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Browsing by Author Michiels, J.J.M.

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Showing results 1 to 8 of 8
Full TextIssue DateTitleAuthor(s)
2007WHO bone marrow features and European clinical, molecular, and pathological (ECMP) criteria for the diagnosis of myeloproliferative disorders.Michiels, J.J.M.; Raeve, H. De; Hebeda, K.M.; Lam, K.H.; Berneman, Z., et al
2006[From gene to disease; primary erythermalgia--a neuropathic disease as a consequence of mutations in a sodium pump gene]Drenth, J.P.H.; Morsche, R.H.M. te; Michiels, J.J.M.
2006The 2001 World Health Organization and updated European clinical and pathological criteria for the diagnosis, classification, and staging of the Philadelphia chromosome-negative chronic myeloproliferative disorders.Michiels, J.J.M.; Raeve, H. De; Berneman, Z.; Bockstaele, D. van; Hebeda, K.M., et al
2005Autosomal dominant erythermalgia associated with a novel mutation in the voltage-gated sodium channel alpha subunit Nav1.7.Michiels, J.J.M.; Morsche, R.H.M. te; Jansen, J.B.M.J.; Drenth, J.P.H.
1997Substance P is not involved in primary and secondary erythermalgiaDrenth, J.P.H.; Michiels, J.J.M.; Joost, T. van
1996Cutaneous pathology in primary erythermalgiaDrenth, J.P.H.; Vuzevski, V.D.; Joost, T. van; Casteels-van Daele, M.; Vermylen, J., et al
1995Acute secondary erythermalgia and hypertension in childrenDrenth, J.P.H.; Michiels, J.J.M.; Ozsoylu, S.
1995Secondary erythermalgia associated with an autoimmune disorder of undetermined significanceDrenth, J.P.H.; Michiels, J.J.M.; Joost, T. Van; Vuzevski, V.D.
Showing results 1 to 8 of 8

 

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