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         Behcets Syndrome:     more books (29)
  1. Behçets Syndrome
  2. Behcet's Disease: A Guide to its Clinical Understanding. Textbook and Atlas by Sungnack Lee, Dongsik Bang, et all 2001-02-15
  3. Behcet's Syndrome
  4. Behcet's Disease: A Contemporary Synopsis by Gary R. Plotkin, John J. Calabro, 1988-02
  5. Adamantiades-Behcet's Disease (Advances in Experimental Medicine and Biology volume 528)
  6. Behcet's Disease by Bertrand Wechsler, 1993-11-01
  7. Immunology of Behcet's Disease
  8. Behcet's Disease (Inflammatory Disease and Therapy)
  9. You Are Not Alone: 15 People with Behcet's by Joanne A Zeis, 1997-04
  10. Behcet's Syndrome Toolkit - Comprehensive Medical Encyclopedia with Treatment Options, Clinical Data, and Practical Information (Two CD-ROM Set) by U.S. Government, 2009-03-14
  11. Behcet's syndrome may respond to infliximab. (Six Cases).: An article from: Skin & Allergy News by Nancy Walsh, 2003-07-01
  12. 21st Century Ultimate Medical Guide to Behcet's Syndrome - Authoritative Clinical Information for Physicians and Patients (Two CD-ROM Set) by PM Medical Health News, 2009-03-14
  13. 2009 Empowered Patient's Complete Reference to Behcet's Syndrome - Diagnosis, Treatment Options, Prognosis (Two CD-ROM Set) by PM Medical Health News, 2009-03-14
  14. Gale Encyclopedia of Medicine: Behcet's syndrome by Kim A. Sharp M.Ln., 2002-01-01

1. BEHCET’S SYNDROME SOCIETY
behcets syndrome Society is the UK patient support group for people with Behcets disease; registered charity number 326679. BEHCET’S SYNDROME SOCIETY.
http://www.behcets.org.uk/
BEHCET’S SYNDROME SOCIETY BEHCET’S SYNDROME SOCIETY

2. Behcets
How is behcets syndrome diagnosed? Behcets can be called either a disease or syndrome ( combination of be mentioned later. behcets syndrome is classically characterized as a triad
http://www.angelsdesign.com/Behcets.htm
BEHCET'S SYNDROME
The symptoms of Behcet's Syndrome
Depend on the area of the body affected. Behcet's syndrome can involve inflammation of many areas of the body. These areas include the arteries that supply blood to the bodies tissues. Behcet's Disease can also affect the veins that take the blood back to the lungs to replenish the oxygen content. Other areas of the body that can be affected by the inflammation of Behcet's Disease include the back of the eyes (retina), brain, joints, skin, and bowels. The mouth and genital ulcers are generally painful and recur in crops. They can range in size from a few millimeters to 20 millimeters in diameter. Inflammation of the eye, which can involve the front of the eye (uvea) causing uveitis, or the back of the eye (retina) causing retinitis, can lead to blindness. It is very important for patients to have this sensitive area monitored by an eye specialist (ophthalmologist). If the arteries become inflamed (arteritis) in patients with Behcet's Disease, it can lead to death of the tissues whose oxygen supply depends on these vessels. This could cause a stroke if affecting the brain, belly pain if affecting the bowel, etc. When veins become inflamed (phlebitis), the inflammation can involve large veins that develop blood clots, which can loosen to cause pulmonary embolism. Symptoms of inflammation of the brain or tissue that covers the brain (meninges) include headaches, neck stiffness, and is often associated with fever. This can cause damage to nervous tissue and lead to weakness of body areas.

3. Encyclopaedia Topic : Behcets Syndrome, Section : Introduction
behcets syndrome. Search. Help. Behcet s disease generally begins when patients are in their 20s or 30s. Behçet s syndrome is rare in the UK.
http://www.nhsdirect.nhs.uk/en.asp?TopicID=601

4. Thalidomide Responsiveness In An Infant With Behcets
HighBeam Research, Free Preview 'Thalidomide Responsiveness in an Infant With behcets syndrome.' Full Membership required for unlimited access. Comprehensive archive of newspapers, magazines
http://rdre1.inktomi.com/click?u=http://www.highbeam.com/library/doc0.asp?docid=

5. Encyclopaedia Topic : Behcets Syndrome, Section : Diagnosis
behcets syndrome. Search. Help. Sections for this topic Blood tests will be needed to rule out other diseases that can be confused with Behcet s syndrome.
http://www.nhsdirect.nhs.uk/en.asp?TopicID=601&AreaID=3618&LinkID=2693

