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Artykuły w czasopismach na temat "Presenile dementia"

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NAKAMURA, SHIGENOBU. "Senile Dementia and Presenile Dementia." Tohoku Journal of Experimental Medicine 161, Supplement (1990): 49–60. http://dx.doi.org/10.1620/tjem.161.supplement_49.

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Pinhorn, A. "Presenile dementia. Dementia classification misleading." BMJ 306, no. 6888 (May 15, 1993): 1343–44. http://dx.doi.org/10.1136/bmj.306.6888.1343-a.

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Järpe, Sven. "PRESENILE DEMENTIA AND HYDROCEPHALUS." Acta Neurologica Scandinavica 46, S43 (January 29, 2009): 89. http://dx.doi.org/10.1111/j.1600-0404.1970.tb02167.x.

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Lying-Tunell, Ulla, Doris Bergquist, Gerhard Böhmer, Hans Olov Malmlund, Olle Marions, and Berndt Söderborg. "STUDIES IN PRESENILE DEMENTIA." Acta Neurologica Scandinavica 46, S43 (January 29, 2009): 90–92. http://dx.doi.org/10.1111/j.1600-0404.1970.tb02168.x.

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Treves, T., A. D. Korczyn, N. Zilber, E. Kahana, Y. Leibowitz, M. Alter, and B. S. Schoenberg. "Presenile dementia in Israel." Alzheimer Disease & Associated Disorders 1, no. 1 (1987): 44. http://dx.doi.org/10.1097/00002093-198701000-00011.

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Whalley, L., G. McGonigal, B. MacLennan, C. McQuade, J. Starr, and B. Thomas. "Presenile dementia: Authors' reply." BMJ 306, no. 6888 (May 15, 1993): 1343–44. http://dx.doi.org/10.1136/bmj.306.6888.1343-c.

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Treves, T., A. D. Korczyn, N. Zilber, E. Kahana, Y. Leibowitz, M. Alter, and B. S. Schoenberg. "Presenile Dementia in Israel." Archives of Neurology 43, no. 1 (January 1, 1986): 26–29. http://dx.doi.org/10.1001/archneur.1986.00520010022014.

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Wright, Christine E., and Paul L. Furlong. "Visual Evoked Potentials in Elderly Patients with Primary or Multi-Infarct Dementia." British Journal of Psychiatry 152, no. 5 (May 1988): 679–82. http://dx.doi.org/10.1192/bjp.152.5.679.

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Flash and pattern-reversal visual evoked potentials (VEP) were recorded in 35 elderly patients with dementia, and 19 controls of equivalent age. Dementia produced a slowing of the major positive (P2) component of the flash VEP but did not affect the latency of the flash P1 component or the P100 pattern-reversal component. This unusual type of abnormality was found in both primary and multi-infarct types of dementia, and has previously been found in primary presenile dementia. The results show that the VEP can be used for the diagnosis of multi-infarct, and primary presenile and senile dementia
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Ernst, B., M. A. Dalby, and A. Dalby. "APHASIC DISTURBANCES IN PRESENILE DEMENTIA." Acta Neurologica Scandinavica 46, S43 (January 29, 2009): 99–100. http://dx.doi.org/10.1111/j.1600-0404.1970.tb02173.x.

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Tonkonogy, Joseph, and Gary S. Moak. "Alois Alzheimer on Presenile Dementia." Topics in geriatrics 1, no. 4 (October 1988): 199–206. http://dx.doi.org/10.1177/089198878800100403.

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Rozprawy doktorskie na temat "Presenile dementia"

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Newens, Andrew J. "The epidemiology of presenile dementia of Alzheimer type." Thesis, University of Newcastle Upon Tyne, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.386740.

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Williams, Ronald N. "Neuropsychological subgroups of dementia of the Alzheimer's type." Virtual Press, 1991. http://liblink.bsu.edu/uhtbin/catkey/774764.

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The present study considered the notion that Neuropsychological subgroups exist within the diagnosis of Dementia of the Alzheimer's Type (DAT). Specifically, the scores on the Cognitive Examination (CAMCOG) of the Cambridge Index of Mental Disorders in the Elderly for 51 DAT patients and 79 normal adults were analyzed via cluster analysis in an attempt to derive meaningful groupings of patients.Results suggested that the CAMCOG was effective in separating normal from impaired individuals. The results also suggested the existence of 4 subgroups within DAT, which were best interpreted as "levels
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Woodburn, Kirstie Jane. "Presenile dementia in Lothian, Scotland : a clinical and genetic analysis." Thesis, University of Edinburgh, 1997. http://hdl.handle.net/1842/21617.

