Geometry.Net - Health_Conditions: Amyloidosis

Florida State University College Of Medicine Digital Library
amyloidosis Clinical Resources. All MD Consult Reference Books for. The Merck Manual17th Ed.1999 Table of contents Chapter 18 amyloidosis Table of contents
http://fsumed-dl.slis.ua.edu/clinical/nephrology/glomerulonephritis/multisystem/

Extractions: Clinical Resources by Topic: Nephrology Amyloidosis Clinical Resources Pediatrics Geriatrics Atlases Radiology ... Miscellaneous Resources See also: Chapter 273: Pathogenesis of Glomerular Injury Table of contents Nonimmunologic Glomerular Injury: Access document Glomerular Adaptation to Nephron Loss: Access document Chapter 275: Glomerulopathies Associated with Multisystem Diseases: Table of contents Hoffman: Hematology: Basic Principles and Practice 3rd Ed.-2000 (MD Consult):
Florida State University College Of Medicine Digital Library
amyloidosis Patient/Family Resources. Miscellaneous. Miscellaneous amyloidosisPatients/Family Resources Healthfinder (US DHHS) Homepage
http://fsumed-dl.slis.ua.edu/patientinfo/nephrology/glomerulonephritis/multi/amy

Extractions: Patient/Family Resources by Topic: Nephrology Amyloidosis Patient/Family Resources Spanish Miscellaneous See also: National Institute of Diabetes and Digestive and Kidney Diseases: Homepage MEDLINE plus Medical Encyclopedia: Table of contents Spanish Miscellaneous Amyloidosis Patients/Family Resources YAHOO - Health:Diseases and Conditions:Amyoidosis
Health Information Resource Database: Amyloidosis Network International, Inc.
amyloidosis Network International, Inc. Abstract. The amyloidosis Network is an informalsupport and information group organized in 1988 by Donald Rasmussen.
http://www.health.gov/NHIC/NHICScripts/Entry.cfm?HRCode=HR2397
Amyloidosis
amyloidosis. Image URL Amyloid, Image URL Amyloid, Image URL Amyloid deposits inglomerulus, Image URL amyloidosis, Image URL amyloidosis, Image URL amyloidosis,
http://www.brisbio.ac.uk/ROADS/subject-listing/amyloidosis.html

Extractions: A collection of medical, dental and veterinary images for use in teaching. Home About the Archive FAQ Terms and Conditions ... Help Amyloid Amyloid Amyloid deposits in glomerulus Amyloid in cortex Amyloid in islets Amyloid in kidney Amyloid in kidney Amyloid in left ventricle Amyloid in liver Amyloid in von Meyenburg complex Amyloidosis Amyloidosis Amyloidosis Amyloidosis Amyloidosis Amyloidosis Amyloidosis Amyloidosis Amyloidosis Amyloidosis Amyloidosis Amyloidosis Amyloidosis Amyloidosis Amyloidosis Amyloidosis and myeloma Amyloidosis in tubules Amyloidosis of tongue Amyloidosis with cholesterolosis Amyloidosis with cholesterolosis Amyloidosis with myeloma Amyloidosis with myeloma Amyloidosis Carcinoid vascular amyloid Carcinoid vascular amyloid Carcinoid vascular amyloid Carcinoid vascular amyloid Cardiac amyloid Generalised primary amyloid Hydronephrosis Nodular amyloidosis Nodular amyloidosis Nodular amyloidosis of perineum Primary amyloid Primary amyloid Primary amyloid Primary amyloid Primary amyloid Primary amyloid Primary amyloid Primary amyloid Primary amyloid Primary amyloid Primary amyloid Pulmonary arterial thrombus Renal amyloidosis Renal amyloidosis Secondary amyloid after bronchiectasis Secondary amyloidosis Severe amyloidosis Severe amyloidosis Strumal ovarian carcinoid Ventricular amyloid stained with iodine
Avera Health - Cardiac Amyloidosis
Cardiac amyloidosis. Cardiac amyloidosis is a disorder caused by deposits of anabnormal protein in the heart tissue, resulting in decreased heart function.
http://www.avera.org/adam/ency/article/000193.htm

Extractions: Different types of amyloidosis are caused by different types of proteins, such as "AL" and "AA." In cardiac amyloidosis there may be associated conduction disturbances (changes in the way the cardiac electrical impulse is transmitted through the heart). Cardiac amyloidosis usually occurs during primary amyloidosis (called AL type amyloidosis). Primary amyloidosis usually accompanies multiple myeloma, a blood disorder in which too much of a certain type of protein is produced. This excess protein is deposited in the heart and in other organs such as the kidney. Deteriorating kidney function also occurs. The heart is less frequently compromised by secondary amyloidosis (called AA type amyloidosis). Senile amyloidosis, however, is a type of secondary amyloidosis which does involve the heart. It is caused by overproduction of a protein different from both the AA and AL types. This particular protein is deposited mainly in the heart, but it can also infiltrate blood vessels. Senile cardiac amyloidosis is becoming more common as the average age of the population increases.
Genesis Health System - Detailed Disease Info - Amyloidosis
amyloidosis. Definition. Types of amyloidosis. The major forms of this diseaseare primary systemic, secondary, and familial or hereditary amyloidosis.
http://www.genesishealth.com/micromedex/detaileddisease/00037170.aspx

