Search

Your search keyword '"Sansone, V. A."' showing total 491 results

Search Constraints

Start Over You searched for: Author "Sansone, V. A." Remove constraint Author: "Sansone, V. A."
491 results on '"Sansone, V. A."'

Search Results

51. Respiratory Trajectories in Type 2 and 3 Spinal Muscular Atrophy in the iSMAC Cohort Study

52. The nonsense mutation stop+4 model correlates with motor changes in Duchenne muscular dystrophy

53. North Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53: A 3 year follow up

54. Different trajectories in upper limb and gross motor function in spinal muscular atrophy

55. Type I SMA “new natural history”: long-term data in nusinersen-treated patients

60. Novel insights on Andersen-Tawil syndrome type 1

61. Age and baseline values predict 12 and 24-month functional changes in type 2 SMA

62. Pulsed electromagnetic fields improve the healing process of Achilles tendinopathy: A pilot study in a rat model

63. Urinary neopterin, a new marker of the neuroinflammatory status in amyotrophic lateral sclerosis

64. Sodium Channel Myotonia Due to Novel Mutations in Domain I of Nav1.4

65. ALS Cognitive Behavioral Screen (ALS-CBS): normative values for the Italian population and clinical usability

66. Gain and loss of abilities in type II SMA: A 12-month natural history study

67. Respiratory function and therapeutic expectations in DMD: Families experience and perspective

68. Age and baseline values predict 12 and 24-month functional changes in type 2 SMA

69. Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase

70. Respiratory Needs in Patients with Type 1 Spinal Muscular Atrophy Treated with Nusinersen

71. MRI patterns of muscle involvement in type 2 and 3 spinal muscular atrophy patients

72. Genetic modifiers of respiratory function in Duchenne muscular dystrophy

88. The role of rehabilitation in the management of late-onset Pompe disease: a narrative review of the level of evidence

89. Correction: Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53 (PLoS ONE (2019) 14:6 (e0218683) DOI: 10.1371/journal.pone.0218683)

94. Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain: Abstracts of Symposia and free communications

98. Thumbs up: Imagined hand movements counteract the adverse effects of post-surgical hand immobilization. Clinical, behavioral, and fMRI longitudinal observations

99. Longitudinal natural history in young boys with Duchenne muscular dystrophy

100. Development of an academic disease registry for spinal muscular atrophy

Catalog

Books, media, physical & digital resources