| 000 | 01589 a2200433 4500 | ||
|---|---|---|---|
| 005 | 20250510213748.0 | ||
| 264 | 0 | _c19791024 | |
| 008 | 197910s 0 0 eng d | ||
| 022 | _a0025-7125 | ||
| 024 | 7 |
_a10.1016/s0025-7125(16)31673-x _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aBosch, E P | |
| 245 | 0 | 0 |
_aMetabolic myopathies. _h[electronic resource] |
| 260 |
_bThe Medical clinics of North America _cJul 1979 |
||
| 300 |
_a759-82 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Review | ||
| 650 | 0 | 4 |
_aAMP Deaminase _xdeficiency |
| 650 | 0 | 4 |
_aCarnitine _xdeficiency |
| 650 | 0 | 4 |
_aCarnitine O-Palmitoyltransferase _xdeficiency |
| 650 | 0 | 4 |
_aCreatine Kinase _xmetabolism |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aGlucan 1,4-alpha-Glucosidase _xdeficiency |
| 650 | 0 | 4 |
_aGlycogen _xmetabolism |
| 650 | 0 | 4 |
_aGlycogen Storage Disease Type II _xmetabolism |
| 650 | 0 | 4 |
_aGlycogen Storage Disease Type III _xmetabolism |
| 650 | 0 | 4 |
_aGlycogen Storage Disease Type V _xmetabolism |
| 650 | 0 | 4 |
_aGlycogen Storage Disease Type VII _xmetabolism |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aLipid Metabolism, Inborn Errors |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMetabolism, Inborn Errors |
| 650 | 0 | 4 |
_aMuscular Diseases _xmetabolism |
| 650 | 0 | 4 |
_aPhosphofructokinase-1 _xdeficiency |
| 650 | 0 | 4 |
_aPhosphorylase a _xdeficiency |
| 650 | 0 | 4 |
_aalpha-Glucosidases _xmetabolism |
| 700 | 1 | _aMunsat, T L | |
| 773 | 0 |
_tThe Medical clinics of North America _gvol. 63 _gno. 4 _gp. 759-82 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/s0025-7125(16)31673-x _zAvailable from publisher's website |
| 999 |
_c154587 _d154587 |
||