Factors predicting survival in ALS: a multicenter Italian study
暂无分享,去创建一个
A. Chiò | G. Mora | G. Logroscino | A. Calvo | R. Tortelli | S. Messina | G. Soraru' | N. Ticozzi | V. Silani | C. Moglia | J. Mandrioli | V. Sansone | C. Caponnetto | M. Monsurrò | K. Marinou | M. Sabatelli | A. Conte | N. Fini | N. Riva | Y. Falzone | P. Volanti | C. Lunetta | F. Trojsi | M. Russo | G. Querin | G. Ferrante | C. Scialò | Kalliopi Marinou
[1] L. Casulari,et al. Prognostic Factors in Amyotrophic Lateral Sclerosis: A Population-Based Study , 2015, PloS one.
[2] D. Fan,et al. Natural history and clinical features of sporadic amyotrophic lateral sclerosis in China , 2015, Journal of Neurology, Neurosurgery & Psychiatry.
[3] Rui Huang,et al. The predictors of survival in Chinese amyotrophic lateral sclerosis patients , 2015, Amyotrophic lateral sclerosis & frontotemporal degeneration.
[4] O. Hardiman,et al. A multidisciplinary clinic approach improves survival in ALS: a comparative study of ALS in Ireland and Northern Ireland , 2014, Journal of Neurology, Neurosurgery & Psychiatry.
[5] Frans Nollet,et al. Prognostic factors for the course of functional status of patients with ALS: a systematic review , 2014, Journal of Neurology.
[6] M. Vinceti,et al. Noninvasive and invasive ventilation and enteral nutrition for ALS in Italy , 2014, Muscle & nerve.
[7] E. Granieri,et al. Epidemiology of amyotrophic lateral sclerosis in Emilia Romagna Region (Italy): A population based study , 2014, Amyotrophic lateral sclerosis & frontotemporal degeneration.
[8] Adriano Chiò,et al. Cognitive correlates in amyotrophic lateral sclerosis: a population-based study in Italy , 2014, Journal of Neurology, Neurosurgery & Psychiatry.
[9] J. Glass,et al. Prognosis and epidemiology of amyotrophic lateral sclerosis: Analysis of a clinic population, 1997–2011 , 2013, Neurology. Clinical practice.
[10] A. Chiò,et al. Amyotrophic lateral sclerosis in Sardinia, insular Italy, 1995–2009 , 2013, Journal of Neurology.
[11] M. Sormani,et al. Clinical epidemiology of ALS in Liguria, Italy , 2013, Amyotrophic lateral sclerosis & frontotemporal degeneration.
[12] P. Andersen,et al. EFNS guidelines on the Clinical Management of Amyotrophic Lateral Sclerosis (MALS) – revised report of an EFNS task force , 2012, European journal of neurology.
[13] M. Vinceti,et al. Changing incidence and subtypes of ALS in Modena, Italy: A 10-years prospective study , 2011, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.
[14] A. Chiò,et al. ALS clinical trials , 2011, Neurology.
[15] O. Hardiman,et al. The syndrome of cognitive impairment in amyotrophic lateral sclerosis: a population-based study , 2011, Journal of Neurology, Neurosurgery & Psychiatry.
[16] S. Paganoni,et al. Body mass index, not dyslipidemia, is an independent predictor of survival in amyotrophic lateral sclerosis , 2011, Muscle & nerve.
[17] M. Sabatelli,et al. Uncovering amyotrophic lateral sclerosis phenotypes: Clinical features and long-term follow-up of upper motor neuron-dominant ALS , 2011, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.
[18] A. Chiò,et al. Phenotypic heterogeneity of amyotrophic lateral sclerosis: a population based study , 2011, Journal of Neurology, Neurosurgery & Psychiatry.
[19] M. Benatar,et al. Enteral tube feeding for amyotrophic lateral sclerosis/motor neuron disease. , 2011, The Cochrane database of systematic reviews.
[20] E. Beghi,et al. The epidemiology and treatment of ALS: Focus on the heterogeneity of the disease and critical appraisal of therapeutic trials , 2011, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.
[21] A. Chiò,et al. Tracheostomy in amyotrophic lateral sclerosis: a 10-year population-based study in Italy , 2010, Journal of Neurology, Neurosurgery & Psychiatry.
[22] D. Annane,et al. Mechanical ventilation for amyotrophic lateral sclerosis/motor neuron disease , 2010, The Cochrane database of systematic reviews.
[23] F. Khan,et al. Multidisciplinary care for adults with amyotrophic lateral sclerosis or motor neuron disease. , 2009, The Cochrane database of systematic reviews.
[24] 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.
[25] E. Beghi,et al. Descriptive epidemiology of amyotrophic lateral sclerosis: new evidence and unsolved issues , 2007, Journal of Neurology, Neurosurgery, and Psychiatry.
[26] P. Shaw,et al. Effects of non-invasive ventilation on survival and quality of life in patients with amyotrophic lateral sclerosis: a randomised controlled trial , 2006, The Lancet Neurology.
[27] W. McGuire,et al. Iron supplementation in enterally fed preterm infants , 2005 .
[28] M. Swash,et al. El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis , 2000, Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases.
[29] M. de Carvalho. Natural history of young-adult amyotrophic lateral sclerosis. , 2009, Neurology.
[30] Robert G. Miller,et al. Riluzole for amyotrophic lateral sclerosis (ALS)/motor neuron disease (MND). , 2007, The Cochrane database of systematic reviews.
[31] H. Mitsumoto,et al. Subcommittee of the American Academy of Neurology Evidence-based Review) : Report of the Quality Standards Management, and Cognitive/behavioral Impairment (an Amyotrophic Lateral Sclerosis: Multidisciplinary Care, Symptom Practice Parameter Update: the Care of the Patient With , 2022 .