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         Hughes Syndrome:     more books (26)
  1. Is sick building syndrome for real?: An article from: Journal of Property Management by Sally S. Hughes, Barbara A. Holt, 1994-07-01
  2. Living with Hughes Syndrome
  3. Hughes Syndrome: Antiphospholipid Syndrome by Khamashta, 2006-01-01
  4. Liberate Yourself from the Success Syndrome by Kent Hughes, Barbara Hughes, 1997-06
  5. Breaking Out of Environmental Illness: Essential Reading for People with Chronic Fatigue Syndrome, Allergies, and Chemical Sensitivities by Robert Sampson M.D., Patricia Hughes B.S.N., 1997-04-01
  6. Culture-Bound Syndromes: Folk Illnesses of Psychiatric and Anthropological Interest (Culture, Illness and Healing)
  7. Stickler: the Elusive Syndrome by Wendy L. Hughes, 2006-11
  8. Supporting Students with Asperger's Syndrome by Mark Hughes, Victoria Milne, et all 2009-04
  9. Reflections: Me & Planet Weirdo by PJ Hughes, 2009-12-01
  10. Serial Murder Syndrome (Serial Murder Syndrome Multiple Personality, False Accusation, Arousal Disorders, Bizarre Human Behavior Uncensored ) by Victor Godot, 2009-10-31
  11. Executive function deficits in autism spectrum disorders and attention-deficit/hyperactivity disorder: Examining profiles across domains and ages [An article from: Brain and Cognition] by F. Happe, R. Booth, et all 2006-06-01
  12. AIDS home care and hospice manual by Anne M Hughes, 1987

21. Lupus UK Factsheet 5 - Lupus And The Brain
brain activity. The second is the clotting disorder associated withsome lupus patients, the antiphospholipid or hughes syndrome. It
http://www.kitzbuhel.demon.co.uk/lupus/faqshets/faqs05.htm
Lupus and the Brain
Back to Lupus Information Doctors throughout the world are now recognising the importance of subtle forms of brain involvement in lupus as well as the more obvious brain problems. Never underestimate brain involvement. It may vary from mild depression, to memory loss, to much more severe problems such as seizures. In general there are two main causes of brain disease in lupus. The first is lupus disease itself which can cause alterations in the brain activity. The second is the clotting disorder associated with some lupus patients, the antiphospholipid or Hughes syndrome . It is very, very important for the doctor to try to distinguish between these two major causes of neurologic involvement as the treatments are clearly very different.
Depression
Depression is an important manifestation of lupus - in some it is the presenting sign of the disease. Many patients and, certainly, many doctors wrongly attribute depression in lupus merely to having a chronic illness and all that goes with it. This is not correct. The disease itself causes depression. Depression is an integral part of lupus in some patients - indeed management of the lupus often itself lifts the depression. The management of depression in lupus rests on a combination of treating the underlying lupus itself as well as possibly adding in antidepressant therapy. One of the medical advances in the last decade has been the introduction of newer milder antidepressants with less of the severe side-effects which so hampered older treatments.

22. SupportPath.com: Antiphospholipid Syndrome
Also called hughes syndrome. Website includes information about hughes syndrome(Antiphospholipid Syndrome), research, and information on support groups.
http://www.supportpath.com/sl_a/antiphospholipid_syndrome.htm
Antiphospholipid Syndrome
Also called: Hughes Syndrome About Us Add-A-Link Email Gallery ... here
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    Hughes Syndrome Foundation
    Website:
    http://www.hughes-syndrome.org/
    Description: The aims of this registered charity: To offer understanding and support to sufferers of Hughes Syndrome; To offer information and education on Hughes Syndrome; To support research into the condition; To raise funds to provide information, education and research. Website includes information about Hughes Syndrome (Antiphospholipid Syndrome), research, and information on support groups.
    Date Added: 08/08/2002
Note: Groups are listed alphabetically by U.S. state and then country.

