000 01514 a2200409 4500
005 20250513204553.0
264 0 _c20000421
008 200004s 0 0 eng d
022 _a1090-3798
024 7 _a10.1053/ejpn.1999.0177
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aGörgen-Pauly, U
245 0 0 _aFamilial pontocerebellar hypoplasia type I with anterior horn cell disease.
_h[electronic resource]
260 _bEuropean journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
_c1999
300 _a33-8 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aAtrophy
_xpathology
650 0 4 _aCerebellum
_xabnormalities
650 0 4 _aDiagnosis, Differential
650 0 4 _aFatal Outcome
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aInfant, Newborn
650 0 4 _aMagnetic Resonance Imaging
650 0 4 _aMotor Neuron Disease
_xcomplications
650 0 4 _aOlivopontocerebellar Atrophies
_xcomplications
650 0 4 _aPedigree
650 0 4 _aPons
_xabnormalities
650 0 4 _aPregnancy
700 1 _aSperner, J
700 1 _aReiss, I
700 1 _aGehl, H B
700 1 _aReusche, E
773 0 _tEuropean journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
_gvol. 3
_gno. 1
_gp. 33-8
856 4 0 _uhttps://doi.org/10.1053/ejpn.1999.0177
_zAvailable from publisher's website
999 _c10680960
_d10680960