Autori: Forcina N*

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Early neurological signs in infants identified through neonatal screening for SMA: do they predict outcome?

Gain and loss of upper limb abilities in Duchenne muscular dystrophy patients: A 24-month study

Early treatment of type II SMA slows rate of progression of scoliosis

Patient reported outcome measure for upper limb in Duchenne muscular dystrophy: correlation with PUL2.0

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?

Long term follow-up of scoliosis progression in type II SMA patients

Oral and Swallowing Abilities Tool (OrSAT) in nusinersen treated patients

Longitudinal Motor Functional Outcomes and Magnetic Resonance Imaging Patterns of Muscle Involvement in Upper Limbs in Duchenne Muscular Dystrophy

Oral and Swallowing Abilities Tool (OrSAT) for Type 1 SMA Patients: Development of a New Module

Point-of-care lung and diaphragm ultrasound in a patient with spinal muscular atrophy with respiratory distress type 1

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