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

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Mercedes Pineda

Hospital Sant Joan de Déu

Passeig de Sant Joan de Déu No. 2

Esplugues

Barcelona

Spain

[email]@hsjdbcn.org

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Hospital Sant Joan de Déu, Passeig de Sant Joan de Déu No. 2, Esplugues, Barcelona, Spain. 2011
  • Department of Pediatric Neurology, Hospital Sant Joan de Déu, Barcelona, Spain. 2004 - 2010
  • Hospital Sant Joan de Deu, Barcelona, Spain. 2009
  • Neuropediatrics Department, Hospital Sant Joan de Déu and Centre for Biomedical Research on Rare Diseases (CIBERER), Barcelona, Spain. 2008
  • S. Neuropediatria i Bioquímica, Unitat Integrada, Hospital Sant Joan de Déu/Hospital Clínic, Universitat de Barcelona, Spain. 2000

References

  1. New agents and approaches to treatment in niemann - pick type C disease. Pérez-Poyato, M.S., Pineda, M. Curr. Pharm. Biotechnol (2011) [Pubmed]
  2. Clinical experience with miglustat therapy in pediatric patients with Niemann-Pick disease type C: a case series. Pineda, M., Perez-Poyato, M.S., O'Callaghan, M., Vilaseca, M.A., Pocovi, M., Domingo, R., Portal, L.R., Pérez, A.V., Temudo, T., Gaspar, A., Peñas, J.J., Roldán, S., Fumero, L.M., de la Barca, O.B., Silva, M.T., Macías-Vidal, J., Coll, M.J. Mol. Genet. Metab. (2010) [Pubmed]
  3. Miglustat in patients with Niemann-Pick disease Type C (NP-C): a multicenter observational retrospective cohort study. Pineda, M., Wraith, J.E., Mengel, E., Sedel, F., Hwu, W.L., Rohrbach, M., Bembi, B., Walterfang, M., Korenke, G.C., Marquardt, T., Luzy, C., Giorgino, R., Patterson, M.C. Mol. Genet. Metab. (2009) [Pubmed]
  4. Idebenone treatment in paediatric and adult patients with Friedreich ataxia: long-term follow-up. Pineda, M., Arpa, J., Montero, R., Aracil, A., Domínguez, F., Galván, M., Mas, A., Martorell, L., Sierra, C., Brandi, N., García-Arumí, E., Rissech, M., Velasco, D., Costa, J.A., Artuch, R. Eur. J. Paediatr. Neurol. (2008) [Pubmed]
  5. Vanishing white matter disease associated with progressive macrocephaly. Pineda, M., R-Palmero, A., Baquero, M., O'Callaghan, M., Aracil, A., van der Knaap, M., Scheper, G.C. Neuropediatrics (2008) [Pubmed]
  6. Cerebral folate deficiency and leukoencephalopathy caused by a mitochondrial DNA deletion. Pineda, M., Ormazabal, A., López-Gallardo, E., Nascimento, A., Solano, A., Herrero, M.D., Vilaseca, M.A., Briones, P., Ibáñez, L., Montoya, J., Artuch, R. Ann. Neurol. (2006) [Pubmed]
  7. Peripheral neuropathy with ataxia in childhood as a result of the G8363A mutation in mitochondrial DNA. Pineda, M., Solano, A., Artuch, R., Andreu, A.L., Playan, A., Vilaseca, M.A., Colomer, J., Briones, P., Casademont, J., Montoya, J. Pediatr. Res. (2004) [Pubmed]
  8. 3-phosphoglycerate dehydrogenase deficiency in a patient with West syndrome. Pineda, M., Vilaseca, M.A., Artuch, R., Santos, S., García González, M.M., Aracil, A., Van Schaftingen, E., Jaeken, J. Dev. Med. Child. Neurol (2000) [Pubmed]
 
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