LEADER 01137nam--2200373---450- 001 990002821310203316 005 20061003105715.0 035 $a000282131 035 $aUSA01000282131 035 $a(ALEPH)000282131USA01 035 $a000282131 100 $a20061003d1980----km-y0itay50------ba 101 $aita 102 $aIT 105 $a||||||||001yy 200 1 $a<> Russia e l'autocoscienza d'Europa$fDieter Groh 210 $aTorino$cEinaudi$d1980 215 $aVII, 436 p.$d21 cm 225 2 $aPiccola biblioteca Einaudi$v405 300 $a[Titolo originale] Russland und das Selbstverstandnis Europas. Ein Beitrag zur europaischen Geistesgeschichte 410 0$12001$aPiccola biblioteca Einaudi 454 1$12001 461 1$1001-------$12001 606 0 $aStoria della Russia 676 $a947 700 1$aGROH,$bDieter$0255236 801 0$aIT$bsalbc$gISBD 912 $a990002821310203316 951 $a947 GRO$b3337 DITESI (armadio 3 I 415) 959 $aBK 969 $aDITESI 979 $aDITESI$b10$c20061003$lUSA01$h1057 996 $aRussia e l'autocoscienza d'Europa$9143550 997 $aUNISA LEADER 05736nam 22007215 450 001 9910300185203321 005 20200630041257.0 010 $a1-4939-0727-1 024 7 $a10.1007/978-1-4939-0727-4 035 $a(CKB)3710000000244331 035 $a(EBL)1964965 035 $a(OCoLC)908082968 035 $a(SSID)ssj0001354138 035 $a(PQKBManifestationID)11987169 035 $a(PQKBTitleCode)TC0001354138 035 $a(PQKBWorkID)11322312 035 $a(PQKB)10792117 035 $a(DE-He213)978-1-4939-0727-4 035 $a(MiAaPQ)EBC1964965 035 $a(iGPub)SPNA0031591 035 $a(PPN)181346729 035 $a(EXLCZ)993710000000244331 100 $a20140916d2015 u| 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aGenomic Applications in Pathology /$fedited by George Jabboure Netto, Iris Schrijver 205 $a1st ed. 2015. 210 1$aNew York, NY :$cSpringer New York :$cImprint: Springer,$d2015. 215 $a1 online resource (616 p.) 300 $aDescription based upon print version of record. 311 $a1-4939-0726-3 320 $aIncludes bibliographical references and index. 327 $aCurrent Massively Parallel Sequencing Technologies: Platforms and Reporting Considerations -- Emerging Next Generation Sequencing Technologies -- Transcriptome Sequencing (RNA-Seq) -- miRNA Expression Assays -- Circulating Tumor Cells: Enrichment and Genomic Applications -- Circulating Cell-free DNA for Molecular Diagnostics and Therapeutic Monitoring -- Genomic Pathology: Training for New Technology -- Implementation of Genomic Sequencing Assays -- Regulatory and Reimbursement Issues in Genomic Testing -- Patents and Proprietary Assays -- Ethical Issues in Clinical Genetics and Genomics -- Transitioning Discoveries from Cancer Genomics Research Laboratories into Pathology Practice -- Bioinformatics Tools in Clinical Genomics -- Next Generation Sequencing for Single Gene Analysis -- Next Generation Sequencing for Gene Panels -- Implementation of Exome Sequencing Assays -- Implementation of Genome Sequencing Assays -- Clinical Information Systems in the Era of Personalized Medicine -- Reporting Clinical Genomic Assay Results and the Role of the Pathologist -- Genomic Applications in Hematologic Oncology -- Genomic Applications in Brain Tumors -- Genomic Applications in Head and Neck Cancers -- Genomic Applications in Breast Carcinoma -- Genomic Applications in Pulmonary Malignancies -- Genomic Applications in Colorectal and Pancreatic Tumors -- Molecular Pathology of Genitourinary Cancers: Translating the Cancer Genome to the Clinic -- Genomic Applications in Gynecologic Malignancies -- Genomic Applications in Epithelial Ovarian Malignancies -- Genomic Applications in Soft Tissue Sarcomas -- Genomic Applications in Inherited Genetic Disorders -- Genomic Applications in Pharmacogenomics -- Sequencing Cell Free DNA in the Maternal Circulation to Screen for Down Syndrome and Other Common Aneuploidies -- Genomic Applications in the Clinical Management of Infectious Diseases. . 330 $aGenomic Applications in Pathology provides a state-of-the art review of the scientific principles underlying next generation genomic technologies and the required bioinformatics approaches to analyses of the daunting amount of data generated by current and emerging genomic technologies. Implementation roadmaps for various clinical assays such as single gene, gene panels, whole exome and whole genome assays are discussed together with issues related to reporting, including the pathologist?s role in interpretation and clinical integration of genomic tests results. Genomic applications for site-specific solid tumors and hematologic neoplasms are detailed, as well as genomic applications in pharmacogenomics, inherited genetic diseases, and infectious diseases. The latest iteration of practice recommendations and guidelines in genomic testing, put forth by stakeholder professional organizations such as the Association for Molecular Pathology  and the College of American Pathologists, are also discussed in the volume, as well as regulatory issues and laboratory accreditation related to genomic testing. Written by experts in the field, Genomic Applications in Pathology provides a comprehensive resource that is of great value to practicing molecular pathologists, hematopathologists, other subspecialized pathologists, general pathologists, pathology trainees, oncologists, and geneticists. 606 $aPathology 606 $aOncology   606 $aLaboratory medicine 606 $aHuman genetics 606 $aPathology$3https://scigraph.springernature.com/ontologies/product-market-codes/H4800X 606 $aOncology$3https://scigraph.springernature.com/ontologies/product-market-codes/H33160 606 $aLaboratory Medicine$3https://scigraph.springernature.com/ontologies/product-market-codes/B15007 606 $aHuman Genetics$3https://scigraph.springernature.com/ontologies/product-market-codes/B12008 615 0$aPathology. 615 0$aOncology  . 615 0$aLaboratory medicine. 615 0$aHuman genetics. 615 14$aPathology. 615 24$aOncology. 615 24$aLaboratory Medicine. 615 24$aHuman Genetics. 676 $a599935 676 $a610 676 $a610724 676 $a611.01816 702 $aNetto$b George Jabboure$4edt$4http://id.loc.gov/vocabulary/relators/edt 702 $aSchrijver$b Iris$4edt$4http://id.loc.gov/vocabulary/relators/edt 906 $aBOOK 912 $a9910300185203321 996 $aGenomic Applications in Pathology$91734969 997 $aUNINA