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The study aim was to identify the population of live patients in the Lothian area of Scotland, with presenile dementia of various aetiologies, and to describe the clinical profiles of each and the patterns of decline which occur, together with any genetic characterisation possible. Cases were identified using the Lothian Psychiatric Case Register. For the demographic data, the CAMDEX (The Cambridge Examination of Mental Disorders of the Elderly) informant interview was used. The behavioural assessment comprised the CAPE-BRS (Clifton Assessment Procedure for the Elderly, Behavioural Rating Scal
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Abeysinghe, Sonali Champika 1959. "Word association in persons with dementia of the Alzheimer type." Thesis, The University of Arizona, 1988. http://hdl.handle.net/10150/276651.

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In an attempt to characterize the nature of semantic memory impairment in persons with dementia of the Alzheimer type (DAT), a free association task, a definition task, and an associate rank ordering task were administered to 10 mildly and 13 moderately impaired DAT subjects, and 14 normal control subjects. The DAT subjects presented a free association response profile that was markedly different from normal controls. Further, DAT subjects provided meaningful definitions to many of the words used as stimuli in the free association task. Relative to controls, DAT subjects demonstrated a deterio
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Knotek, Peter Cyril 1963. "Consistency of response on a semantic memory task in persons with dementia of the Alzheimer type." Thesis, The University of Arizona, 1988. http://hdl.handle.net/10150/276669.

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The purpose of this investigation was to determine the test-retest response consistency rate on a semantic memory task in persons with dementia of the Alzheimer type (DAT). Ten mildly and 13 moderately impaired DAT subjects and 14 normal controls matched for age, years of education, and estimated IQ participated in this study. The Peabody Picture Vocabulary Test (PPVT) was administered twice to each subject with a seven day inter-test interval. The mild and moderate DAT subjects responded inconsistently to significantly more PPVT items than normal controls. When the effects of guessing were co
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Clarnette, Roger M. "Predictors of cognitive decline in those with subjective memory complaint." University of Western Australia. School of Psychiatry and Clinical Neurosciences, 2008. http://theses.library.uwa.edu.au/adt-WU2008.0245.

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[Truncated abstract] Background: Dementia, largely due to Alzheimer's disease (AD), is a major public health problem. The early identification of disease is an important challenge for clinicians because treatment of AD is now available. A simple and accurate means of stratifying risk for AD and identifying early disease is needed so that risk factor modification and treatment can occur optimally. To date, despite many attempts, an accurate means of standardising an approach to the assessment of subtle cognitive symptoms has not been developed. A subjective complaint of poor memory has been ide
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Singleton, Andrew B. "Genetic aspects of dementia." Thesis, University of Newcastle Upon Tyne, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.299652.

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Smadja, Annie. "Maladie de Lyme et syndrome démentiel : étude clinique et biologique chez 66 malades d'hôpital psychiatrique." Bordeaux 2, 1988. http://www.theses.fr/1988BOR25125.

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Książki na temat "Presenile dementia"

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1935-, Kertesz Andrew, and Munoz David G, eds. Pick's disease and Pick complex. New York: Wiley-LISS, 1998.

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C, Baldwin Robert, and Murray Michelle, eds. Younger people with dementia: A multidisciplinary approach. London: Martin Dunitz, 2003.

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Dementia, Scottish Action on, ed. Dementia in Scotland: Priorities for care,strategies for change. (Edinburgh): (Scottish Action on Dementia), 1986.

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Osborn, Averil. Developing local services and action for dementia sufferers and their carers: Some principles and pointers. Edinburgh: Age Concern Scotland, 1988.

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Henig, Robin Marantz. The myth of senility: The truth about the brain and aging. Washington, D.C: American Association of Retired Persons, 1985.

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The myth of senility: The truth about the brain and aging. Washington, D.C: American Association of Retired Persons, 1988.

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Maryland. Governor's Task Force on Alzheimer's Disease and Related Disorders. The Maryland report on Alzheimer's disease and related disorders. [Baltimore, Md.]: The Task Force, 1985.

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S, Burns Alistair, ed. Ageing and dementia: A methodological approach. London: E. Arnold, 1993.

