient with juvenile hemochromatosis.

D. Trono, B. Mangeat, T. Matthes, 2004, Haematologica.

Different pathophysiological mechanisms of intramitochondrial iron accumulation in acquired and congenital sideroblastic anemia caused by mitochondrial DNA deletion

P. Rustin, T. Matthes, P. Beris, 2006, European journal of haematology.

Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome.

S. Antonarakis, S. Deutsch, T. Schwede, 2003, Blood.

The D 1424 N MYH 9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly / Fechtner syndrome

S. Antonarakis, S. Deutsch, T. Schwede, 2003 .

for the phenotypes in May-Hegglin anomaly / Fechtner syndrome mutation results in an unstable protein responsible MYH 9 Asp

S. Antonarakis, S. Deutsch, T. Schwede, 2003 .

Lentiviral PU.1 overexpression restores differentiation in myeloid leukemic blasts

S. Durual, V. Piguet, T. Matthes, 2007, Leukemia.