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.