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AndrÉ Castanheira, Michael Swash & Mamede De Carvalho. (2022) Percutaneous gastrostomy in amyotrophic lateral sclerosis: a review. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 23:3-4, pages 176-189.
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Polona Klavžar, Blaž Koritnik, Lea Leonardis, Leja Dolenc Grošelj, Mojca Kirbiš, Stanka Ristić Kovačič, Polona Klinar, Maja Pohar Perme & Janez Zidar. (2020) Improvements in the multidisciplinary care are beneficial for survival in amyotrophic lateral sclerosis (ALS): experience from a tertiary ALS center. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 21:3-4, pages 203-208.
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Manisha Kak, Naoum P. Issa, Raymond P. Roos, Bobbie Jean Sweitzer, Ori Gottlieb, Amy Guralnick, Steven R. White, Carol E. Semrad, Betty Soliven, Joumana Baroody & Kourosh Rezania. (2017) Gastrostomy tube placement is safe in advanced amyotrophic lateral sclerosis. Neurological Research 39:1, pages 16-22.
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. (2014) SESSION 1 JOINT OPENING SESSION. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 15:sup1, pages 1-56.
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Michal Sarfaty, Beatrice Nefussy, Ditza Gross, Yami Shapira, Nachum Vaisman & Vivian E. Drory. (2013) Outcome of percutaneous endoscopic gastrostomy insertion in patients with amyotrophic lateral sclerosis in relation to respiratory dysfunction. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 14:7-8, pages 528-532.
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Articles from other publishers (14)
Adrienne Sulistyo, Agessandro Abrahao, Maria Eliza Freitas, Benjamin Ritsma & Lorne Zinman. (2023) Enteral tube feeding for amyotrophic lateral sclerosis/motor neuron disease. Cochrane Database of Systematic Reviews 2023:8.
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Xi Chen, Jiawen Xu, Jingyan Guo, Ting Ye, Baocheng Zhao, Shiming Fang, Yan Chen & Yi Dong. (2023) A Predictive Model and Survival Analysis for Tube Feeding in ALS Patients: A Prospective Cohort Study in a Chinese ALS Clinic. Acta Neurologica Scandinavica 2023, pages 1-13.
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Munira Essat, Elizabeth Coates, Mark Clowes, Daniel Beever, Gemma Hackney, Sean White, Theocharis Stavroulakis, Vanessa Halliday & Christopher McDermott. (2022) Understanding the current nutritional management for people with amyotrophic lateral sclerosis - A mapping review. Clinical Nutrition ESPEN 49, pages 328-340.
Crossref
Crossref
L. Brylev, V. Fominykh, V. Chernenkaia, I. Chernenkiy, K. Gorbachev, A. Ataulina, A. Izvekov, M. Monakhov, A. Olenichev, S. Orlov, I. Turin, M. Loginov, S. Rautbart, A. Baymukanov, V. Parshikov, V. Demeshonok, A. Yakovlev, T. Druzhkova, A. Guekht & N. Gulyaeva. (2021) Stress load and neurodegeneration after gastrostomy tube placement in amyotrophic lateral sclerosis patients. Metabolic Brain Disease 36:8, pages 2473-2482.
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Leila Bond, Paulamy Ganguly, Nishad Khamankar, Nolan Mallet, Gloria Bowen, Braden Green & Cassie S. Mitchell. (2019) A Comprehensive Examination of Percutaneous Endoscopic Gastrostomy and Its Association with Amyotrophic Lateral Sclerosis Patient Outcomes. Brain Sciences 9:9, pages 223.
Crossref
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Nimish J. Thakore, Brittany R. Lapin, Erik P. Pioro & Loutfi S. Aboussouan. (2019) Variation in noninvasive ventilation use in amyotrophic lateral sclerosis. Neurology 93:3.
Crossref
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Osama A. Khairoalsindi & Ahmad R. Abuzinadah. (2018) Maximizing the Survival of Amyotrophic Lateral Sclerosis Patients: Current Perspectives. Neurology Research International 2018, pages 1-12.
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Mamede de CarvalhoClifton L. Gooch. (2017) The yin and yang of gastrostomy in the management of ALS. Neurology 89:14, pages 1435-1436.
Crossref
Crossref
Erin McDonnellDavid SchoenfeldSabrina PaganoniNazem Atassi. (2017) Causal inference methods to study gastric tube use in amyotrophic lateral sclerosis. Neurology 89:14, pages 1483-1489.
Crossref
Crossref
Sarah Martin, Ahmad Al Khleifat & Ammar Al-Chalabi. (2017) What causes amyotrophic lateral sclerosis?. F1000Research 6, pages 371.
Crossref
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Sabrina Paganoni, Chafic Karam, Nanette Joyce, Richard Bedlack & Gregory T. Carter. (2015) Comprehensive rehabilitative care across the spectrum of amyotrophic lateral sclerosis. NeuroRehabilitation 37:1, pages 53-68.
Crossref
Crossref
V. Brunaud-Danel, V. Tiffreau, N. Danel-Buhl, T. Perez, C. Moreau, A. Destee, D. Devos & L. Defebvre. (2015) Comment prendre en charge un malade atteint de SLA ?. Pratique Neurologique - FMC 6:1, pages 13-18.
Crossref
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Jean-Claude Desport, Pierre Jésus & Philippe Fayemendy. (2014) Gastrostomies et nutrition entérale lors des maladies neuromusculaires. Nutrition Clinique et Métabolisme 28:3, pages 181-188.
Crossref
Crossref
Philippe Corcia, Caroline Ingre, Helene Blasco, Rayomand Press, Julien Praline, Catherine Antar, Charlotte Veyrat-Durebex, Yves-Olivier Guettard, William Camu, Peter M Andersen, Patrick Vourc'h & Christian R Andres. (2012) Homozygous SMN2 deletion is a protective factor in the Swedish ALS population. European Journal of Human Genetics 20:5, pages 588-591.
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