6. Jo's Story
A story submitted by Jo Durant who has Behcet's Syndrome of the Professors at GOSH diagnosed me with behcets syndrome, and I was admitted to hospital for just the support branch of the behcets syndrome Society. I cannot thank them
http://www.behcetsuk.org/Stories/jo.html
Close page
Jo's Story
Hi all. My name is Jo Durant, I live in Northampton, England. For years I have been embarrassed to talk about my Behcets, and its symptoms, but reading all these amazingly honest stories, I am beginning to accept.
I am a 16 year old student, who loves all the "normal" things-socializing (when I have the energy!) music, and I am mad keen on art and animal rights. I am a vegan.
When I was 9 months I began getting fevers and skin lesions, and over the years my symptoms just got worse. I was a mystery-none of the Doctors could work out what it was, for a while they thought I had Crohn's Disease. Then when I was 7, I was rushed to Great Ormond Street Children's Hospital in London. I had developed oral and genital ulcers along with other mystery symptoms which are now familiar to me-aching joints, extreme fatigue. One of the Professors at GOSH diagnosed me with Behcets Syndrome, and I was admitted to hospital for just over a week. I was pumped full of antibiotics, so I can't really remember much that went on. When I came out I was put on Colchicine, which I have been told helps the skin and eyes.
I was then rushed into Great Ormond Street again when I was 11-my symptoms had started all over again. I was admitted, and I was tried on so many different drugs. In the end I was put on Thalidomide. A controversial drug if ever there was one! But I am a sensible teenager (a rare find!) I feel that when you live with something as rare and serious and Behcets, you grow up ten times quicker than others.

7. Behcet's Syndrome
For Medical Professionals only, registration required. Behcet's syndrome,
http://www.amersham-health.com/medcyclopaedia/Volume III 1/Behcets syndrome.html
Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Behcet's syndrome, (Halushi Behcet, 1889–1948, Turkish dermatologist), a chronic inflammatory disorder of unknown cause involving the small blood vessels and characterized by a classic triad of recurrent oral and genital ulcerations with ocular inflammation. Many other sites can be affected, including the skin, joints, and cardiovascular, neurologic and gastrointestinal organs. Joint manifestations involving a single joint or only a few joints appear in more than 50% of patients. The knees are the predominant site of articular involvement. Patients may have joint effusion, stiffness, warmth and tenderness, but permanent changes are rare. An elevated erythrocyte sedimentation rate, a strongly positive C-reactive protein, and elevation of alpha-2 globulin levels during the acute phase of the disease are typical features. Radiographic findings, which may resemble those of rheumatoid arthritis or related disorders, include osteoporosis, soft tissue swelling, and rarely joint space narrowing and osseous erosions. Sacroiliac joint abnormalities may sometimes be seen, and sacroiliitis can simulate the changes in ankylosing spondylitis or other seronegative spondyloarthropathies.
DR
The Encyclopaedia of Medical Imaging Volume III:1 Contacts GE Healthcare Making Waves

8. International Rare Disease Support Network (IRDSN)
Bacterial Pneumonia. Balantidiasis. BallerGerold Syndrome. Bannayan-Riley-Ruvalcaba Syndrome Beckers Nevus. Beckwith-Wiedmann Syndrome. behcets syndrome. Bejel. Bell's Palsy
http://www.angelfire.com/biz5/raredisorders/b.html
var cm_role = "live" var cm_host = "angelfire.lycos.com" var cm_taxid = "/memberembedded"
B If you are unable to locate the rare disease/disorder support group you are interested in; or, you are experiencing difficulty with any link(s), please send me an E-mail message informing me of this problem. irdsn@RareDiseaseSupport.org B-Cell Lymphomas
Babesiosis

