Amyloid and Amyloidosis
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Front Matter....Pages i-xx Front Matter....Pages 1-1 A Brief History of International Symposia on Amyloidosis....Pages 3-8 Statistical Analysis of Amyloid Activities Since 1950 — Basis for an Autonomous Journal....Pages 9-14 Front Matter....Pages 15-15 Anti-Casein Antibodies in the Serum of Patients with Al Amyloidosis....Pages 17-22 Experimental Systemic Amyloidosis in Mice-Induction of Amyloidosis by Immunization with Syngeneic Organ Extracts and Immunological Investigation....Pages 23-28 Secondary Amyloidosis Associated with Chronic Arthritis in Rabbits....Pages 29-34 Cloning and Sequence Analysis of cDNAs Encoding Mouse C-Reactive Protein....Pages 35-40 Systemic Amyloidosis: Tissue Specific Variability in the Primary Structure of Amyloid Proteins....Pages 41-43 Fourier Transform Infrared Spectroscopy of Air-Dried and Heavy Water Suspended AA and AL Amyloid Fibril Preparations of Different Species....Pages 45-50 Replacement of SAA from the HDL-SAA Complex by APO AI and APO AII: HDL has Higher Binding Capacity for SAA than for AA....Pages 51-56 apoSAA and AA: Precursor and Product Revisited....Pages 57-62 SAA2 Deposition in the Spleen of the Mouse....Pages 63-68 In Vitro Formation of Amyloid Fibrils from Murine Serum Amyloid a Protein (SAA)....Pages 69-73 Induced AA Amyloid in Hamster: On the Amyloid Enhancing Factor and Protein AA-Cross Reacting Components of Intermediate Molecular Weight....Pages 75-80 Deposition of Amyloid a Fibrils in Spleen is Accompanied by Decreased Hepatic and Splenic and Increased Macrophage Serum Amyloid a Expression....Pages 81-86 Immunolocalization of Heparan Sulfate Proteoglycans to AA Amyloid Deposition Sites in Spleen and Liver During Experimental Amyloidosis....Pages 87-93 Renal Peritubular Amyloid Deposition in the Experimental Murine Amyloidosis....Pages 95-100 Ultrastructural Study of the Spleen in Experimental Murine Amyloidosis Using the Protein A-Gold Immunocytochemical Technique....Pages 101-106 Experimental Amyloidosis of Rabbit Induced by Saponin....Pages 107-112 Ultrastructural Investigation of Spontaneously Occurring Amyloidosis in White Pekin Ducks....Pages 113-118 Enhanced Degradation of Serum Amyloid Protein SAA in vivo by Proteolytic Enzymes....Pages 119-124 Front Matter....Pages 15-15 Degradation Studies on Plasma Prealbumin....Pages 125-130 Protease and Protease Inhibitors in Familial Amyloidotic Polyneuropathy....Pages 131-135 A Study of Dipeptidyl Aminopeptidase IV in the Sera of Japanese FAP Patients....Pages 137-142 Front Matter....Pages 143-143 Primary Structure of A V K II Light Chain from a Patient with Amyloid Arthropathy....Pages 145-150 Molecular Heterogeneity of Amyloid Fibril Proteins in Primary Amyloidosis....Pages 151-156 The Amino Acid Sequence of a Carbohydrate-Containing Immuno-Globulin-Light-Chain-Type Amyloid Fibril Protein (AL)....Pages 157-162 Structural Analysis of a Lambda IV Primary Amyloid Protein....Pages 163-168 AL Amyloidosis (MIY) with Intestinal Tract Involvements and the Chemical Analysis of its BJP (MIY, NIG-84)....Pages 169-173 Lambda Predominance of Bence Jones Protein (BJP) in AL Amyloidosis Among Japanese Patients....Pages 175-178 Immunohistochemical Typing of Tissues from 100 Patients with Systemic Amyloidosis....Pages 179-184 Expression