23. Hughes Syndrome
Live Learn. hughes syndrome. Rare blood disorder, Antiphospholipid Antibody SyndromeAKA hughes syndrome. hughes syndrome Foundation. I Support hughes syndrome.
http://pages.ivillage.com/ashley_dea/liveandlearn/id6.html
'); document.writeln(' Click Here! Hughes Syndrome Home About Site About Me My Life Story ... Contact Me Rare blood disorder, Antiphospholipid Antibody Syndrome AKA Hughes Syndrome I was diagnosed with Hughes Syndrome at age 15, but I was sick long before that. Doctors are still finding things out about this disease. The main thing it does is make your blood clot more than it should. A blood clot is what usually gets the disease noticed. When I was 15 I had a clot in my right leg, from my knee to my pelvic area. And some of it broke off into my lungs too. It sure was an experience for me. Hughes Syndrome causes other problems too, just because its an auto-immune disease. It makes the immune system weak and my body fights against itself. It can't tell the good from the bad, so it attacks the good. Hughes Syndrome loves to mimic other diseases, like MS, and Lupus. In fact, some people with Lupus have Hughes Syndrome, and vice-versa. There are two different types of the antiphospholipid antibody. Some people can have the antibody and still live normal lives. But if you have the one that people with Lupus have, often called the Lupus Anticoagulant, then you may have problems. Some people have even been misdiagnosed with MS, when they really had Hughes Syndrome. Hughes Syndrome may run in the family, it has been known to cluster in families.

24. Camera Stella Syndrome (Leonard Hughes Syndrome, Spondyloendochromatosis, Spondy
HOME Camera Stella Syndrome (Leonard hughes syndrome, Spondyloendochromatosis,Spondyloepimetaphyseal Dysplasia). Camera Stella syndrome;
http://www.bdid.com/camera.htm

HOME
Camera Stella Syndrome (Leonard Hughes Syndrome, Spondyloendochromatosis, Spondyloepimetaphyseal Dysplasia)

25. Birth Disorder Information Directory - Y
Young hughes syndrome (XLinked Mental Retardationwith Short Stature and Obesity)
http://www.bdid.com/defecty.htm

HOME
Y
Yim Ebbin Syndrome (Amelia Cleft Lip and Palate with Hydrocephalus and Iris Coloboma) Yorifuji Okuno Syndrome (Pancreatic Hypoplasia with Diabetes and Heart Disease) Yoshimura Takeshita Syndrome (Deafness with Tubular Acidosis and Anemia, Hoyeraal Hreidarsson Syndrome) Young Hughes Syndrome (X-Linked Mental Retardation with Short Stature and Obesity) Young Maders Syndrome Young McKeever Squier Syndrome (Fatal Infantile Encephalopathy with Olivopontocerebellar Hypoplasia; Olivopontocerebellar Hypoplasia, Lethal Type) Young Simpson Syndrome (Mental Retardation with Unusual Facies and Hypothyroidism) Young Syndrome Yunis Varon Syndrome (Cleidocranial Dysplasia with Micrognathia, Absent Thumbs, and Distal Aphalangia)

26. Fertility Friends
hughes syndrome. (The Antiphospholipid Syndrome). At the present time I am goingthrough lots of blood tests to find out whether or not I have hughes syndrome.
http://www.fertilityfriends.co.uk/?m=c&c=322

27. Hughes Syndrome - The Syndrome Behind The Name (otherwise Known
hughes syndrome the Syndrome behind the Name (otherwise known as AntipholipidSyndrome) Click here for article written by Graham RV Hughes, MD.
http://212.199.79.240/imaj/oct99-9.htm

