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dr. J.M.P.J. (Hans) Breur MD

dr. J.M.P.J. (Hans) Breur MD

Associate Professor - medical

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Research Output (164)

Long-term outcomes and complications of transvenous pacemaker implantation in small infants.

Vos L.M., Blank A.C., Kammeraad J., Freund M.W., Breur J.M.P.J. 2014,

Five years of Kawasaki disease in the Netherlands: a national surveillance study.

Tacke C.E., Breunis W.B., Rodrigues Pereira R., Breur J.M.P.J., Giltay J.C., van Haaften G. 2014, In: The Pediatric infectious disease journal. 33 , p. 793-797 5 p.

Congenital cardiac, aortic arch, and vascular bed anomalies in PHACE syndrome (from the International PHACE Syndrome Registry)

Bayer Michelle L., Frommelt Peter C., Blei Francine, Breur Johannes M.P.J., Cordisco Maria R., Frieden Ilona J., Goddard Deborah S., Holland Kristen E., Krol Alfons L., Maheshwari Mohit, Metry Denise W., Morel Kimberly D., North Paula E., Pope Elena, Shieh Joseph T., Southern James F., Wargon Orli, Siegel Dawn H., Drolet Beth A. 15 Dec 2013, In: American Journal of Cardiology. 112 , p. 1948-1952 5 p.

Treatment of infantile haemangiomas with atenolol:comparison with a historical propranolol group

de Graaf M., Raphaël M.F. , Breugem C.C., Knol M.J., Bruijnzeel - Koomen C.A.F.M., Kon M., Breur J.M.P.J., Pasmans S.G.M.A. Dec 2013, In: Journal of Plastic, Reconstructive & Aesthetic Surgery. 66 , p. 1732-1740 9 p.

Hemangiomen: wanneer en hoe te behandelen?

Totte J.E.E., Breugem C.C., de Graaf M., Toonstra J., Raphael M.F., Breur G.J., Speleman L., Breur J.M.P.J., Pasmans S.G.M.A. 2013, In: Huisarts en Wetenschap. 56 , p. 74-78 5 p.

Evaluatie van de waarde van aanvullend onderzoek voorafgaand en tijdens de behandeling van infantiele hemangiomen met beta-blokkers.

Vlasveld F., Raphael M.F., Breugem C.C., de Graaf M., Slieker M.G., Pasmans S.G.M.A., Breur J.M.P.J. 2013,

Dominant missense mutations in ABCC9 cause Cantu syndrome

Harakalova M., van Harssel J.J.T., Terhal P.A., van Lieshout S., Duran K.J., Renkens I.J., Amor D.J., Wilson L.C., Kirk E.P., Turner C.L.S., Shears D., Garcia-Minaur S., Lees M.M., Ross A., Venselaar H., Vriend G., Takanari H., Rook M.B., van der Heyden M.A.G., Asselbergs F.W., Breur J.M.P.J., Swinkels M.E.M., Scurr I.J., Smithson S.F., Knoers V.V.A.M., van der Smagt J.J., Nijman I.J., Kloosterman W.P., van Haelst M.M., van Haaften G.W., Cuppen E.P.J.G. 11 May 2012,

Dominant missense mutations in potassium channel cause Cantu syndrome

van Haaften G.W., Harakalová M., van Harssel J.J.T., Terhal P.A., van Lieshout S., Duran K.J., Renkens I.J., Armor D., Wilson L., Kirk E., Turner C.L.S., Shears D., Garcia-Minaur S., Lees M.M., Ross A., Venselaar H., Vriend G., Takanari H., Rook M., van der Heyden M., Asselbergs F.W., Breur Hans M., Swinkels M.E., Scurr I.J., Knoers V.V.A.M., van der Smagt J.J., Nijman I.J., Kloosterman W.P., van Haelst M.M., Cuppen E.P.J.G. 21 Mar 2012,

Dominant missense mutations in ABCC9 cause Cantú syndrome

Harakalova M., van Harssel J.J.T., Terhal P.A., van Lieshout S., Duran K.J., Renkens I.J., Amor D.J., Wilson L.C., Kirk E.P., Turner C.L., Shears D., Garcia-Minaur S., Lees M.M., Ross A., Venselaar H., Vriend G., Takanari H., Rook M.B., van der Heyden M.A. , Asselbergs F.W., Breur J.M.P.J., Swinkels M.E., Scurr I.J., Smithson S.F., Knoers V.V.A.M., van der Smagt J.J., Nijman I.J., Kloosterman W.P., van Haelst M.M., van Haaften G.W., Cuppen E.P.J.G. 2012, In: Nature Genetics. 44 , p. 793-796 4 p.

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