نتایج جستجو برای: kayser

تعداد نتایج: 275  

2017
Anne Chatton Bengt Kayser

INTRODUCTION: In affluent countries habitual physical activity (PA) levels are low while participation of middle-aged people in road running events is increasing. We compared PA determinants of runners aged 50+ to those of a general population sample of similar age in Switzerland. METHOD: Cross-sectional study comparing 580 road running event participants to 1,067 general population subjects. B...

Journal: :Gut 2006
A Rühl

brain mapping. IEEE Signal Process Mag 2001;18:14–30. 23 Kayser J, Tenke CE. Trusting in or breaking with convention: towards a renaissance of principal components analysis in electrophysiology. Clin Neurophysiol 2005;116:1747–53. 24 Friston K. Modes or models: a critique on independent component analysis for fMRI. Trends Cogn Sci 1998;2:373–5. 25 Delorme A, Makeig S. EEGLAB: an open source too...

2008
A. R. LORIMER J. MCGEE S. G. MCALPINE

CONGENITAL hepatic fibrosis is an uncommon cause of portal hypertension and usually presents as alimentary bleeding in childhood or adolescence. The occurrence in more than one member of a family has been described (Kerr et al., 1961; Campbell et al., 1958). This report concerns four members of one family who have presented with clinical features attributable to congenital hepatic fibrosis. Pat...

2014
Shih-Min Lin Jy-Been Liang Ke-Hung Chien Yi-Hao Chen Jiann-Torng Chen Da-Wen Lu Chi-Ting Horng

Purpose: To report a case of asymptomatic Wilson’s disease (WD) in which the identification of a Kayser-Fleischer (K-F) ring and its characterization by confocal biomicroscopy led to the diagnosis. Methods: Case report. Results: Confocal biomicroscopy showed clustered, highly reflective, and round foci in Descemet’s membrane, which we believed to be depositions of copper in this patient with as...

1994
R Aleksan A Le Yaouanc L Oliver J.-C Raynal

To help the difficult determination of the angle γ of the unitarity triangle, Aleksan, Dunietz and Kayser have proposed the modes of the type K − D + s , common to B s and ¯ B s. We point out that it is possible to gain in statistics by a sum over all modes with ground state mesons in the final state, i.e. s. The delicate point is the relative phase of these different contributions to the dilut...

2018
Takahiro Amano Tokuhiro Matsubara Tsutomu Nishida Hiromi Shimakoshi Akiyoshi Shimoda Aya Sugimoto Kei Takahashi Kaori Mukai Masashi Yamamoto Shiro Hayashi Sachiko Nakajima Koji Fukui Masami Inada

A 64-year-old woman was referred to our hospital with jaundice of the bulbar conjunctiva and general fatigue. After admission, she developed hepatic encephalopathy and was diagnosed with fulminant hepatitis based on the American Association for the Study of Liver Disease (AASLD) position paper. Afterwards, additional laboratory findings revealed that serum ceruloplasmin levels were reduced, uri...

Journal: :Antimicrobial agents and chemotherapy 1993
K J Shaw H Munayyer P N Rather R S Hare G H Miller

The ant(4')-IIa gene was previously cloned from Pseudomonas aeruginosa on a 1.6-kb DNA fragment (G. A. Jacoby, M. J. Blaser, P. Santanam, H. Hächler, F. H. Kayser, R. S. Hare, and G. H. Miller, Antimicrob. Agents Chemother. 34:2381-2386, 1990). In the current study, the ant(4')-IIa gene was localized by gamma-delta mutagenesis. A region of approximately 600 nucleotides which contained the ant(4...

2009
Chandramouli Chandrasekaran Asif A. Ghazanfar Sascha Tyll Carsten Nicolas Boehler Eike Budinger Hans-Jochen Heinze Ryan J. Morrill Luis Lemus

[PDF] [Full Text] [Abstract] , October 27, 2009; 106 (43): 18362-18366. PNAS Shawn A. Steckenfinger and Asif A. Ghazanfar Monkey visual behavior falls into the uncanny valley [PDF] [Full Text] [Abstract] , October 13, 2010; 30 (41): 13609-13623. J. Neurosci. and Jon Driver Toemme Noesselt, Sascha Tyll, Carsten Nicolas Boehler, Eike Budinger, Hans-Jochen Heinze Visual Detection Sensitivity S...

2016
Qi-Jie Zhang Liu-Qing Xu Chong Wang Wei Hu Ning Wang Wan-Jin Chen

RATIONALE Wilson's disease (WD) is an autosomal recessive inherited disorder of copper metabolism with excellent prognosis if treated timely. However, WD is usually prone to neglect and misdiagnosis at an early stage. We reported a rare WD pedigree, and the clinical features, laboratory tests, and gene mutations were analyzed in detail. PATIENT CONCERNS The patient was a 17-year-old and 136-c...

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