81. Entrez PubMed Click here to read Remission of Behcet s syndrome with tumour necrosis factor alpha blocking therapy. Goossens PH, Verburg RJ, Breedveld FC. http://arthritis-research.com/pubmed/11350856

Entrez PubMed Nucleotide Protein ... Books Search PubMed Protein Nucleotide Structure Genome Books CancerChromosomes 3D Domains Domains Gene GEO GEO DataSets HomoloGene Journals MeSH NCBI Web Site OMIM PMC PopSet SNP Taxonomy UniGene UniSTS for Limits Preview/Index History Clipboard ... Text Version Entrez PubMed Overview FAQ Tutorial New/Noteworthy ... E-Utilities PubMed Services Journals Database MeSH Database Single Citation Matcher Batch Citation Matcher ... Cubby Related Resources Order Documents NLM Gateway TOXNET Consumer Health ... PubMed Central Summary Brief Abstract Citation ASN.1 MEDLINE XML UI List LinkOut Related Articles Cited in Books CancerChrom Links Domain Links 3D Domain Links GEO DataSet Links Gene Links Genome Links GEO Links HomoloGene Links Nucleotide Links OMIM Links PMC Links Cited in PMC PopSet Links Protein Links SNP Links Structure Links UniSTS Links Show: Sort Author Journal Pub Date Text File Clipboard E-mail Order Ann Rheum Dis. 2001 Jun;60(6):637. Related Articles, Links Remission of Behcet's syndrome with tumour necrosis factor alpha blocking therapy. Goossens PH, Verburg RJ, Breedveld FC. Department of Rheumatology, Leiden University Medical Centre, The Netherlands.

82. Behcet S Syndrome . Behcet s syndrome is a chronic disease that involves multiple body systems. The disease...... jsp, Behcet s syndrome. Definition. A http://www.lifesteps.com/gm/Atoz/ency/behcets_syndrome_pr.jsp

83. InteliHealth: Behcet's Syndrome Health A to Z, Reviewed by the Faculty of Harvard Medical School Behcet s syndrome http://sushi.intelihealth.com/IH/ihtIH/WSIHW000/9339/9540.html

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84. Entrez PubMed Click here to read Treatment of intestinal Behcet s syndrome with chimeric tumour necrosis factor alpha antibody. Travis SP, Czajkowski http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Abstra

85. Entrez PubMed Click here to read Labyrinthine involvement in Behcet s syndrome. Pollak L, Luxon LM, Haskard DO. Department of NeuroOtology, National http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citati

86. Birth Disorder Information Directory - BA-BL Behcet Disease/syndrome (AdamantiadesBehcet s syndrome; Halushi-Behcet s syndrome; Oculo-Bucco-Genital syndrome; Touraine s Aphthosis; Triple Symptom Complex http://www.bdid.com/defectba.htm

HOME Ba-Bl B-K Mole Syndrome See Melanoma, Familial/Cutaneous Malignant Type Bader Syndrome (Odontomatosis Aortae Oesophagus Stenosis, Odontoma Dysphagia Syndrome) bader syndrome ODONTOMA-DYSPHAGIA SYNDROME BADS Syndrome See Black Locks with Albinism and Deafness Syndrome Baelz Syndrome (Cheilitis Glandularis) baelz syndrome CHEILITIS GLANDULARIS Bagatelle Cassidy Syndrome (Macrocephaly Short Limbs Deafness) bagatelle cassidy syndrome Bahemuka Brown Syndrome (Spastic Paraplegia Facial Cutaneous Lesions) bahemuka brown syndrome Baker Vinters Syndrome (Hydrocephalus Craniosynostosis Bifid Nose) baker vinters syndrome Ballard Syndrome (Brachydactyly, Combined B and E Types; Pitt Williams Brachydactyly) ballard syndrome BRACHYDACTYLY, COMBINED B AND E TYPES Baller Gerold Syndrome See Craniosynostosis-Radial Aplasia Syndrome Ballinger Wallace Syndrome (Diabetes-Deafness Syndrome, Maternally Transmitted; Diabetes Mellitus, Noninsulin-Dependent/Type II, with Deafness) Ballinger-wallace syndrome DIABETES-DEAFNESS SYNDROME, MATERNALLY TRANSMITTED Bamboo Hair Syndrome See Netherton Disease Bamforth Syndrome (Hypothyroidism, Athyroidal, with Spiky Hair and Cleft Palate)

