000 | 02789nam a22004455i 4500 | ||
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001 | 978-1-4614-0653-2 | ||
003 | DE-He213 | ||
005 | 20140220083239.0 | ||
007 | cr nn 008mamaa | ||
008 | 120312s2012 xxu| s |||| 0|eng d | ||
020 |
_a9781461406532 _9978-1-4614-0653-2 |
||
024 | 7 |
_a10.1007/978-1-4614-0653-2 _2doi |
|
050 | 4 | _aRC321-580 | |
072 | 7 |
_aPSAN _2bicssc |
|
072 | 7 |
_aMED057000 _2bisacsh |
|
082 | 0 | 4 |
_a612.8 _223 |
100 | 1 |
_aAhmad, Shamim I. _eeditor. |
|
245 | 1 | 0 |
_aNeurodegenerative Diseases _h[electronic resource] / _cedited by Shamim I. Ahmad. |
264 | 1 |
_aNew York, NY : _bSpringer US, _c2012. |
|
300 |
_aXXXII, 390p. 71 illus. _bonline resource. |
||
336 |
_atext _btxt _2rdacontent |
||
337 |
_acomputer _bc _2rdamedia |
||
338 |
_aonline resource _bcr _2rdacarrier |
||
347 |
_atext file _bPDF _2rda |
||
490 | 1 |
_aAdvances in Experimental Medicine and Biology, _x0065-2598 ; _v724 |
|
505 | 0 | _aAcute Disseminated Encephalomyelitis -- Age‑Related Macular Degeneration -- Arachnoid Cysts -- Autism Spectrum Disorders: Information for Pediatricians Supporting Families of Young Children on the Spectrum -- Autosomal Recessive Charcot‑Marie‑Tooth Neuropathy -- Creutzfeldt‑Jakob Disease -- Epigenetics in Autism and other Neurodevelopmental Diseases -- Epilepsy and Epileptic Syndrome -- Frontotemporal Lobar Degeneration -- Gerstmann‑ Sträussler ‑Scheinker Disease -- Juvenile Neuronal Ceroid Lipofuscinoses -- Kuru: The First Prion Disease -- Leukodystrophies -- Machado‑Joseph Disease and other Rare Autosomal Dominant Spinocerebellar Ataxias -- Neurodegenerations Induced by Organophosphorous Compounds -- Mitochondrial Importance in Alzheimer’s, Huntington’s and Parkinson’s Diseases -- Multiple Sclerosis -- Myotonic Dystrophy Type 1 or Steinert’s Disease -- Neurodegeneration in Diabetes Mellitus -- Neurofibromatoses -- Oxidative Stress in Developmental Brain Disorders -- Oxidative Stress and Mitochondrial Dysfunction in Down Syndrome -- Pick’s Disease -- Premature Aging Syndrome -- The Savant Syndrome and its Possible Relationship to Epilepsy -- Sjogren‑Larsson Syndrome -- The Spinocerebellar Ataxias: Clinical Aspects and Molecular Genetics -- Tourette Syndrome. | |
520 | _aNo back cover text. | ||
650 | 0 | _aMedicine. | |
650 | 0 | _aNeurosciences. | |
650 | 1 | 4 | _aBiomedicine. |
650 | 2 | 4 | _aNeurosciences. |
650 | 2 | 4 | _aBiomedicine general. |
710 | 2 | _aSpringerLink (Online service) | |
773 | 0 | _tSpringer eBooks | |
776 | 0 | 8 |
_iPrinted edition: _z9781461406525 |
830 | 0 |
_aAdvances in Experimental Medicine and Biology, _x0065-2598 ; _v724 |
|
856 | 4 | 0 | _uhttp://dx.doi.org/10.1007/978-1-4614-0653-2 |
912 | _aZDB-2-SBL | ||
999 |
_c100899 _d100899 |