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Eugenio Mercuri

Department of Child Neurology and Psychiatry

Catholic University

Italy

[email]@ic.ac.uk

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Child Neurology and Psychiatry, Catholic University, Italy. 2007
  • Department of Paediatrics & Neonatal Medicine, Imperial College School of Medicine, Hammersmith Hospital, Du Cane Road, UK. 1999 - 2005
  • Dubowitz Neuromuscular Centre, Department of Paediatrics, Hammersmith Hospital, London, UK. 2000 - 2004
  • Department of Paediatrics and Neonatal Medicine, Hammersmith Campus, London, UK. 1999 - 2003
  • Department of Pediatrics, Hammersmith Campus, Imperial College School of Medicine, London, United Kingdom. 2003
  • Department of Paediatrics, Dubowitz Neuromuscular Centre, Hammersmith Hospital, Imperial College, UK. 2002

References

  1. Muscle MRI in inherited neuromuscular disorders: past, present, and future. Mercuri, E., Pichiecchio, A., Allsop, J., Messina, S., Pane, M., Muntoni, F. J. Magn. Reson. Imaging (2007) [Pubmed]
  2. The development of vision. Mercuri, E., Baranello, G., Romeo, D.M., Cesarini, L., Ricci, D. Early Hum. Dev. (2007) [Pubmed]
  3. Muscle imaging in clinical practice: diagnostic value of muscle magnetic resonance imaging in inherited neuromuscular disorders. Mercuri, E., Jungbluth, H., Muntoni, F. Curr. Opin. Neurol. (2005) [Pubmed]
  4. Neonatal cerebral infarction and neuromotor outcome at school age. Mercuri, E., Barnett, A., Rutherford, M., Guzzetta, A., Haataja, L., Cioni, G., Cowan, F., Dubowitz, L. Pediatrics (2004) [Pubmed]
  5. Visual function at school age in children with neonatal encephalopathy and low Apgar scores. Mercuri, E., Anker, S., Guzzetta, A., Barnett, A.L., Haataja, L., Rutherford, M., Cowan, F., Dubowitz, L., Braddick, O., Atkinson, J. Arch. Dis. Child. Fetal Neonatal Ed. (2004) [Pubmed]
  6. Extreme variability of phenotype in patients with an identical missense mutation in the lamin A/C gene: from congenital onset with severe phenotype to milder classic Emery-Dreifuss variant. Mercuri, E., Poppe, M., Quinlivan, R., Messina, S., Kinali, M., Demay, L., Bourke, J., Richard, P., Sewry, C., Pike, M., Bonne, G., Muntoni, F., Bushby, K. Arch. Neurol. (2004) [Pubmed]
  7. Congenital muscular dystrophy with short stature, proximal contractures and distal laxity. Mercuri, E., Lampe, A., Straub, V., Yuva, Y., Longman, C., Wright, M., Brown, S., Sewry, C., Bonnemann, C., Kinali, M., Brockington, M., Hausser, I., Hilton Jones, D., Voit, T., Bushby, K., Muntoni, F. Neuropediatrics (2004) [Pubmed]
  8. Phenotypic spectrum associated with mutations in the fukutin-related protein gene. Mercuri, E., Brockington, M., Straub, V., Quijano-Roy, S., Yuva, Y., Herrmann, R., Brown, S.C., Torelli, S., Dubowitz, V., Blake, D.J., Romero, N.B., Estournet, B., Sewry, C.A., Guicheney, P., Voit, T., Muntoni, F. Ann. Neurol. (2003) [Pubmed]
  9. Neurologic examination of preterm infants at term age: comparison with term infants. Mercuri, E., Guzzetta, A., Laroche, S., Ricci, D., vanhaastert, I., Simpson, A., Luciano, R., Bleakley, C., Frisone, M.F., Haataja, L., Tortorolo, G., Guzzetta, F., de Vries, L., Cowan, F., Dubowitz, L. J. Pediatr. (2003) [Pubmed]
