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Developmental Medicine and Child Neurology
|
July 20, 2007
Visual function in infants with non-syndromic craniosynostosis
D 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 study
E 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 age
E Mercuri, L Haataja, A Guzzetta, et al.
Neuromuscular Disorders : NMD
|
May 17, 2006
POMT2 mutation in a patient with 'MEB-like' phenotype
E 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 dystrophy
M 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 findings
S 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 status
E 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 imaging
E 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 cardiomyopathy
M 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 locus
L Hartley, M Kinali, R Knight, et al.
Page
of 15
Search research articles
Search
Showing results (91-100 of 150) with videos related to
Sort By:
Page
of 15
Developmental Medicine and Child Neurology
|
July 20, 2007
Visual function in infants with non-syndromic craniosynostosis
D 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 study
E 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 age
E Mercuri, L Haataja, A Guzzetta, et al.
Neuromuscular Disorders : NMD
|
May 17, 2006
POMT2 mutation in a patient with 'MEB-like' phenotype
E 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 dystrophy
M 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 findings
S 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 status
E 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 imaging
E 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 cardiomyopathy
M 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 locus
L Hartley, M Kinali, R Knight, et al.
Page
of 15