000 01734 a2200505 4500
005 20250517222052.0
264 0 _c20191202
008 201912s 0 0 eng d
022 _a1758-1001
024 7 _a10.1177/0004563218785190
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSeeman, Tomáš
245 0 0 _aHypomagnesaemia is absent in children with autosomal dominant polycystic kidney disease.
_h[electronic resource]
260 _bAnnals of clinical biochemistry
_c01 2019
300 _a90-94 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aCentral Nervous System Diseases
_xblood
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aCross-Sectional Studies
650 0 4 _aDental Enamel
_xabnormalities
650 0 4 _aDiabetes Mellitus, Type 2
_xblood
650 0 4 _aDiagnosis, Differential
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aHypercalciuria
_xblood
650 0 4 _aInfant
650 0 4 _aInfant, Newborn
650 0 4 _aKidney Diseases, Cystic
_xblood
650 0 4 _aMagnesium
_xblood
650 0 4 _aMale
650 0 4 _aNephrocalcinosis
_xblood
650 0 4 _aPolycystic Kidney, Autosomal Dominant
_xblood
650 0 4 _aPolycystic Kidney, Autosomal Recessive
_xblood
650 0 4 _aPrevalence
650 0 4 _aRenal Tubular Transport, Inborn Errors
_xblood
700 1 _aFořtová, Magdaléna
700 1 _aSopko, Bruno
700 1 _aPrůša, Richard
700 1 _aPohl, Michael
700 1 _aJohn, Ulrike
773 0 _tAnnals of clinical biochemistry
_gvol. 56
_gno. 1
_gp. 90-94
856 4 0 _uhttps://doi.org/10.1177/0004563218785190
_zAvailable from publisher's website
999 _c28503223
_d28503223