نتایج جستجو برای: disease progress curve

تعداد نتایج: 1734701  

Journal: :Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin 2013
E Schwartz E Meltzer M Mendelson A Tooke F Steiner P Gautret B Friedrich-Jaenicke M Libman H Bin A Wilder-Smith Dj Gubler D O Freedman P Parola

In April 2013, ten cases of dengue fever in travellers returning from Luanda, Angola, to five countries on four continents, were reported to the globally distributed GeoSentinel Surveillance network. Dengue virus serotype 1 was identified in two cases. The findings indicate that a major dengue outbreak is currently ongoing in Luanda. This report illustrates how cases from an emerging arboviral ...

1997
Sylvain Lizotte Brahim Chaib-draa

the Management of Dependences between Activities Sylvain Lizotte & Brahim Chaib-draa Computer Science Department, Laval University, Ste-Foy, PQ, Canada, G1K 7P4 e-mail: {lizotte,chaib}@ift.ulaval.ca Short form of the title: Coordination = Management of Dependences Author to whom correspondence should be sent: B. Chaib-draa Mailing address: Département Informatique, Pav. Pouliot, Université Lava...

2008
ROBERT G. OJEMANN ROBERTO C. HEROS

SPONTANEOUS BRAIN HEMORRHAGE accounts for about 10% of all strokes and is associated with a high morbidity and mortality rate." While the incidence of stroke due to occlusive cerebrovascular disease has declined the incidence of intracerebral hemorrhage has remained relatively stable. The syndromes that result from brain hemorrhage are sufficiently characterized to permit their clinical recogni...

Journal: :Rinsho shinkeigaku = Clinical neurology 2013
Yoshio Tsuboi

Treatment for prion disease: recent progress

2017
Laura Bognar Andras Vereczkei Ors Peter Horvath

c 2017 The Korean Society of Neurogastroenterology and Motility J Neurogastroenterol Motil, Vol. 23 No. 4 October, 2017 www.jnmjournal.org TO THE EDITOR: We read with interest the article entitled “Is Gastroesophageal Reflux Disease and Achalasia Coincident or Not” published in January 2017, by Jung and Park. The title raises a very interesting question, however, in the end, the question remain...

Journal: :Blood 2016
Leslie V Parise Nancy Berliner

Despite a long history of knowing the genetic cause of sickle cell disease (SCD), progress in developing treatments to prevent painful vaso-occlusive crises and the other myriad of associated symptoms has, until recently, been disappointingly slow. As long ago as 1949, Pauling et al described sickle cell anemia as a molecular disease, with two other groups convincingly describing it as an inher...

2015
Lin Chen Hongyun Huang wei-Ming Duan Gengsheng Mao

License. The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. Permissions beyond the scope of the License are administered by Dove Medical Press Limited. Information on how to request permission may be f...

2011
Paul J Martin

255 PRF deficiency occurs not only with allelic variants characterized by mutations in the coding region of the gene. McIlroy et al. reported that the occurrence of a C/T polymorphism at position-398 of the proximal promoter region of the PRF1 gene was associated with decreased quantities of PRF in CTLs in HIV infected patients. A decrease of about 50% of control PRF levels was observed in hete...

2010
Wonjin Ji Ilho Ha

Alzheimer's disease, the most common cause of dementia, is characterized by two major pathological hallmarks: amyloid plaques and neurofibrillary tangles. Based on these two indicators, an amyloid cascade hypothesis was proposed, and accordingly, most current therapeutic approaches are now focused on the removal of β-amyloid peptides (Aβ from the brain. Additionally, strategies for blocking tau...

Journal: :Postepy higieny i medycyny doswiadczalnej 2013
Karolina Pytka Małgorzata Zygmunt Barbara Filipek

Parkinson's disease (PD) is a chronic, progressive disease of the central nervous system (CNS), characterized by a slow loss of dopaminergic neurons in the substantia nigra, leading to significant decrease in dopamine (DA) levels in the striatum. Currently used drugs, such as levodopa (L-DOPA), amantadine, dopamine agonists (D) or anticholinergic drugs, are not effective enough, and do not elim...

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