| 000 | 01646 a2200469 4500 | ||
|---|---|---|---|
| 005 | 20250511191615.0 | ||
| 264 | 0 | _c19920402 | |
| 008 | 199204s 0 0 eng d | ||
| 022 | _a0340-6199 | ||
| 024 | 7 |
_a10.1007/BF01958956 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aBertini, E | |
| 245 | 0 | 0 |
_aPeripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiency. _h[electronic resource] |
| 260 |
_bEuropean journal of pediatrics _cFeb 1992 |
||
| 300 |
_a121-6 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_a3-Hydroxyacyl CoA Dehydrogenases _xdeficiency |
| 650 | 0 | 4 | _aAcyl-CoA Dehydrogenase, Long-Chain |
| 650 | 0 | 4 | _aBiochemical Phenomena |
| 650 | 0 | 4 | _aBiochemistry |
| 650 | 0 | 4 | _aBiopsy |
| 650 | 0 | 4 |
_aCardiomyopathy, Hypertrophic _xcomplications |
| 650 | 0 | 4 |
_aFatty Acid Desaturases _xdeficiency |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aFibroblasts _xenzymology |
| 650 | 0 | 4 |
_aHeart Failure _xetiology |
| 650 | 0 | 4 |
_aHereditary Sensory and Motor Neuropathy _xcomplications |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 |
_aRetinitis Pigmentosa _xcomplications |
| 650 | 0 | 4 |
_aSural Nerve _xpathology |
| 700 | 1 | _aDionisi-Vici, C | |
| 700 | 1 | _aGaravaglia, B | |
| 700 | 1 | _aBurlina, A B | |
| 700 | 1 | _aSabatelli, M | |
| 700 | 1 | _aRimoldi, M | |
| 700 | 1 | _aBartuli, A | |
| 700 | 1 | _aSabetta, G | |
| 700 | 1 | _aDiDonato, S | |
| 773 | 0 |
_tEuropean journal of pediatrics _gvol. 151 _gno. 2 _gp. 121-6 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/BF01958956 _zAvailable from publisher's website |
| 999 |
_c1543836 _d1543836 |
||