Extractions: Facility Information DeWitt Comm Hosp Genesis Medical Ctr Illini Hospital Genesis Health Grp VNA Amyloidosis is a progressive, incurable, metabolic disease characterized by abnormal deposits of protein in one or more organs or body systems. Amyloid proteins are manufactured by malfunctioning bone marrow. Amyloidosis, which occurs when accumulated amyloid deposits impair normal body function, can cause organ failure or death . It is a rare disease, occurring in about eight of every 1,000,000 people. It affects males and females equally and usually develops after the age of 40. At least 15 types of amyloidosis have been identified. Each one is associated with deposits of a different kind of protein. The major forms of this disease are primary systemic, secondary, and familial or hereditary amyloidosis. There is also another form of amyloidosis associated with Alzheimer's disease Primary systemic amyloidosis usually develops between the ages of 50 and 60. With about 2,000 new cases diagnosed annually, primary systemic amyloidosis is the most common form of this disease in the United States. Also known as light-chain-related amyloidosis, it may also occur in association with multiple myeloma (bone marrow cancer).
Amyloidosis
amyloidosis. What is it? Who gets it? amyloidosis occurs in only eightof every one million people. Symptoms usually occur after age 40.
http://www.hmc.psu.edu/healthinfo/a/amyloidosis.htm
ESynopsis Of Amyloidosis Of The Kidney
eSynopsis of amyloidosis of Kidney From the Electonic Synopsis of Pathology, theUniversity of Connecticut School of Medicine, Department of Pathology.
http://esynopsis.uchc.edu/S264.htm
MSN Health -
amyloidosis Important It is possible that the main title of the reportamyloidosis is not the name you expected. Please check the
http://content.health.msn.com/NR/internal.asp?GUID={E6072C1F-29B8-4DD3-A4FB-E3B5
VETERINARY INFORMATION SERVICE
VETERINARY INFORMATION SERVICE. Familial amyloidosis in Abyssinian Cats. Mostamyloidosis is etiopathic; that is no underlying cause can be found.
http://www.pressenter.com/~dvmvis/amyloid.htm
Human Immunology And Cancer Program-Primary Systemic Amyloidosis
Human Immunology and Cancer Program Primary Systemic amyloidosis (ALamyloidosis). The Human Immunology Cancer Program has focused
http://gsm.utmck.edu/amyloid/primary.htm

Extractions: The proteins associated with this type of amyloid are composed of antibody-related molecules (immunoglobulins) that are involved in the body's defense against infection. They are made by plasma cells in the bone marrow and are secreted into the blood stream. For unknown reasons, a single population or clone of plasma cells grows excessively (such as occurs in multiple myeloma and other conditions). This leads to an increased production and secretion of these proteins, some of which eventually can form amyloid. Because they result from the proliferation of a single (i.e., monoclonal) plasma cell, the antibodies produced are termed monoclonal immunoglobulins or M-components. One particular type of M-component - Bence Jones protein - was named after its discoverer, Dr. Henry Bence Jones, over 150 years ago. This protein represents a portion of the antibody molecule called the light chain; thus, when this material deposits as amyloid, the resulting condition is designated light-chain or AL amyloidosis. Features of Primary (AL) Amyloidosis The primary (AL) form of amyloidosis is relatively uncommon, with an incidence of approximately 1 per 100,000 population; it is estimated that about 2,000-3,000 new cases are diagnosed each year. The disorder typically is manifested during the fifth or sixth decade of life and is apparently non-inheritable. Because it is fairly rare, it is often overlooked as a cause of organ dysfunction until late in the course of the disease.
Amyloid En Amyloidosis
Amyloid and amyloidosis. Clinical information for patients and doctors aboutsystemic amyloidosis diagnosis and therapy of amyloid deposition.
http://www.amyloid.nl/
Hemic And Lymphatic Diseases
ChediakHigashi Syndrome histopathol. images - Univ of New Mexico (US).amyloidosis About amyloidosis Skinner et al. - Boston U. (US);
http://www.mic.ki.se/Diseases/c15.html
Amyloidosis Of The Kidney
amyloidosis of Kidney From the Virtual Pathology Museum, Department ofPathology, University of Connecticut Health Center. Renal amyloidosis.
http://radiology.uchc.edu/eAtlas/GU/1347.htm
Amyloidosis
amyloidosis. amyloidosis is a progressive, incurable, metabolic disease characterizedby abnormal deposits of protein in one or more organs or body systems.
http://www.healthatoz.com/healthatoz/Atoz/ency/amyloidosis.html