Bacterial Endocarditis
...
RETURN HOME

9. HONselect - Behcet's Syndrome
English Behcet s Syndrome, Triple-Symptom Complex - Behcet Syndrome - behcets syndrome - Complex, Triple-Symptom - Syndrome, Behcet s - Triple Symptom
http://www.hon.ch/HONselect/RareDiseases/C07.465.075.html
List of rare diseases: English Deutsch
Language:
MeSH term:
Accepted terms:
English: Behcet's Syndrome - Triple-Symptom Complex
- Behcet Syndrome
- Behcets Syndrome
- Complex, Triple-Symptom
- Syndrome, Behcet's
- Triple Symptom Complex
Français: BEHCET, SYNDROME - APHTOSE BEHCET-TOURAINE Deutsch: Behçet-Syndrom - Trisymptomkomplex - Morbus Beçet Español: SINDROME DE BEHCET - COMPLEJO DE SINTOMA TRIPLE Português: SINDROME DE BEHCET - COMPLEXO DE TRIPLO SINTOMA HONselect ressources Definition: Yes Articles: Yes Images: No News: No Conferences: No Clinical trials: Yes Web sites: English Yes Français Yes Deutsch No Español No Português No Home About us Site map Feedback ... HONewsletter http://www.hon.ch/HONselect/RareDiseases/C07.465.075.html Last modified: Wed Apr 28 2004

10. Behcet S Syndrome
behcets syndrome behcets syndrome Pharmacotherapy for behcets syndrome This page was last reviewed/updated on 03/16/2004 Copyright © 2002 The Arthritis
http://www.arthritis.ca/look at research/cochrane reviews/behcets/default.asp?s=

11. Pharmacotherapy For Behcets Syndrome
Pharmacotherapy for behcets syndrome Pharmacotherapy for behcets syndrome Background behcets syndrome is a multisystemic disorder with recurrent oral and
http://www.arthritis.ca/look at research/cochrane reviews/behcets/pharmacotherap

12. Behcet's Syndrome
Behcet s syndrome,. Print this article, It is more common in males of eastern Mediterranean origin. Behcet s syndrome and Crohn s disease.
http://www.amershamhealth.com/medcyclopaedia/Volume IV 1/BEHCETS SYNDROME.asp
Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Behcet's syndrome, (Halushi Behcet, 1889–1948, Turkish dermatologist), chronic inflammatory disorder of unknown origin involving the small blood vessels and characterized by recurrent aphthous ulcers of the oral and pharyngeal mucous membranes and the genitalia, skin lesions, severe uveitis, retinal vasculitis and optic atrophy. It also frequently involves also the joints, the gastrointestinal system and central nervous system. It is more common in males of eastern Mediterranean origin. Behcet's syndrome and Crohn's disease Involvement of the small vessels of the small intestine by vasculitis may produce a pathological, clinical and radiological appearance that closely resembles the findings seen in Crohns disease . An association of Behcet’s and Crohn’s disease has been reported in the literature. On enteroclysis, lesions of the small bowel, particularly small aphthous ulcers, are visible as small punctiform collections of barium surrounded by a thin radiolucent halo.
ALB
The Encyclopaedia of Medical Imaging Volume IV:1 Contacts GE Healthcare Making Waves

13. Behcet's Syndrome
Behcet s syndrome,. Print this article, (Halushi Behcet, 18891948, Turkish dermatologist), a chronic inflammatory disorder of unknown
http://www.amershamhealth.com/medcyclopaedia/medical/Volume III 1/BEHCETS SYNDRO
Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Behcet's syndrome, (Halushi Behcet, 18891948, Turkish dermatologist), a chronic inflammatory disorder of unknown cause involving the small blood vessels and characterized by a classic triad of recurrent oral and genital ulcerations with ocular inflammation. Many other sites can be affected, including the skin, joints, and cardiovascular, neurologic and gastrointestinal organs. Joint manifestations involving a single joint or only a few joints appear in more than 50% of patients. The knees are the predominant site of articular involvement. Patients may have joint effusion, stiffness, warmth and tenderness, but permanent changes are rare. An elevated erythrocyte sedimentation rate, a strongly positive C-reactive protein, and elevation of alpha-2 globulin levels during the acute phase of the disease are typical features. Radiographic findings, which may resemble those of rheumatoid arthritis or related disorders, include osteoporosis, soft tissue swelling, and rarely joint space narrowing and osseous erosions. Sacroiliac joint abnormalities may sometimes be seen, and sacroiliitis can simulate the changes in ankylosing spondylitis or other seronegative spondyloarthropathies.
DR
The Encyclopaedia of Medical Imaging Volume III:1
Contacts
GE Healthcare Making Waves

14. PharmGKB: Behcet's Syndrome
Alternate Names Behcet Syndrome; behcets syndrome; Complex, TripleSymptom; Syndrome, Behcet s; Triple Symptom Complex; Triple-Symptom Complex.
http://www.pharmgkb.org/do/serve?objId=PA443488&objCls=Disease