28. Hughes Syndrome And Chronic Fatigue Syndrome
hughes syndrome and Chronic Fatigue Syndrome. © MMII, Ken Lassesen, MS. Iwas also her first patient to become symptom free. hughes syndrome.
http://lassesen.com/cfids/familyhistory.htm
Hughes Syndrome and Chronic Fatigue Syndrome
© MMII, Ken Lassesen, M.S. In 1999, I had sudden onset CFS while I was employed by Microsoft. Microsoft offers self-insured medical insurance that is extremely liberal for all practical purposes there was no deductible or restrictions on any tests that my MD wish to try – of course, living in the US meant a wealth of private facilities and laboratories. As a result of this blessing, not only did I go into full remission from CFS but my wife and two daughters had an accurate diagnosis of their odd symptoms and rational treatment started. Our class of CFS appears to be a variant of Hughes Syndrome (formerly called Antiphospholipid antibody syndrome (APS)). The first paper on this variant was published in 1999 by David Berg and others [i] . Add to this blessing, our existing family practice MD believed that CFS was very real and that she had no treatment for it – but she was willing to listen, learn and cooperate if I could present hard, peer-review research. I was her first CFS patient that she had seen 2 weeks before onset and 2 weeks after onset – very dramatically illustrating the changes. I was also her first patient to become symptom free.
Hughes Syndrome
Hughes syndrome is caused by antibodies that result in deficiency of certain enzymes, such as

29. Hughes Syndrome Testing
The following tests are used to exclude hughes syndrome (and variants)as being the cause of CFS. All tests must be negative (there
http://lassesen.com/cfids/isac.htm
Hughes Syndrome Testing
Home
Up Hughes Syndrome Testing Pathogens Other Tests The following tests are used to exclude Hughes Syndrome (and variants) as being the cause of CFS. All tests must be negative (there are many variants of Hughes Syndrome).
Immune System Activation of Coagulation Panel
For detection of "sticky blood" there are several tests. The usual US-CFS test is the ISAC Panel from Hemex laboratories (http://www.hemex.com)
Anticardiolipin Antibodies
This is a cheap test, but it requires two positive tests 6 months apart for a positive result. . It is suggested as a possible pre-ISAC panel test to justify the ISAC expense. (Note: a negative results does not imply a negative ISAC panel)
Lupus Anticoagulant
The name does not imply Lupus rather an antibody that is also seen with Lupus. Moderate number of positive results.
Wasserman Reaction
This is a very old syphilis test, a positive test does not imply syphilis, rather one form of Hughes Syndrome. Least amount of positive results. Experience
APS-Hughes
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30. Divvy's Home Page
hughes syndrome The Blood Disease that Mimics MS - Could you have been given thewrong diagnosis? by Judy Graham. hughes syndrome is easy and cheap to treat.
http://www.btinternet.com/~mcbiffa/hughes.html

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MS Links Fun Links Contact me
Hughes Syndrome - The Blood Disease that Mimics MS - Could you have been given the wrong diagnosis? by Judy Graham
Case History Jeremiah Sheehan a successful London architect, knows how devastating it is to be told you have MS, and then how stressful to hear it might be something else that you have never heard of and requires completely different treatment. "I had so many things going wrong that I was described by one doctor as a medical chaosity, and although my story is a harrowing one I do feel I have been given a reprieve." Jeremiah, 45, one of the key designers of the much acclaimed Rainforest Cafe in Piccadilly, had always been careful about his health. One of his favourite pastimes was hill-walking. But it was whilst in Scottish Highlands four years ago that he noticed a dramatic change in his health. I had this paralysing fatigue that made it hard for me to even get back to the car. I thought it might be linked to asthma I had suffered from for many years." But other symptoms developed. "I started having double vision, the beginnings of optic neuritis. Then I began to trip up and had problems with my balance. I had something called drop foot where I couldn't lift my toes so I would fall over them. I was getting badly bruised, at one point I ended up in casualty with dislocated ribs and gashes, I looked as though I had been in a war. The doctors didn't know what was wrong."

31. Sticky Blood Explained By Kay Thackray
The description by Graham Hughes of the antiphospholipid syndrome orhughes syndrome is one of the medical landmarks of the 20th century.
http://www.author.co.uk/thackray/
Kay Thackray
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The description by Graham Hughes of the "antiphospholipid syndrome" or Hughes Syndrome is one of the medical landmarks of the 20th century. Here is a disease, a medical discovery, which should turn such fashions around. In a series of brilliant clinical observations, Dr Hughes, not only pieced together what is now clearly a common and important disease, but also, with his team, set up the blood tests and treatment guidelines, which are used world-wide.
This was not an anecdotal observation. It was a prime example of meticulous clinical observation and dogged determination. Hughes Syndrome is now recognised as a major new disease. It has been described, by Dr Josep Font of Barcelona as, "one of the 2 new diseases (with AIDS) of the 20th century". Despite being 20 years old, and being of major importance in the diagnosis of strokes, migraine, multiple sclerosis, and miscarriage, the syndrome is still under diagnosed by doctors. This book by Kay Thackray is an important contribution to the understanding of the syndrome.

