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 (11-20 of 168) with videos related to

Pageof 17
Sort By:
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 9, 2001
Visual disorders in children with brain lesions: 1. Maturation of visual function in infants with neonatal brain lesions: correlation with neuroimagingA Guzzetta, G Cioni, F Cowan, et al.
Neuromuscular Disorders : NMD|June 7, 2011
173rd ENMC International Workshop: congenital muscular dystrophy outcome measures 5-7 March 2010, Naarden, The NetherlandsC G Bönnemann, A Rutkowski, E Mercuri, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|April 9, 1999
Incidence of cranial ultrasound abnormalities in apparently well neonates on a postnatal ward: correlation with antenatal and perinatal factors and neurological statusE Mercuri, L Dubowitz, S P Brown, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 1, 1994
Acetazolamide without frusemide in the treatment of post-haemorrhagic hydrocephalusE Mercuri, J C Faundez, F Cowan, et al.
Gene Therapy|June 1, 2017
Therapeutic approaches for spinal muscular atrophy (SMA)M Scoto, R S Finkel, E Mercuri, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 5, 2002
Remission of clinical signs in early duchenne muscular dystrophy on intermittent low-dosage prednisolone therapyV Dubowitz, M Kinali, M Main, et al.
Brain & Development|November 1, 1993
Autosomal recessive congenital cerebellar atrophy. A clinical and neuropsychological studyF Guzzetta, E Mercuri, S Bonanno, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 19, 2000
Diaphragmatic spinal muscular atrophy with bulbar weaknessE Mercuri, F Goodwin, C Sewry, et al.
Journal of Lipid Research|June 4, 1998
Simple detection of a point mutation in LDL receptor gene causing familial hypercholesterolemia in southern Italy by allele-specific polymerase chain reactionA Cantafora, I Blotta, E Mercuri, et al.
Neuropediatrics|December 1, 1993
Familial unilateral and bilateral occipital calcifications and epilepsyG Tortorella, A Magaudda, E Mercuri, et al.
Pageof 17

Showing results (11-20 of 168) with videos related to

Sort By:
Pageof 17
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 9, 2001
Visual disorders in children with brain lesions: 1. Maturation of visual function in infants with neonatal brain lesions: correlation with neuroimagingA Guzzetta, G Cioni, F Cowan, et al.
Neuromuscular Disorders : NMD|June 7, 2011
173rd ENMC International Workshop: congenital muscular dystrophy outcome measures 5-7 March 2010, Naarden, The NetherlandsC G Bönnemann, A Rutkowski, E Mercuri, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|April 9, 1999
Incidence of cranial ultrasound abnormalities in apparently well neonates on a postnatal ward: correlation with antenatal and perinatal factors and neurological statusE Mercuri, L Dubowitz, S P Brown, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 1, 1994
Acetazolamide without frusemide in the treatment of post-haemorrhagic hydrocephalusE Mercuri, J C Faundez, F Cowan, et al.
Gene Therapy|June 1, 2017
Therapeutic approaches for spinal muscular atrophy (SMA)M Scoto, R S Finkel, E Mercuri, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 5, 2002
Remission of clinical signs in early duchenne muscular dystrophy on intermittent low-dosage prednisolone therapyV Dubowitz, M Kinali, M Main, et al.
Brain & Development|November 1, 1993
Autosomal recessive congenital cerebellar atrophy. A clinical and neuropsychological studyF Guzzetta, E Mercuri, S Bonanno, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 19, 2000
Diaphragmatic spinal muscular atrophy with bulbar weaknessE Mercuri, F Goodwin, C Sewry, et al.
Journal of Lipid Research|June 4, 1998
Simple detection of a point mutation in LDL receptor gene causing familial hypercholesterolemia in southern Italy by allele-specific polymerase chain reactionA Cantafora, I Blotta, E Mercuri, et al.
Neuropediatrics|December 1, 1993
Familial unilateral and bilateral occipital calcifications and epilepsyG Tortorella, A Magaudda, E Mercuri, et al.
Pageof 17