Manejo nutricional de la esclerosis lateral amiotrófica: resumen de recomendaciones
暂无分享,去创建一个
C. Wanden-Berghe | Grupo de trabajo Senpe | J. Hernández | J. González | N. V. Casas | A. C. Blanco | M. ª. D. D. O. García | Francisca Margarita Lozano Fuster | Victoria Avilés | Rosana Ashbaugh Enguídanos | Isabel Ferrero López | J. B. M. Soria | Irene Bretón Lesmes | José Manuel Moreno Villares
[1] Jianbo Hao,et al. Serum uric acid levels in patients with amyotrophic lateral sclerosis: a meta-analysis , 2018, Scientific Reports.
[2] S. Selkirk,et al. Nutrition management methods effective in increasing weight, survival time and functional status in ALS patients: a systematic review , 2018, Amyotrophic lateral sclerosis & frontotemporal degeneration.
[3] P. Singer,et al. ESPEN guideline clinical nutrition in neurology. , 2017, Clinical nutrition.
[4] J. Bach,et al. Use of Noninvasive Ventilation During Feeding Tube Placement , 2017, Respiratory Care.
[5] D. Schoenfeld,et al. Causal inference methods to study gastric tube use in amyotrophic lateral sclerosis , 2017, Neurology.
[6] J. Little,et al. Identification of risk factors associated with onset and progression of amyotrophic lateral sclerosis using systematic review and meta‐analysis , 2017, Neurotoxicology.
[7] M. Vinceti,et al. Percutaneous endoscopic gastrostomy, body weight loss and survival in amyotrophic lateral sclerosis: a population-based registry study , 2017, Amyotrophic lateral sclerosis & frontotemporal degeneration.
[8] M. Galea,et al. Symptomatic treatments for amyotrophic lateral sclerosis/motor neuron disease. , 2017, The Cochrane database of systematic reviews.
[9] N. Issa,et al. Gastrostomy tube placement is safe in advanced amyotrophic lateral sclerosis , 2017, Neurological research.
[10] W. Camu,et al. The Use of Peripherally Inserted Central Catheter in Amyotrophic Lateral Sclerosis Patients at a Later Stage , 2016, European Neurology.
[11] Giancarlo Logroscino,et al. Population-Based Evidence that Survival in Amyotrophic Lateral Sclerosis Is Related to Weight Loss at Diagnosis , 2016, Neurodegenerative Diseases.
[12] L. Machtoub,et al. Clinical Features of Amyotrophic Lateral Sclerosis , 2015 .
[13] L. Genton,et al. Should patients with ALS gain weight during their follow-up? , 2015, Nutrition.
[14] K. Morrison. Gastrostomy in patients with amyotrophic lateral sclerosis (ProGas): a prospective cohort study , 2015, The Lancet Neurology.
[15] O. Hardiman,et al. End-of-life management in patients with amyotrophic lateral sclerosis , 2015, The Lancet Neurology.
[16] P. Corcia,et al. Nutritional assessment of amyotrophic lateral sclerosis in routine practice: Value of weighing and bioelectrical impedance analysis , 2015, Muscle & nerve.
[17] S. Petri,et al. Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: a prospective observational study , 2015, Journal of Neurology.
[18] J. Lou,et al. Hypercaloric enteral nutrition in patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled phase 2 trial , 2014, The Lancet.
[19] D. Matthews,et al. Estimating daily energy expenditure in individuals with amyotrophic lateral sclerosis. , 2014, The American journal of clinical nutrition.
[20] S. Petri,et al. Weight loss, dysphagia and supplement intake in patients with amyotrophic lateral sclerosis (ALS): impact on quality of life and therapeutic options , 2013, BMC Neurology.
[21] D. Czell,et al. Outcomes of Percutaneous Endoscopic Gastrostomy Tube Insertion in Respiratory Impaired Amyotrophic Lateral Sclerosis Patients Under Noninvasive Ventilation , 2013, Respiratory Care.
[22] D. Greenwood. Nutrition management of amyotrophic lateral sclerosis. , 2013, Nutrition in clinical practice : official publication of the American Society for Parenteral and Enteral Nutrition.
[23] M. Inghilleri,et al. Nutritional and metabolic support in patients with amyotrophic lateral sclerosis. , 2012, Nutrition.
[24] A. Al-Chalabi,et al. Eating-derived pleasure in amyotrophic lateral sclerosis as a predictor of non-oral feeding , 2012, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.
[25] B. Giometto,et al. Nutritional intervention for amyotrophic lateral sclerosis. , 2012, Minerva gastroenterologica e dietologica.
[26] C. Crisci,et al. Amyotrophic lateral sclerosis: Ethical challenges. , 2011, Neurology. Clinical practice.
[27] C. Pichard,et al. Nutritional state, energy intakes and energy expenditure of amyotrophic lateral sclerosis (ALS) patients. , 2011, Clinical nutrition.
[28] V. Meininger,et al. Safety of home parenteral nutrition in patients with amyotrophic lateral sclerosis: A French national survey , 2011, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.
[29] C. Parsons,et al. Amyotrophic Lateral Sclerosis , 2011, Neurology.
[30] J. Kassubek,et al. Patients with elevated triglyceride and cholesterol serum levels have a prolonged survival in amyotrophic lateral sclerosis , 2011, Journal of Neurology.
[31] O. Hardiman,et al. Management of Amyotrophic Lateral Sclerosis , 2010 .
[32] E. Beghi,et al. Prognostic factors in ALS: A critical review , 2009, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.
[33] J. Pouget,et al. Enteral and parenteral nutrition in the later stages of ALS: An observational study , 2009, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.
[34] R. Olney,et al. Enteral tube feeding for amyotrophic lateral sclerosis/motor neuron disease. , 2006, The Cochrane database of systematic reviews.
[35] M. Piquet. [Nutritional approach for patients with amyotrophic lateral sclerosis]. , 2006, Revue neurologique.
[36] B. Beaufrère,et al. Validation of bioelectrical impedance analysis in patients with amyotrophic lateral sclerosis. , 2003, The American journal of clinical nutrition.