Extractions: Definition Amyloidosis is a progressive, incurable, metabolic disease characterized by abnormal deposits of protein in one or more organs or body systems. Description Amyloid proteins are manufactured by malfunctioning bone marrow. Amyloidosis, which occurs when accumulated amyloid deposits impair normal body function, can cause organ failure or death . It is a rare disease, occurring in about eight of every 1,000,000 people. It affects males and females equally and usually develops after the age of 40. At least 15 types of amyloidosis have been identified. Each one is associated with deposits of a different kind of protein. Types of amyloidosis The major forms of this disease are primary systemic, secondary, and familial or hereditary amyloidosis. There is also another form of amyloidosis associated with Alzheimer's disease Primary systemic amyloidosis usually develops between the ages of 50 and 60. With about 2,000 new cases diagnosed annually, primary systemic amyloidosis is the most common form of this disease in the United States. Also known as light-chain-related amyloidosis, it may also occur in association with multiple myeloma (bone marrow cancer Secondary amyloidosis is a result of chronic infection or inflammatory disease. It is often associated with:
Amyloidosis-Kidney Disease
amyloidosisKidney Disease. amyloidosis Support Network - amyloidosis SupportNetwork - The Network's primary function is to link those affected by
http://www.health-nexus.com/amyloidosis-kidney_disease.htm

Extractions: Health-Nexus.Net Health-Nexus.Org The #1 Health information site Search Health-Nexus for: Match ALL words Match ANY word Email this page to a friend ! Post a question or comment on our Message Board Home Page Health Specialties Health News ... Alternative Health Options Substance Abuse Animal Health Search: Books Magazines Video Keywords: Find it Here Amyloidosis-Kidney Disease THE MERCK MANUAL - Amyloidosis ...Disorders Chapter 18. Amyloidosis Topics [General] [General] Amyloidosis: Accumulation in the tissues...different biochemical types of amyloidosis, etiologic mechanisms may...For example, in secondary amyloidosis (see below), a defect in...
Amyloidosis
HOME amyloidosis. HEAD AND NECK MANIFESTATIONS OF amyloidosis; amyloidosis; TRACHEALamyloidosis; Amyloid Treatment and Research Center; amyloidosis IX. HOME
http://www.bdid.com/amyloidosis.htm

Extractions: HOME Familial Lichen Lichen Renal Visceral Finnish Type German Type Icelandic Type Meretoja Type Oculoleptomeningeal Type of Gingiva and Conjuctiva, with Mental Retardation (Hornova Dlurosova Syndrome) Ohio Type Ostertag Type Primary Localized Cutaneous Systemic Nonneuropathic Type I Type V (Amyloid Cranial Neuropathy with Lattice Corneal Dystrophy, Amyloidosis Due to Mutant Gelsolin, Finnish Type Amyloidosis, Meretoja Type Amyloidosis) Type VI (Icelandic Type Amyloidosis) Type VII (Oculoleptomeningeal Type Amyloidosis, Ohio Type Amyloidosis)
Department Of Health - Amyloidosis
amyloidosis Links Ask an Oncologist about amyloidosis Ask a Board Certified Oncologistquestions about amyloidosis. http//www.amyloidosis.org. Information.
http://www.doh.state.fl.us/amyloidosis.html

Extractions: Amyloidosis Support Network - The Network's primary function is to link those affected by amyloidosis, to further support resources, and to educate the public and professionals so that the disease can be recognized earlier and appropriately treated. http://www.amyloidosis.org Information Amyloidosis is a group of diseases in which one or more organ systems in the body accumulate deposits of abnormal proteins. Although amyloidosis is not cancer, it is very serious. It is disabling or life threatening. However, growing awareness of the condition seems to be leading to substantial new research and treatment alternatives. These are the major types of amyloidosis which are all very different from each other: Primary A myloidosis is a plasma cell disorder that originates in the bone marrow and is usually treated with chemotherapy. It is the most common type of amyloidosis in the United States, with estimates of up to 2000 cases diagnosed each year, and occasionally occurs with multiple myeloma. The deposits in this type of the disease are made up of immunoglobulin light chain proteins that may be deposited in any bodily tissues or organs. The disease results when enough amyloid protein builds up in one or more organs to cause the organ(s) to malfunction. The heart, kidneys, nervous system and gastrointestinal tract are most often affected.
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Expert commentary on management of a patient with amyloidosis before and afterkidney transplantation. Focus On Renal biopsy revealed amyloidosis.
http://www.medscape.com/viewarticle/440308
Amyloidpage
Amyloid Treatment and Research Program Boston University School of Medicine. MarthaSkinner, MD, Director Rodney H. Falk, MD, Assoc. Director. Coordinators.
http://medicine.bu.edu/amyloid/Amyloid1.htm

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