Bibliografías temáticas / FAMILIAL AMYOTROPHIC LATERAL SCLEROSIS / Libros

Libros sobre el tema "FAMILIAL AMYOTROPHIC LATERAL SCLEROSIS"

Siga este enlace para ver otros tipos de publicaciones sobre el tema: FAMILIAL AMYOTROPHIC LATERAL SCLEROSIS.
Autor: Grafiati
Publicado: 11 de septiembre de 2023

Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros

Elija tipo de fuente:

Consulte los 50 mejores mejores libros para su investigación sobre el tema "FAMILIAL AMYOTROPHIC LATERAL SCLEROSIS".

Junto a cada fuente en la lista de referencias hay un botón "Agregar a la bibliografía". Pulsa este botón, y generaremos automáticamente la referencia bibliográfica para la obra elegida en el estilo de cita que necesites: APA, MLA, Harvard, Vancouver, Chicago, etc.

También puede descargar el texto completo de la publicación académica en formato pdf y leer en línea su resumen siempre que esté disponible en los metadatos.

Explore libros sobre una amplia variedad de disciplinas y organice su bibliografía correctamente.

1

Hiroshi, Mitsumoto, ed. Amyotrophic lateral sclerosis: A guide for patients and families. 3a ed. New York, NY: Demos Health, 2009.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
2

Hiroshi, Mitsumoto y Munsat Theodore L. 1930-, eds. Amyotrophic lateral sclerosis: A guide for patients and families. 2a ed. New York: Demos, 2001.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
3

Massachusetts. Bureau of Environmental Health. Environmental Epidemiology Program. The Amyotrophic Lateral Sclerosis (ALS) Disease Registry: Frequently asked questions for patients and families. Boston, Mass.]: Massachusetts Department of Public Health, Bureau of Environmental Health, Environmental Epidemiology Program, 2009.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
4

Brown, Robert H., Michael Swash y Piera Pasinelli. Amyotrophic Lateral Sclerosis. 2a ed. London: CRC Press, 2021. http://dx.doi.org/10.1201/9781003076445.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
5

Cosi, V., Ann C. Kato, W. Parlette, P. Pinelli y M. Poloni, eds. Amyotrophic Lateral Sclerosis. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4684-5302-7.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
6

MD, Brown Robert H., Swash Michael y Pasinelli Piera, eds. Amyotrophic lateral sclerosis. 2a ed. Abingdon [England]: Informa Healthcare, 2006.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
7

National Institute of Neurological Disorders and Stroke (U.S.). Office of Communications and Public Liaison, ed. Amyotrophic lateral sclerosis. Bethesda, Md: U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, 2000.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
8

1949-, Chad David A. y Pioro Erik P. 1955-, eds. Amyotrophic lateral sclerosis. Philadelphia: F.A. Davis, 1998.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
9

Hiroshi, Mitsumoto, Przedborski Serge y Gordon Paul H, eds. Amyotrophic lateral sclerosis. Boca Raton: Taylor & Francis, 2006.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
10

Clifford, Rose F., ed. Amyotrophic lateral sclerosis. New York, N.Y: Demos, 1990.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
11

1947-, Brown Robert H., Meininger Vincent y Swash Michael, eds. Amyotrophic lateral sclerosis. London: Martin Dunitz, 2000.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
12

Returning to earth. New York: Grove Press, 2007.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
13

A, Murray Christine, ed. Amyotrophic lateral sclerosis: New research. New York: Nova Biomedical Books, 2006.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
14

1941-, Smith Richard Alan, ed. Handbook of amyotrophic lateral sclerosis. New York: Dekker, 1992.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
15

Ludwig, Gutmann y Mitsumoto Hiroshi, eds. Advances in amyotrophic lateral sclerosis. Boston, Mass: Little, Brown, 1996.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
16

G, Farrell Jason, ed. New amyotrophic lateral sclerosis research. New York: Nova Biomedical Books, 2008.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
17

