MARC record from Internet Archive

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001 ocn656365967
003 OCoLC
005 20200513191141.0
008 100817s2009 ne a ob 101 0 eng d
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007 cr cn|||||||||
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020 $a9789048128136
020 $a9048128137
020 $z9789048128129$q(alk. paper)
020 $z9048128129$q(alk. paper)
024 7 $a10.1007/978-90-481-2813-6$2doi
035 $a(OCoLC)656365967$z(OCoLC)570638520$z(OCoLC)609973232$z(OCoLC)647898944$z(OCoLC)712789958$z(OCoLC)767181093$z(OCoLC)985038799$z(OCoLC)1005765598$z(OCoLC)1044268475$z(OCoLC)1056387274$z(OCoLC)1066625568$z(OCoLC)1078054649$z(OCoLC)1086942438$z(OCoLC)1105601913$z(OCoLC)1112567796
037 $a978-90-481-2812-9$bSpringer$nhttp://www.springerlink.com
050 4 $aRC925
060 4 $aW1$bAD559 v.652 2009
060 4 $aWE 550$bI685i 2009
072 7 $aMED$x065000$2bisacsh
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111 2 $aInternational Symposium on Rare Diseases$d(2008 :$cValencia, Spain)
245 10 $aInherited neuromuscular diseases :$btranslation from pathomechanisms to therapies /$c[edited by] Carmen Espino s, Vicente Felipo, Francesc Palau.
260 $aDordecht :$bSpringer,$c℗♭2009.
300 $a1 online resource (xiii, 304 pages) :$billustrations
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 ;$vv. 652
504 $aIncludes bibliographical references and index.
505 0 $aPreface; Contents; Contributors; 1 Pathology and Diagnosis of Muscular Dystrophies; 2 Standards of Care for Duchenne Muscular Dystrophy: Brief Treat-NMD Recommendations; 3 Genetics and Pathogenesis of Distal Muscular Dystrophies; 4 Phenotype Variations in Early Onset Pompe Disease: Diagnosis and Treatment Results with Myozyme; 5 Diseases of the Human Mitochondrial Oxidative Phosphorylation System; 6 Mitochondrial Diseases: A Cross-Talk Between Mitochondrial and Nuclear Genomes; 7 Mitochondrial Disorders Due to Nuclear OXPHOS Gene Defects; 8 Coenzyme Q10 Deficiencies in Neuromuscular Diseases.
520 $aPresents the development of neuromuscular diseases as a whole, including muscular dystrophies, mitochondrial disorders, peripheral neuropathies, spinal muscular atrophy, motoneurone disease and Friedreich ataxia. This title offers a review of inherited neuromuscular diseases under different approaches: genetics, pathomechanisms, and treatments.
588 0 $aPrint version record.
650 0 $aMusculoskeletal system$xDiseases.
650 12 $aNeuromuscular Diseases.
650 22 $aGenetic Diseases, Inborn.
650 7 $aMEDICAL$xOrthopedics.$2bisacsh
650 7 $aHEALTH & FITNESS$xDiseases$xMusculoskeletal.$2bisacsh
650 7 $aMEDICAL$xRheumatology.$2bisacsh
650 7 $aSciences de la vie.$2eclas
650 7 $aBiome decine.$2eclas
650 7 $aMusculoskeletal system$xDiseases.$2fast$0(OCoLC)fst01030019
650 7 $aNeuromuskula re Krankheit$2gnd
650 7 $aAngeborene Krankheit$2gnd
651 7 $aValencia.$2swd
655 2 $aCongress.
655 4 $aElectronic books.
700 1 $aEspino s, Carmen.
700 1 $aFelipo, Vicente.
700 1 $aPalau, Francesc.
776 08 $iPrint version:$aInternational Symposium on Rare Diseases (2008 : Valencia, Spain).$tInherited neuromuscular diseases.$dDordecht : Springer, ℗♭2009$z9789048128129$z9048128129$w(DLC) 2009936205$w(OCoLC)401151193
830 0 $aAdvances in experimental medicine and biology ;$vv. 652.
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856 40 $3SpringerLink$uhttps://doi.org/10.1007/978-90-481-2813-6
856 40 $3SpringerLink$uhttps://link.springer.com/openurl?genre=book&isbn=978-90-481-2812-9
856 40 $3SpringerLink$uhttp://link.springer.com/10.1007/978-90-481-2813-6
856 40 $3SpringerLink$uhttp://www.library.yorku.ca/e/resolver/id/1928771$zAn electronic book accessible through the World Wide Web; click for information
856 40 $uhttps://0-link-springer-com.pugwash.lib.warwick.ac.uk/10.1007/978-90-481-2813-6$zConnect to Springer e-book
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856 $uhttps://discover.gcu.ac.uk/discovery/openurl?institution=44GLCU_INST&vid=44GLCU_INST:44GLCU_VU2&?u.ignore_date_coverage=true&rft.mms_id=991002487317003836$p5372085030003836$xStGlGCU
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