000 01441 a2200433 4500
005 20250515000800.0
264 0 _c20051202
008 200512s 0 0 eng d
022 _a0174-304X
024 7 _a10.1055/s-2005-872808
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBarone, R
245 0 0 _aCongenital insensitivity to pain with Anhidrosis (NTRK1 mutation) and early onset renal disease: clinical report on three sibs with a 25-year follow-up in one of them.
_h[electronic resource]
260 _bNeuropediatrics
_cAug 2005
300 _a270-3 p.
_bdigital
500 _aPublication Type: Comparative Study; Journal Article
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aB-Lymphocytes
_xmetabolism
650 0 4 _aCD5 Antigens
_xmetabolism
650 0 4 _aChild
650 0 4 _aDNA Mutational Analysis
_xmethods
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aHypohidrosis
_xetiology
650 0 4 _aImmunoglobulin G
_xurine
650 0 4 _aLongitudinal Studies
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aPain Insensitivity, Congenital
_xcomplications
650 0 4 _aReceptor, trkA
_xgenetics
650 0 4 _aSiblings
700 1 _aLempereur, L
700 1 _aAnastasi, M
700 1 _aParano, E
700 1 _aPavone, P
773 0 _tNeuropediatrics
_gvol. 36
_gno. 4
_gp. 270-3
856 4 0 _uhttps://doi.org/10.1055/s-2005-872808
_zAvailable from publisher's website
999 _c15774004
_d15774004