87. Brain Foundation - Behcet's Disease Although the exact cause remains unclear, Behcet s syndrome is thought to arise as a result of an autoimmune response, that is, when the body s defense http://www.brainaustralia.org.au/AZ_of_Brain_Disorders/behcets_disease

Home About Us The Brain Healthy Brain ... Site Map DHTML_MENU_rel_path = '/squizlib/dhtml_menu/images/'; Behcet’s Disease Description Behcet's disease is a rare, chronic, lifelong disease that affects mainly young adults, with men having more severe symptoms than women do. Although the exact cause remains unclear, Behcet's syndrome is thought to arise as a result of an autoimmune response, that is, when the body's defense mechanism malfunctions and begins to attack its own tissues. The syndrome involves inflammation of blood vessels throughout the body. Symptoms include recurrent oral ulcers, recurrent genital ulcers, and eye inflammation It may also cause various types of skin lesions, arthritis, bowel inflammation, and meningitis (inflammation of the membranes of the brain and spinal cord). The symptoms usually flare up then go into remission. The time between attacks tends to be unpredictable; it can be as short as a few days, or it can be long as years before a person has another episode. Behcet's syndrome affects men five to 10 times more frequently than women. On average, the first symptoms appear between the ages of 10 and 30. Treatment Although Behcet's syndrome can be a chronic condition, most symptoms diminish over time. Treatment, therefore, focuses on the symptoms. Vasculitis and inflammatory eye disease will require glucocorticoids and perhaps other immunosuppressive drugs. Mouth sores may be treated with glucocorticoids in the form of mouthwash or paste. Colchicine, thalidomide and dapsone may be helpful for the skin or joint disease. Joint inflammation may require anti-inflammatory agents, pain medications, physical therapy and, occasionally, other immunosuppressive medications.

88. Genetic And Rare Diseases Information Center - Office Of Rare Diseases Disease Behcet syndrome. Synonyms AdamantiadesBehcet s syndrome. Halushi-Behcet s syndrome. Oculo-Bucco-Genital syndrome. Touraine s Aphthosis. http://ord.aspensys.com/asp/diseases/diseaseinfo.asp?ID=848

89. Behcet's Syndrome . Behcet s syndrome is a chronic disease that involves multiple body systems.......Encyclopedia Index B. Behcet s syndrome. Definition. http://www.rwjhamilton.org/Atoz/ency/behcets_syndrome.asp

Encyclopedia Index B Behcet's syndrome Definition A group of symptoms that affect a variety of body systems, including musculoskeletal, gastrointestinal, and the central nervous system. These symptoms include ulceration of the mouth or the genital area, skin lesions , and inflammation of the uvea (an area around the pupil of the eye). Description Behcet's syndrome is a chronic disease that involves multiple body systems. The disease is named for a Turkish dermatologist, Hulusi Behcet, who first reported a patient with recurrent mouth and genital ulcers along with uveitis in 1937. The disease occurs worldwide, but is most prevalent in Japan, the Middle East, and in the Mediterranean region. There is a wider prevalence among males than females in a ratio of two to one. Causes and symptoms The cause of Behcet's syndrome is unknown. Symptoms include recurring ulcers in the mouth or the genital area, skin lesions, arthritis that affects mainly the knees and ankles, pain and irritation in the eyes, and fever . The mouth and genital ulcers tend to occur in multiples and can be quite painful. In the mouth, these ulcers are generally found on the tongue, gums, and the inside of the lips or jaws. In the genital area, the ulcers usually occur on the penis and scrotum in males and on the vulva of women. The eye inflammation can lead to blindness.

