• 9098 Citations
  • 47 h-Index
19982019
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Fingerprint Dive into the research topics where Pasquale Striano is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 37 Similar Profiles
Epilepsy Medicine & Life Sciences
Seizures Medicine & Life Sciences
Myoclonic Epilepsy Medicine & Life Sciences
Mutation Medicine & Life Sciences
Brain Diseases Medicine & Life Sciences
Electroencephalography Medicine & Life Sciences
etiracetam Medicine & Life Sciences
Intellectual Disability Medicine & Life Sciences

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Research Output 1998 2019

Abnormal circadian rhythm in patients with GRIN1-related developmental epileptic encephalopathy

Scala, M., Amadori, E., Fusco, L., Marchese, F., Capra, V., Minetti, C., Vari, M. S. & Striano, P., May 24 2019, In : European Journal of Paediatric Neurology.

Research output: Contribution to journalArticle

Brain Diseases
Circadian Rhythm
Sleep
Crying
Inborn Genetic Diseases

AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders

SYNAPS Study Group, Dec 1 2019, In : Nature Communications. 10, 1, 3094.

Research output: Contribution to journalArticle

Open Access
AMPA Receptors
mutations
disabilities
Brain Diseases
disorders

An observational study of fixed-dose Tanacetum parthenium nutraceutical preparation for prophylaxis of pediatric headache

Moscano, F., Guiducci, M., Maltoni, L., Striano, P., Ledda, M. G., Zoroddu, F., Raucci, U., Villa, M. P. & Parisi, P., Mar 12 2019, In : Italian Journal of Pediatrics. 45, 1, p. 36

Research output: Contribution to journalArticle

Tanacetum parthenium
Dietary Supplements
Observational Studies
Headache
Pediatrics
1 Citation (Scopus)

Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment

Deciphering Developmental Disorders Study & SYNAPS Study Group, Apr 4 2019, In : American Journal of Human Genetics. 104, 4, p. 721-730 10 p.

Research output: Contribution to journalArticle

Open Access
Vesicle-Associated Membrane Protein 2
SNARE Proteins
Synaptic Membranes
Membrane Fusion
Mutation

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