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Amyloid and Related Disorders (Record no. 19783)

000 -LEADER
fixed length control field 06747nam a22004695i 4500
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20140310150647.0
007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION
fixed length control field cr nn 008mamaa
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 120331s2012 xxu| s |||| 0|eng d
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9781607613893
978-1-60761-389-3
050 #4 - LIBRARY OF CONGRESS CALL NUMBER
Classification number RB1-214
082 04 - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 616.07
Edition number 23
264 #1 -
-- Totowa, NJ :
-- Humana Press,
-- 2012.
912 ## -
-- ZDB-2-SME
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Picken MD, PhD, FASN, Maria M.
Relator term editor.
245 10 - IMMEDIATE SOURCE OF ACQUISITION NOTE
Title Amyloid and Related Disorders
Medium [electronic resource] :
Remainder of title Surgical Pathology and Clinical Correlations /
Statement of responsibility, etc edited by Maria M. Picken MD, PhD, FASN, Ahmet Dogan, M.D., Ph.D., Guillermo A. Herrera, M.D.
300 ## - PHYSICAL DESCRIPTION
Extent XVIII, 425p. 223 illus., 180 illus. in color.
Other physical details online resource.
440 1# - SERIES STATEMENT/ADDED ENTRY--TITLE
Title Current Clinical Pathology
505 0# - FORMATTED CONTENTS NOTE
Formatted contents note Aspects of the History and Nomenclature of Amyloid and Amyloidosis.-Amyloid Diseases at the Molecular Level: General Overview and Focus on AL Amyloidosis -- AA Amyloidosis -- The Hereditary Amyloidoses -- Dialysis-Associated Amyloidosis -- Localized Amyloidoses and Amyloidoses Associated with Aging Outside the Central Nervous System -- Cerebrovascular Amyloidoses -- Differential Diagnosis of Amyloid in Surgical Pathology: Organized Deposits and Other Material in the Differential Diagnosis of Amyloidosis -- Light / Heavy Chain Deposition Disease as a Systemic Disorder -- Glomerulonephritis with Non-Organized Monoclonal Immunoglobulin Deposits -- Pathologies of Renal and Systemic Intracellular Paraprotein Storage: Crystalopathies and Beyond -- Diagnosis of Amyloid Using Congo Red -- Diagnosis of Minimal Amyloid Deposits using the Congo Red Fluorescence Method -- Thioflavin T stain -- Fat Tissue Analysis in the Management of Patients with Systemic Amyloidosis -- Generic Diagnosis of Amyloid -- Routine Use of Amyloid Typing on Formalin-fixed Paraffin Sections from 626 Patients by Immunohistochemistry -- Amyloid Typing.-Options for Amyloid Typing in Renal Pathology -- Amyloid Typing: Immuno-Electron Microscopy -- Classification of Amyloidosis by Mass Spectrometry Based Proteomics -- Laboratory Support for Diagnosis of Amyloidosis -- Bone Marrow Biopsy and Its Utility in the Diagnosis of AL Amyloidosis and Other Plasma Cell Dyscrasias -- Laboratory Methods for the Diagnosis of Hereditary Amyloidoses -- Amyloidoses of the Kidney and Genitourinary Tract -- Cardiac Amyloidoses -- Amyloidosis of the Gastrointestinal Tract and Liver -- Peripheral Nerve Amyloidosis -- Clinical and Pathologic Issues in Patients with Amyloidosis -- Emerging Therapies for Amyloidosis -- Modern Therapies in AA Amyloidosis -- Medicolegal Issues of Amyloidosis -- Amyloidosis from the Patient’s Perspective. Aspects of the History and Nomenclature of Amyloid and Amyloidosis.-Amyloid Diseases at the Molecular Level: General Overview and Focus on AL Amyloidosis -- AA Amyloidosis -- The Hereditary Amyloidoses -- Dialysis-Associated Amyloidosis -- Localized Amyloidoses and Amyloidoses Associated with Aging Outside the Central Nervous System -- Cerebrovascular Amyloidoses -- Differential Diagnosis of Amyloid in Surgical Pathology: Organized Deposits and Other Material in the Differential Diagnosis of Amyloidosis -- Light / Heavy Chain Deposition Disease as a Systemic Disorder -- Glomerulonephritis with Non-Organized Monoclonal Immunoglobulin Deposits -- Pathologies of Renal and Systemic Intracellular Paraprotein Storage: Crystalopathies and Beyond -- Diagnosis of Amyloid Using Congo Red -- Diagnosis of Minimal Amyloid Deposits using the Congo Red Fluorescence Method -- Thioflavin T stain -- Fat Tissue Analysis in the Management of Patients with Systemic Amyloidosis -- Generic Diagnosis of Amyloid -- Routine Use of Amyloid Typing on Formalin-fixed Paraffin Sections from 626 Patients by Immunohistochemistry -- Amyloid Typing.