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51. Electrodiagnosis of Guillain-Barre syndrome in the International GBS Outcome Study: Differences in methods and reference values

52. Targeted transcript analysis in muscles from patients with genetically diverse congenital myopathies

53. Electrodiagnosis of Guillain-Barre syndrome in the International GBS Outcome Study:Differences in methods and reference values

54. Frequency, entity and determinants of fatigue in Charcot–Marie–Tooth disease.

55. Centronuclear myopathies: genotype–phenotype correlation and frequency of defined genetic forms in an Italian cohort

56. Intravenous immunoglobulin versus intravenous methylprednisolone for chronic inflammatory demyelinating polyradiculoneuropathy: a randomised controlled trial

65. Frequency and time to relapse after discontinuing 6-month therapy with IVIg or pulsed methylprednisolone in CIDP

73. RFC1 expansions are a common cause of idiopathic sensory neuropathy

74. Chronic inflammatory demyelinating polyradiculoneuropathy: Can we make a diagnosis in patients not fulfilling electrodiagnostic criteria?

79. PMP22 messenger RNA levels in skin biopsies: testing the effectiveness of a Charcot–Marie–Tooth 1A biomarker

80. Validation of the Italian version of the Neuropathic Pain Symptom Inventory in peripheral nervous system diseases

81. The impact of symptoms on daily life as perceived by patients with Charcot-Marie-Tooth type 1A disease

82. Large scale genotype–phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy

83. Interpretation of the Epigenetic Signature of Facioscapulohumeral Muscular Dystrophy in Light of Genotype-Phenotype Studies

87. Cutaneous sensory and autonomic denervation in progressive supranuclear palsy

90. Neuropathy and levodopa in Parkinsonʼs disease: Evidence from a multicenter study

96. GDAP1 mutations in Italian axonal Charcot–Marie–Tooth patients: Phenotypic features and clinical course

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