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E Mercuri

Showing results (61-70 of 168) with videos related to

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Biochemical Society Transactions|May 1, 1996
The protein defect in congenital muscular dystrophyC A Sewry, I Naom, M D'Alessandro, et al.
Neurology|April 13, 2000
Early and severe presentation of autosomal dominant Emery-Dreifuss muscular dystrophy (EMD2)E Mercuri, A Y Manzur, H Jungbluth, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 19, 2000
An unusual case of hyperekplexiaH Jungbluth, M I Rees, A Y Manzur, et al.
Neuropediatrics|June 10, 2005
Assessment of visual function in children with methylmalonic aciduria and homocystinuriaD Ricci, M Pane, F Deodato, et al.
Developmental Medicine and Child Neurology|May 23, 2001
Visual function in children with hemiplegia in the first years of lifeA Guzzetta, B Fazzi, E Mercuri, et al.
Neuropediatrics|August 1, 1996
Visual outcome in children with congenital hemiplegia: correlation with MRI findingsE Mercuri, M Spanò, G Bruccini, et al.
Neuropediatrics|July 13, 1999
Neonatal neurological examination in infants with hypoxic ischaemic encephalopathy: correlation with MRI findingsE Mercuri, A Guzzetta, L Haataja, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|September 1, 1996
Visual function and perinatal focal cerebral infarctionE Mercuri, J Atkinson, O Braddick, et al.
Pediatrics|January 26, 1999
Early prognostic indicators of outcome in infants with neonatal cerebral infarction: a clinical, electroencephalogram, and magnetic resonance imaging studyE Mercuri, M Rutherford, F Cowan, et al.
Annals of Tropical Paediatrics|February 24, 2001
Neonatal neurological testing in resource-poor settingsR McGready, J Simpson, S Panyavudhikrai, et al.
Pageof 17

Showing results (61-70 of 168) with videos related to

Sort By:
Pageof 17
Biochemical Society Transactions|May 1, 1996
The protein defect in congenital muscular dystrophyC A Sewry, I Naom, M D'Alessandro, et al.
Neurology|April 13, 2000
Early and severe presentation of autosomal dominant Emery-Dreifuss muscular dystrophy (EMD2)E Mercuri, A Y Manzur, H Jungbluth, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 19, 2000
An unusual case of hyperekplexiaH Jungbluth, M I Rees, A Y Manzur, et al.
Neuropediatrics|June 10, 2005
Assessment of visual function in children with methylmalonic aciduria and homocystinuriaD Ricci, M Pane, F Deodato, et al.
Developmental Medicine and Child Neurology|May 23, 2001
Visual function in children with hemiplegia in the first years of lifeA Guzzetta, B Fazzi, E Mercuri, et al.
Neuropediatrics|August 1, 1996
Visual outcome in children with congenital hemiplegia: correlation with MRI findingsE Mercuri, M Spanò, G Bruccini, et al.
Neuropediatrics|July 13, 1999
Neonatal neurological examination in infants with hypoxic ischaemic encephalopathy: correlation with MRI findingsE Mercuri, A Guzzetta, L Haataja, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|September 1, 1996
Visual function and perinatal focal cerebral infarctionE Mercuri, J Atkinson, O Braddick, et al.
Pediatrics|January 26, 1999
Early prognostic indicators of outcome in infants with neonatal cerebral infarction: a clinical, electroencephalogram, and magnetic resonance imaging studyE Mercuri, M Rutherford, F Cowan, et al.
Annals of Tropical Paediatrics|February 24, 2001
Neonatal neurological testing in resource-poor settingsR McGready, J Simpson, S Panyavudhikrai, et al.
Pageof 17