| 000 | 01837 a2200541 4500 | ||
|---|---|---|---|
| 005 | 20250514195313.0 | ||
| 264 | 0 | _c20040910 | |
| 008 | 200409s 0 0 eng d | ||
| 022 | _a1590-1874 | ||
| 024 | 7 |
_a10.1007/s10072-004-0246-z _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aMariotti, C | |
| 245 | 0 | 0 |
_aAtaxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families. _h[electronic resource] |
| 260 |
_bNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology _cJul 2004 |
||
| 300 |
_a130-7 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 |
_aAtaxia _xdiagnosis |
| 650 | 0 | 4 |
_aCarrier Proteins _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aFollow-Up Studies |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aItaly |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aNervous System Diseases _xdiagnosis |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aVitamin E _xtherapeutic use |
| 650 | 0 | 4 |
_aVitamin E Deficiency _xdiagnosis |
| 700 | 1 | _aGellera, C | |
| 700 | 1 | _aRimoldi, M | |
| 700 | 1 | _aMineri, R | |
| 700 | 1 | _aUziel, G | |
| 700 | 1 | _aZorzi, G | |
| 700 | 1 | _aPareyson, D | |
| 700 | 1 | _aPiccolo, G | |
| 700 | 1 | _aGambi, D | |
| 700 | 1 | _aPiacentini, S | |
| 700 | 1 | _aSquitieri, F | |
| 700 | 1 | _aCapra, R | |
| 700 | 1 | _aCastellotti, B | |
| 700 | 1 | _aDi Donato, S | |
| 773 | 0 |
_tNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology _gvol. 25 _gno. 3 _gp. 130-7 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/s10072-004-0246-z _zAvailable from publisher's website |
| 999 |
_c15000154 _d15000154 |
||