National Institute of Neurological Disorders and Stroke (U.S.). Office of Communications and Public Liaison. ALS (Amyotrophic lateral sclerosis) fact sheet. Bethesda, MD: National Institutes of Health, 2010.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
18

Motor neurone diseases: Amyotrophic lateral sclerosis. London: Chapman & Hall, 1995.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
19

author, Sands Michael 1962, ed. Hold on, let go: Facing ALS with courage and hope. [North Vancouver, British Columbia]: Influence Publishing, 2015.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
20

Behind those eyes: Our journey with ALS. Renfrew, Ont: General Store Publishing House, 2013.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
21

T, Caroscio James, ed. Amyotrophic lateral sclerosis: A guide to patient care. New York: Thieme, 1986.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
22

Respiratory management of ALS: Amyotrophic lateral sclerosis. Sudbury, Mass: Jones and Bartlett, 2009.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
23

Serratrice, Georges. Pathogenesis and therapy of amyotrophic lateral sclerosis. Philadelphia: Lippincott-Raven, 1995.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
24

Munsat, Theodore L. y Hiroshi Mitsumoto. Amyotrophic Lateral Sclerosis: A Guide for Patients and Families. Demos Medical Publishing, 2001.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
25

Amyotrophic Lateral Sclerosis: A Guide for Patients and Families. ReadHowYouWant.com, Limited, 2010.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
26

Mitsumoto, Hiroshi. Amyotrophic Lateral Sclerosis: A Guide for Patients and Families. Springer Publishing Company, Incorporated, 2009.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
27

Lulé, Dorothée, Albert C. Ludolph y Andrea Kübler. Psychological morbidity in amyotrophic lateral sclerosis: Depression, anxiety, hopelessness. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198757726.003.0003.

Texto completo
Resumen
Amyotrophic lateral sclerosis is a devastating condition with progressive loss of movement, speech, and respiratory function, and no available cure. Following the development of clinical symptoms and after receiving a diagnosis, patients may develop psychological morbidity, such as depression, anxiety, and hopelessness. However, many patients adjust successfully in the course of the disease and maintain good psychological well-being, so that a decline in psychological well-being does not necessarily accompany loss of physical function. There are several major determinants of good psychological adjustment to chronic and terminal disease—intrinsic factors such as coping strategies and internal locus of control, and extrinsic factors such as high (perceived and actual) social support by families and multidisciplinary professional teams. Providing care with a holistic view of the patient is probably the most effective approach to supporting patients’ psychosocial adjustment to the disease and minimizing depression, anxiety, and hopelessness.
Los estilos APA, Harvard, Vancouver, ISO, etc.
28

Watermeyer, Tamlyn J. y Laura H. Goldstein. Psychological research in amyotrophic lateral sclerosis: Past, present, and future. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198757726.003.0001.

Texto completo
Resumen
This chapter, of particular interest to those interested in psychological treatments for people with amyotrophic lateral sclerosis (ALS), outlines earlier work that sought to identify correlates of reduced well-being and quality of life in people with ALS and delineates possible targets for intervention. In this context, the chapter then evaluates several studies that have investigated psychological interventions for optimizing well-being in people with ALS and their caregivers. The chapter reviews current efforts to address the paucity of interventional research in this patient group, focusing on five therapies that have so far been evaluated for treatment efficacy. These therapies include hypnosis, mindfulness, cognitive behavioural therapy, expressive disclosure therapy, and dignity therapy. The main findings from these studies and their clinical implications for people with ALS and their families are discussed. Recommendations for future research are considered, together with a discussion of the implementation of such interventions in therapeutic or multidisciplinary settings.
Los estilos APA, Harvard, Vancouver, ISO, etc.
29

Mitsumoto, Hiroshi. Amyotrophic Lateral Sclerosis: A Guide for Patients and Families, Third Edition. Springer Publishing Company, Incorporated, 2009.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
30

Amyotrophic Lateral Sclerosis: A Guide for Patients and Families, 3rd Edition. ReadHowYouWant.com, Limited, 2011.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
31

