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Results: 5

Authors: Lemmink, HH Tuyt, L Knol, G Krikke, E Vellenga, E
Citation: Hh. Lemmink et al., Identification of LIL-STAT in monocytic leukemia cells and monocytes afterstimulation with interleukin-6 or interferon gamma, BLOOD, 98(13), 2001, pp. 3849-3852

Authors: Konrad, M Vollmer, M Lemmink, HH Van den Heuvel, LPWJ Jeck, N Vargas-Poussou, R Lakings, A Ruf, R Deschenes, G Antignac, C Guay-Woodford, L Knoers, NVAM Seyberth, HW Feldmann, D Hildebrandt, F
Citation: M. Konrad et al., Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome, J AM S NEPH, 11(8), 2000, pp. 1449-1459

Authors: Vollmer, M Jeck, N Lemmink, HH Vargas, R Feldmann, D Konrad, M Beekmann, F van den Heuvel, LPWJ Deschenes, G Guay-Woodford, LM Antignac, C Seyberth, HW Hildebrandt, F Knoers, NVAM
Citation: M. Vollmer et al., Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31, NEPH DIAL T, 15(7), 2000, pp. 970-974

Authors: Van der Loop, FTL Monnens, LAH Schroder, CH Lemmink, HH Breuning, MH Timmer, EDJ Smeets, HJM
Citation: Ftl. Van Der Loop et al., Identification of COL4 A5 defects in Alport's syndrome by immunohistochemistry of skin (vol 55, pg 1217, 1999), KIDNEY INT, 56(6), 1999, pp. 2337-2337

Authors: van der Loop, FTL Monnens, LAH Schroder, CH Lemmink, HH Breuning, MH Timmer, EDJ Smeets, HJM
Citation: Ftl. Van Der Loop et al., Identification of COL4A5 defects in Alport's syndrome by immunohistochemistry of skin, KIDNEY INT, 55(4), 1999, pp. 1217-1224
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