High metabolic level in patients with familial amyotrophic lateral sclerosis

References

• Kunst CB. Complex genetics of amyotrophic lateral sclerosis. Am J Hum Genet. 2004; 75: 933–47
   PubMed Web of Science ®Google Scholar
• Gros-Louis F, Gaspar C, Rouleau G. Genetics of familial and sporadic amyotrophic lateral sclerosis. Biochim Biophys Acta. 2006; 1762: 956–72
   PubMed Web of Science ®Google Scholar
• Kasarskis EJ, Berryman S, Vanderleest JG, Schneider AR, McClain CJ. Nutritional status of patients with amyotrophic lateral sclerosis: relation to the proximity of death. Am J Clin Nutr. 1996; 63: 130–7
   PubMed Web of Science ®Google Scholar
• Desport JC, Preux PM, Magy L, Boirie Y, Vallat JM, Beaufrère B, et al. Factors correlated with hypermetabolism in patients with amyotrophic lateral sclerosis. Am J Clin Nutr. 2001; 74: 328–34
   PubMed Web of Science ®Google Scholar
• Desport JC, Torny F, Lacoste M, Preux PM, Couratier P. Hypermetabolism in ALS: correlations with clinical and paraclinical parameters. Neurodegenerative Dis. 2005; 2: 202–7
   PubMed Web of Science ®Google Scholar
• Dupuis L, Oudart H, René F, Gonzalez de Aguilar JL, Loeffler JP. Evidence for defective energy homeostasis in amyotrophic lateral sclerosis: benefit of a high-energy diet in a transgenic mouse model. Proc Natl Acad Sci USA. 2004; 101: 11159–64
   PubMed Web of Science ®Google Scholar
• Jafari-Schluep HF, Khoris J, Mayeux-Portas V, Hand C, Rouleau G, Camu W. Groupe Français d'Etude des Maladies du Motoneurone. Les anomalies du gène superoxyde dismutase 1 dans la sclérose latérale amyotrophique familiale : corrélations phénotype/génotype et implications pratiques. Expérience française et revue de la littérature. Rev Neurol (Paris) 2004; 160: 44–50
   PubMed Web of Science ®Google Scholar
• Brooks BR, Miller RG, Swash M, Munsat TL. World Federation of Neurology Research Group on Motor Neuron Diseases. El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord. 2000; 1: 293–9
   PubMed Web of Science ®Google Scholar
• Medical Resarch Council. Aid to the investigation of peripheral nerve injury. In: Medical Research Council. War memorandum, 2nd edn. London: His Majesty's Stationery Office; 1943. pp 11–46.
   Google Scholar
• The ALS CNTF treatment study (ACTS) phase I-II Study Group. The Amyotrophic Lateral Sclerosis Functional Rating Scale. Assessment of activities of daily living in patients with amyotrophic lateral sclerosis. Arch Neurol. 1996;53:141–7.
   PubMed Web of Science ®Google Scholar
• Ferrannini E. The theoretical bases of indirect calorimetry: a review. Metabolism. 1988; 37: 287–301
   PubMed Web of Science ®Google Scholar
• Harris JA, Benedict FG. A biometric study of basal metabolism in man. Carnegie Institute of Washington, Washington, DC 1919
   Google Scholar
• Desport JC, Preux PM, Bouteloup-Demange C, Clavelou P, Beaufrère B, Bonnet C, et al. Validation of bioelectrical impedance analysis in patients with amyotrophic lateral sclerosis. Am J Clin Nutr. 2003; 77: 1179–85
   PubMed Web of Science ®Google Scholar
• Dupuis L, di Scala F, René F, de Tapia M, Oudart H, Pradat PF, et al. Up-regulation of mitochondrial uncoupling protein 3 reveals an early muscular metabolic defect in amyotrophic lateral sclerosis. FASEB J. 2003; 17: 2091–3
   PubMed Web of Science ®Google Scholar
• Criscuolo F, Mozo J, Hurtaud C, Nübel T, Bouillaud F. UCP2, UCP3, avUCP, what do they do when proton transport is not stimulated? Possible relevance to pyruvate and glutamine metabolism. Biochim Biophys Acta. 2006; 1757: 1284–91
   PubMed Web of Science ®Google Scholar
• Manfredi G, Xu Z. Mitochondrial dysfunction and its role in motor neuron degeneration in ALS. Mitochondrion. 2005; 5: 77–87
   PubMed Web of Science ®Google Scholar
• Afifi AK, Aleu FP, Goodgold J, MacKay B. Ultrastructure of atrophic muscle in amyotrophic lateral sclerosis. Neurology. 1966; 16: 475–81
   PubMed Web of Science ®Google Scholar
• Hirano A, Donnenfeld H, Sasaki S, Nakano I. Fine structural observations of neurofilamentous changes in amyotrophic lateral sclerosis. J Neuropathol Exp Neurol. 1984; 43: 461–70
   PubMed Web of Science ®Google Scholar
• Sasaki S, Iwata M. Impairment of fast axonal transport in the proximal axons of anterior horn neurons in amyotrophic lateral sclerosis. Neurology. 1996; 47: 535–40
   PubMed Web of Science ®Google Scholar
• Wiedemann FR, Winkler K, Kuznetsov AV, Bartels C, Vielhaber S, Feistner H, et al. Impairment of mitochondrial function in skeletal muscle of patients with amyotrophic lateral sclerosis. J Neurol Sci. 1998; 156: 65–72
   PubMed Web of Science ®Google Scholar
• Vielhaber S, Kunz D, Winkler K, Wiedemann FR, Kirches E, Feistner H. Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis. Brain. 2000; 123: 1339–48
   PubMed Web of Science ®Google Scholar
• Desport JC, Preux PM, Truong TC, Vallat JM, Sautereau D, Couratier P. Nutritional status is a prognostic factor for survival in ALS patients. Neurology. 1999; 53: 1059–63
   PubMed Web of Science ®Google Scholar
• Heffernan C, Jenkinson C, Holmes T, Feder G, Kupfer R, Leigh PN, et al. Nutritional management in MND/ALS patients: an evidence based review. Amyotroph Lateral Scler Other Motor Neuron Disord. 2004; 5: 72–83
   PubMed Web of Science ®Google Scholar