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Frontotemporal disorders: Information for patients, families, and caregivers. Bethesda, Md.]: National Institutes of Health, National Institute on Aging, 2010.

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Scarbrough, Michael R. Alzheimer's disease & presenile dementia: Subject analysis with reference bibliography. Washington, D.C: ABBE Publishers, 1987.

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Części książek na temat "Presenile dementia"

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Zichlin, Miriam. "Presenile Dementia." In Encyclopedia of Clinical Neuropsychology, 2014. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-0-387-79948-3_1140.

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Zichlin, Miriam. "Presenile Dementia." In Encyclopedia of Clinical Neuropsychology, 1. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-56782-2_1140-2.

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Zichlin, Miriam. "Presenile Dementia." In Encyclopedia of Clinical Neuropsychology, 2792. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-57111-9_1140.

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Treves, Therese, Nelly Zilber, Amos D. Korczyn, Esther Kahana, Yaffa Leibowitz, Milton Alter, and Bruce S. Schoenberg. "The Epidemiology of Alzheimer’s Type Presenile Dementia in Israel." In Advances in Behavioral Biology, 169–75. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4613-2179-8_22.

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Gambi, D., M. Onofrj, M. Basciani, C. Censoni, and A. Faricelli. "Acute effects of L-acetylcarnetine (LAC) on quantitative EEG (QEEG) and visual evoked potentials (VEPS) in patients affected by senile, presenile and alcoholic dementia. Comparison with L-carne tine." In Atherosclerosis and Cardiovascular Diseases, 483–89. Dordrecht: Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3205-0_64.

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Xia, Weiming, and Dennis J. Selkoe. "Role of presenilin in APP processing and Aβ production." In Neuroscientific Basis of Dementia, 183–91. Basel: Birkhäuser Basel, 2001. http://dx.doi.org/10.1007/978-3-0348-8225-5_21.

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Kudo, Takashi, Kazunori Imaizumi, Taiichi Katayama, Naoya Sato, Yuka Nakano, Yuka Jinno, Yuko Segawa, Junji Takeda, Masaya Tohyama, and Masatoshi Takeda. "Impairment of response to ER stress in presenilin 1 mutant." In Neuroscientific Basis of Dementia, 193–99. Basel: Birkhäuser Basel, 2001. http://dx.doi.org/10.1007/978-3-0348-8225-5_22.

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Yoshiike, Yuji, and Akihiko Takashima. "Presenilin-Based Transgenic Models of Alzheimer’s Dementia." In Neuromethods, 415–37. Totowa, NJ: Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60761-898-0_21.

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Thinakaran, Gopal, Carlos A. Saura, Taisuke Tomita, Toshiyuki Honda, and Takeshi Iwatsubo. "Lessons from presenilin domain analysis: endoproteolytic processing and enhanced Aβ42 production mediated by FAD-linked variants." In Neuroscientific Basis of Dementia, 167–75. Basel: Birkhäuser Basel, 2001. http://dx.doi.org/10.1007/978-3-0348-8225-5_19.

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Morganti, Francesca. "Experiencing Dementia from Inside: The Expediency of Immersive Presence." In Lecture Notes of the Institute for Computer Sciences, Social Informatics and Telecommunications Engineering, 55–70. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-25872-6_5.

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Streszczenia konferencji na temat "Presenile dementia"

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Innocencio, Giovanna de Camargo, Paulo Roberto Hernandes Júnior, Juliana de Souza Rosa, Patrick de Abreu Cunha Lopes, and Jhoney Francieis Feitosa. "Epidemiological profile of Dementia in the state of São Paulo in the last 5 years." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.175.

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Background: dementia is a syndrome characterized by the presence of a progressive deficit in cognitive function, with interference in social and occupational activities, with risk factors varying with genetic and environmental stressors. The differential diagnosis must identify potentially reversible conditions, of different etiologies, such as metabolic changes, intoxications, and nutritional deficiencies. In primary degenerative dementias and sequelae forms, the etiological diagnosis carries therapeutic and prognostic implications. Objectives: to analyse the current epidemiological profile o
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Méndez, Lorena López. "Un gesto una historia: proyecto artístico como herramienta de identidad y reminiscencia en personas mayores con Demencia temprana." In IV Congreso Internacional de Investigación en Artes Visuales. ANIAV 2019. Imagen [N] Visible. Valencia: Universitat Politècnica de València, 2019. http://dx.doi.org/10.4995/aniav.2019.8963.

