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

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Aicardi Syndrome Medicine & Life Sciences
Interferons Medicine & Life Sciences
Mutation Medicine & Life Sciences
Living Donors Medicine & Life Sciences
REM Sleep Behavior Disorder Medicine & Life Sciences
Tissue Donors Medicine & Life Sciences
Ketogenic Diet Medicine & Life Sciences
Genes Medicine & Life Sciences

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Research Output 2017 2019

  • 34 Citations
  • 3 h-Index
  • 12 Article

Living Kidney Donation Is Recipient Age Sensitive and Has a High Rate of Donor Organ Disqualifications

Gregorini, M., Martinelli, V., Ticozzelli, E., Canevari, M., Fasoli, G., Pattonieri, E. F., Erasmi, F., Valente, M., Esposito, P., Contardi, A., Grignano, M. A., Pietrabissa, A., Abelli, M. & Rampino, T., Jan 1 2019, (Accepted/In press) In : Transplantation Proceedings.

Research output: Contribution to journalArticle

Living Donors
Tissue Donors
Kidney
Kidney Transplantation
Transplantation

Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review

Garau, J., Cavallera, V., Valente, M., Tonduti, D., Sproviero, D., Zucca, S., Battaglia, D., Battini, R., Bertini, E., Cappanera, S., Chiapparini, L., Crasà, C., Crichiutti, G., Dalla Giustina, E., D'Arrigo, S., De Giorgis, V., De Simone, M., Galli, J., La Piana, R., Messana, T. & 19 others, Moroni, I., Nardocci, N., Panteghini, C., Parazzini, C., Pichiecchio, A., Pini, A., Ricci, F., Saletti, V., Salvatici, E., Santorelli, F. M., Sartori, S., Tinelli, F., Uggetti, C., Veneselli, E., Zorzi, G., Garavaglia, B., Fazzi, E., Orcesi, S. & Cereda, C., May 26 2019, In : Journal of Clinical Medicine. 8, 5

Research output: Contribution to journalArticle

Aicardi Syndrome
Interferons
Molecular Biology
Mutation
Genes

Overall cognitive profiles in patients with GLUT1 Deficiency Syndrome

De Giorgis, V., Masnada, S., Varesio, C., Chiappedi, M. A., Zanaboni, M., Pasca, L., Filippini, M., Macasaet, J. A., Valente, M., Ferraris, C., Tagliabue, A. & Veggiotti, P., Feb 4 2019, In : Brain and Behavior. p. e01224

Research output: Contribution to journalArticle

Ketogenic Diet
Diet
Aptitude
Facilitative Glucose Transport Proteins
Tin

The spectrum of intermediate SCN8A-related epilepsy

Johannesen, K. M., Gardella, E., Encinas, A. C., Lehesjoki, A-E., Linnankivi, T., Petersen, M. B., Lund, I. C. B., Blichfeldt, S., Miranda, M. J., Pal, D. K., Lascelles, K., Procopis, P., Orsini, A., Bonuccelli, A., Giacomini, T., Helbig, I., Fenger, C. D., Sisodiya, S. M., Hernandez-Hernandez, L., Krithika, S. & 25 others, Rumple, M., Masnada, S., Valente, M., Cereda, C., Giordano, L., Accorsi, P., Bürki, S. E., Mancardi, M., Korff, C., Guerrini, R., von Spiczak, S., Hoffman-Zacharska, D., Mazurczak, T., Coppola, A., Buono, S., Vecchi, M., Hammer, M. F., Varesio, C., Veggiotti, P., Lal, D., Brünger, T., Zara, F., Striano, P., Rubboli, G. & Møller, R. S., May 10 2019, In : Epilepsia. 60, 5, p. 830-844 15 p.

Research output: Contribution to journalArticle

Epilepsy
Brain Diseases
Intellectual Disability
Seizures
Muscle Hypotonia

A Novel Mutation in the Stalk Domain of KIF5A Causes a Slowly Progressive Atypical Motor Syndrome

Filosto, M., Piccinelli, S. C., Palmieri, I., Necchini, N., Valente, M., Zanella, I., Biasiotto, G., Lorenzo, D. D., Cereda, C. & Padovani, A., Dec 22 2018, In : Journal of Clinical Medicine. 8, 1

Research output: Contribution to journalArticle

Amyotrophic Lateral Sclerosis
Hereditary Spastic Paraplegia
Mutation
Phenotype
Genes