LEADER 01280nam0-2200313 --450 001 9910801895403321 005 20240207162122.0 100 $a20240207d1961----kmuy0itay5050 ba 101 0 $aeng 102 $aNL 105 $a 001yy 200 1 $aPrinciples and applications of paper electrophoresis$fby Ch. Wunderly$gwith a foreword by P. König 210 $aAmsterdam [etc.]$cElsevier$d©1961 215 $aXII, 253 p.$cill.$d19 cm 225 1 $aElsevier Monographs. Chemistry section$v11$aElsevier publishing company$c$3IT\ICCU\MILV\023317 314 $aProfessor, Chemistry Faculty, University of Cincinnati, Cincinnati, Ohio, U.S.A.$9IT\ICCU\AQ1V\002812 314 $aMember of scientific Staff, Medical University Clinic, Zurich, Switzerland$9IT\ICCU\TSAV\010387 314 $aPioneer of paper electrophoresis, São Paulo, Brasil$9IT\ICCU\UBOV\692684 676 $a631$v22$zita 700 1$aWunderly,$bCharlie$0313555 702 1$aOesper,$bRalph Edward$f<1886-1977> 702 1$aKönig,$bPaul$c 801 0$aIT$bUNINA$gREICAT$2UNIMARC 901 $aBK 912 $a9910801895403321 952 $aA PAT 947$b694/2024$fFAGBC 959 $aFAGBC 996 $aPrinciples and applications of paper electrophoresis$93877185 997 $aUNINA LEADER 04911nam 22005535 450 001 9911007465103321 005 20250630210209.0 010 $a3-031-85967-7 024 7 $a10.1007/978-3-031-85967-0 035 $a(CKB)39124603400041 035 $a(DE-He213)978-3-031-85967-0 035 $a(MiAaPQ)EBC32145025 035 $a(Au-PeEL)EBL32145025 035 $a(EXLCZ)9939124603400041 100 $a20250530d2025 u| 0 101 0 $aeng 135 $aur||||||||||| 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 10$aAtlas of Interstitial Lung Disease Pathology $eWith High Resolution CT Correlations /$fby Andrew Churg, Nestor L. Müller 205 $a3rd ed. 2025. 210 1$aCham :$cSpringer Nature Switzerland :$cImprint: Springer,$d2025. 215 $a1 online resource (XVI, 300 p. 419 illus., 336 illus. in color.) 311 08$a3-031-85966-9 327 $aGeneral Approach to Interstitial Lung Disease: Clinical, Radiologic, and Pathologic Considerations -- Imaging in Interstitial Lung Disease -- Biopsy Choices and Handling in Interstitial Lung Disease -- Acute Interstitial Pneumonia (AIP) -- Organizing Pneumonia (OP) -- Usual Interstitial Pneumonia (UIP) -- Nonspecific Interstitial Pneumonia (NSIP) -- Respiratory Bronchiolitis with Interstitial Lung Disease (RBILD), Smoking-Related Interstitial Fibrosis (SRIF), and Desquamative Interstitial Pneumonia (DIP) -- Combined Pulmonary Fibrosis with Emphysema -- Langerhans Cell Histiocytosis -- Introduction to Granulomatous Forms of Interstitial Lung Disease -- Hypersensitivity Pneumonitis -- Sarcoid -- Miscellaneous Granulomatous Forms of Interstitial Lung Disease -- Eosinophilic Pneumonias -- Pulmonary Alveolar Proteinosis -- Lymphangioleiomyomatosis -- Drug Reactions Producing Interstitial Lung Disease -- Lymphoid and Hematopoietic Processes Producing a Pattern of Interstitial Lung Disease -- Bronchiolitis -- Interstitial Lung Disease in Patients with Connective tissue Diseases and Interstitial Pneumonias with Autoimmune Features -- Pneumoconioses Producing a Pattern of Interstitial Lung Disease -- Mimics of Interstitial Lung Disease. 330 $aThis objective of this atlas is to serve as an updated diagnostic resource that allows pathologists to diagnose interstitial lung disease (ILD) when they encounter it in biopsies. Pathologists often struggle in this area due to the numerous different and sometimes overlapping entities encompassed by term ?ILD?. ILD pathology is unique in that diagnostic accuracy always requires correlation with the clinical and particularly the radiologic findings. This is different from most areas of pathology in which only minimal clinical/radiologic information will allow an accurate diagnosis. By including CT findings, pathologists will know what to look for in radiology reports or when talking with radiologists. A further recent development has been the increasingly widespread use of transbronchial cryobiopsy for diagnosing interstitial lung disease. What is becoming evident, however, is that there is astonishingly little in the way of pathologic guidance for making diagnoses with cryobiopsies, and pathologists struggle with them. Advances in understanding the genetics of ILD have led to realization that there are major overlaps in the genetic abnormalities associated with a UIP pattern, even if the underlying disease is fibrotic hypersensitivity pneumonitis or connective tissue disease. A new idea is that of telomeropathy; i.e. the finding that patients with short telomeres are particularly likely to develop fibrotic lung disease, and, most importantly, should not be treated with immunosuppressive agents. Atlas of Interstitial Lung Disease: Pathology with High Resolution CT Correlations 3rd Edition is primarily directed toward non-expert pathologists who encounter interstitial lung disease specimens, as well as radiologists who want some understanding of the pathologic basis for the imaging findings. The book incorporates current clinical/radiological/pathologic guidelines and provides information on how to apply them to biopsy specimens. 606 $aPathology 606 $aRespiratory organs$xDiseases 606 $aRadiology 606 $aPathology 606 $aPneumology 606 $aRadiology 615 0$aPathology. 615 0$aRespiratory organs$xDiseases. 615 0$aRadiology. 615 14$aPathology. 615 24$aPneumology. 615 24$aRadiology. 676 $a616.07 700 $aChurg$b Andrew$4aut$4http://id.loc.gov/vocabulary/relators/aut$0918367 702 $aMüller$b Nestor L$4aut$4http://id.loc.gov/vocabulary/relators/aut 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9911007465103321 996 $aAtlas of Interstitial Lung Disease Pathology$92962042 997 $aUNINA