90. MeSH-D Terms Associated To MeSH-C Term Behcet S Syndrome MeSHD terms associated to MeSH-C term Behcet s syndrome, G2D Home. The number indicates the strength of the association of the corresponding http://www.bork.embl-heidelberg.de/g2d/c2d.pl?Behcet's_Syndrome:unknown

91. The Health Network - Your Complete Online Health Centre Behcet’s syndrome is both a chronic (long term) and recurrent condition. OUTCOMES While the course of Behcet’s syndrome is long, the ulcers usually heal. http://www.healthnetwork.com.au/search-display.php?cat=condition&name=BEHCET'S S

92. Behcet's Disease pain. Systemic corticosteroids continue to be useful therapy for most manifestations of Behcet s syndrome. Corticosteroid therapy http://www.wnep.com/global/story.asp?s=1230763

93. EMedHome.com Archives Of Featured Articles, Clinical Cases, Clinical Pearls, And click on images to enlarge What is your diagnosis? Behcet s syndrome Behcet s syndrome is a multisystem disorder whose etiology remains obscure. http://www.emedhome.com/features_archive-detail.cfm?FID=113

94. Rev Electron Biomed / Electron J Biomed 2003;1(3):161-169. Foyaca Et Al. NEURO-B NEUROBEHCET S syndrome TREATED WITH HERBAL MEDICATION. 7. -Kidd D, Steuer A, Denman AM, Rudge P. Neurological complications in Behcet’s syndrome. http://biomed.uninet.edu/2003/n3/foyaca.html

ISSN: 1697-090X Inicio Home Indice del volumen Volume index ... Contacto/Contact: NEURO-BEHCET'S SYNDROME TREATED WITH HERBAL MEDICATION. *Foyaca-Sibat H, **Ibañez-Valdés LdeF. *Department of Neurology, **Department of Family Medicine. University of Transkei. Umtata. South Africa. foyaca @ intekom.co.za Rev Electron Biomed / Electron J Biomed 2003;1(3):161-169. Comment Reviewer Dr. Felix Conde Martín . Hospital Can Misses. Ibiza. España Comment Reviewer Prof. Fidel Fernández Fernández . Universidad de Cantabria. Santander. España. Abstract KEY WORDS Introduction. are summarized in Table I. Pallis and Fudge in 1956 and Wadia and Williams in 1957, described the clinical manifestations of NBS for the first time and they established three different types such as: 1) Brainstem disturbances, 2) Meningomyelitis, and 3) Confusional syndrome, dementia, Parkinsonism, pseudobulbar palsy and quadriparesis. Vascular complications as a result of vasculitis of the vasa vasorum or dural venous sinus thrombosis, intracranial hypertension, polymiositis, and peripheral neuropathy, spinal cord lesions, optic neuropathy , and vestibulocochlear involvement have been reported The course is relapsing-remitting, secondary progressive or primary progressive and the most commonly affected area is the brain stem with other additional symptoms or signs, and hemispherical involvement with mental changes. Factors suggesting a poor prognosis are repeated attacks, incomplete recovery, progressive disease course, and high level of CSF leucocytosis during acute attack

95. Ann Rheum Dis -- Abstracts: Chamberlain 37 (5): 459 Download to Citation Manager. Annals of the Rheumatic Diseases, 1978, Vol 37, 459465. PAPERS. A family study of Behcet s syndrome. MA Chamberlain. http://www.annrheumdis.com/cgi/content/abstract/37/5/459

HOME HELP FEEDBACK SUBSCRIPTIONS ... Email this link to a friend eLetters: Submit a response to this article Similar articles found in: Ann Rheum Dis Online PubMed PubMed Citation This Article has been cited by: other online articles Search PubMed for articles by: Chamberlain, M. A. Alert me when: new articles cite this article Download to Citation Manager Annals of the Rheumatic Diseases, 1978, Vol 37, 459-465 PAPERS A family study of Behcet's syndrome MA Chamberlain The first-degree family members of patients with Behcet's syndrome were investigated to determine (1) whether there was a familial aggregation of Behcet's syndrome or of its component features, (2) whether there was an increased incidence of sacro-iliitis in these families, and (3) whether a link exists between Behcet's syndrome and spondarthritides in first-degree relatives. Of the 226 relatives and patients seen, 21 patients with definite Behcet's syndrome and their 71 relatives were analysed in some detail. Orogenital ulceration was found in 2 mothers of probands; 1 patient had psoriasis and Behcet's but neither disease featured in the pedigree.

