نتایج جستجو برای: jacob disease

تعداد نتایج: 1492846  

2015
Alan Peres Valente Paula da Cunha Pinho Leandro Tavares Lucato

Creutzfeldt-Jacob disease (CJD) is a rare condition caused by a pathogenic prion protein that evolves with rapidly progressive dementia and death. The clinical presentation may sometimes be misleading. Magnetic Resonance Imaging (MRI) aids diagnosis with patterns that can guide or confirm clinical hypotheses. Two cases of rapidly progressive dementia with ataxia, myoclonus and restricted diffus...

2015
P Jolliet L Besbes F Abroug J Ben Kheli M Besbes J-M Arnal F Daviaud J-D Chiche B Lortat-Jacob J-L Diehl N Lerolle A Mercat K Razazi C Brun-Buisson S Bertini A Corrado J Texereau L Brochard

An international phase iii randomised trial on the efficacy of helium/oxygen during spontaneous breathing and intermittent non-invasive ventilation for severe exacerbations of chronic obstructive pulmonary disease (the E.C.H.O.trial) P Jolliet, L Besbes, F Abroug, J Ben Kheli, M Besbes, J-M Arnal, F Daviaud, J-D Chiche, B Lortat-Jacob, J-L Diehl, N Lerolle, A Mercat, K Razazi, C Brun-Buisson, S...

2014
SRIRAM POTHAPREGADA

So-called ‘Saharanpur encephalitis,’ with high case fatality, used to occur annually, post-monsoon, in Western districts of Uttar Pradesh (UP). Over 2 decades, Indian Council of Medical Research (ICMR) and National Centre for Disease Control (NCDC) staff failed to diagnose it. A team of volunteer investigators (T Jacob John, virologist; VM Vashishtha, pediatrician; NC Nayak, pathologist; Amod K...

2011
Thomas Behnisch PingAn YuanXiang Philipp Bethge Suhel Parvez Ying Chen Jin Yu Anna Karpova Julietta U. Frey Marina Mikhaylova Michael R. Kreutz

BACKGROUND In recent years a number of potential synapto-nuclear protein messengers have been characterized that are thought to be involved in plasticity-related gene expression, and that have the capacity of importin- mediated and activity-dependent nuclear import. However, there is a surprising paucity of data showing the nuclear import of such proteins in cellular models of learning and memo...

Journal: :Annals of clinical and laboratory science 1997
J A Knight

The laboratory examination of cerebrospinal fluid (CSF) continues to play an important role in the clinical diagnosis and treatment of various disorders of the central nervous system (CNS). The major conditions currently include, as they have in the past, infectious diseases, neoplastic processes, multiple sclerosis, other demyelinating disorders, and intracerebral hemorrhage. Recent publicatio...

2008
Jacob Steinhardt Thomas Jefferson

We investigate subsets of the symmetric group with structure similar to that of a graph. The “trees” of these subsets correspond to minimal conjugate generating sets of the symmetric group. There are two main theorems in this paper. The first is a characterization of minimal conjugate generating sets of Sn. The second is a generalization of a result due to Feng characterizing the automorphism g...

Journal: :Veterinary pathology 2011
B F Porter B C Lewis J F Edwards J Alroy B J Zeng P A Torres K N Bretzlaff E H Kolodny

The G(M2) gangliosidoses are a group of lysosomal storage diseases caused by defects in the genes coding for the enzyme hexosaminidase or the G(M2) activator protein. Four Jacob sheep from the same farm were examined over a 3-year period for a progressive neurologic disease. Two lambs were 6-month-old intact males and 2 were 8-month-old females. Clinical findings included ataxia in all 4 limbs,...

2011
E. Thompson

Department of Psychology University of Ghana. Legon-Accra School of Counselling and Educational Psychology Indiana University-Purdue University, Indianapolis (IUPUI) Indianapolis, Indiana USA Corresponding Author: Samuel Atindanbila ___________________________________________________________________________ This paper is aimed at describing the practices of African Traditional Healers, highligh...

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