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Fingerprint Dive into the research topics where Maria Nolano is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 19 Similar Profiles
Skin Medicine & Life Sciences
Nerve Fibers Medicine & Life Sciences
Biopsy Medicine & Life Sciences
Charcot-Marie-Tooth Disease Medicine & Life Sciences
Touch Medicine & Life Sciences
Mechanoreceptors Medicine & Life Sciences
Tooth Medicine & Life Sciences
Peripheral Nervous System Diseases Medicine & Life Sciences

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Research Output 1986 2019

  • 3597 Citations
  • 27 h-Index
  • 100 Article
  • 3 Conference contribution
  • 1 Chapter
  • 1 Letter

A Delphi consensus statement of the Neuropathic Pain Special Interest Group of the Italian Neurological Society on pharmacoresistant neuropathic pain

Neuropathic Pain Special Interest Group of the Italian Neurological Society, Apr 2 2019, In : Neurological Sciences.

Research output: Contribution to journalArticle

Public Opinion
Advisory Committees
Patient Care

Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination

SYNAPS Study Group, Oct 1 2019, In : Brain : a journal of neurology. 142, 10, p. 2948-2964 17 p.

Research output: Contribution to journalArticle

Ranvier's Nodes
Demyelinating Diseases
Protein Isoforms
Inborn Genetic Diseases

Cooling the skin for assessing small-fibre function

Leone, C., Dufour, A., Di Stefano, G., Fasolino, A., Di Lionardo, A., La Cesa, S., Galosi, E., Valeriani, M., Nolano, M., Cruccu, G. & Truini, A., Apr 10 2019, In : Pain.

Research output: Contribution to journalArticle

Evoked Potentials
Facial Pain

Alterations of autophagy in the peripheral neuropathy Charcot-Marie-Tooth type 2B

Colecchia, D., Stasi, M., Leonardi, M., Manganelli, F., Nolano, M., Veneziani, B. M., Santoro, L., Eskelinen, E-L., Chiariello, M. & Bucci, C., 2018, In : Autophagy. 14, 6, p. 930-941 12 p.

Research output: Contribution to journalArticle

Peripheral Nervous System Diseases
GTP Phosphohydrolases

A novel SCN9A splicing mutation in a compound heterozygous girl with congenital insensitivity to pain, hyposmia and hypogeusia

Marchi, M., Provitera, V., Nolano, M., Romano, M., Maccora, S., D'Amato, I., Salvi, E., Gerrits, M., Santoro, L. & Lauria, G., Sep 2018, In : Journal of the Peripheral Nervous System. 23, 3, p. 202-206 5 p.

Research output: Contribution to journalArticle

Congenital Pain Insensitivity
Missense Mutation