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

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Angels García-Cazorla

Neurology Department

Hospital Sant Joan de Déu

Universitat de Barcelona

Passeig Sant Joan de Déu

Spain

[email]@hsjdbcn.org

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Neurology Department, Hospital Sant Joan de Déu, Universitat de Barcelona, Passeig Sant Joan de Déu, Spain. 2008 - 2009
  • Neurology Department, Hospital Sant Joan de Déu, University of Barcelona and Centre for Biomedical Research on Rare Diseases (CIBERER), Instituto de Salud Carlos III, Spain. 2007 - 2009
  • Department of Pediatrics, Centre Hospitalier Universitaire Necker Enfants-Malades, Paris, France. 2005 - 2006
  • Metabolic Diseases Unit, Department of Pediatrics and Biochemistry, Centre Hospitalier Universitaire Necker Enfants-Malades, Université René Descartes, France. 2006
  • Neuropaediatric Unit, Hospital Sant Joan de Déu, Barcelona, Spain. 2004

References

  1. Mental retardation and inborn errors of metabolism. García-Cazorla, A., Wolf, N.I., Serrano, M., Moog, U., Pérez-Dueñas, B., Póo, P., Pineda, M., Campistol, J., Hoffmann, G.F. J. Inherit. Metab. Dis. (2009) [Pubmed]
  2. Inborn errors of metabolism and motor disturbances in children. García-Cazorla, A., Wolf, N.I., Serrano, M., Pérez-Dueñas, B., Pineda, M., Campistol, J., Fernández-Alvarez, E., Colomer, J., DiMauro, S., Hoffmann, G.F. J. Inherit. Metab. Dis. (2009) [Pubmed]
  3. Mitochondrial diseases associated with cerebral folate deficiency. Garcia-Cazorla, A., Quadros, E.V., Nascimento, A., Garcia-Silva, M.T., Briones, P., Montoya, J., Ormazábal, A., Artuch, R., Sequeira, J.M., Blau, N., Arenas, J., Pineda, M., Ramaekers, V.T. Neurology (2008) [Pubmed]
  4. Mitochondrial diseases mimicking neurotransmitter defects. Garcia-Cazorla, A., Duarte, S., Serrano, M., Nascimento, A., Ormazabal, A., Carrilho, I., Briones, P., Montoya, J., Garesse, R., Sala-Castellvi, P., Pineda, M., Artuch, R. Mitochondrion (2008) [Pubmed]
  5. Secondary abnormalities of neurotransmitters in infants with neurological disorders. García-Cazorla, A., Serrano, M., Pérez-Dueñas, B., González, V., Ormazábal, A., Pineda, M., Fernández-Alvarez, E., Campistol, J.M., Artuch, R.M. Dev. Med. Child. Neurol (2007) [Pubmed]
  6. Pyruvate carboxylase deficiency: metabolic characteristics and new neurological aspects. García-Cazorla, A., Rabier, D., Touati, G., Chadefaux-Vekemans, B., Marsac, C., de Lonlay, P., Saudubray, J.M. Ann. Neurol. (2006) [Pubmed]
  7. Mitochondrial respiratory chain deficiencies expressing the enzymatic deficiency in the hepatic tissue: a study of 31 patients. Garcia-Cazorla, A., De Lonlay, P., Rustin, P., Chretien, D., Touati, G., Rabier, D., Slama, A., Saudubray, J.M. J. Pediatr. (2006) [Pubmed]
  8. Long-term follow-up of neonatal mitochondrial cytopathies: a study of 57 patients. García-Cazorla, A., De Lonlay, P., Nassogne, M.C., Rustin, P., Touati, G., Saudubray, J.M. Pediatrics (2005) [Pubmed]
  9. White matter alterations associated with chromosomal disorders. García-Cazorla, A., Sans, A., Baquero, M., García-Bargo, M.D., Arellano, M., Poo, P., Gean, E., Campistol, J. Dev. Med. Child. Neurol (2004) [Pubmed]
  10. Infectious acute hemicerebellitis. García-Cazorla, A., Oliván, J.A., Pancho, C., Sans, A., Boix, C., Campistol, J. J. Child Neurol. (2004) [Pubmed]
 
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