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Neuromuscular Disorders : NMD|August 12, 2017
Longitudinal assessments in discordant twins with SMAMarika Pane, Leonardo Lapenta, Emanuela Abiusi, et al.
CNS Drugs|August 18, 2019
An Integrated Safety Analysis of Infants and Children with Symptomatic Spinal Muscular Atrophy (SMA) Treated with Nusinersen in Seven Clinical TrialsBasil T Darras, Michelle A Farrar, Eugenio Mercuri, et al.
European Journal of Human Genetics : EJHG|November 4, 2004
Phenylbutyrate increases SMN gene expression in spinal muscular atrophy patientsChristina Brahe, Tiziana Vitali, Francesco D Tiziano, et al.
Human Genetics|August 3, 2005
A homozygous COL6A2 intron mutation causes in-frame triple-helical deletion and nonsense-mediated mRNA decay in a patient with Ullrich congenital muscular dystrophyLaura Lucarini, Betti Giusti, Rui-Zhu Zhang, et al.
Neuromuscular Disorders : NMD|September 18, 2012
Muscle MRI in Becker muscular dystrophyGiorgio Tasca, Elisabetta Iannaccone, Mauro Monforte, et al.
The Pediatric Infectious Disease Journal|May 15, 2020
Children's Healthcare During Corona Virus Disease 19 Pandemic: the Italian ExperienceDanilo Buonsenso, Roberta Onesimo, Piero Valentini, et al.
Annals of Clinical and Translational Neurology|November 4, 2020
Nusinersen in type 0 spinal muscular atrophy: should we treat?Eloisa Tiberi, Simonetta Costa, Marika Pane, et al.
Ophthalmology|September 5, 2017
Follow-up to Age 4 Years of Treatment of Type 1 Retinopathy of Prematurity Intravitreal Bevacizumab Injection versus Laser: Fluorescein Angiographic FindingsDomenico Lepore, Graham E Quinn, Fernando Molle, et al.
Epilepsy Research|July 22, 2009
Giant subcortical heterotopia involving the temporo-parieto-occipital region: a challenging cause of drug-resistant epilepsyFederica Novegno, Domenica Battaglia, Daniela Chieffo, et al.
Molecular Neurobiology|November 26, 2024
High Expression of SMN circ4-2b-3 in SMA I Children Treated with Nusinersen is Associated with Improved Motor OutcomesMarika Guerra, Alberto Marini, Vittoria Pagliarini, et al.
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