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         Antiphospholipid Syndrome:     more books (36)
  1. Positive Options for Antiphospholipid Syndrome (APS): Self-Help and Treatment by Triona Holden, 2003-03
  2. Hughes Syndrome: Antiphospholipid Syndrome
  3. Antiphospholipid Syndrome in Systemic Autoimmune Diseases, Volume 10 (Handbook of Systemic Autoimmune Diseases)
  4. The Antiphospholipid Syndrome II: Autoimmune Thrombosis (Pt. 2)
  5. The Antiphospholipid Syndrome by Ronald A. Asherson, Ricard Cervera, et all 1996-08-05
  6. Antiphospholipid Syndrome - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by ICON Health Publications, 2004-08-31
  7. Hughes Syndrome: Patients' Guide by Graham Hughes, 2001-04-02
  8. Antiphospholipid Thrombosis Syndromes, An Issue of Hematology/Oncology Clinics (The Clinics: Internal Medicine) by Roger L. Bick MDPhDFACP, William Baker, 2008-02-19
  9. Clinical Approach to Antiphospholipid Antibodies
  10. Dermatoses are often the first sign of APS.(Dermatology)(Antiphospholipid syndrome): An article from: Internal Medicine News by Jeff Evans, 2004-12-01
  11. Dermatoses are often the first sign of APS.(Dermatology)(Antiphospholipid syndrome): An article from: Internal Medicine News by Jeff Evans, 2004-12-01
  12. Catastrophic antiphospholipid syndrome
  13. Criteria for antiphospholipid syndrome revised.(Rheumatology): An article from: Internal Medicine News by Nancy Walsh, 2006-06-01
  14. Lifelong anticoagulant Tx warranted for APS.(Cardiovascular Medicine)(antiphospholipid syndrome): An article from: Internal Medicine News by Jeff Evans, 2004-10-01

101. Antiphospholipid Syndrome: What Is It?
antiphospholipid syndrome is an autoimmune disorder in which the body makes antibodies to its own phospholipids or plasma proteins.
http://arthritis.about.com/b/a/130561.htm
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Antiphospholipid Syndrome: What Is It?
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December 05, 2004
Antiphospholipid Syndrome: What Is It?
Antiphospholipid syndrome is an autoimmune disorder in which the body makes antibodies to its own phospholipids or plasma proteins. Antiphospholipid syndrome (APS) can occur in individuals without any associated disease. This is called primary APS. The disorder may also occur with systemic lupus erythematosus (SLE) or another rheumatic or autoimmune disorder. This is called secondary APS. Antiphospholipid antibodies can be found in as many as 50% of people with lupus and in 1-5% of the rest of the population. About Guide to Rare Diseases Mary Kugler explains with more details , including the fact women with APS may have frequent miscarriages or premature births Email to a Friend
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102. Hotdog Express Version 1.0 Document
Features background information, message board, chat room, and related links.
http://www.mindspring.com/~waxman/
Antiphospholipid Antibody Syndrome (APS) On The Net
This Page Was Created On 3/22/98, Last Modified On 12/18/99
Our MESSAGE Board on Delphi is up and running. Its a YEAR old, and there are Thousands of messages for you to look at! Lots of people like YOU who also have APS who want to talk. Come Join US!! See Below For Link!!
Information and Links concerning Antiphospholipid Antibody Syndrome, Antiphospholipid Syndrome, APLS, APS
This Site Was Created By Mark Waxman Keywords: Antiphospholipid Antibody Syndrome, Antibodies, APLS, APS, Blood, Clot, Clotting, Disorder, Heart, Lupus
The information presented here is for informational and educational purposes only and should not be used for diagnostic or treatment purposes, in other words, they are not a substitute for medical care or treatment by a qualified professional. If you believe that you have Antiphospholipid Antibody Syndrome, see your Doctor or Healthcare Professional immediately. The author of this web page is NOT a Doctor or Healthcare Professional but IS an individual who has been diagnosed with Antiphospholipid Antibody Syndrome.
What Is Antiphospholipid Antibody Syndrome, (APS)?

