نتایج جستجو برای: monilia laxa
تعداد نتایج: 831 فیلتر نتایج به سال:
Marie-José Côté, Canadian Food Inspection Agency, Ottawa Laboratory (Fallowfield), Centre for Plant Quarantine Pests, 3851 Fallowfield Road, Ottawa, Ontario, Canada, K2H 8P9; Marie-Claude Tardif, Health Canada, Food Directorate, Building #7, Tunney’s Pasture, P.L. 0700E1, Ottawa, Ontario, Canada K1A 0L2; and Allison J. Meldrum, Canadian Food Inspection Agency, Ottawa Laboratory (Fallowfield), C...
Ashford (1917) and a number of subsequent workers regarded monilias, particularly Monilia psilosis, as the cause of sprue. Several species of the genus Monilia have been implicated in the causation of sprue and this disease was at one time regarded as moniliasis of the digestive tract. Although the result of recent work has shown that this view is no longer justifiable, there is a tendency for ...
Cutis laxa is a heterogeneous condition characterized by redundant, sagging, inelastic, and wrinkled skin. The inherited forms of this disease are rare and can have autosomal dominant, autosomal recessive, or X-linked inheritance. Three of the autosomal recessive cutis laxa syndromes, namely cutis laxa IIA (ARCL2A), cutis laxa IIB (ARCL2B), and geroderma osteodysplastica (GO), have very similar...
بیماری پوسیدگی قهوه ای یکی از مهم ترین بیماری های درختان میوه هسته دار بوده که بوسیله گونه های مختلفی از قارچ monilia ایجاد می شود. در این بررسی تعداد 70 نمونه از شکوفه و میوه های مشکوک به آلودگی در طی سال های 1390-1389 از شهرستان های استان گلستان جمع آوری شدند. امکان تولید آپوتسیوم در شرایط باغ، کرت های آزمایشی مزرعه، سایه و آزمایشگاه بررسی شد. کنترل بیماری با مقایسه تاثیر چند سم (اکسی کلرور م...
BACKGROUND Cutis laxa is an acquired or inherited condition characterized by redundant, pendulous and inelastic skin. Autosomal dominant cutis laxa has been described as a benign disease with minor systemic involvement. OBJECTIVE To report a family with autosomal dominant cutis laxa and a young girl with sporadic cutis laxa, both with variable expression of an aortic aneurysmal phenotype rang...
Hereditary cutis laxa comprises a heterogeneous group of connective tissue disorders characterized by loose skin and variable systemic involvement. Autosomal dominant and recessive as well as X-linked forms have been described. Some dominant forms are caused by mutations in the elastine gene (ELN). The X-linked form is now classified in the group of copper transport diseases. The genetic defect...
Cutis laxa (CL) is a rare congenital and acquired disorder characterized by loose and redundant skin with reduced elasticity. Three types of congenital cutis laxa have been recognized. Other findings are pulmonary emphysema, bronchiectasia, hernia and diverticulosis. We describe a female neonate involved by cutis laxa syndrome and a positive family history. We focus on the radiologic findings o...
at the Unao Hospital Laboratory, we have come across forms closely resembling the Monilia tropicalis of Castellani, together with spirochetes, pneumococci and Micrococcus catarrhalis. In a few there were staphylococci, streptococci and seldom fusiform bacilli. The first case we saw in 1923 was a female of a well-to-do family and the appearance of Monilia reminded us of the articles published in...
Cutis laxa, clinically characterized by loose and pendulous skin related to loss of elastic tissue, is a rare heterogeneous condition. It is classified into congenital and acquired types. We report a case of generalized acquired cutis laxa type 1 in a young man following pruritic urticarial plaques. We have done a brief review of literature.
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