of Plasma Cell-Associated Non-Light Chain Antigens in Patients with Plasma Cell Dyscrasia and Amyloidosis....Pages 185-190 Use of Various Electroimmune Techniques in the Diagnosis and Follow-Up of Patients with AL Amyloidosis....Pages 191-196 Front Matter....Pages 197-197 The Structure of Protein AA and its Correlation to the Tissue Distribution of Amyloid....Pages 199-203 Amino Acid Sequence Composition of AA Amyloid Fibrils in Cystic Fibrosis....Pages 205-209 Phylogenetic Analysis of Amyloid a Protein....Pages 211-216 Characterization of Serum Amyloid a (SAA) Protein in the Sheep....Pages 217-222 Structural Studies of SAA and AA from Horse and Cow....Pages 223-228 SAA Versus CRP Serum Levels in Different Inflammatory Conditions, Studied by Elisa Using Polyclonal Anti-AA and Monoclonal Anti-SAA Antibodies....Pages 229-233 Monoclonal Antibody to SAAL 1–3 Isomer Better Discriminant of the Acute Phase Reaction to Cancer and Monitor of Disease Progression than the Polyclonal Antibody to Human AA....Pages 235-240 Monoclonal Antibody Against Synthesized Short Peptides Corresponding to Human Amyloid a Protein....Pages 241-246 Front Matter....Pages 197-197 Diagnosis of AA-Amyloidosis Using Monoclonal Antibodies: Application to Paraffin and Ultrathin Sections as Well as to Urinary Sediments....Pages 247-252 Influence of Serum Amyloid A on Human Lecithin : Cholesterol Acyltransferase Activity....Pages 253-258 Structure and Variation in the Human Serum Amyloid A Gene Family....Pages 259-263 Serum Amyloid A: Characterization of Three cDNAS in One Individual and Complete Structure of their Corresponding Protein Products....Pages 265-269 Regulation of Human SAA Gene Expression....Pages 271-276 Localization of Amyloid SAA Gene Expression in Mouse Liver by in Situ Hybridization....Pages 277-282 Rat Liver and Lung Express Serum Amyloid A Related mRNAs....Pages 283-287 Identification of Cells Expressing SAA 3 mRNA by in Situ Hybridization....Pages 289-292 Diverse Gene Structure for Serum Amyloid a Protein in Wild Mice....Pages 293-297 Front Matter....Pages 299-299 Two New DNA-Based Tests for Mutations Causing Familial Amyloidotic Polyneuropathy....Pages 301-305 Epitope Mapping of TTR (Prealbumin) and TTR(Met 30 ) with Monoclonal Antibodies....Pages 307-310 Amyloid Fibril Formation by Polymerization of Abnormal Transthyretin....Pages 311-316 Demonstration of Transthyretin (Prealbumin) Variants in Italian Kindreds with Familial Amyloidotic Polyneuropathy....Pages 317-321 Abnormal Transthyretin in Familial Amyloidotic Polyneuropathy in Japan and Sweden....Pages 323-328 Elderly Asymptomatic Carriers and Late-Onset Cases of Familial Amyloidotic Polyneuropathy Detected by Radioimmunoassay....Pages 329-334 Studies on the Fate of Normal and Variant Prealbumin in the Circulation....Pages 335-341 Studies on Transthyretin Metabolism in the Nervous System....Pages 343-348 Alpha-Adrenergic Receptors in Familial Amyloidotic Polyneuropathy....Pages 349-354 DNA Tests for Four Prealbumin Mutations in Hereditary Amyloidosis....Pages 355-360 Prealbumin Gene Expression in Control Subjects and Individuals with Familial Amyloidotic Polyneuropathy....Pages 361-364 Front Matter....Pages 299-299 Diagnosis of Familial Amyloid Polyneuropathy by Recombinant DNA Techniques in Relation with Clinical Features....Pages 365-370 Haplotype Analisis