96. Ann Rheum Dis -- Abstracts: Bird Stewart 45 (4): 265 PAPERS. Genetic analysis of families of patients with Behcet s syndrome data incompatible with autosomal recessive inheritance. JA Bird Stewart. http://www.annrheumdis.com/cgi/content/abstract/45/4/265

HOME HELP FEEDBACK SUBSCRIPTIONS ... Email this link to a friend eLetters: Submit a response to this article Similar articles found in: Ann Rheum Dis Online PubMed PubMed Citation This Article has been cited by: other online articles Search PubMed for articles by: Bird Stewart, J. A. Alert me when: new articles cite this article Download to Citation Manager Annals of the Rheumatic Diseases, 1986, Vol 45, 265-268 PAPERS Genetic analysis of families of patients with Behcet's syndrome: data incompatible with autosomal recessive inheritance JA Bird Stewart Data on families with Behcet's syndrome were analysed to test a hypothesis of autosomal recessive inheritance. Fifteen families from the UK and nine from Turkey were included. There were 27 individuals with Behcet's syndrome according to the Japanese criteria and 119 unaffected individuals. There were no affected parents in the families. The 'goodness of fit' test of Elandt-Johnson was applied to the distribution of affected individuals in these families, and the data were found to be incompatible with autosomal recessive inheritance. HLA associations were also examined in patients and

97. Behçet's Syndrome Hamuryudan V, et al Systemic interferon alpha2b treatment in Behcet syndrome. J Rheumatol 1994;211098-1100; Kaklamni VG, Vaiopoulos G, Koklomonis PG. http://www.5mcc.com/Assets/SUMMARY/TP0115.html

DESCRIPTION: Rare multisystem, chronic disease characterized by oral and genital mucocutaneous ulcerations, skin rashes, arthritis, thrombophlebitis, uveitis, colitis, and neurologic symptoms. Endemic in Japan and Northeastern Mediterranean region. System(s) affected: Skin/Exocrine, Reproductive, Nervous, Renal/Urologic, Musculoskeletal Genetics: One report in a mother and newborn (A. Fam, Ann Rheumatic Dis 1981;40:509-512). Very rarely familial. Incidence/Prevalence in USA: In other countries, per 100,000 Japan: 10 Iran: 16-100 Germany: 2 Saudi Arabia: 20 Predominant age: 3rd to 4th decades Predominant sex: CAUSES: Unknown Classified as vasculopathy or autoimmune HLA-B5 alloantigen relationship Possible environmental toxin - heavy metals, pesticides Possibly English walnuts or Ginkgo nuts Fibrinolysis abnormality One report associated with HIV infection (C. Stein, J Rheumatol 1991;18,1427-8) Synonyms: Mucocutaneous ocular syndrome Franceschetti-Valero syndrome ICD-9-CM: REFERENCES: Shimizu T, et al: Behcet disease. Semin Arthritis Rheum 1979; 8:223-260 Chaleby K: Clin Chem 1987;33:1679-1681

98. NZORD Support Groups Postal address PO Box 117, Kaikohe Phone 09 401 0429 Email bechets.info@nzord.org.nz Personal stories of people affected by Behcet s syndrome Click here to http://www.nzord.org.nz/internal.asp?CategoryID=100006&ArticleID=100126

99. Health Library - support groups. Behcet s syndrome. This information is provided as a resource and does not constitute an endorsement for any group. It http://myhealth.barnesjewish.org/library/healthguide/selfhelp/topic.asp?hwid=shc

100. Gimenei >> Health >> Conditions_and_Diseases >> Musculoskeletal_Disorders >> Con Gimenei.com, Search for Scope All Words, Results per page 10. Request Timeout 2, http://www.gimenei.com/directory/top/Health/Conditions_and_Diseases/Musculoskele

Search for: Scope: All Words Any Word Phrase Results per page: Request Timeout: Search Depth: Gimenei Health Conditions and Diseases Musculoskeletal Disorders ... Connective Tissue Behcet's Syndrome DVD: DVD: The China Syndrome DVD: Book: You Are Not Alone: 15 People With Behcet's - So you've just been given the diagnosis of Behcet's Disease, a rare autoimmune rheumatic condition that seemingly no one has ever heard of before. I have the disease myself, and I enjoyed reading how others like me are coping. This book offers in-depth personal stories of Americans who deal with Behcet's Disease on a daily basis and can help you feel less alone. Check out Joanne Zeis's other books and resources too for the best patient information available!

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