نتایج جستجو برای: but mps

تعداد نتایج: 2058103  

2014
Serena Del Turco Giuseppina Basta Alessandro Mazzarisi Debora Battaglia Teresa Navarra Michele Coceani Massimiliano Bianchi Mathis Schlueter Paolo Marraccini

BACKGROUND Circulating microparticles (MPs) have been reported to be associated with coronary artery disease (CAD). In this study, we explored the relationship between MPs procoagulant activity and characteristics of atherosclerotic plaque detected by 64-slice computed tomography angiography (CTA). METHODS In 127 consecutive patients with CAD but without acute coronary syndrome and who underw...

2015
Yohei Sato Masako Fujiwara Hiroshi Kobayashi Michio Yoshitake Kazuhiro Hashimoto Yuji Oto Hiroyuki Ida

Mucopolysaccharidosis (MPS) is an inherited metabolic disease caused by deficiency of the enzymes needed for glycosaminoglycan (GAG) degradation. MPS type I is caused by the deficiency of the lysosomal enzyme alpha-l-iduronidase and is classified into Hurler syndrome, Scheie syndrome, and Hurler-Scheie syndrome based on disease severity and onset. Cardiac complications such as left ventricular ...

Journal: :Revista do Hospital das Clinicas 2000
L M Albano S S Sugayama D R Bertola C E Andrade C Y Utagawa F Puppi H B Nader L Toma J Coelho S Leistner M Burin R Giugliani A K Chong

UNLABELLED The mucopolysaccharidoses (MPS) are a heterogeneous group of inborn errors of lysosomal glycosaminoglycan (GAG) metabolism. The importance of this group of disorders among the inborn errors of metabolism led us to report 19 cases. METHOD We performed clinical, radiological, and biochemical evaluations of the suspected patients, which allowed us to establish a definite diagnosis in ...

Journal: :Arquivos de neuro-psiquiatria 2006
Marcos C Lange Hélio A G Teive André R Troiano Marco Bitencourt Vaneuza A M Funke Daniela C Setúbal José Zanis Neto Carlos R Medeiros Lineu C Werneck Ricardo Pasquini Carmen M S Bonfim

Bone marrow transplantation (BMT) is a therapeutic option for patients with genetic storage diseases. Between 1979 and 2002, eight patients, four females and four males (1 to 13 years old) were submitted to this procedure in our center. Six patients had mucopolysaccharidosis (MPS I in 3; MPS III in one and MPS VI in 2), one had adrenoleukodystrophy (ALD) and one had Gaucher disease. Five patien...

Journal: :Journal of applied physiology 2015
Stephen R Thom Michael Bennett Neil D Banham Walter Chin Denise F Blake Anders Rosen Neal W Pollock Dennis Madden Otto Barak Alessandro Marroni Costantino Balestra Peter Germonpre Massimo Pieri Danilo Cialoni Phi-Nga Jeannie Le Christopher Logue David Lambert Kevin R Hardy Douglas Sward Ming Yang Veena B Bhopale Zeljko Dujic

Decompression sickness (DCS) is a systemic disorder, assumed due to gas bubbles, but additional factors are likely to play a role. Circulating microparticles (MPs)--vesicular structures with diameters of 0.1-1.0 μm--have been implicated, but data in human divers have been lacking. We hypothesized that the number of blood-borne, Annexin V-positive MPs and neutrophil activation, assessed as surfa...

2014
Songwang Hou Doris Grillo Carol L. Williams J. Andrew Wasserstrom Igal Szleifer Ming Zhao

Cancer cell-derived micro-particles (MPs) play important regulatory roles on cellular and system levels. These activities are attributed in part to protein factors carried by MPs. However, recruitment strategies for sequestering certain protein factors in MPs are poorly understood. In the current study, using exogenous and endogenously expressed phospholipid-binding probes, we investigated the ...

2017
Nils Rother Elmar Pieterse Jelle Lubbers Luuk Hilbrands Johan van der Vlag

OBJECTIVE Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by the presence of autoantibodies against nuclear components. Lupus nephritis (LN) is the major cause of morbidity and mortality in patients with SLE. Central to the pathogenesis of SLE is the accumulation of cellular waste, especially apoptotic microparticles (MPs), which stimulates diverse immune reactions inc...

Journal: :International journal of clinical and experimental pathology 2015
Fang Ma Hengchao Liu Yong Shen Yingjie Zhang Shaojun Pan

The ischemia-protective mechanism of remote precondition has been a mystery for a long time. Little was known about details of the inter-organ cardio-protective. Microvesicles, also known as microparticles (MPs), are small membrane-vesicles budding from the plasma membrane of cell. Recent studies have indicated MPs to be an important messenger in various biological processes. Our research mainl...

Journal: :Vox sanguinis 2008
O Rubin D Crettaz G Canellini J-D Tissot N Lion

BACKGROUND AND OBJECTIVES Microparticles (MPs) are small phospholipid vesicles of less than 1 microm, shed in blood flow by various cell types. These MPs are involved in several biological processes and diseases. MPs have also been detected in blood products; however, their role in transfused patients is unknown. The purpose of this study was to characterize those MPs in blood bank conditions. ...

Journal: :Blood 2011
Jakub Tolar In-Hyun Park Lily Xia Chris J Lees Brandon Peacock Beau Webber Ron T McElmurry Cindy R Eide Paul J Orchard Michael Kyba Mark J Osborn Troy C Lund John E Wagner George Q Daley Bruce R Blazar

Mucopolysaccharidosis type I (MPS IH; Hurler syndrome) is a congenital deficiency of α-L-iduronidase, leading to lysosomal storage of glycosaminoglycans that is ultimately fatal following an insidious onset after birth. Hematopoietic cell transplantation (HCT) is a life-saving measure in MPS IH. However, because a suitable hematopoietic donor is not found for everyone, because HCT is associated...

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