of Familial Amyloidotic Polyneuropathy: an Evidence for Multiple Origins of the Val→met Mutation....Pages 371-376 DNA Polymorphisms Analysis in Families with Familial Amyloidotic Polyneuropathy (FAP) from Different Ethnic Origins....Pages 377-382 RFLP Analysis of Mutated Transthyretin in Vitreous Amyloidosis....Pages 383-386 Familial Amyloidotic Polyneuropathy in Sweden — RFLP Analysis in Patients and in Healthy Controls....Pages 387-392 A Potential Animal Model for Familial Amyloidotic Polyneuropathy Through Introduction of Human Mutant Transthyretin Gene Into Mice....Pages 393-398 Toward Establishment of an Animal Model for Familial Amyloidotic Polyneuropathy: Generation and Characterization of Transgenic Mice....Pages 399-404 Localization of Prealbumin mRNA in Fetal and Adult Mice....Pages 405-409 Front Matter....Pages 411-411 Is the Homozygous State for Hereditary Amyloid Neuropathy (HAN) — Type I (Portuguese, Andrade) Incompatible with Early Intrauterine Life?....Pages 413-418 Familial Amyloid Polyneuropathy: A Clinical Scale for the Evaluation of the Peripheral Neuropathy....Pages 419-423 Familial Amyloidotic Polyneuropathy: Screening of the Population at Risk in Portugal....Pages 425-428 Familial Amyloid Polyneuropathy (Portuguese Type): Study of Asymptomatic Carriers....Pages 429-434 Late-Onset Forms of Familial Amyloid Polyneuropathy (Portuguese Type): A Reappraisal....Pages 435-439 Genetic Study of Late-Onset in Hereditary Amyloid Neuropathy (HAN) — Type I (Portuguese, Andrade)....Pages 441-446 Genetic Expression of a Variant Prealbumin in Typical and Late-Onset Japanese Family with Familial Amyloidotic Polyneuropathy....Pages 447-451 Natural History of the ECG Abnormalities in FAP Portuguese Type: A Follow-Up Study with ECG, Holter Monitoring and Intracardiac Electrophysiological Study....Pages 453-457 Development of High-Grade Ventricular Arrhythmias in Familial Amyloid Polyneuropathy....Pages 459-464 Early Detection of Amyloid Heart Disease by Technetium-99M-Pyrophosphate Single-Photon Emission-Computed Tomography : A Study with Familial Amyloid Polyneuropathy....Pages 465-469 Impaired Left Ventricular Diastolic Properties in Patients with Familial Amyloid Polyneuropathy : A Study by Computerized M-Mode Echocardiography....Pages 471-473 Noninvasive Evaluation of Left Ventricular Systolic and Diastolic Time Intervals in Familial Amyloid Polyneuropathy....Pages 475-480 Front Matter....Pages 411-411 Molecular Analysis of a Variant Type of Familial Amyloidotic Polyneuropathy (FAP) Showing Cerebellar Ataxia and Pyramidal Tract Signs....Pages 481-486 Morphometric Study on Changes in Sural Nerves and Comparison with Clinical Manifestations in Familial Amyloidosis....Pages 487-491 Sural Nerve Biopsy in Familial Amyloidotic Polyneuropathy: A Morphological and Morphometric Polyneuropathy....Pages 493-498 Clinicopathological Studies on Nephropathy of Familial Amyloid Polyneuropathy in Japan....Pages 499-504 Pathology of Familial Amyloidotic Polyneuropathy Occurring in Kumamoto....Pages 505-510 Pathological Sutdies on Familial Amyloidosis....Pages 511-516 Front Matter....Pages 517-517 A Unique Protein that Shares a Common Epitope with Senile Plaque in Alzheimer’s Disease Brain....Pages 519-523 Preparation of a Monoclonal Antibody Against a Synthetic Brain Amyloid Beta Peptide(N1–10) and Distribution