| 000 | 03527nam a22005415i 4500 | ||
|---|---|---|---|
| 001 | 978-0-387-32442-5 | ||
| 003 | DE-He213 | ||
| 005 | 20250710083949.0 | ||
| 007 | cr nn 008mamaa | ||
| 008 | 100301s2006 xxu| s |||| 0|eng d | ||
| 020 |
_a9780387324425 _a99780387324425 |
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| 024 | 7 |
_a10.1007/0-387-32442-9 _2doi |
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| 082 | 0 | 4 |
_a611 _223 |
| 100 | 1 |
_aHollyfield, Joe G. _eeditor. |
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| 245 | 1 | 0 |
_aRetinal Degenerative Diseases _h[recurso electrónico] / _cedited by Joe G. Hollyfield, Robert E. Anderson, Matthew M. LaVail. |
| 264 | 1 |
_aBoston, MA : _bSpringer US, _c2006. |
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| 300 |
_aXXII, 562 p. _bonline resource. |
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| 336 |
_atext _btxt _2rdacontent |
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| 337 |
_acomputer _bc _2rdamedia |
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_arecurso en línea _bcr _2rdacarrier |
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_atext file _bPDF _2rda |
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| 490 | 1 |
_aAdvances in Experimental Medicine and Biology, _x0065-2598 ; _v572 |
|
| 505 | 0 | _aFrom the contents Genetic Factors Modifying Clinical Expression of Autosomal Dominant Rp -- Disease-Associated Variants of The Rod-Derived Cone Viability Factor (Rdcvf) In Leber Congenital Amaurosis. Rod-Derived Cone Viability Variants in Lca -- Leber Congenital Amaurosis: Survey of The Genetic Heterogeneity, Refinement of The Clinical Definition and Phenotype-Genotype Correlations as A Strategy For Molecular Diagnosis. Clinical and Molecular Survey in Lca -- A First Locus For Isolated Autosomal Recessive Optic Atrophy (Roa1) Maps To Chromosome 8q21-Q22 -- Rcc1-Like Domain and ORF15: Essentials in Rpgr Gene -- Choroidal Neovascularization in Patients with Adult-Onset Foveomacular Dystrophy Caused by Mutations in the Rds/Peripherin Gene -- Biochemical Characterisation of the C1QTNF5 Gene Associated With Late-Onset Retinal Degeneration. A Genetic Model of Age-Related Macular Degeneration -- Bietti Crystalline Corneoretinal Dystrophy Associated with Cyp4v2 Gene Mutations -- Fundus Appearance Of Choroideremia Using Optical Coherence Tomograpy -- A2e, A Fluorophore Of Rpe Lipofuscin, Can Destabilie Membrane -- Amino-Retinoid Compounds in The Human Retinal Pigment Epithelium -- Annexins In Bruch's Membrane and Drusen -- Molecular Mechanisms of Photoreceptor Degeneration in RP Caused by Impdh1 Mutations. | |
| 520 | _aRetinal Degenerations is the result of the International Symposium on Retinal degeneration which has become perhaps the most important research meeting in the field. THe topics in this volume explore the etiology, cellular mechanisms, epidemiology, genetics, models and potential therapeutic measures for the blinding diseases of retinitis pigmentosa and age-related macular degeneration. | ||
| 650 | 0 | _aMEDICINE. | |
| 650 | 0 | _aHUMAN ANATOMY. | |
| 650 | 0 | _aOPHTHALMOLOGY. | |
| 650 | 0 | _aEPIDEMIOLOGY. | |
| 650 | 0 | _aQUALITY OF LIFE. | |
| 650 | 0 | _aLIFE SCIENCES. | |
| 650 | 0 |
_aQUALITY OF LIFE _xRESEARCH. |
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| 650 | 1 | 4 | _aMEDICINE & PUBLIC HEALTH. |
| 650 | 2 | 4 | _aANATOMY. |
| 650 | 2 | 4 | _aOPHTHALMOLOGY. |
| 650 | 2 | 4 | _aQUALITY OF LIFE RESEARCH. |
| 650 | 2 | 4 | _aEPIDEMIOLOGY. |
| 650 | 2 | 4 | _aLIFE SCIENCES, GENERAL. |
| 700 | 1 |
_aAnderson, Robert E. _eeditor. |
|
| 700 | 1 |
_aLaVail, Matthew M. _eeditor. |
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| 710 | 2 | _aSpringerLink (Online service) | |
| 773 | 0 | _tSpringer eBooks | |
| 776 | 0 | 8 |
_iPrinted edition: _z9780387284644 |
| 830 | 0 |
_aAdvances in Experimental Medicine and Biology, _x0065-2598 ; _v572 |
|
| 856 | 4 | 0 |
_uhttp://dx.doi.org/10.1007/0-387-32442-9 _zVer el texto completo en las instalaciones del CICY |
| 912 | _aZDB-2-SME | ||
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