15. Community Information Directory (CINDI)
behcets syndrome Society Address 3 Church Close. Town HUNGERFORD. County Berkshire. Postcode RG17 8PU view map. Telephone 0151 644 6909 (helpline).
http://apps.newham.gov.uk/cindi/a2z/Organisation.asp?OrgID=9107

16. Behcets Syndrome Society
Organisation behcets syndrome Society. Comment Formed Who is it for People with behcets syndrome their families. How to Contact Contact
http://www.guide-information.org.uk/guide/search_index_detail.lasso?RecID=G6128

17. DermIS / Main Menu / DOIA / Behçet's Disease / Info
SYNDROME, BEHCET TRIPLE SYMPTOM COMPLEX, Behcet s, Behcet s disease, Behcet s disease, NOS, behcets syndrome, Behcet s Syndrome, Behcet s syndrome, NOS, Complex
http://dermis.multimedica.de/doia/diagnose.asp?zugr=d&lang=e&diagnr=136100&topic

18. News View
behcets syndrome Down by the oriental medicine! from Okmedic. behcets syndrome is the disease that was found in 1937 by Turkish doctor whose name is Behcets.
http://www.okmedic.com/news/news_view.html?board=h_news&idno=60&language=eng

19. Service AB7Be N°3
behcets syndrome Society official UK support group for sufferers of Behcets Disease. Includes information on the disease, and similar disorders.
http://membres.lycos.fr/behcet/serv03.htm
AB (Amicale de Behcet en Belgique)
  • Behcet 's Association
    THE AMERICAN BEHCET 'S ASSOCIATION PO Box 54063 Minneapolis, MN 55454-0063 HOTLINE: 1-800-7 BEHCET S BEHCET 'S DISEASE NO KNOW CAUSE NO CURE ONLY HOPE - BEHCET 'S DISEASE - A RATE AND MYSTIFYING ILLNESS - WHAT ARE THE...
    Trouvé par: Excite, FAST Search, HotBot, Lycos, MSN Web Search, WebCrawler
    http://www.w2.com/
    behcet s.html Traduire ... 's Syndrome
    sufferer of this chronic rheumatoid condition provides information and support for others. Includes a bulletin board. Behcet 's Disease
    Trouvé par: FAST Search, HotBot, MSN Web Search, Yahoo!
    http://www.alexknight.clara.net/
    behcet s-syndrome/ Traduire ... 's Disease
    Who to Contact American Behcet 's Disease Association P.O. Box 280242 Memphis, TN 38168-0240 (800) 7 BEHCET S Website: http://pweb.netcom.com/~mharting/ behcet .html
    Trouvé par: HotBot, MSN Web Search, WebCrawler
    http://familyvillage.wisc.edu/lib_
    behcet .htm Traduire ... SYNDROME ADAMANTIADES - BEHCET `S SYNDROME American Behcet s Disease Association ``The American Behcet 's Disease association's goal is to provide support and information to people with Behcet 's Diseaseand their families and to educate the medical community about Behcet 's Disease.`` PO BOX 280242 Memphis, TN. 38168-0240 1-800-7
  • 20. Behcets Syndrome
    BEHÇET s SYNDROME. Epidemiology Behçet s syndrome is a rare condition, most cases having been reported from the Middle East and Japan.
    http://www.od.mah.se/depts/webodont/behcets_syndrome.html

    AltaVista
    PubMed/Medline/NIH
    ICD-10 / DA-3: Synonyms: BS, BD, Definition - Keywords: This aphthous stomatitis ocular inflammation , and genital ulcerations Epidemiology: and the presenting age is usually between 15 and 45 years. There seems to have been an increased incidence during the last decades. Aetiology and pathogenesis: The aetiology is unknown. Infections due to virus, bacteria and mycoplasma have been discussed, and lately autoimmunity. The basic pathological mechanism seems to be a deposition of circulating immune complexes in small vessels, causing vasculitis. Clinical features: Oral lesions are present in 90% of the cases ( Fig. 3033 ) . These are indistinguishable from those of RAU , and include all three forms of ulceration - MiAU, MjAU and HU. Only about 3% of all patients with RAU have BS, and progression of RAU to BS is rare. Eye involvement occurs in 80% of the cases with uveitis - and eventually hypopyon, conjunctivitis and/or keratitis. Severe eye lesions eventually causing blindness. Genital aphthous lesions are present in 65% of the cases with lesions on the penis, scrotum and/or vulva (labiae majora et minora).

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