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Browsing by Author Michiels, J.J.M.
Showing results 1 to 8 of 8
| Full Text | Issue Date | Title | Author(s) | | 2007 | WHO 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. |
| 2006 | The 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 |
| 2005 | Autosomal 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. |
| 1997 | Substance P is not involved in primary and secondary erythermalgia | Drenth, J.P.H.; Michiels, J.J.M.; Joost, T. van |
| 1996 | Cutaneous pathology in primary erythermalgia | Drenth, J.P.H.; Vuzevski, V.D.; Joost, T. van; Casteels-van Daele, M.; Vermylen, J., et al |
| 1995 | Acute secondary erythermalgia and hypertension in children | Drenth, J.P.H.; Michiels, J.J.M.; Ozsoylu, S. |
| 1995 | Secondary erythermalgia associated with an autoimmune disorder of undetermined significance | Drenth, J.P.H.; Michiels, J.J.M.; Joost, T. Van; Vuzevski, V.D. |
Showing results 1 to 8 of 8
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