Articles by author

TFR2-related haemochromatosis in the Netherlands: a cause of arthralgia in young adulthood
Issue: March 2017, Volume: 75, Number: 2

T.M.A. Peters, A.F.M. Meulders, K. Redert, M.L.H. Cuijpers, A.J.M. Rennings, M.C.H. Janssen, N.M.A. Blijlevens, D.W. Swinkels

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A novel mutation in mitochondrial DNA in a patient with diabetes, deafness and proteinuria
Issue: December 2016, Volume: 74, Number: 10

A.Y. Adema, M.C.H. Janssen, J.W. van der Heijden

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Dysphagia, malnutrition and gastrointestinal problems in patients with mitochondrial disease caused by the m3243A>G mutation
Issue: January 2015, Volume: 73, Number: 1

P. de Laat, H.E.E. Zweers, S. Knuijt, J.A.M. Smeitink, G.J.A. Wanten, M.C.H. Janssen

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Adult issues in phenylketonuria
Issue: January 2009, Volume: 67, Number: 1

M.P.A. Hoeks, M. den Heijer, M.C.H. Janssen

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Hereditary haemochromatosis
Issue: December 2007, Volume: 65, Number: 11

M.C.H. Janssen

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Local and systemic thrombolytic therapy for acute deep venous thrombosis
Issue: March 2005, Volume: 63, Number: 3

M.C.H. Janssen, H. Wollersheim, L.J. Schultze-Kool, Th. Thien

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