Nutritional assessment of amyotrophic lateral sclerosis in routine practice: Value of weighing and bioelectrical impedance analysis

Prediagnostic body fat and risk of death from amyotrophic lateral sclerosis: The EPIC cohort

(2013) V. Gallo et al.   NEUROLOGY

Clinical epidemiology of ALS in Liguria, Italy

(2012) Monica Bandettini di Poggio et al.   Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Premorbid body mass index and risk of amyotrophic lateral sclerosis

(2012) Éilis J. O'Reilly et al.   Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Phenotypic heterogeneity of amyotrophic lateral sclerosis: a population based study

(2011) A. Chio et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Amyotrophic lateral sclerosis

(2011) Matthew C Kiernan et al.   LANCET

Body mass index, not dyslipidemia, is an independent predictor of survival in amyotrophic lateral sclerosis

(2011) Sabrina Paganoni et al.   MUSCLE & NERVE

What does body mass index measure in amyotrophic lateral sclerosis and why should we care?

(2011) Edward J. Kasarskis   MUSCLE & NERVE

A decrease in body mass index is associated with faster progression of motor symptoms and shorter survival in ALS

(2010) Ali Jawaid et al.   Amyotrophic Lateral Sclerosis

Assessing change in body composition in children with Duchenne muscular dystrophy: Anthropometry and bioelectrical impedance analysis versus dual-energy X-ray absorptiometry

(2010) Elise Mok et al.   CLINICAL NUTRITION

Progression in ALS is not linear but is curvilinear

(2010) Paul H. Gordon et al.   JOURNAL OF NEUROLOGY

Patients with elevated triglyceride and cholesterol serum levels have a prolonged survival in amyotrophic lateral sclerosis

(2010) J. Dorst et al.   JOURNAL OF NEUROLOGY

Alteration of nutritional status at diagnosis is a prognostic factor for survival of amyotrophic lateral sclerosis patients

(2010) B. Marin et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Malnutrition at the time of diagnosis is associated with a shorter disease duration in ALS

(2010) Nadège Limousin et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Energy metabolism in amyotrophic lateral sclerosis

(2010) Luc Dupuis et al.   LANCET NEUROLOGY

Incidence of amyotrophic lateral sclerosis in the Limousin region of France, 1997–2007

(2009) Benoit Marin et al.   Amyotrophic Lateral Sclerosis

Hypermetabolism in ALS patients: an early and persistent phenomenon

(2009) C. Bouteloup et al.   JOURNAL OF NEUROLOGY

Practice Parameter update: The care of the patient with amyotrophic lateral sclerosis: Drug, nutritional, and respiratory therapies (an evidence-based review): Report of the Quality Standards Subcommittee of the American Academy of Neurology

(2009) R. G. Miller et al.   NEUROLOGY

Prognostic significance of bioelectrical impedance phase angle in advanced cancer: Preliminary observations

(2009) Lidia Santarpia et al.   NUTRITION

Phase angle is a prognostic factor for survival in amyotrophic lateral sclerosis

(2008) Jean-Claude Desport et al.   Amyotrophic Lateral Sclerosis

Prevalence and clinical implications of sarcopenic obesity in patients with solid tumours of the respiratory and gastrointestinal tracts: a population-based study

(2008) Carla MM Prado et al.   LANCET ONCOLOGY

Dyslipidemia is a protective factor in amyotrophic lateral sclerosis

(2008) L. Dupuis et al.   NEUROLOGY