Briggs, John, Jerry Beller, Beller Health y Brain Research. Amyotrophic Lateral Sclerosis: Guide for Patients, Families, Caregivers, and Medical Professionals. Independently Published, 2020.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
32

Rice, Ed. If They Could Only Hear Me: A collection of personal stories about ALS and the families that have been affected. BookSurge Publishing, 2005.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
33

Aguirre, T. Genetic and Functional Studies of the Cu/Zn Superoxide Dismutase Gene in Belgian Patients with Familial or Sporadic Amyotrophic Lateral Sclerosis. Leuven University Press, 1998.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
34

I Found My Tribe. Penguin Random House, 2018.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
35

I Found My Tribe. Charnwood, 2018.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
36

I found my tribe. 2018.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
37

Fitzmaurice, Ruth. I Found My Tribe. Penguin Random House, 2017.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
38

Hamri, Sanaa y Craig Brewer. Empire. 2017.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
39

1972-, Williams Jennifer y Suggs Rob, eds. Tenacious: How God used a terminal diagnosis to turn a family and a football team into champions. 2013.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
40

Hayertz, Marchelle. Amyotrophic Lateral Sclerosis Treatment : Amyotrophic Lateral Sclerosis Treatment and Management: Amyotrophic Lateral Sclerosis Pronunciation. Independently Published, 2021.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
41

Mitsumoto, Hiroshi, Serge Przedborski y Paul H. Gordon. Amyotrophic Lateral Sclerosis. Taylor & Francis Group, 2005.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
42

Pagnini, Francesco y Zachary Simmons, eds. Amyotrophic Lateral Sclerosis. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198757726.001.0001.

Texto completo
Resumen
Amyotrophic lateral sclerosis: Understanding and optimizing quality of life and psychological well-being presents a comprehensive and up-to-date review of the enhancement of the lives of people with amyotrophic lateral sclerosis (ALS) and their caregivers. ALS is a progressive, fatal neurodegenerative disorder. No current medical therapy can reverse or stop its progression, and the promotion of quality of life and psychological well-being is a central component of ALS care. Health care professionals who work in this field should incorporate attention to psychological, emotional, and relational aspects of the disease into their approach to care. This book provides some of the knowledge and direction necessary for optimizing the quality of care for individuals with ALS and their caregivers. Topics discussed include an ALS-centred view of quality of life, depressive features, anxiety, resilience, cognitive impairment, complementary and alternative medicines, and psychological research. Specific elements of ALS, such as end-of-life concerns and bulbar dysfunction, are described through the lens of their psychological impact. There is extensive discussion of the development of new psychological treatments, as well as the impact and incorporation of new technologies, with the goal of fostering optimal quality of life and psychological well-being as key parts of a holistic approach to care for the patients and for those who are close to such individuals.
Los estilos APA, Harvard, Vancouver, ISO, etc.
43

Ferraiuolo, Laura y Stephen J. Kolb. Amyotrophic Lateral Sclerosis. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0026.

Texto completo
Resumen
An overriding mystery of ALS pathogenesis orbits around the molecular basis of selective motor neuron vulnerability and clouds our view. There are likely mechanisms involved in the initiation of motor neuron loss and mechanisms involved in the progression of motor neuron loss once initiated. Motor neuron vulnerability is likely related to the unique biological characteristics of these cells. This chapter introduces central molecular pathways that appear to be involved in the pathogenesis of ALS, and highlights why dysregulation of these mechanisms could lead to motor neuron death. Indeed, there are likely mechanisms involved in the initiation of motor neuron loss and mechanisms involved in the progression of motor neuron loss once initiated. Our task is to determine those mechanisms that are relevant to ALS pathogenesis that may be targeted therapeutically to prevent onset and/or halt progression.
Los estilos APA, Harvard, Vancouver, ISO, etc.
44

Harms, Matthew B. y Timothy M. Miller. Amyotrophic Lateral Sclerosis. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0027.