103. Antiphospholipid Antibody Syndrome, APS, APLS, Hughes Syndrome, Sticky Blood, Cl
Medical research information on APLS, APS, APLAS or Hughes syndrome and related blood disorders.
http://apls.freelinuxhost.com/index.html
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Rate this site! 1 - Worst 10 - Best AOL customers click here for E-mail information Do you have problems with your balance and posture. Try the Wobble cushion Click here To enter the 1st World survey of APS patient symptoms Anti Phospholipid Syndrome This site is intended as a research resource for medical professionals, patients and families who wish to learn more about a little known lethal, yet treatable, blood disorder that causes hypercoagulation. Early signs of this disease are often diagnosed as many different disorders before being correctly diagnosed. This inability to correctly diagnose is not due to any form of medical inefficiency, but is due to the disease only being recognised in the last 9 years, and it's ability to mimic the symptoms of a number of well known and documented diseases. Even though I have a clinical diagnosis of APLS, wear an SOS Talisman bracelet and carry a medical fact card on me, in an emergency the Accident and Emergency doctors still insist on treating the possibly catastrophic events as a Migraine. I hope this site will help to raise the awareness of many doctors and health care professionals, and give help and the comfort of understanding the problems to patients and their families.

104. Quick Registration
Delphi message board and chat room for anyone with an interest in the disorder. Requires free registration.
http://forums.delphiforums.com/apssupport/start
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105. Search Result For "Antiphospholipid-Antibody Syndrome"
NOAH pages containing antiphospholipidAntibody syndrome antiphospholipid Antibody syndrome; Arthritis and Pregnancy; When Pregnancy Is Complicated By
http://www.noah-health.org/search/results.php?lang=1&keyword=Antiphospholipid-An

106. Antiphospholipid Antibody Syndrome
Rheumatology Diffuse Lupus Anticoagulant antiphospholipid.
http://www.fpnotebook.com/RHE18.htm
Home About Links Index ... Editor's Choice document.write(code); Advertisement Rheumatology Diffuse Assorted Pages Amyloidosis Antiphospholipid Antibody Syndrome Systemic Lupus Erythematosus Polymyalgia Rheumatica ... Medication Causes of Myositis Antiphospholipid Antibody Syndrome Antiphospholipid Syndrome Book Home Page Cardiovascular Medicine Dentistry Dermatology Emergency Medicine Endocrinology Gastroenterology Geriatric Medicine Gynecology Hematology and Oncology HIV Infectious Disease Jokes Laboratory Neonatology Nephrology Neurology Obstetrics Ophthalmology Orthopedics Otolaryngology Pediatrics Pharmacology Practice Management Prevention Psychiatry Pulmonology Radiology Rheumatology Sports Medicine Surgery Urology Chapter Rheumatology Index Bone Cardiovascular Medicine Dermatology Diffuse Examination Infectious Disease Intra-Articular Disorders Laboratory General Marfans Myofascial Neurology Osteoarthritis Pain Pediatrics Pharmacology Procedure Radiology RA Spondylitis Symptom Evaluation Page Diffuse Index Amyloidosis Behcet's Syndrome Lupus Anticoagulant Antiphospholipid Lupus Systemic Polymyalgia Rheumatica Polymyositis Background Polymyositis DDx Polymyositis Evaluation Polymyositis Management Polymyositis Types Idiopathic Sjogren's Syndrome Systemic Sclerosis
  • Pathophysiology Recurrent thrombosis of any size vessel May have no link with SLE despite early associations Diagnosis Major clinical associations Venous thrombosis Deep Vein Thrombosis Pulmonary Embolism Arterial thrombosis Cerebrovascular Accident (CVA) Transient Ischemic Attack s Myocardial Infarction Gangrene
  • 107. Diagnosing Antiphospholipid Antibody Syndrome - College Of American Pathologists
    The diagnosis was primary antiphospholipid antibody syndrome. The patient has been on coumadin therapy for four months and has not experienced any transient
    http://www.cap.org/apps/docs/cap_today/case_study/coag1.html
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    Diagnosing antiphospholipid antibody syndrome
    March 1999
    Coagulation Case Study Jeffrey S. Dlott, MD Douglas A. Triplett, MD
    Editor's note: This is the second in a series of articles focusing on laboratory evaluation of coagulation disorders. Each article contains a clinical history, laboratory results, an algorithm for evaluating either an abnormal coagulation screening test or a clinical abnormality (bleeding or thrombosis), and a final diagnosis. A major goal of this series is to provide an overview of how specific coagulation abnormalities can be evaluated in the clinical laboratory. Clinical history . The patient is a 39-year-old Caucasian male who at age 30 had a left anterior myocardial infarction. Shortly thereafter the patient experienced his first of several strokes. Residual deficits include memory loss and expressive aphasia. Multiple neurologic and cardiac imaging studies have failed to demonstrate an etiology. Laboratory findings have repeatedly demonstrated a prolonged activated partial throm-boplastin time and borderline thrombocytopenia. The initial laboratory findings are shown in Table 1 The differential diagnosis was based on lupus anticoagulant plus or minus other an-ti-phospholipid anti-bodies versus specific factor inhibitors or factor deficiency. (See

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