Melanie Schranz

Mutations in SPINT2 Cause a Syndromic Form of Congenital Sodium Diarrhea

Peter Heinz‐Erian, Thomas Müller, Birgit Krabichler et al. · The American Journal of Human Genetics · 2009 · 123 citations · Full text

Genetic Disorder, Genetics, Pathogenesis +7

Hepatic but not brain iron is rapidly chelated by deferasirox in aceruloplasminemia due to a novel gene mutation

Armin Finkenstedt, Elisabeth Wolf, Elmar Höfner et al. · Journal of Hepatology · 2010 · 81 citations · Full text

Activation and inactivation of the iron hormone hepcidin: Biochemical characterization of prohepcidin cleavage and sequential degradation to N-terminally truncated hepcidin isoforms

Melanie Schranz, Rania Bakry, Marc Creus et al. · Blood Cells Molecules and Diseases · 2009 · 26 citations

Biochemistry, Natural Sciences, Metalloprotein +10

Impact of D181V and A69T on the function of ferroportin as an iron export pump and hepcidin receptor

Roman Praschberger, Melanie Schranz, William J. Griffiths et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 2014 · 23 citations · Full text

Biochemistry, Iron Metabolism, Natural Sciences +9

MNGIE Syndrome: Liver Cirrhosis Should Be Ruled Out Prior to Bone Marrow Transplantation

Armin Finkenstedt, Melanie Schranz, Sylvia Bösch et al. · JIMD Reports · 2012 · 22 citations · Full text