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.
Crossref
Carolina Parra-Cantu, Jennifer M. Martinez-Thompson, Forrest B. Linch, Tasha L. Welch, Claudia Z. Chou, Adele K. Pattinson, Nathan P. Staff & Melissa Neisen. (2023) Radiologically Inserted Gastrostomy Tube Placement Guided by the Assessment and Primary Palliative Care Provided by an Amyotrophic Lateral Sclerosis Multidisciplinary Clinic: A Single-Arm Retrospective Clinical Study. American Journal of Hospice and Palliative Medicine®, pages 104990912311805.
Crossref
Eleanor James, Cathy Ellis, Ruth Brassington, Sivakumar Sathasivam & Carolyn A Young. (2022) Treatment for sialorrhea (excessive saliva) in people with motor neuron disease/amyotrophic lateral sclerosis. Cochrane Database of Systematic Reviews 2022:5.
Crossref
Jordi Greoles Cano. (2022) La gastrostomía endoscópica percutánea (PEG) como procedimiento para mejorar la supervivencia de los pacientes con esclerosis lateral amiotrófica (ELA). Atención Primaria 54:4, pages 102286.
Crossref
Mohammed K. Ismail & Shreesh Shrestha. 2022. Neuromuscular Disorders. Neuromuscular Disorders
79
96
.
Maggie A. Kuhn & Lisa Marie Williams. 2020. Neurologic and Neurodegenerative Diseases of the Larynx. Neurologic and Neurodegenerative Diseases of the Larynx
131
141
.
Ezekiel Oluwasayo Ijaopo & Ruth Oluwasolape Ijaopo. (2019) Tube Feeding in Individuals with Advanced Dementia: A Review of Its Burdens and Perceived Benefits. Journal of Aging Research 2019, pages 1-16.
Crossref
Claudia Tarlarini, Lucia Catherine Greco, Andrea Lizio, Francesca Gerardi, Valeria Ada Sansone & Christian Lunetta. (2018) Taste changes in amyotrophic lateral sclerosis and effects on quality of life. Neurological Sciences 40:2, pages 399-404.
Crossref
Toni L. Glover & Benzi M. Kluger. 2019. Geriatric Neurology. Geriatric Neurology
545
561
.
Fang Cui, Liuqing Sun, Jianmei Xiong, Jianyong Li, Yangang Zhao & Xusheng Huang. (2018) Therapeutic effects of percutaneous endoscopic gastrostomy on survival in patients with amyotrophic lateral sclerosis: A meta-analysis. PLOS ONE 13:2, pages e0192243.
Crossref
Rosa Burgos, Irene Bretón, Emanuele Cereda, Jean Claude Desport, Rainer Dziewas, Laurence Genton, Filomena Gomes, Pierre Jésus, Andreas Leischker, Maurizio Muscaritoli, Kalliopi-Anna Poulia, Jean Charles Preiser, Marjolein Van der Marck, Rainer Wirth, Pierre Singer & Stephan C. Bischoff. (2018) ESPEN guideline clinical nutrition in neurology. Clinical Nutrition 37:1, pages 354-396.
Crossref
Ashley A. Waito, Teresa J. Valenzano, Melanie Peladeau-Pigeon & Catriona M. Steele. (2017) Trends in Research Literature Describing Dysphagia in Motor Neuron Diseases (MND): A Scoping Review. Dysphagia 32:6, pages 734-747.
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
Matthew Kurien, Jake Williams & David S. Sanders. (2016) Malnutrition in healthcare settings and the role of gastrostomy feeding. Proceedings of the Nutrition Society 76:3, pages 352-360.
Crossref
Josef Finsterer & Claudia Stöllberger. (2017) Emergencies in motoneuron disease. Internal and Emergency Medicine 12:5, pages 641-650.
Crossref
M.-H. Soriani & C. Desnuelle. (2017) Care management in amyotrophic lateral sclerosis. Revue Neurologique 173:5, pages 288-299.
Crossref
Kazuaki Nagashima, Natsumi Furuta, Kouki Makioka, Yukio Fujita, Masaki Ikeda & Yoshio Ikeda. (2017) An analysis of prognostic factors after percutaneous endoscopic gastrostomy placement in Japanese patients with amyotrophic lateral sclerosis. Journal of the Neurological Sciences 376, pages 202-205.
Crossref
Theocharis Stavroulakis & Christopher J. McDermott. 2017. Nutrition in Neurologic Disorders. Nutrition in Neurologic Disorders
91
104
.
Theocharis Stavroulakis & Christopher J McDermott. (2016) Enteral feeding in neurological disorders. Practical Neurology 16:5, pages 352-361.
