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