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Enrico Bertini

    • 70h-indexImpact measure calculated using publication and citation counts. Updated daily.
    • 19498CitationsNumber of citations received by Enrico's publications. Updated daily.

    Co-authors (3614)

    • Maria Angelica Palomino

    Publications (5)

    • Early neurodevelopmental assessment in Duchenne muscular dystrophy

      • Pane M
      • Scalise R
      • Berardinelli A
      • et al.
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    • Identification of a deep intronic mutation in the COL6A2 gene by a novel custom oligonucleotide CGH array designed to explore allelic and genetic heterogeneity in collagen VI-related myopathies

      • Bovolenta M
      • Neri M
      • Martoni E
      • et al.
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    • Prenatal ultrasound and magnetic resonance imaging features in a fetus with Walker-Warburg syndrome

      • Strigini F
      • Vallerianit A
      • Cecchi M
      • et al.
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    • Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome

      • Valente E
      • Silhavy J
      • Brancati F
      • et al.
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    • NPHP1 gene deletion is a rare cause of Joubert syndrome related disorders.

      • Castori M
      • Valente E
      • Donati M
      • et al.
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