of an Immunoreactivity in Serum....Pages 525-530 Biochemical and Molecular Studies of Native and Synthetic B-Amyloid Protein in Alzheimer’s Disease....Pages 531-536 β-Amyloid cDNA Cloned from Alzheimer’s Disease Brain....Pages 537-541 α-1-Antichymotrypsin, a Serine Protease Inhibitor, is a Component of the Amyloid Deposits in Alzheimer’s Disease....Pages 543-548 Immunohistochemical Study of Alzheimer Disease Using Antibodies to Synthetic Amyloid and Fibronectin....Pages 549-553 Monoclonal Antibody AM34 Detects New Proteins Associated with Secondary Amyloidosis....Pages 555-560 Corpora Amylacea in Aging and Alzheimer’s Brain: Immunolocalization of Chondroitin Sulfate and Heparan Sulfate Proteoglycans....Pages 561-566 Ubiquitin: A Newly Identified Component of Paired Helical Filaments....Pages 567-572 Ultrastructure of Amyloid Fibrils in Alzheimer’s Disease and Down’s Syndrome....Pages 573-578 An Isolate of Families with Hereditary Cystatin C Amyloid Angiopathy and Cerebral Haemorrhage in the South of Iceland....Pages 579-584 Distribution of Cystatin C Amyloid Deposits in the Icelandic Patients with Hereditary Cystatin C Amyloid Angiopathy....Pages 585-590 Studies on the Cystatin C Gene in Patients with Hereditary Cystatin C Amyloid Angiopathy (HCCAA) with Cerebral Haemorrhage....Pages 591-596 Possibly “Familial” Cerebral Amyloid Angiopathy in Japan: Immunohistochemical Identification of Gamma-Trace....Pages 597-602 Front Matter....Pages 603-603 Beta-2 Microglobulin Amyloidosis....Pages 605-610 Chemical Analysis of Beta 2 -Microglobulin Derived Amyloid in Patients on Long-Term Hemodialysis....Pages 611-616 Coexistence of B 2 -Microglobulin-Derived Amyloid Deposits and Ectopic Calcification in the Heart of a Chronic Hemodialysis Patient....Pages 617-622 β 2 -Microglobulin Binding to Collagen : An Amyloidogenic Factor in Chronic Hemodialysis Patients....Pages 623-627 New Adsorbents for Extracorporeal Removal of β 2 -Microglobulin....Pages 629-634 Characterization of a Prealbumin Variant in Familial Amyloid Cardiomyopathy of Danish Origin....Pages 635-640 Senile Cardiovascular Amyloid: Lack of Evidence for Differences Between Amyloid Fibril Protein and Normal Transthyretin....Pages 641-645 Amyloid Fibril Protein in Finnish Hereditary Amyloidosis....Pages 647-652 Biochemical Characterization of Amyloid Protein in Primary Lichen Amyloidosis....Pages 653-656 Immunological Examination of Senile Amyloidosis of the Temporal Artery....Pages 657-659 Isolated Atrial Amyloid (IAA): A Cardiac Amyloid of Endocrine Origin....Pages 661-666 The Nature of the Amyloid in the Islets of Langerhans: A Novel Polypeptide Hormone?....Pages 667-671 Relationships of Islet Amyloid Polypeptide (IAPP) to Spontaneous Diabetes in Adult Cats....Pages 673-678 Serum Clearance Rate of Senile Amyloid Related Apolipoprotein A-II is Accelerated with Increasing Age in Senescence Accelerated Mouse (SAM)....Pages 679-683 AS SAM Amyloidosis is Present in Aging Mice of Many Strains, not Only in SAM....Pages 685-690 Immunohistochemical Studies of Age-Associated Amyloid Deposition in the Joint of Senescence-Accelerated Mouse (SAM)....Pages 691-694 Biochemical and Genetic Characterization of Murine Senile Amyloidosis....Pages 695-700 Front Matter....Pages 701-701 Possible Derivation of Cutaneous Amyloid from Degenerating Collagen Fibers: Ultrastructural, Immunohistological Studies Employing Anticollagen Antibodies....Pages 703-708 Immunohistochemical Staining Properties of Cutaneous Amyloidosis Using Anti-Keratin Monoclonal Antibodies....Pages 709-713 Reactivity of Immunoglobulins on Amyloid in Lichenoid and Macular Amyloidoses with Epidermal Keratin....Pages 715-720 Front Matter....Pages 701-701 Amyloid Deposition and Elastic Fiber in Cutaneous Amyloidosis....Pages 721-726 Amyloid in the Skin of Patients Undergoing Long-Term Hemodialysis....Pages 727-730 Histochemical and Ultrastructural Studies on the Pigment Abnormality in Cutaneous Amyloidosis....Pages 731-736 Hepatic Amyloidosis (AL): The Natural History in 80 Patients....Pages 737-742 Gastrointestinal Manifestations in Systemic Amyloidosis....Pages 743-748 Amyloid Localized to Tenosynovium at Carpal Tunnel Release: The Natural History of 124 Cases....Pages 749-754 Analysis of Paraproyein Deposition in the Kidney: Therapeutic Approach to Renal Amyloidosis....Pages 755-758 Immunohistochemical and Ultrastructural Studies of Amyloid Deposition in Squamous Cell Carcinoma of Uterine Cervix....Pages 759-764 An Autopsy Case of Recessive Dystrophic Epidermolysis Bullosa Complicating Secondary Systemic Amyloidosis....Pages 765-769 Systemic Amyloidosis Associated with Giant Lymph Node Hyperplasia....Pages 771-776 Amyloidosis Associated with Systemic Lupus Erythematosus....Pages 777-782 An Autopsied Case of Systemic Light Chain Deposition Disease (LCDD): The Relationship between LCDD and AL Amyloidosis....Pages 783-788 Immunohistochemical Classification of Amyloidosis and Immunohistochemistry of Fibrillar Nephropathy on Routinely Processed Plastic-Embedded Tissues....Pages 789-794 Histologic Characterization of Amyloidosis Based on Amyloid Proteins....Pages 795-799 The Subcutaneous Fat Aspirate: A Controlled and Blinded Evaluation of the Technique in the Diagnosis of Primary Amyloidosis (AL)....Pages 801-805 Three-Dimensional Analysis of Heart and Kidney in Primary Amyloidosis with Neural Involvement....Pages 807-812 Front Matter....Pages 813-813 DMSO Therapy Using Dermal Application to Patients with Systemic Amyloidosis....Pages 815-819 Systemic Amyloidosis: A Clinical Survey of 162 Cases....Pages 821-826 Natural History of Ogawa Village Type Familial Amyloid Polyneuropathy in Japan....Pages 827-832 Colchicine Analogues in Experimental Murine Amyloidogenesis....Pages 833-837 Front Matter....Pages 813-813 Evaluation of Serum Variant Prealbumin Levels, and its Behavior after Plasma Exchange for Familial Amyloidotic Polyneuropathy (Type 1)....Pages 839-844 Periodic Plasma Exchanges in the Treatment of Familial Amyloid Polyneuropathy: Preliminary Results....Pages 845-849 Treatment of Autonomic Dysfunction with L-Threo-3,4-Dihydroxyphenylserine in Patients with Familial Amyloidotic Polyneuropathy: A Multicenter Study....Pages 851-856 Treatment of Autonomic Disorders of Familial Amyloid Polyneuropathy with L-Threo-3,4-Dihydroxyphenyserine....Pages 857-861 Treatment of Orthostatic Hypotension in Familial Amyloidotic Polyneuropathy with L-Threo-3,4-Dihydroxyphenylserine....Pages 863-868 Insulin for Nausea in Familial Amyloid Polyneuropathy....Pages 869-874 Pacemaker Treatment in Familial Amyloid Polyneuropathy....Pages 875-877 Back Matter....Pages 879-885
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