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Knoers Nine V.
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http://hub.abes.fr/bmj/periodical/jmg/2013/volume_50/issue_5/B35958AFB1536AAFE053120B220A26C8/authorship/33
http://hub.abes.fr/bmj/periodical/jnnp/2010/volume_81/issue_10/B35A82167E0C4C40E053120B220AF6DD/authorship/6
http://hub.abes.fr/oup/periodical/ndt/2001/volume_16/issue_1/101093ndt16148/authorship/4
http://hub.abes.fr/oup/periodical/hmg/2007/volume_16/issue_5/101093hmgddm016/authorship/10
http://hub.abes.fr/bmj/periodical/jmg/2012/volume_49/issue_8/B35958AFB0986AAFE053120B220A26C8/authorship/12
http://hub.abes.fr/oup/periodical/ndt/2008/volume_23/issue_10/101093ndtgfn229/authorship/9
http://hub.abes.fr/oup/periodical/ndt/2000/volume_15/issue_7/101093ndt157970/authorship/14
http://hub.abes.fr/oup/periodical/ndt/2004/volume_19/issue_3/101093ndtgfg574/authorship/3
http://hub.abes.fr/oup/periodical/ndt/2003/volume_18/issue_3/101093ndt183512/authorship/7
http://hub.abes.fr/oup/periodical/ndt/2004/volume_19/issue_5/101093ndtgfg474/authorship/6
http://hub.abes.fr/bmj/periodical/jmg/2011/volume_48/issue_6/B35958AFAFF66AAFE053120B220A26C8/authorship/13
http://hub.abes.fr/bmj/periodical/jmg/2001/volume_38/issue_3/B3598D6B5D3D7CBEE053120B220A90C5/authorship/7
http://hub.abes.fr/springer/periodical/439/1995/volume_96/issue_1/B9279D37F10C5861E053120B220A3025/authorship/9
http://hub.abes.fr/springer/periodical/467/1995/volume_9/issue_2/B8CBB510C28E4191E053120B220A87AF/authorship/2
http://hub.abes.fr/springer/periodical/467/1996/volume_10/issue_4/B8CBB510C5B64191E053120B220A87AF/authorship/9
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Autosomal recessive hypophosphataemic rickets with hypercalciuria is not caused by mutations in the type II renal sodium/phosphate cotransporter gene
Effects of chemical chaperones on partially retarded NaCl cotransporter mutants associated with Gitelman's syndrome in a mouse cortical collecting duct cell line
Characterization of a recurrent 15q24 microdeletion syndrome
Evaluating PVALB as a candidate gene for SLC12A3-negative cases of Gitelman's syndrome
Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31
Bladder function impairment in aquaporin-2 defective nephrogenic diabetes insipidus
Exclusion of mutations in FXYD2, CLDN16 and SLC12A3 in two families with primary renal Mg2+ loss
Linkage of Gitelman syndrome to the thiazide-sensitive sodium-chloride cotransporter gene with identification of mutations in Dutch families
Discovery of aquaporins: a breakthrough in research on renal water transport
Clinical phenotype of nephrogenic diabetes insipidus in females heterozygous for a vasopressin type 2 receptor mutation
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