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La presente comunicación, expone un proyecto artístico titulado “Usuario en Línea”, compuesto por un archivo configurado por una serie de fotografías de personas en actitud de trabajar en diferentes profesiones, sujetos anónimos pero reconocibles a través de objetos que configuran la imagen y dan paso a descubrir cuál es el trabajo que desarrolla la persona representada. Este proyecto posteriormente fue vinculado y dio paso a la elaboración de uno de los talleres realizados en el Centro de Referencia Estatal de Atención a Personas con Enfermedad de Alzheimer y otras Demencias (CREA) del Imsers
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Bertoldi, Lucas de Oliveira Pinto, Beatriz Cassarotti, Isabela Silva Souza, Alana Strucker Barbosa, Eduardo Silveira Marques Branco, Isabela Badan Fernandes, Paula Carolina Grande Nakazato, et al. "Case Report: Creutzfeld- Jakob disease, onset with ataxia and absence of dementia." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.614.

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Context: Creutzfeld Jakob disease, a rare prion disease that leads to rapidly progressive dementia and movement disorders, through its pathophysiology will determine brain damage. Regardless of the cause, the course of the disease will be rapid and will invariably lead to death. Objective: The reason why the case is described is due to the low incidence of this disease and its unusual course in the case described. Case report: A 67-year-old male, had a personal history of smoking and obesity . Referred to our service due to sudden ataxia, in the presence of an unchanged MRI scan. The first sym
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Souto, Emília Correia, Carolina Maria Marin, Gustavo Carvalho Costa, Igor Braga Farias, Bruno de Mattos Lombardi Badia, Icaro França Navarro Pinto, Roberta Ismael Lacerda Machado, Paulo Victor Sgobbi de Souza, Wladimir Bocca Vieira de Rezende Pinto, and Acary Souza Bulle Oliveira. "Family with atypical Parkinsonism due to CHCHD10 gene mutation." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.502.

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Introduction: Parkinson’s disease - PD is the second most common agerelated neurodegenerative disorder. Characterized by a variety of motor and non-motor symptoms that relate to the loss of dopaminergic neurons in the midbrain black substance. Although most cases of PD are sporadic, 5–10% of patients have monogenetic mutations with a description of more than 20 genes for the familial form. Mitochondrial mutation in CHCHD10 has also been reported to be associated with a wide spectrum of neurodegenerative disorders, including PD. Objectives: Description of a rare recently described genetic cause
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Costa, Matheus Gomes Reis, Victor Bertani Andrade, and Carla Jamile Jabar Menezes. "Clinical-epidemiological profile of the patient hospitalized with Dementia in the state of São Paulo." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.451.

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Background: Dementia syndromes have a progressive and varied nature, causing cognitive and functional decay. Therefore, understanding the epidemiology of this disease is important for its screening. Objectives: To present the patients hospitalized in the state of São Paulo clinical-epidemiological profile, between March 2011 and February 2021. Design and settings: Descriptive, retrospective, and quantitative epidemiological study. Methodology: The data were collected in Sistema de Informação Hospitalares do Sistema Único de Saúde. The number of hospitalizations and mortality rate were analyzed
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Oliveira, Danielle de, Marina Grigoli, Paloma Zanarelli, Patrícia Manzine, and Márcia Cominetti. "INCREASED EXPRESSION OF SOLUBLE INACTIVE ADAM10 IN PATIENTS WITH ALZHEIMER’S DISEASE AND TYPE 2 DIABETES MELLITUS." In XIII Meeting of Researchers on Alzheimer's Disease and Related Disorders. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1980-5764.rpda003.

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Background: DM2 (type 2 diabetes mellitus) can lead to higher risk of developing AD (Alzheimer’s disease). Previous results show that soluble inactive ADAM10 (A Disintegrin And Metalloprotease 10) plasma levels are increased in AD. Objectives: To compare plasma ADAM10 levels between cognitively healthy participants, patients with AD and with the concomitant presence of AD and DM2. Methods: Plasma samples from 36 individuals aged 60 years or more were analyzed, divided into 4 groups: Cognitively and metabolically preserved, AD, DM2 and concomitant presence of AD and DM2. Blood was collected and
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Tavares-Junior, Jose Wagner, Pedro Braga-Neto, Manoel Sobreira Neto, Danilo Oliveira, Carmem Gomes, Safira Gaspar, Emmanuelle Sobreira, Werbety Lucas Feitosa, Leticia Chaves Cunha, and Raquel Montenegro. "LONG-COVID COGNITIVE IMPAIRMENT: COGNITIVE ASSESSMENT AND APOLIPOPROTEIN E (APOE) GENOTYPING CORRELATION IN A BRAZILIAN COHORT." In XIII Meeting of Researchers on Alzheimer's Disease and Related Disorders. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1980-5764.rpda030.