Crossref
Kota Bokuda, Toshio Shimizu, Kazuhiro Imamura, Akihiro Kawata, Kazuhiko Watabe, Masaharu Hayashi, Yuki Nakayama, Eiji Isozaki & Imaharu Nakano. (2016) Predictive factors for prognosis following unsedated percutaneous endoscopic gastrostomy in ALS patients. Muscle & Nerve 54:2, pages 277-283.
Crossref
R. Tortelli, M. Copetti, F. Panza, A. Fontana, R. Cortese, R. Capozzo, A. Introna, E. D'Errico, S. Zoccolella, S. Arcuti, D. Seripa, I. L. Simone & G. Logroscino. (2016) Time to generalization and prediction of survival in patients with amyotrophic lateral sclerosis: a retrospective observational study. European Journal of Neurology 23:6, pages 1117-1125.
Crossref
Theocharis Stavroulakis, Wendy O Baird, Susan K Baxter, Theresa Walsh, Pamela J Shaw & Christopher J McDermott. (2016) The impact of gastrostomy in motor neurone disease: challenges and benefits from a patient and carer perspective. BMJ Supportive & Palliative Care 6:1, pages 52-59.
Crossref
Suresh Kumar Chhetri, Belinda Fay Bradley, Tahir Majeed & Robert William Lea. (2016) Motor neurone disease in Lancashire and South Cumbria in North West England and an 8year experience with enteral nutrition. Journal of Clinical Neuroscience 24, pages 47-51.
Crossref
Cumara B. O'Carroll, Amelia K. Adcock & Bart M. Demaerschalk. 2015. Evidence‐Based Neurology: Management of Neurological Disorders. Evidence‐Based Neurology: Management of Neurological Disorders
219
234
.
. (2015) Gastrostomy in patients with amyotrophic lateral sclerosis (ProGas): a prospective cohort study. The Lancet Neurology 14:7, pages 702-709.
Crossref
L. P. Greenaway, N. H. Martin, V. Lawrence, A. Janssen, A. Al-Chalabi, P. N. Leigh & L. H. Goldstein. (2015) Accepting or declining non-invasive ventilation or gastrostomy in amyotrophic lateral sclerosis: patients’ perspectives. Journal of Neurology 262:4, pages 1002-1013.
Crossref
Rubika Balendra, Ashley Jones, Naheed Jivraj, I Nick Steen, Carolyn A Young, Pamela J Shaw, Martin R Turner, P Nigel Leigh & Ammar Al-Chalabi. (2015) Use of clinical staging in amyotrophic lateral sclerosis for phase 3 clinical trials. Journal of Neurology, Neurosurgery & Psychiatry 86:1, pages 45-49.
Crossref
Patricia Stanich, Adriana Leico Oda, Cristina Cleide dos Santos Salvioni & Acary Souza Bulle Oliveira. 2015. Diet and Nutrition in Dementia and Cognitive Decline. Diet and Nutrition in Dementia and Cognitive Decline
1115
1123
.
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
Cristina Cleide dos Santos Salvioni, Patricia Stanich, Claudinéa S. Almeida & Acary Souza Bulle Oliveira. (2014) Nutritional care in motor neurone disease/ amyotrophic lateral sclerosis. Arquivos de Neuro-Psiquiatria 72:2, pages 157-163.
Crossref
Namita A. Goyal & Tahseen Mozaffar. (2014) Respiratory and Nutritional Support in Amyotrophic Lateral Sclerosis. Current Treatment Options in Neurology 16:2.
Crossref
Sonja Körner, Melanie Hendricks, Katja Kollewe, Antonia Zapf, Reinhard Dengler, Vincenzo Silani & Susanne Petri. (2013) Weight loss, dysphagia and supplement intake in patients with amyotrophic lateral sclerosis (ALS): impact on quality of life and therapeutic options. BMC Neurology 13:1.
Crossref
Pei-Ning Wang. (2013) Promoting palliative care in patients with motor neuron disease in Taiwan. Journal of the Chinese Medical Association 76:7, pages 361-362.
Crossref
Zachary Simmons. 2013. Neurological Rehabilitation. Neurological Rehabilitation
483
498
.
Marlia M. Braun, Matt Osecheck & Nanette C. Joyce. (2012) Nutrition Assessment and Management in Amyotrophic Lateral Sclerosis. Physical Medicine and Rehabilitation Clinics of North America 23:4, pages 751-771.
Crossref
Chad Kawa, James Stewart, Kristen Hilden, Douglas G. Adler, Christopher Tietze, Mark B. Bromberg & John C. Fang. (2012) A Retrospective Study of Nurse-Assisted Propofol Sedation in Patients With Amyotrophic Lateral Sclerosis Undergoing Percutaneous Endoscopic Gastrostomy. Nutrition in Clinical Practice 27:4, pages 540-544.
