References
- Schwarz S, Husstedt I, Bertram HP, Kuchelmeister K. Amyotrophic lateral sclerosis after accidental injection of mercury. J Neurol Neurosurg Psychiatry 1996; 60: 698
- Andersen PM. Genetics of sporadic ALS. Amyotroph Lateral Scler Other Motor Neuron Disord 2001; 2(1)S37–41
- Siddique T. What is missing in ALS. Lancet Neurol 2008; 7: 289–90
- Youssoufian H, Pyeritz RE. Mechanisms and consequences of somatic mosaicism in humans. Nat Rev Genet 2002; 3: 748–58
- Beck JA, Poulter M, Campbell TA, Uphill JB, Adamson G, Geddes JF, et al. Somatic and germline mosaicism in sporadic early-onset Alzheimer's disease. Hum Mol Genet 2004; 13: 1219–24
- Shaw PJ, Tomkins J, Slade JY, Usher P, Curtis A, Bushby K, et al. CNS tissue Cu/Zn superoxide dismutase (SOD1) mutations in motor neuron disease (MND). Neuroreport 1997; 8: 3923–7
- Pamphlett R. Somatic mutation: a cause of sporadic neurodegenerative diseases?. Med Hypotheses 2004; 62: 679–82
- Boillee S, Yamanaka K, Lobsiger CS, Copeland NG, Jenkins NA, Kassiotis G, et al. Onset and progression in inherited ALS determined by motor neurons and microglia. Science 2006; 312: 1389–92
- Nagai M, Re DB, Nagata T, Chalazonitis A, Jessell TM, Wichterle H, et al. Astrocytes expressing ALS-linked mutated SOD1 release factors selectively toxic to motor neurons. Nat Neurosci 2007; 10: 615–22
- Ogino S, Kawasaki T, Brahmandam M, Yan L, Cantor M, Namgyal C, et al. Sensitive sequencing method for KRAS mutation detection by pyrosequencing. J Mol Diagn 2005; 7: 413–21
- Xiao W, Oefner PJ. Denaturing high-performance liquid chromatography: a review. Hum Mutat 2001; 17: 439–74
- Yu B, Sawyer NA, Caramins M, Yuan ZG, Saunderson RB, Pamphlett R, et al. Denaturing high performance liquid chromatography: high throughput mutation screening in familial hypertrophic cardiomyopathy and SNP genotyping in motor neuron disease. J Clin Pathol 2005; 58: 479–85
- Restagno G, Gomez A, Lombardo F, Cocco E, Calvo A, Ghiglione P, et al. The IVS1 +319 t > a of SOD1 gene is not an ALS-causing mutation. Amyotroph Lateral Scler Other Motor Neuron Disord 2005; 6: 45–9
- Conforti FL, Sprovieri T, Mazzei R, Ungaro C, Tessitore A, Tedeschi G, et al. Sporadic ALS is not associated with VAPB gene mutations in southern Italy. J Negat Results Biomed 2006; 5: 7
- Brooks BR, Miller RG, Swash M, Munsat TL. El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord 2000; 1: 293–9
- Lloyd CM, Richardson MP, Brooks DJ, Al-Chalabi A, Leigh PN. Extramotor involvement in ALS: PET studies with the GABA(A) ligand [(11)C]flumazenil. Brain 2000; 123: 2289–96
- Luquin N, Yu B, Trent RJ, Morahan JM, Pamphlett R. An analysis of the entire SOD1 gene in sporadic ALS. Neuromuscul Disord 2008; 18: 545–52
- Krypuy M, Newnham GM, Thomas DM, Conron M, Dobrovic A. High resolution melting analysis for the rapid and sensitive detection of mutations in clinical samples: KRAS codon 12 and 13 mutations in non-small cell lung cancer. BMC Cancer 2006; 6: 295
- Thomas RK, Nickerson E, Simons JF, Janne PA, Tengs T, Yuza Y, et al. Sensitive mutation detection in heterogeneous cancer specimens by massively parallel picoliter reactor sequencing. Nat Med 2006; 12: 852–5