Results 61 to 70 of about 730,915 (232)

Scrotal doppler ultrasonography in behcet?s disease [PDF]

open access: yes, 2010
Behçet hastalığı vaskülit ile karakteize multisistemik bir hastalıktır. İlk olarak Hulusi Behçet tarafından 1937 yılında tariflenmiştir. Tekrarlayan oral-genital ülserler ve üveit triadı ile meydana çıkar.
Aktaş, Ünal
core  

Endovascular repair of a dual abdominal aortic aneurysm in Behcet's disease

open access: yesTurkish Journal of Vascular Surgery, 2019
Behcet's disease is an inflammatory multisystemic vasculitis characterized by orogenic ulcers and ocular lesions and its etiology is still unknown. The incidence of aortic aneurysms is 2 to 6% in patients with Behcet's disease and 18% of these ...
Elif Coşkun   +3 more
doaj  

Experimental Therapeutic Solutions for Behcet’s Disease

open access: yesJournal of Experimental Pharmacology, 2021
Burçin Cansu Bozca, Erkan Alpsoy Akdeniz University School of Medicine, Department of Dermatology and Venereology, Antalya, TurkeyCorrespondence: Erkan AlpsoyAkdeniz University School of Medicine, Department of Dermatology and Venereology, Antalya,
Bozca BC, Alpsoy E
doaj  

Rare vasculitis types and obstetric and neonatal outcomes – A population‐based study

open access: yesInternational Journal of Gynecology &Obstetrics, EarlyView.
Abstract Objective Vasculitis is an infrequent pathology among reproductive‐aged women. While data exists regarding pregnancy outcomes in the more common vasculitis subtypes, data is limited regarding these outcomes in rare vasculitis subtypes. We aimed to compare pregnancy and perinatal outcomes between women who suffered from rare types of vasculitis
Uri Amikam   +4 more
wiley   +1 more source

The genetic landscape of congenital diarrheas and very early onset inflammatory bowel disease in the Middle East

open access: yesJPGN Reports, EarlyView.
Abstract Objectives Monogenic causes of congenital diarrheas and enteropathies (CoDE) and very early onset inflammatory bowel disease (VEOIBD) are mostly recessive and therefore more prevalent in populations with increased consanguinity rates. To assess the genetic basis of these disorders in a likely high‐prevalence population, we established a multi ...
Lily Gillette   +21 more
wiley   +1 more source

Behcet\u27s Disease [PDF]

open access: yes, 2022
This video provides an overview of Behcet\u27s Disease, a rare vasculitis of unknown ...
Harinee Arunachalam, MSIV; Sean Gratton, MD
core  

Juvenile Gangrenous Vasculitis of the Scrotum or Scrotum Lipschütz Ulcers

open access: yesJEADV Clinical Practice, EarlyView.
ABSTRACT Lipschütz genital ulcers are traditionally described in adolescent females and often linked to acute viral infections. Their male counterpart remains poorly characterised. We report a 59‐year‐old man with sudden onset of unilateral necrotic ulcers on the scrotum and inguinal region following a brief febrile episode and mild pharyngitis ...
Francesco Bellinato   +2 more
wiley   +1 more source

Identification of multiple independent susceptibility loci in the HLA region in Behcet's disease [PDF]

open access: yes, 2013
Behcet's disease is an inflammatory disease characterized by recurrent oral and genital ulcers and significant organ involvement. Localizing the genetic association between HLA-B*51 and Behcet's disease and exploring additional susceptibility ...
DİRESKENELİ, RAFİ HANER
core   +1 more source

Triggering of Koebner Phenomenon by Picosecond Laser in a Psoriatic Patient: Clinical and Immunopathologic Insights

open access: yesLasers in Surgery and Medicine, EarlyView.
ABSTRACT Objectives To report the first case of Koebner phenomenon induced by picosecond laser treatment in a patient with psoriasis. We analyzed the clinical and histopathological features and discussed the possible mechanism by which the laser's photomechanical effect triggered the reaction.
Teppei Sakai, Koya Sonoda, Jun Omatsu
wiley   +1 more source

A strong association between HLA-B(*)5101 and Behcet's disease in Greek patients [PDF]

open access: yes, 1997
Behcet's disease is known to be associated with HLA-B51, one of the split antigens of HLA-B5, among many different ethnic groups. In a Greek population, an increased incidence of HLA-B5 in the patient group has also been reported.
Isobe, K.   +12 more
core  

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