Crossref
Jong Seok BaeYoon-Ho HongWonKi BaekEun Hee SohnJoong-Yang ChoByung-Jo KimSeung Hyun Kim. (2012) Current Status of the Diagnosis and Management of Amyotrophic Lateral Sclerosis in Korea: A Multi-Center Cross-Sectional Study. Journal of Clinical Neurology 8:4, pages 293.
Crossref
Benoît Marin, Pierre Jésus, Pierre-Marie Preux, Philippe Couratier & Jean-Claude Desport. (2011) Troubles nutritionnels lors de la sclérose latérale amyotrophique (SLA). Nutrition Clinique et Métabolisme 25:4, pages 205-216.
Crossref
Katja Kollewe, Sonja Körner, Reinhard Dengler & Susanne Petri. 2011. Diet and Nutrition in Palliative Care. Diet and Nutrition in Palliative Care
379
389
.
Carolyn A Young, Cathy Ellis, Julia Johnson, Sivakumar Sathasivam & Nicky Pih. (2011) Treatment for sialorrhea (excessive saliva) in people with motor neuron disease/amyotrophic lateral sclerosis. Cochrane Database of Systematic Reviews.
Crossref
Rossella Spataro, Leonardo Ficano, Federico Piccoli & Vincenzo La Bella. (2011) Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: Effect on survival. Journal of the Neurological Sciences 304:1-2, pages 44-48.
Crossref
Hans Dieter Katzberg & Michael Benatar. (2011) Enteral tube feeding for amyotrophic lateral sclerosis/motor neuron disease. Cochrane Database of Systematic Reviews.
Crossref
Maureen A Lefton-Greif, Thomas O Crawford, Sharon McGrath-Morrow, Kathryn A Carson & Howard M Lederman. (2011) Safety and caregiver satisfaction with gastrostomy in patients with Ataxia Telangiectasia. Orphanet Journal of Rare Diseases 6:1, pages 23.
Crossref
Mohammad K. Ismail. 2011. Neuromuscular Disorders: Treatment and Management. Neuromuscular Disorders: Treatment and Management
51
60
.
Mitsuko Ushikubo, Mina Kanbe, Mieko Sukawa, Chieko Tomita & Sachiyo Hoshikawa. (2010) Continuing Care between Hospital and Home about Percutaneous Endoscopic Gastrostomy Based on the Experience of Patients with Amyotrophic Lateral Sclerosis. The Kitakanto Medical Journal 60:2, pages 135-141.
Crossref
R. G. MillerC. E. JacksonE. J. KasarskisJ. D. EnglandD. ForshewW. JohnstonS. KalraJ. S. KatzH. MitsumotoJ. RosenfeldC. ShoesmithM. J. StrongS. C. Woolley. (2009) Practice Parameter update: The care of the patient with amyotrophic lateral sclerosis: Drug, nutritional, and respiratory therapies (an evidence-based review). Neurology 73:15, pages 1218-1226.
Crossref
Philip Van Damme & Wim Robberecht. (2009) Recent advances in motor neuron disease. Current Opinion in Neurology 22:5, pages 486-492.
Crossref
M.-H. Soriani & C. Desnuelle. (2009) Épidémiologie de la SLA. Revue Neurologique 165:8-9, pages 627-640.
Crossref
Amelia Romero Merlos & Rita Bonet Bolós. (2009) Revisión del manejo dietético y nutricional de los pacientes con esclerosis lateral amiotrófica. Actividad Dietética 13:1, pages 10-16.
Crossref
P. Clavelou, C. Bouteloup, J.-C. Desport, L. Ouchachne, N. Guy, G. Besson & P. Couratier. (2009) Effets de la gastrostomie sur la survie et la qualité de vie des patients atteints de sclérose latérale amyotrophique (SLA). Revue Neurologique 165, pages S24-S25.
Crossref
Robert G. Miller, Fred Anderson, Benjamin Rix Brooks, Hiroshi Mitsumoto, Walter G. Bradley & Steven P. Ringel. (2009) Outcomes research in amyotrophic lateral sclerosis: Lessons learned from the amyotrophic lateral sclerosis clinical assessment, research, and education database. Annals of Neurology 65:S1, pages S24-S28.
Crossref
Jeffrey Rosenfeld & Amy Ellis. (2008) Nutrition and Dietary Supplements in Motor Neuron Disease. Physical Medicine and Rehabilitation Clinics of North America 19:3, pages 573-589.
Crossref
Jeremy M. Shefner. (2008) Designing Clinical Trials in Amyotrophic Lateral Sclerosis. Physical Medicine and Rehabilitation Clinics of North America 19:3, pages 495-508.
Crossref
Jau-Shin Lou. (2008) Fatigue in Amyotrophic Lateral Sclerosis. Physical Medicine and Rehabilitation Clinics of North America 19:3, pages 533-543.