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Background: COVID-19 neurological manifestations were demonstrated during the pandemic, including cognitive impairment. Objectives: To determine the prevalence of cognitive and behavioral complaints (such as dementia, MCI or SCD) in a outpatient sample with recent SARS-COV2 infection. Specific: Evaluate the association of cognitive impairment with the presence of the polymorphism found in the APOE gene and with respiratory disease. Methodology: Observational, longitudinal, prospective clinical study. Inclusion criteria: patients with confirmed Covid-19. Patients are evaluated in an outpatient
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Casiddu, Niccolò, Francesco Burlando, Claudia Porfirione, and Annapaola Vacanti*. "Si–Robotics: an assistive experimental robot." In Intelligent Human Systems Integration (IHSI 2022) Integrating People and Intelligent Systems. AHFE International, 2022. http://dx.doi.org/10.54941/ahfe1001025.

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SiRobotics is a European-funded project that involves 17 partners among companies and universities, which worked together to design and develop novel solutions of collaborative assistive ICT robotics with advanced capabilities to support caregivers, users and families in healthcare services, while acting with a socially acceptable behavior. The aim of the project is to support weak users in their daily activities, whether they live in home environments or elder care facilities; assessing the progress of their physical and cognitive decline, i.e. cognitive frailty, dementia, mild cognitive impa
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Faur, Maria Eduarda, Emily Stefhani Keil, Gabriel Augusto Corti, Maria Eduarda Angelo de Mendonça Filet, Raddib Eduardo Noleto da Nóbrega de Oliveira, Rafael Pereira Guimarães, Thábata Emanuelle Martins Nunes, Gustavo da Cunha Ribas, Carla Heloísa Cabral Moro, and Alexandre Luiz Longo. "Creutzfeldt-Jakob disease: case report strongly suspicious with 14- 3-3 protein missing." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.059.

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Context: The Creutzfeldt-Jakob disease (CJd) is a rare spongiform encephalopathy caused by a prion. In clinical practice the presence of 14- 3-3 protein can be a insensitive marker of sporadic CJd, well as absent for genetic CJd and new variantes, being susceptible to false negatives. Case report: V.L, male, 57 years old, previously rigid, who presented na insidious picture of memory loss and a progressive functional decline for one month and a half. On admission, he was alert, non-contacting, with evidente myoclonus in the upper and lower members and spasticity in lower members. The picture i
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Silva, Vinícius de Oliveira, Lucas Costa Lins, and Elton Marcio Marques Coelho. "Clinical-epidemiological profile of the hospitalized patient with Alzheimer in the State of São Paulo." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.701.

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Background: Alzheimer’s Disease (AD) is the most common form of dementia and its prevalence practically doubles every five years from the age of 60. The progression of the disease determines cognitive deterioration, impairment of basic daily activities and the need for multiple hospitalizations. Objectives: Characterize the clinical-epidemiological profile of hospitalizations for Alzheimer’s in the state of São Paulo, in the period from 2015 to 2019. Design and Setting: Epidemiological, descriptive and retrospective study with quantitative analysis. Methods: Data provided from the Hospital Mor
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Raporty organizacyjne na temat "Presenile dementia"

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Hauer, Klaus, Ilona Dutzi, Christian Werner, Jürgen M. Bauer, and Phoebe Ullrich. Implementation of intervention programs specifically tailored for patients with CI in early rehabilitation during acute hospitalization: a scoping review protocol. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, October 2022. http://dx.doi.org/10.37766/inplasy2022.10.0067.

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Review question / Objective: What is the current status of implementation of interventional programs on early functional rehabilitation during acute, hospital-based medical care, specifically tailored for older patients with CI and what are the most appropriate programs or program components to support early rehab in this specific population? This study combines a systematic umbrella review with a scoping review. While an umbrella review synthesizes knowledge by summarizing existing review papers, a scoping review aims to provide an overview of an emerging area, extracting concepts and identif
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