32. Peter Elwood
hughes syndrome causes many of the strokes that affect people under45 years old. It is preventable, as are many cases of migraine
http://www.aspirin-foundation.com/edin_7.htm
Aspirin and the Anti-Phospholipid Syndrome G raham Hughes is consultant rheumatologist at the Guy’s and St Thomas’ Hospital Trust, where he set up, in the Rayne Institute, the Lupus Arthritis Research Unit. He is Editor of the Journal Lupus. His main research interest is in systemic lupus erythematosus (SLE), not in itself a rare disease. However, he is seeing more and more people with anti-phospholipid syndrome, named internationally in 1992 as Hughes’ syndrome. W omen with it have recurrent spontaneous abortions, arterial and venous thromboses, and early myocardial infarctions. His interest in the disease started in 1975, in Jamaica, where he found women with ‘Jamaican neuropathy’, with meningomyelopathy, false positive syphilis tests, and thromboses in veins and arteries. In 1983 he wrote of recurrent thrombosis, abortion, cerebral disease, lupus and a circulating protein pro-coagulant co-factor, as the anti-phospholipid syndrome L ater in 1983, he added thrombocytopenia, livido reticularis, teenage migraine, demyelinating disease, Budd Chiari syndrome and dementia to the list of signs and symptoms. His colleague Nigel Harris developed the tests, and the offending pro-coagulant protein beta-2GP-1 is now well studied. Other protein co-factors that promote clotting include prothrombin. Dr Hughes’ group showed that people who possess anti-phospholipid antibodies and prothrombin antibodies have a 60% risk of thrombosis, and that many develop dementia.

33. Peter Elwood
hughes syndrome – Sticky Blood, Obstetrics and the GP, Dr Hughesfirst became interested in the syndrome that now bears his name
http://www.aspirin-foundation.com/the_aspirin_age6.htm
Hughes Syndrome – Sticky Blood, Obstetrics and the GP Dr Hughes first became interested in the syndrome that now bears his name in the early 1970s, when studying systemic lupus erythematosus (SLE). In 1983, he gave the Prosser-White Oration, in which he described women with multiple thromboses, neurological disease, thrombocytopenia, livedo reticularis, headaches, migraine, epilepsy, chorea, multiple abortions, peripheral thrombosis, Budd Chiari syndrome and early death from stroke. Many were thought to have 'lupus' but had negative antinuclear antibody tests. The diagnosis was changed to anti-phospholipid syndrome when it was found they had anti-phospholipid antibodies, then was renamed Hughes syndrome when Dr Hughes' part in discovering it was recognised. It is often unrecognised. Of 146 women with primary stroke, 7% had anti-PL antibody. In 55 Italian people under 45 years old with strokes, 20% had anti-PL syndrome: four of the ten went on to have further strokes. Dr Hughes has a weekly clinic of 800 patients, many of whom complain of memory loss. Many know precisely when their INR has fallen, because their dysarthria or headache returns when it falls from 3.2 to 2.9. One sufferer, an author, needs an INR of 3.4: if it falls to 3.1 she writes nonsense.

34. Mypharmacy
Shop Health Books Sheldon Press Living with hughes syndrome, Living withhughes syndrome Living with hughes syndrome information Price £6.99.
http://www.mypharmacy-secure.co.uk/acatalog/Shop_Living_with_Hughes_Syndrome_364
Health information Medicines Alternative medicines Health products ... Sheldon Press Living with Hughes Syndrome
Living with Hughes Syndrome
Living with Hughes Syndrome information

Price:

35. Babyloss - A Home On The Web For Miscarriage Information And Support
hughes syndrome Foundation hughes syndrome (antiphospholipid syndrome) 'stickyblood' is characterised by arterial and venous blood clotting and is an
http://homepages.which.net/~charlotte.cornwall/babyloss/support/support.html
home information support forums ... library SUPPORT
Communities and organisations dedicated to help you. online communities babyloss forums click here for support and friendship from fellow parents experiencing pregnancy loss StillFathers.org Still Fathers is a new resource for men who have experienced stillbirth, infant death, or miscarriage, and provides support, encouragement, and 'a place to touch base'. Remember Our Angels
http://www.geocities.com/rememberourangels2002/index.html
Pregnancy and Infant Loss
the home of the US Awareness campaign. Amongst the useful info and support is a list of remembrance ceremonies Born Too Soon
Following 5 losses, Paula Craven has set up this support website and also written leaflets for use at her local hospital. Please visit her website where you will be assured of comfort and understanding. soc.support.pregnancy.loss

36. Arthritis Research Campaign | Antiphospholipid Syndrome
Available from the hughes syndrome Foundation hughes syndrome A Patient's Guide,by Dr Graham Hughes, SpringerVerlag London, 2001, ISBN 1852334576, 63 pp.
http://www.arc.org.uk/about_arth/booklets/6059/6059.htm

scotland + n. ireland

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What is antiphospholipid syndrome (APS)?
Antiphospholipid syndrome (APS) is a disorder in which the blood has a tendency to clot too quickly ('sticky blood' syndrome). The clotting can affect any vein or artery in the body, resulting in a wide range of symptoms. These are described below. (The medical words in italics are explained in more detail in the Glossary at the end of the booklet.)
History of APS
Most of the early work leading to the detailed description of APS was carried out in the early 1980s by Dr Graham Hughes and his colleagues while studying a disease called lupus (see ARC booklet ' Lupus '). In lupus the immune system goes into 'overdrive' and produces a huge variety of excess antibodies . While studying lupus it became clear that some patients had a tendency to form blood clots in arteries and veins. This clotting was associated with a particular antibody which 'attacks' phospholipids - hence the term antiphospholipid antibodies . It was discovered that the syndrome could exist in people without lupus. This is now known as APS or primary antiphospholipid syndrome.
What are the main signs and symptoms?

37. The Miscarriage Association
hughes syndrome FOUNDATION. hughes syndrome Foundation a site offering supportand information regarding hughes syndrome (antiphospholipid syndrome).
http://www.miscarriage.association.care4free.net/links.htm

38. Ivanhoe's Medical Breakthroughs - Discussion Groups
Antiphospholipid Antibody Syndrome (aka hughes syndrome) KuddleUpWthMe 10/07/02» RE Antiphospholipid Antibody Syndrome (aka hughes syndrome) Eyzkrazy4u 10
http://www.ivanhoe.com/discussion/p_discussion.cfm?forumID=3&action=msglist

39. Springer-Verlag London: Medicine
hughes syndrome A Patient's Guide Graham RV Hughes £7.99; 2001; 63pages;205x135mm; Softcover; 185233-457-6. As with any delicate
http://www.springer.co.uk/medicine_showcase.htm
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Positron Emission Tomography
Basic Science and Clinical Practice

Peter E Valk, Dale L Bailey, David W Townsend and Michael N Maisey (Eds)
A comprehensive and contemporary reference work covering the basic science and clinical applications of positron emission tomography (PET). This book reflects the tremendous increase in interest in PET as both a clinical and research imaging modality in the past 10 years. Written by experts in the field and edited by those involved in PET development, and training of scientists and medical specialists.
Positron Emission Tomography - basic science and clinical practice thoroughly explains the principles, clinical applications and economic aspects of PET today. Chapters go into detail on PET applications in oncology, the central nervous system, cardio-respiratory systems, infectious diseases and pediatrics. Discussions are also found on technology design and evaluation, PET in drug discovery and development in imaging gene expression and therapy. Peter E Valk MB BS FRACP is based in the Northern California PET Imaging Center, Sacramento, CA USA

40. Bokpris.com - Hughes Syndrome: Patients' Guide
hughes syndrome Patients' Guide Jämför priser, frakt och leveranstidenpå böcker i svenska och utländska Internetbutiker.
http://www.bokpris.com/1852334576
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