Texto completo
Resumen
Recent advances in sequencing technologies have dramatically expanded the number of genes associated with amyotrophic lateral sclerosis, including rare but highly penetrant causative mutations as well as common risk alleles. This chapter discusses these gene discoveries and how they have implicated a diverse array of biological pathways essential for motor neuron health and have begun to inform our understanding of ALS pathogenesis as a heterogeneous and multistep process. Insights from these discoveries are leading to a new generation of targeted therapies directed at specific genes and are poised to inform how patients with amyotrophic lateral sclerosis are evaluated and treated in the clinic.
Los estilos APA, Harvard, Vancouver, ISO, etc.
45

Wainger, Brian J. Amyotrophic Lateral Sclerosis. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0028.

Texto completo
Resumen
Mouse and cellular models of ALS including stem cells have revealed tremendous insight into the molecular processes that lead to ALS. Models of ALS and other neurodegenerative diseases have led to emergent molecular themes that span several diseases. Future models must account for neuronal subtype specificity of different neurodegenerative diseases, particularly between tightly related diseases such as FTD and ALS. Human iPSC-derived motor neurons offer promise both with regard to the use of human cells and in particular the ability to model sporadic disease, which is critically important given the overwhelming abundance of sporadic disease in ALS and other neurodegenerative diseases.
Los estilos APA, Harvard, Vancouver, ISO, etc.
46

Harris, Brent T., Galam A. Khan y Saed Sadeghi. Amyotrophic Lateral Sclerosis. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0029.

Texto completo
Resumen
Although the basic gross and microscopic pathological changes in amyotrophic lateral sclerosis (ALS) have been known for more than 100 years, emerging technology and research into the cellular and molecular changes found in this disease are challenging our understanding about the pathogenesis and pathophysiology. All cell types of the CNS/PNS as well as circulating immune cells have been implicated in the pathology of ALS. Numerous genes, their proteins, and environmental factors have also been associated. However, we still do not understand the specific gene-environmental interactions that bring about and drive this devastating disease in most cases. This short chapter does not address the causal factors and molecular pathogeneses that have been hypothesized and actively researched in the pathology of ALS-as these are discussed in other sections of this text. Here, it shows and discusses the basic pathological changes at the tissue and cellular levels that help to establish the pathological diagnosis of ALS at autopsy.
Los estilos APA, Harvard, Vancouver, ISO, etc.
47

Mitsumoto, Hiroshi, Serge Przedborski y Paul H. Gordon, eds. Amyotrophic Lateral Sclerosis. CRC Press, 2005. http://dx.doi.org/10.1201/b14133.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
48

Sattler, Rita y Jeffrey Rothstein. Amyotrophic Lateral Sclerosis. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199794591.003.0063.

Texto completo
Resumen
This is a digitally enhanced text. Readers can also see the coverage of this topic area in the second edition of Neuroglia. The second edition of Neuroglia was first published digitally in Oxford Scholarship Online and the bibliographic details provided, if cited, will direct people to that version of the text. Readers can also see the coverage of this topic area in the ...
Los estilos APA, Harvard, Vancouver, ISO, etc.
49

Araki, Toshiyuki, ed. Amyotrophic Lateral Sclerosis. Exon Publications, 2021. http://dx.doi.org/10.36255/exonpublications.amyotrophiclateralsclerosis.2021.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
50

1952-, Brown Robert H., Meininger Vincent y Swash Michael, eds. Amyotrophic lateral sclerosis. London: Martin Dunitz, 2000.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
También puede estar interesado en las bibliografías sobre el tema "FAMILIAL AMYOTROPHIC LATERAL SCLEROSIS" para otros tipos de fuentes:
Artículos de revistas Tesis
Ofrecemos descuentos en todos los planes premium para autores cuyas obras están incluidas en selecciones literarias temáticas. ¡Contáctenos para obtener un código promocional único!

Pasar a la bibliografía