  10. Neonatal cerebral infarction and visual function at school age. Mercuri, E., Anker, S., Guzzetta, A., Barnett, A., Haataja, L., Rutherford, M., Cowan, F., Dubowitz, L., Braddick, O., Atkinson, J. Arch. Dis. Child. Fetal Neonatal Ed. (2003) [Pubmed]
  11. Neonatal brain MRI and motor outcome at school age in children with neonatal encephalopathy: a review of personal experience. Mercuri, E., Barnett, A.L. Neural Plast. (2003) [Pubmed]
  12. Selective muscle involvement on magnetic resonance imaging in autosomal dominant Emery-Dreifuss muscular dystrophy. Mercuri, E., Counsell, S., Allsop, J., Jungbluth, H., Kinali, M., Bonne, G., Schwartz, K., Bydder, G., Dubowitz, V., Muntoni, F. Neuropediatrics (2002) [Pubmed]
  13. Collagen VI involvement in Ullrich syndrome: a clinical, genetic, and immunohistochemical study. Mercuri, E., Yuva, Y., Brown, S.C., Brockington, M., Kinali, M., Jungbluth, H., Feng, L., Sewry, C.A., Muntoni, F. Neurology (2002) [Pubmed]
  14. MRI lesions and infants with neonatal encephalopathy. Is the Apgar score predictive?. Mercuri, E., Rutherford, M., Barnett, A., Foglia, C., Haataja, L., Counsell, S., Cowan, F., Dubowitz, L. Neuropediatrics (2002) [Pubmed]
  15. Clinical and imaging findings in six cases of congenital muscular dystrophy with rigid spine syndrome linked to chromosome 1p (RSMD1). Mercuri, E., Talim, B., Moghadaszadeh, B., Petit, N., Brockington, M., Counsell, S., Guicheney, P., Muntoni, F., Merlini, L. Neuromuscul. Disord. (2002) [Pubmed]
  16. A short protocol for muscle MRI in children with muscular dystrophies. Mercuri, E., Pichiecchio, A., Counsell, S., Allsop, J., Cini, C., Jungbluth, H., Uggetti, C., Bydder, G. Eur. J. Paediatr. Neurol. (2002) [Pubmed]
  17. Muscle MRI findings in a three-generation family affected by Bethlem myopathy. Mercuri, E., Cini, C., Counsell, S., Allsop, J., Zolkipli, Z., Jungbluth, H., Sewry, C., Brown, S.C., Pepe, G., Muntoni, F. Eur. J. Paediatr. Neurol. (2002) [Pubmed]
  18. Early diagnostic and prognostic indicators in full term infants with neonatal cerebral infarction: an integrated clinical, neuroradiological and EEG approach. Mercuri, E. Minerva Pediatr. (2001) [Pubmed]
  19. Early and severe presentation of autosomal dominant Emery-Dreifuss muscular dystrophy (EMD2). Mercuri, E., Manzur, A.Y., Jungbluth, H., Bonne, G., Muchir, A., Sewry, C., Schwartz, K., Muntoni, F. Neurology (2000) [Pubmed]
  20. Congenital muscular dystrophy with secondary merosin deficiency and normal brain MRI: a novel entity?. Mercuri, E., Sewry, C.A., Brown, S.C., Brockington, M., Jungbluth, H., DeVile, C., Counsell, S., Manzur, A., Muntoni, F. Neuropediatrics (2000) [Pubmed]
  21. Vincristine treatment revealing asymptomatic hereditary motor sensory neuropathy type 1A. Mercuri, E., Poulton, J., Buck, J., Broadbent, V., Bamford, M., Jungbluth, H., Manzur, A.Y., Muntoni, F. Arch. Dis. Child. (1999) [Pubmed]
  22. Cerebral infarction in the newborn infant: review of the literature and personal experience. Mercuri, E., Cowan, F. Eur. J. Paediatr. Neurol. (1999) [Pubmed]
 
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