نتایج جستجو برای: bullosa

تعداد نتایج: 3547  

Journal: :acta medica iranica 0
m. h. baradaranfar m. labibi

the presence of anatomic variations of paranasal sinuses must be noted in order to attain a full understanding and accurate diagnosis of chronic sinusitis. the frequency of anatomic variations in chronic sinusitis is different in various studies. the purpose of this study is to assess the frequency of anatomic variations in chronic sinusitis patients admitted to otolaryngology ward of shahid sa...

Journal: :Anais brasileiros de dermatologia 2010
Zilda Najjar Prado de Oliveira Alexandre M Périgo Lígia M I Fukumori Valéria Aoki

Immunological mapping, an immunofluorescence technique, is currently the method most used to diagnose and differentiate the principal types of hereditary epidermolysis bullosa, since this technique is capable of determining the level of cleavage of this mechanobullous disease.

Journal: :Journal of neonatal surgery 2015
Mahdi Ben Dhaou Saloua Ammar Hamdi Louati Hayet Zitouni Mohamed Jallouli Riadh Mhiri

Epidermolysis bullosa (EB) is an inherited blistering disorder characterized by the fragility of the skin and mucous membranes. Extracutaneous manifestations can be associated. We report a unique concomitant occurrence of EB and hypertrophic pyloric stenosis in a newborn.

Journal: :Proceedings of the Royal Society of Medicine 1929

Journal: :Molecular medicine 1998
J L Arbiser J D Fine D Murrell A Paller S Connors K Keough E Marsh J Folkman

BACKGROUND Patients with recessive dystrophic epidermolysis bullosa (RDEB) have deficiencies of collagen type VII and have elevated levels of fibroblast collagenase, and a greatly increased risk of cutaneous squamous cell carcinoma. Patients with other genetic blistering disorders do not have elevated collagenase or an increased risk of squamous cell carcinoma, despite chronic wounding. The con...

Journal: :British journal of nursing 2008
Elizabeth Pillay

This article is the first in a series of three focusing on the causes, clinical presentation, complications and care of adult patients affected by epidermolysis bullosa (EB), a group of rare genetic skin fragility disorders. Although the condition is rare, in some cases it presents extreme challenges both to those affected and those involved in the care of the EB patient; therefore, these artic...

Journal: :Nihon Naibunpi Gakkai zasshi 1990
F Nakamura H Rakugi K Fukuo M Nakamaru F Masugi T Onishi T Ogihara K Hashimoto T Kozuka K Yoshikawa

Epidermolysis bullosa is a group of disorders whose common primary feature is the formation of blisters following trivial trauma. Recessive dystrophic epidermolysis bullosa (RDEB), a subtype of epidermolysis bullosa, is frequently associated with growth retardation. This growth retardation has been reported to be caused by trophopathy following protein loss through skin lesions. Endocrine disor...

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