نتایج جستجو برای: intermediate syndrome

تعداد نتایج: 746925  

2014
Isabella Eckerle Victor M. Corman Marcel A. Müller Matthias Lenk Rainer G. Ulrich Christian Drosten

Replicative capacity of Middle East respiratory syndrome coronavirus (MERS-CoV) was assessed in cell lines derived from livestock and peridomestic small mammals on the Arabian Peninsula. Only cell lines originating from goats and camels showed efficient replication of MERS-CoV. These results provide direction in the search for the intermediate host of MERS-CoV.

Journal: :Haematologica 2009
Akos Czibere Ingmar Bruns Bärbel Junge Raminder Singh Guido Kobbe Rainer Haas Ulrich Germing

To further clarify the role of ribosomal protein S14 (RPS14) in myelodysplastic syndrome, we examined RPS14 transcription in bone marrow derived CD34+ cells from patients with non-5q- myelodysplastic syndrome and found a reduced expression of RPS14 in 51 of 72 (71%) patients. MDS patients with an intermediate-1 risk (INT-1) score according to the international prognostic scoring system and low ...

Journal: :iranian journal of applied language studies 2015
mohammad hassan chehrazad parviz ajideh

test method facet is one of the factors which can have an influence on the test takers’ performance. the purpose of the current study was to investigate the effects of two different response types, multiple-choice cloze and multiple-choice test, on the pre-intermediate and intermediate test takers’ reading comprehension performance. to this end, 40 pre-intermediate and intermediate learners par...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تبریز 1348

چکیده ندارد.

2012
Eun Soo Jeong Min Jeong Kim Seung Hyen Yoo Dong Hyun Kim Jin Sung Jung Nam Ho Koo Se Heon Chang

Intramural hematoma of the esophagus (IHE) is an uncommon form of esophageal injury, which may be an intermediate of mucosal tear (Mallory-Weiss syndrome) or transmural rupture (Boerhaave's syndrome). To date, the pathogenesis of IHE has not been well documented. IHE may occur within the submucosal layer of the esophagus following dissection of the mucosa. The most commonly presented symptoms a...

2017
Tu-Anh Tran

Muckle-Wells syndrome (MWS) is a rare autoinflammatory disorder. It is due to NLRP3 gene mutations, responsible for excessive caspase-1 activation and interleukin 1β processing. MWS is the intermediate phenotype of severity of cryopyrin-associated periodic syndrome. Urticarial rash, conjunctivitis, recurrent fever, arthralgia, and fatigue are the main clinical manifestations of MWS. Yet, sensor...

Journal: :Neurosurgery 1996
M Cerdà-Esteve E Cuadrado-Godia J J Chillaron C Pont-Sunyer G Cucurella M Fernández A Goday J F Cano-Pérez A Rodríguez-Campello J Roquer

Hyponatremia is the most frequent electrolyte disorder in critically neurological patients. Cerebral salt wasting syndrome (CSW) is defined as a renal loss of sodium during intracranial disease leading to hyponatremia and a decrease in extracellular fluid volume. The pathogenesis of this disorder is still not completely understood. Sympathetic responses as well as some natriuretic factors play ...

2009
Gianluca Di Micco

The clinical presentation of ischaemic heart disease includes stable and unstable angina pectoris, silent ischaemia, myocardial infarction, heart failure and sudden death [1]. For many years, unstable angina has been considered an intermediate syndrome between chronic stable angina and acute myocardial infarction. In recent years, its pathophysiology has been clarified and acute coronary syndro...

Journal: :Developmental cell 2013
Devangini Gandhi Andrei Molotkov Ekatherina Batourina Kerry Schneider Hanbin Dan Maia Reiley Ed Laufer Daniel Metzger Fengxia Liang Yi Liao Tung-Tien Sun Bruce Aronow Roni Rosen Josh Mauney Rosalyn Adam Carolina Rosselot Jason Van Batavia Andrew McMahon Jill McMahon Jin-Jin Guo Cathy Mendelsohn

The urothelium is a multilayered epithelium that serves as a barrier between the urinary tract and blood, preventing the exchange of water and toxic substances. It consists of superficial cells specialized for synthesis and transport of uroplakins that assemble into a tough apical plaque, one or more layers of intermediate cells, and keratin 5-expressing basal cells (K5-BCs), which are consider...

2014
Travis A. Dittmer Nidhi Sahni Nard Kubben David E. Hill Marc Vidal Rebecca C. Burgess Vassilis Roukos Tom Misteli

Laminopathies are a collection of phenotypically diverse diseases that include muscular dystrophies, cardiomyopathies, lipodystrophies, and premature aging syndromes. Laminopathies are caused by >300 distinct mutations in the LMNA gene, which encodes the nuclear intermediate filament proteins lamin A and C, two major architectural elements of the mammalian cell nucleus. The genotype-phenotype r...

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