Crossref
Paula Leslie. (2008) Food for Thought: How Do Patients With ALS Decide About Having a PEG?. Perspectives on Swallowing and Swallowing Disorders (Dysphagia) 17:1, pages 33-39.
Crossref
Nicky Grundy, Sivakumar Sathasivam, Cathy Ellis & Julia Johnson. 1996. Cochrane Database of Systematic Reviews. Cochrane Database of Systematic Reviews.
Toshio Shimizu, Hideaki Hayashi, Hitoshi Inoue, Kazuhiro Imamura & Kiyomitsu Oyanagi. (2008) Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis -Relation of respiratory function at the time of PEG to survival length-. Rinsho Shinkeigaku 48:10, pages 721-726.
Crossref
David S. Seres. 2008. Nutrition and Gastrointestinal Disease. Nutrition and Gastrointestinal Disease
299
318
.
Adrian N. Holm & Todd H. Baron. (2007) Palliative Use of Percutaneous Endoscopic Gastrostomy and Percutaneous Endoscopic Cecostomy Tubes. Gastrointestinal Endoscopy Clinics of North America 17:4, pages 795-803.
Crossref
Aleksandar Radunović, Hiroshi Mitsumoto & P Nigel Leigh. (2007) Clinical care of patients with amyotrophic lateral sclerosis. The Lancet Neurology 6:10, pages 913-925.
Crossref
Lauren B. ElmanDavid J. HoughtonGregory F. WuHoward I. HurtigClyde E. MarkowitzLeo McCluskey. (2007) Palliative Care in Amyotrophic Lateral Sclerosis, Parkinson's Disease, and Multiple Sclerosis. Journal of Palliative Medicine 10:2, pages 433-457.
Crossref
Paul H. Gordon & Hiroshi Mitsumoto. 2007. Motor neuron disorders and related diseases. Motor neuron disorders and related diseases
389
424
.
Douglas Mitchell. 2007. Evidence‐based Neurology: Management of Neurological Disorders. Evidence‐based Neurology: Management of Neurological Disorders
234
243
.
Ailsa Brotherton & Christina Lyons. (2006) The impact of HETF for adults with neurological conditions. British Journal of Community Nursing 11:12, pages 511-518.
Crossref
Adam Czaplinski, Albert A. Yen & Stanley H. Appel. (2006) Amyotrophic lateral sclerosis: early predictors of prolonged survival. Journal of Neurology 253:11, pages 1428-1436.
Crossref
Susan E Langmore, Edward J Kasarskis, Maria Laura Manca & Richard K Olney. 1996. Cochrane Database of Systematic Reviews. Cochrane Database of Systematic Reviews.
A.C. Ludolph. (2006) 135th ENMC International Workshop: Nutrition in Amyotrophic Lateral Sclerosis 18–20 of March 2005, Naarden, The Netherlands. Neuromuscular Disorders 16:8, pages 530-538.
Crossref
LINDA GANZINI. (2006) Artificial nutrition and hydration at the end of life: Ethics and evidence. Palliative and Supportive Care 4:2, pages 135-143.
Crossref
C. Bouteloup. (2006) Quels sont les moyens de suppléance de la fonction alimentaire et leurs indications?. Revue Neurologique 162, pages 309-319.
Crossref
M.-A. Piquet. (2006) Approche nutritionnelle des patients atteints de Sclérose Latérale Amyotrophique. Revue Neurologique 162, pages 177-187.
Crossref
Zachary Simmons. (2005) Management Strategies for Patients With Amyotrophic Lateral Sclerosis From Diagnosis Through Death. The Neurologist 11:5, pages 257-270.
Crossref
M.D. Ballesteros pomar & A. Arés luque. (2005) Nutrición basada en la evidencia en las enfermedades neurológicas. Endocrinología y Nutrición 52, pages 97-101.
Crossref
P. KaufmannG. LevyJ. L.P. ThompsonM. L. DelBeneV. BattistaP. H. GordonL. P. RowlandB. LevinH. Mitsumoto. (2005) The ALSFRSr predicts survival time in an ALS clinic population. Neurology 64:1, pages 38-43.
Crossref
Jane Skelton. (2005) Nursing role in the multidisciplinary management of motor neurone disease. British Journal of Nursing 14:1, pages 20-24.
Crossref
Paul H. Gordon. (2005) Advances in clinical trials for amyotrophic lateral sclerosis. Current Neurology and Neuroscience Reports 5:1, pages 48-54.
Crossref
Heidi Klingbeil, Heather R Baer & Pamela E Wilson. (2004) Aging with a disability 11No commercial party having a direct financial interest in the results of the research supporting this article has or will confer a benefit upon the authors(s) or upon any organization with which the author(s) is/are associated.. Archives of Physical Medicine and Rehabilitation 85, pages 68-73.
Crossref