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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Andoni Echaniz-Laguna

Département de Neurologie

Hôpital Civil


67091 Strasbourg



Name/email consistency: high



  • Département de Neurologie, Hôpital Civil, BP426, 67091 Strasbourg, France. 2004 - 2010
  • Inserm, U692, Laboratoire de Signalisations Moléculaires et Neurodégénérescence, Strasbourg, France. 2008
  • Service des Maladies du Système Nerveux et du Muscle, Clinique Neurologique, Hĵpital Civil de Strasbourg, France. 2002


  1. Muscle phosphorylase b kinase deficiency revisited. Echaniz-Laguna, A., Akman, H.O., Mohr, M., Tranchant, C., Talmant-Verbist, V., Rolland, M.O., Dimauro, S. Neuromuscul. Disord. (2010) [Pubmed]
  2. A novel variation in the Twinkle linker region causing late-onset dementia. Echaniz-Laguna, A., Chanson, J.B., Wilhelm, J.M., Sellal, F., Mayençon, M., Mohr, M., Tranchant, C., Mousson de Camaret, B. Neurogenetics (2010) [Pubmed]
  3. Myopathies in the elderly: a hospital-based study. Echaniz-Laguna, A., Mohr, M., Lannes, B., Tranchant, C. Neuromuscul. Disord. (2010) [Pubmed]
  4. Electrophysiological studies in a mouse model of Schwartz-Jampel syndrome demonstrate muscle fiber hyperactivity of peripheral nerve origin. Echaniz-Laguna, A., Rene, F., Marcel, C., Bangratz, M., Fontaine, B., Loeffler, J.P., Nicole, S. Muscle. Nerve (2009) [Pubmed]
  5. Teaching neuroimages: Chronic inflammatory demyelinating polyradiculoneuropathy causing spinal cord compression. Echaniz-Laguna, A., Philippi, N. Neurology (2009) [Pubmed]
  6. Histone deacetylase inhibitors: therapeutic agents and research tools for deciphering motor neuron diseases. Echaniz-Laguna, A., Bousiges, O., Loeffler, J.P., Boutillier, A.L. Curr. Med. Chem. (2008) [Pubmed]
  7. Subtle central and peripheral nervous system abnormalities in a family with centronuclear myopathy and a novel dynamin 2 gene mutation. Echaniz-Laguna, A., Nicot, A.S., Carré, S., Franques, J., Tranchant, C., Dondaine, N., Biancalana, V., Mandel, J.L., Laporte, J. Neuromuscul. Disord. (2007) [Pubmed]
  8. NDRG1-linked Charcot-Marie-Tooth disease (CMT4D) with central nervous system involvement. Echaniz-Laguna, A., Degos, B., Bonnet, C., Latour, P., Hamadouche, T., Lévy, N., Leheup, B. Neuromuscul. Disord. (2007) [Pubmed]
  9. Muscular mitochondrial function in amyotrophic lateral sclerosis is progressively altered as the disease develops: a temporal study in man. Echaniz-Laguna, A., Zoll, J., Ponsot, E., N'guessan, B., Tranchant, C., Loeffler, J.P., Lampert, E. Exp. Neurol. (2006) [Pubmed]
  10. A study of three patients with amyotrophic lateral sclerosis and a polyneuropathy resembling CIDP. Echaniz-Laguna, A., Degos, B., Mohr, M., Kessler, R., Urban-Kraemer, E., Tranchant, C. Muscle. Nerve (2006) [Pubmed]
  11. Novel Lamp-2 gene mutation and successful treatment with heart transplantation in a large family with Danon disease. Echaniz-Laguna, A., Mohr, M., Epailly, E., Nishino, I., Charron, P., Richard, P., Guiraud-Chaumeil, C., Tranchant, C. Muscle. Nerve (2006) [Pubmed]
  12. A family with early-onset and rapidly progressive X-linked spinal and bulbar muscular atrophy. Echaniz-Laguna, A., Rousso, E., Anheim, M., Cossée, M., Tranchant, C. Neurology (2005) [Pubmed]
  13. Chronic inflammatory demyelinating polyradiculoneuropathy in patients with liver transplantation. Echaniz-Laguna, A., Battaglia, F., Ellero, B., Mohr, M., Jaeck, D. Muscle. Nerve (2004) [Pubmed]
  14. Homozygous exon 7 deletion of the SMN centromeric gene (SMN2): a potential susceptibility factor for adult-onset lower motor neuron disease. Echaniz-Laguna, A., Guiraud-Chaumeil, C., Tranchant, C., Reeber, A., Melki, J., Warter, J.M. J. Neurol. (2002) [Pubmed]
  15. Mitochondrial respiratory chain function in skeletal muscle of ALS patients. Echaniz-Laguna, A., Zoll, J., Ribera, F., Tranchant, C., Warter, J.M., Lonsdorfer, J., Lampert, E. Ann. Neurol. (2002) [Pubmed]
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