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E Mercuri

Showing results (91-100 of 150) with videos related to

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Developmental Medicine and Child Neurology|July 20, 2007
Visual function in infants with non-syndromic craniosynostosisD Ricci, G Vasco, G Baranello, et al.
Neuropediatrics|October 8, 1998
Orientation-reversal and phase-reversal visual evoked potentials in full-term infants with brain lesions: a longitudinal studyE Mercuri, O Braddick, J Atkinson, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|May 18, 1999
Visual function in term infants with hypoxic-ischaemic insults: correlation with neurodevelopment at 2 years of ageE Mercuri, L Haataja, A Guzzetta, et al.
Neuromuscular Disorders : NMD|May 17, 2006
POMT2 mutation in a patient with 'MEB-like' phenotypeE Mercuri, A D'Amico, A Tessa, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 30, 2007
Predictive factors for the development of scoliosis in Duchenne muscular dystrophyM Kinali, M Main, J Eliahoo, et al.
Clinical Anatomy (New York, N.Y.)|August 17, 2018
Brain morphometry of preschool age children affected by autism spectrum disorder: Correlation with clinical findingsS Lucibello, T Verdolotti, F M Giordano, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Cognitive abilities in children with congenital muscular dystrophy: correlation with brain MRI and merosin statusE Mercuri, J Gruter-Andrew, J Philpot, et al.
Pediatrics|August 2, 2000
Head growth in infants with hypoxic-ischemic encephalopathy: correlation with neonatal magnetic resonance imagingE Mercuri, D Ricci, F M Cowan, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 21, 2004
Diagnostic difficulties in a case of primary systemic carnitine deficiency with idiopathic dilated cardiomyopathyM Kinali, S E Olpin, P T Clayton, et al.
Neuromuscular Disorders : NMD|January 24, 2007
A congenital myopathy with diaphragmatic weakness not linked to the SMARD1 locusL Hartley, M Kinali, R Knight, et al.
Pageof 15

Showing results (91-100 of 150) with videos related to

Sort By:
Pageof 15
Developmental Medicine and Child Neurology|July 20, 2007
Visual function in infants with non-syndromic craniosynostosisD Ricci, G Vasco, G Baranello, et al.
Neuropediatrics|October 8, 1998
Orientation-reversal and phase-reversal visual evoked potentials in full-term infants with brain lesions: a longitudinal studyE Mercuri, O Braddick, J Atkinson, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|May 18, 1999
Visual function in term infants with hypoxic-ischaemic insults: correlation with neurodevelopment at 2 years of ageE Mercuri, L Haataja, A Guzzetta, et al.
Neuromuscular Disorders : NMD|May 17, 2006
POMT2 mutation in a patient with 'MEB-like' phenotypeE Mercuri, A D'Amico, A Tessa, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 30, 2007
Predictive factors for the development of scoliosis in Duchenne muscular dystrophyM Kinali, M Main, J Eliahoo, et al.
Clinical Anatomy (New York, N.Y.)|August 17, 2018
Brain morphometry of preschool age children affected by autism spectrum disorder: Correlation with clinical findingsS Lucibello, T Verdolotti, F M Giordano, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Cognitive abilities in children with congenital muscular dystrophy: correlation with brain MRI and merosin statusE Mercuri, J Gruter-Andrew, J Philpot, et al.
Pediatrics|August 2, 2000
Head growth in infants with hypoxic-ischemic encephalopathy: correlation with neonatal magnetic resonance imagingE Mercuri, D Ricci, F M Cowan, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 21, 2004
Diagnostic difficulties in a case of primary systemic carnitine deficiency with idiopathic dilated cardiomyopathyM Kinali, S E Olpin, P T Clayton, et al.
Neuromuscular Disorders : NMD|January 24, 2007
A congenital myopathy with diaphragmatic weakness not linked to the SMARD1 locusL Hartley, M Kinali, R Knight, et al.
Pageof 15