-Options for Amyloid Typing in Renal Pathology -- Amyloid Typing: Immuno-Electron Microscopy -- Classification of Amyloidosis by Mass Spectrometry Based Proteomics -- Laboratory Support for Diagnosis of Amyloidosis -- Bone Marrow Biopsy and Its Utility in the Diagnosis of AL Amyloidosis and Other Plasma Cell Dyscrasias -- Laboratory Methods for the Diagnosis of Hereditary Amyloidoses -- Amyloidoses of the Kidney and Genitourinary Tract -- Cardiac Amyloidoses -- Amyloidosis of the Gastrointestinal Tract and Liver -- Peripheral Nerve Amyloidosis -- Clinical and Pathologic Issues in Patients with Amyloidosis -- Emerging Therapies for Amyloidosis -- Modern Therapies in AA Amyloidosis -- Medicolegal Issues of Amyloidosis -- Amyloidosis from the Patient’s Perspective.
520 ## - SUMMARY, ETC.
Summary, etc Abnormal proteins are known to be associated with various pathologies. Most notably, these include amyloidoses, monoclonal protein deposits associated with plasma cell dyscrasia/multiple myeloma, cryoglobulins and various related organized and non-organized deposits. Amyloid and Related Disorders presents an overview of the most recent developments in this area including clinical presentation, etiology, pathogenesis, and differential diagnosis. The rationale for various therapies, including transplantation, is discussed and tissue diagnosis (its pitfalls and strategies for avoiding them) and laboratory support are included.   The involvement of all major organ systems including renal/genitourinary, cardiac, gastrointestinal, pulmonary, peripheral nerve/central nervous system, soft tissue and bone marrow pathology is covered.  This approach provides a unifying concept of these pathologic processes, which have systemic involvement, and which have, hitherto, not been universally appreciated. Awareness of these diseases among a wider audience of pathologists may increase the rate of their diagnosis as well as that of earlier diagnosis. This volume will be invaluable to specialized and general pathologists as well as cytopathologists; other medical professionals may also benefit from this concise update on the systemic amyloidoses.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Medicine.
Topical term or geographic name as entry element Internal medicine.
Topical term or geographic name as entry element Nephrology.
Topical term or geographic name as entry element Pathology.
Topical term or geographic name as entry element Medicine & Public Health.
Topical term or geographic name as entry element Pathology.
Topical term or geographic name as entry element Nephrology.
Topical term or geographic name as entry element Internal Medicine.
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Dogan, M.D., Ph.D., Ahmet.
Relator term editor.
Personal name Herrera, M.D., Guillermo A.
Relator term editor.
710 2# - ADDED ENTRY--CORPORATE NAME
Corporate name or jurisdiction name as entry element SpringerLink (Online service)
773 0# - HOST ITEM ENTRY
Title Springer eBooks
776 08 - ADDITIONAL PHYSICAL FORM ENTRY
Display text Printed edition:
International Standard Book Number 9781607613886
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier http://dx.doi.org/10.1007/978-1-60761-389-3
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme
Item type E-Book
Copies
Price effective from Permanent location Date last seen Not for loan Date acquired Source of classification or shelving scheme Koha item type Damaged status Lost status Withdrawn status Current location Full call number
2014-04-07AUM Main Library2014-04-07 2014-04-07 E-Book   AUM Main Library616.07
Languages: 
English |
العربية