Nicola Forcina
Rome, Italy
Last Updated: 09/26/2026
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Found 25 publications
Compound Heterozygous COA7 Variants Presenting With Childhood-Onset Axonal Neuropathy in 2 Siblings.
Compound Heterozygous COA7 Variants Presenting With Childhood-Onset Axonal Neuropathy in 2 Siblings.
Journal: Neurology. Genetics
Published: June 11, 2025
Early neurological signs in infants identified through neonatal screening for SMA: do they predict outcome?
Journal: European journal of pediatrics
Published: January 17, 2024
Gain and loss of upper limb abilities in Duchenne muscular dystrophy patients: A 24-month study.
Journal: Neuromuscular disorders : NMD
Published: August 18, 2023
Early treatment of type II SMA slows rate of progression of scoliosis.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: June 26, 2023
Patient reported outcome measure for upper limb in Duchenne muscular dystrophy: correlation with PUL2.0.
Journal: Neuromuscular disorders : NMD
Published: April 18, 2023
Longitudinal Analysis of PUL 2.0 Domains in Ambulant and Non-Ambulant Duchenne Muscular Dystrophy Patients: How do they Change in Relation to Functional Ability?
Journal: Journal of neuromuscular diseases
Published: April 17, 2023
Long term follow-up of scoliosis progression in type II SMA patients.
Journal: Neuromuscular disorders : NMD
Published: September 01, 2022
Oral and Swallowing Abilities Tool (OrSAT) in nusinersen treated patients.
Journal: Archives of disease in childhood
Published: January 25, 2022
Longitudinal Motor Functional Outcomes and Magnetic Resonance Imaging Patterns of Muscle Involvement in Upper Limbs in Duchenne Muscular Dystrophy.
Journal: Medicina (Kaunas, Lithuania)
Published: September 25, 2021
Oral and Swallowing Abilities Tool (OrSAT) for Type 1 SMA Patients: Development of a New Module.
Journal: Journal of neuromuscular diseases
Published: May 24, 2021
Early Gross Motor Milestones in Duchenne Muscular Dystrophy.
Journal: Journal of neuromuscular diseases
Published: May 03, 2021
Last Updated: 09/26/2026