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

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Antonio Orlacchio

Centro Europeo di Ricerca sul Cervello -Istituto di Ricovero e Cura a Carattere Scientifico Santa Lucia

64 Via del Fosso di Fiorano

Rome 00143

Italy

[email]@hsantalucia.it

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Centro Europeo di Ricerca sul Cervello -Istituto di Ricovero e Cura a Carattere Scientifico Santa Lucia, 64 Via del Fosso di Fiorano, Rome 00143, Italy. 2004 - 2010
  • Laboratorio di Neurogenetica, CERC-IRCCS Santa Lucia, Rome, Italy and Dipartimento di Neuroscienze, Università di Roma "Tor Vergata", Italy. 2008
  • Laboratorio di Neurogenetica, I.R.C.C.S. Santa Lucia, Via Ardeatina 354, 00179, Italy. 2002 - 2006
  • Laboratory of Neurogenetics, University of Rome Tor Vergata, Italy. 2004

References

  1. SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis. Orlacchio, A., Babalini, C., Borreca, A., Patrono, C., Massa, R., Basaran, S., Munhoz, R.P., Rogaeva, E.A., St George-Hyslop, P.H., Bernardi, G., Kawarai, T. Brain (2010) [Pubmed]
  2. Stem cells: an overview of the current status of therapies for central and peripheral nervous system diseases. Orlacchio, A., Bernardi, G., Orlacchio, A., Martino, S. Curr. Med. Chem. (2010) [Pubmed]
  3. Silver syndrome variant of hereditary spastic paraplegia: A locus to 4p and allelism with SPG4. Orlacchio, A., Patrono, C., Gaudiello, F., Rocchi, C., Moschella, V., Floris, R., Bernardi, G., Kawarai, T. Neurology (2008) [Pubmed]
  4. The apolipoprotein E2 isoform is associated with accelerated onset of coronary artery disease in systemic lupus erythematosus. Orlacchio, A., Bruce, I.N., Rahman, P., Kawarai, T., Bernardi, G., St George-Hyslop, P.H., Gladman, D.D., Urowitz, M.B. Med. Sci. Monit. (2008) [Pubmed]
  5. RNA interference as a tool for Alzheimer's disease therapy. Orlacchio, A., Bernardi, G., Orlacchio, A., Martino, S. Mini. Rev. Med. Chem (2007) [Pubmed]
  6. Neuroacanthocytosis associated with a defect of the 4.1R membrane protein. Orlacchio, A., Calabresi, P., Rum, A., Tarzia, A., Salvati, A.M., Kawarai, T., Stefani, A., Pisani, A., Bernardi, G., Cianciulli, P., Caprari, P. BMC. Neurol (2007) [Pubmed]
  7. Research actuality in the genetics of stroke. Orlacchio, A., Bernardi, G. Clin. Exp. Hypertens. (2006) [Pubmed]
  8. Clinical and genetic study of a large SPG4 Italian family. Orlacchio, A., Kawarai, T., Gaudiello, F., Totaro, A., Schillaci, O., Stefani, A., Floris, R., St George-Hyslop, P.H., Sorbi, S., Bernardi, G. Mov. Disord. (2005) [Pubmed]
  9. New locus for hereditary spastic paraplegia maps to chromosome 1p31.1-1p21.1. Orlacchio, A., Kawarai, T., Gaudiello, F., St George-Hyslop, P.H., Floris, R., Bernardi, G. Ann. Neurol. (2005) [Pubmed]
  10. Lack of association between Alzheimer's disease and the promoter region polymorphisms of the nicastrin gene. Orlacchio, A., Kawarai, T., Polidoro, M., Paterson, A.D., Rogaeva, E., Orlacchio, A., St George-Hyslop, P.H., Bernardi, G. Neurosci. Lett. (2004) [Pubmed]
  11. A new SPG4 mutation in a variant form of spastic paraplegia with congenital arachnoid cysts. Orlacchio, A., Gaudiello, F., Totaro, A., Floris, R., St George-Hyslop, P.H., Bernardi, G., Kawarai, T. Neurology (2004) [Pubmed]
  12. Hereditary spastic paraplegia: clinical genetic study of 15 families. Orlacchio, A., Kawarai, T., Totaro, A., Errico, A., St George-Hyslop, P.H., Rugarli, E.I., Bernardi, G. Arch. Neurol. (2004) [Pubmed]
  13. Association study of the 5-hydroxytryptamine(6) receptor gene in Alzheimer's disease. Orlacchio, A., Kawarai, T., Paciotti, E., Stefani, A., Orlacchio, A., Sorbi, S., St George-Hyslop, P.H., Bernardi, G. Neurosci. Lett. (2002) [Pubmed]
  14. Association analysis between Alzheimer's disease and the Nicastrin gene polymorphisms. Orlacchio, A., Kawarai, T., Polidoro, M., Stefani, A., Orlacchio, A., St George-Hyslop, P.H., Bernardi, G. Neurosci. Lett. (2002) [Pubmed]
  15. Clinical and genetic study of a large Italian family linked to SPG12 locus. Orlacchio, A., Kawarai, T., Rogaeva, E., Song, Y.Q., Paterson, A.D., Bernardi, G., St George-Hyslop, P.H. Neurology (2002) [Pubmed]
 
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