000 01639 a2200529 4500
005 20250515201325.0
264 0 _c20100315
008 201003s 0 0 eng d
022 _a1439-3824
024 7 _a10.1055/s-0029-1231074
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aProchazkova, D
245 0 0 _aWilson's disease: monocentric experiences over a period of 10 years [corrected].
_h[electronic resource]
260 _bKlinische Padiatrie
_cDec 2009
300 _a419-24 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAdenosine Triphosphatases
_xgenetics
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aAlleles
650 0 4 _aCation Transport Proteins
_xgenetics
650 0 4 _aCeruloplasmin
_xdeficiency
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aCopper
_xurine
650 0 4 _aCopper-Transporting ATPases
650 0 4 _aDiagnosis, Differential
650 0 4 _aFemale
650 0 4 _aFollow-Up Studies
650 0 4 _aGenetic Carrier Screening
650 0 4 _aHepatolenticular Degeneration
_xdiagnosis
650 0 4 _aHumans
650 0 4 _aLiver Function Tests
650 0 4 _aLiver Transplantation
650 0 4 _aMale
650 0 4 _aNeurologic Examination
650 0 4 _aRetrospective Studies
650 0 4 _aYoung Adult
700 1 _aPouchla, S
700 1 _aMejzlik, V
700 1 _aKonecna, P
700 1 _aMichalek, J
700 1 _aBartosova, D
700 1 _aHrstkova, H
773 0 _tKlinische Padiatrie
_gvol. 221
_gno. 7
_gp. 419-24
856 4 0 _uhttps://doi.org/10.1055/s-0029-1231074
_zAvailable from publisher's website
999 _c19394989
_d19394989