| 000 | 01697 a2200505 4500 | ||
|---|---|---|---|
| 005 | 20250512093513.0 | ||
| 264 | 0 | _c19701103 | |
| 008 | 197011s 0 0 eng d | ||
| 022 | _a0001-6314 | ||
| 024 | 7 |
_a10.1111/j.1600-0404.1970.tb02177.x _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aGamstorp, I | |
| 245 | 0 | 0 |
_aMetabolic neuropathies and myopathies in infancy and childhood. _h[electronic resource] |
| 260 |
_bActa neurologica Scandinavica _c1970 |
||
| 300 |
_a109-119 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Review | ||
| 650 | 0 | 4 | _aAbnormalities, Multiple |
| 650 | 0 | 4 | _aAlpha-Globulins |
| 650 | 0 | 4 | _aCardiomegaly |
| 650 | 0 | 4 | _aCerebrospinal Fluid Proteins |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aDiabetes Mellitus |
| 650 | 0 | 4 | _aDiffuse Cerebral Sclerosis of Schilder |
| 650 | 0 | 4 |
_aGlucosidases _xmetabolism |
| 650 | 0 | 4 | _aGlucosyltransferases |
| 650 | 0 | 4 | _aGlycogen Storage Disease |
| 650 | 0 | 4 | _aHeart Defects, Congenital |
| 650 | 0 | 4 | _aHeart Diseases |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aHypogonadism |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aIntellectual Disability |
| 650 | 0 | 4 |
_aMetabolism, Inborn Errors _xcomplications |
| 650 | 0 | 4 |
_aMuscles _xenzymology |
| 650 | 0 | 4 |
_aMuscular Atrophy _xcongenital |
| 650 | 0 | 4 |
_aMuscular Diseases _xchemically induced |
| 650 | 0 | 4 | _aObesity |
| 650 | 0 | 4 |
_aPeripheral Nervous System Diseases _xetiology |
| 650 | 0 | 4 | _aPolyradiculopathy |
| 650 | 0 | 4 | _aPorphyrias |
| 650 | 0 | 4 | _aRefsum Disease |
| 650 | 0 | 4 | _aSerum Albumin |
| 773 | 0 |
_tActa neurologica Scandinavica _gvol. 46 _gno. S43 _gp. 109-119 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/j.1600-0404.1970.tb02177.x _zAvailable from publisher's website |
| 999 |
_c4201096 _d4201096 |
||