Biomaterial Database

HLA antigens associated with Behçet's disease. 1977

F Ersoy, and I Berkel, and T Firat, and H Kazokoğlu

UI	MeSH Term	Description	Entries
D008875	Middle Aged	An adult aged 45 - 64 years.	Middle Age
D006649	Histocompatibility Antigens	A group of antigens that includes both the major and minor histocompatibility antigens. The former are genetically determined by the major histocompatibility complex. They determine tissue type for transplantation and cause allograft rejections. The latter are systems of allelic alloantigens that can cause weak transplant rejection.	Transplantation Antigens,Antigens, Transplantation,Histocompatibility Antigen,LD Antigens,SD Antigens,Antigen, Histocompatibility,Antigens, Histocompatibility,Antigens, LD,Antigens, SD
D006801	Humans	Members of the species Homo sapiens.	Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000293	Adolescent	A person 13 to 18 years of age.	Adolescence,Youth,Adolescents,Adolescents, Female,Adolescents, Male,Teenagers,Teens,Adolescent, Female,Adolescent, Male,Female Adolescent,Female Adolescents,Male Adolescent,Male Adolescents,Teen,Teenager,Youths
D000328	Adult	A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available.	Adults
D001528	Behcet Syndrome	Rare chronic inflammatory disease involving the small blood vessels. It is of unknown etiology and characterized by mucocutaneous ulceration in the mouth and genital region and uveitis with hypopyon. The neuro-ocular form may cause blindness and death. SYNOVITIS; THROMBOPHLEBITIS; gastrointestinal ulcerations; RETINAL VASCULITIS; and OPTIC ATROPHY may occur as well.	Behcet Disease,Behcet's Disease,Behcet's Syndrome,Triple-Symptom Complex,Adamantiades-Behcet Disease,Behcet Triple Symptom Complex,Behçet Disease,Old Silk Route Disease,Triple Symptom Complex,Adamantiades Behcet Disease,Adamantiades-Behcet Diseases,Behçet Diseases,Symptom Complex, Triple,Triple Symptom Complices

Related Publications

F Ersoy, and I Berkel, and T Firat, and H Kazokoğlu

[HLA antigens and Behçet's disease (author's transl)].

February 1978, Nippon Ganka Gakkai zasshi,

F Ersoy, and I Berkel, and T Firat, and H Kazokoğlu

HLA antigens in a Japanese family with Behçet's disease.

October 1994, Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie,

F Ersoy, and I Berkel, and T Firat, and H Kazokoğlu

HLA antigens in Behçet's disease with refractory ocular attacks.

April 1987, Tissue antigens,

F Ersoy, and I Berkel, and T Firat, and H Kazokoğlu

Specific histocompatibility antigens associated with Behçet's disease.

October 1975, American journal of ophthalmology,

F Ersoy, and I Berkel, and T Firat, and H Kazokoğlu

HLA antigens in familial Behçet's disease in Ireland.

November 1998, British journal of rheumatology,

F Ersoy, and I Berkel, and T Firat, and H Kazokoğlu

HLA-DR and DQ antigens in Chinese patients with Behçet's disease.

February 1993, Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology,

F Ersoy, and I Berkel, and T Firat, and H Kazokoğlu

Behçet's disease: lack of correlation of clinical manifestations with HLA antigens.

February 1981, Tissue antigens,

F Ersoy, and I Berkel, and T Firat, and H Kazokoğlu

HLA antigens in a family with Behçet's syndrome.

January 1986, Acta medica Scandinavica,

F Ersoy, and I Berkel, and T Firat, and H Kazokoğlu

HLA antigens and Adamantiades-Behçet's disease (A-BD) in Greeks.

January 1988, Clinical and experimental rheumatology,

F Ersoy, and I Berkel, and T Firat, and H Kazokoğlu

Behçet's disease associated with one of the HLA-B51 subantigens, HLA-B* 5101.

October 1993, American journal of ophthalmology,