Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

E Mercuri

Showing results (111-120 of 150) with videos related to

Pageof 15
Sort By:
Neuromuscular Disorders : NMD|June 6, 2000
Minicore myopathy in children: a clinical and histopathological study of 19 casesH Jungbluth, C Sewry, S C Brown, et al.
Neurology|May 24, 2006
Expanding the clinical spectrum of POMT1 phenotypeA D'Amico, A Tessa, C Bruno, et al.
Neuromuscular Disorders : NMD|February 13, 2001
Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle alpha-actin (ACTA1) geneH Jungbluth, C A Sewry, S C Brown, et al.
Neuropediatrics|December 21, 2006
Neurological examination at 6 to 9 months in infants with cystic periventricular leukomalaciaD Ricci, F Cowan, M Pane, et al.
Muscle & Nerve|March 17, 2005
Extreme variability of skeletal and cardiac muscle involvement in patients with mutations in exon 11 of the lamin A/C geneE Mercuri, S C Brown, P Nihoyannopoulos, et al.
Brain : a Journal of Neurology|April 6, 2006
Disease severity in dominant Emery Dreifuss is increased by mutations in both emerin and desmin proteinsF Muntoni, G Bonne, L G Goldfarb, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|November 11, 2006
Maturation of cerebral electrical activity and development of cortical folding in young very preterm infantsE Biagioni, M F Frisone, S Laroche, et al.
Neuromuscular Disorders : NMD|August 19, 2003
Muscle magnetic resonance imaging in patients with congenital muscular dystrophy and Ullrich phenotypeE Mercuri, C Cini, A Pichiecchio, et al.
Neuropediatrics|May 31, 2003
General movements detect early signs of hemiplegia in term infants with neonatal cerebral infarctionA Guzzetta, E Mercuri, G Rapisardi, et al.
Neuromuscular Disorders : NMD|March 4, 2021
Longitudinal data of neuropsychological profile in a cohort of Duchenne muscular dystrophy boys without cognitive impairmentR Battini, S Lenzi, S Lucibello, et al.
Pageof 15

Showing results (111-120 of 150) with videos related to

Sort By:
Pageof 15
Neuromuscular Disorders : NMD|June 6, 2000
Minicore myopathy in children: a clinical and histopathological study of 19 casesH Jungbluth, C Sewry, S C Brown, et al.
Neurology|May 24, 2006
Expanding the clinical spectrum of POMT1 phenotypeA D'Amico, A Tessa, C Bruno, et al.
Neuromuscular Disorders : NMD|February 13, 2001
Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle alpha-actin (ACTA1) geneH Jungbluth, C A Sewry, S C Brown, et al.
Neuropediatrics|December 21, 2006
Neurological examination at 6 to 9 months in infants with cystic periventricular leukomalaciaD Ricci, F Cowan, M Pane, et al.
Muscle & Nerve|March 17, 2005
Extreme variability of skeletal and cardiac muscle involvement in patients with mutations in exon 11 of the lamin A/C geneE Mercuri, S C Brown, P Nihoyannopoulos, et al.
Brain : a Journal of Neurology|April 6, 2006
Disease severity in dominant Emery Dreifuss is increased by mutations in both emerin and desmin proteinsF Muntoni, G Bonne, L G Goldfarb, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|November 11, 2006
Maturation of cerebral electrical activity and development of cortical folding in young very preterm infantsE Biagioni, M F Frisone, S Laroche, et al.
Neuromuscular Disorders : NMD|August 19, 2003
Muscle magnetic resonance imaging in patients with congenital muscular dystrophy and Ullrich phenotypeE Mercuri, C Cini, A Pichiecchio, et al.
Neuropediatrics|May 31, 2003
General movements detect early signs of hemiplegia in term infants with neonatal cerebral infarctionA Guzzetta, E Mercuri, G Rapisardi, et al.
Neuromuscular Disorders : NMD|March 4, 2021
Longitudinal data of neuropsychological profile in a cohort of Duchenne muscular dystrophy boys without cognitive impairmentR Battini, S Lenzi, S Lucibello, et al.
Pageof 15