Research output per year
Research output per year
Personal profile
Academic discipline
MEDS-12/A - Neurology
Fingerprint
Dive into the research topics where Serenella Servidei is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 1 Similar Profiles
Collaborations and top research areas from the last five years
Recent external collaboration on country level (based on research outputs with Scopus ID). Dive into details by clicking on the dots.
-
Cross-cultural adaptation of the Italian version of the "Child and Youth Mental Health Instrument for Developmental Disabilities" (I-ChYMH-DD)
Sforza, E., Leoni, C., De, R. E., Bellani, J., Viscogliosi, G., Di, P. A., Zampino, M., Fischetto, R., Pane, M., Rigante, D., Servidei, S., Primiano, G. A., Onesimo, R., Carfì, A. & Giuseppe, Z., 2026, In: THE ITALIAN JOURNAL OF PEDIATRICS. 2026, 52(1):66, p. 1-5 5 p.Research output: Contribution to journal › Article
-
Cross-cultural adaptation of the Italian version of the “Child and Youth Mental Health Instrument for Developmental Disabilities” (I-ChYMH-DD)
Sforza, E., Leoni, C., De Rosa, E., Bellani, J., Viscogliosi, G., Di Paola, A., Zampino, M., Fischetto, R., Pane, M., Rigante, D., Servidei, S., Primiano, G. A., Onesimo, R., Carfì, A. & Zampino, G., 2026, In: THE ITALIAN JOURNAL OF PEDIATRICS. 52, 1, p. 1-5 5 p.Research output: Contribution to journal › Article
-
Do rare genetic conditions exhibit a specific phonotype? A comprehensive description of the vocal traits associated with Crisponi/Cold-Induced Sweating Syndrome type 1.
Calà, F., Sforza, E., D'Alatri, L., Frassineti, L., Manfredi, C., Onesimo, R., Rigante, D., Pane, M., Servidei, S., Primiano, G. A., Crisponi, G., Crisponi, L., Leoni, C., Lanatà, A. & Zampino, G., 2025, In: Genes. 2025, 16: 881, p. 1-10 10 p.Research output: Contribution to journal › Article
-
Ophthalmological signs and sensorimotor evaluation in mitochondrial chronic progressive external ophthalmoplegia: a multidisciplinary prospective study
Savino, G., Giannuzzi, F., Cima, V., Brando, D., Fossataro, C., Servidei, S., Savastano, M. C. & Primiano, G. A., 2025, In: BMC Ophthalmology. 25, 1, p. N/A-N/AResearch output: Contribution to journal › Article
-
Predictors of Neurotoxicity in a Large Cohort of Italian Patients Undergoing Anti-CD19 Chimeric Antigen Receptor (CAR) T-Cell Therapy
Modoni, A., Vollono, C., Galli, E., Capriati, L., Sora', F., Hohaus, S., Servidei, S., Piccirillo, N., Calabresi, P. & Sica, S., 2025, In: Brain and Behavior. 15, 9, p. N/A-N/AResearch output: Contribution to journal › Article
Datasets
-
Isolated light chain deposition disease neuropathy in a patient with multiple myeloma
Romano, A. (Creator), Riso, V. (Creator), Bisogni, G. (Creator), Di Paolantonio, A. (Contributor), Rossi, E. (Creator), Sabatelli, M. (Creator), Servidei, S. (Creator) & Luigetti, M. (Creator), Taylor & Francis, 2019
DOI: 10.6084/m9.figshare.9937802, https://tandf.figshare.com/articles/Isolated_light_chain_deposition_disease_neuropathy_in_a_patient_with_multiple_myeloma/9937802
Dataset
-
Progressive axonal polyneuropathy in a mitochondrial disorder: an uncommon association with familial amyloid neuropathy
Luigetti, M. (Creator), Primiano, G. (Creator), Bisogni, G. (Creator), Cuccagna, C. (Creator), Carrozzo, R. (Creator), Obici, L. (Creator), Bernardo, D. (Creator), Sancricca, C. (Creator) & Servidei, S. (Creator), Taylor & Francis, 2019
DOI: 10.6084/m9.figshare.7729367, https://tandf.figshare.com/articles/Progressive_axonal_polyneuropathy_in_a_mitochondrial_disorder_an_uncommon_association_with_familial_amyloid_neuropathy/7729367
Dataset
-
CACNA1A-p.Thr501Met mutation associated with familial hemiplegic migraine: a family report
Romozzi, M. (Creator), Primiano, G. (Creator), Rollo, E. (Creator), Travaglini, L. (Creator), Calabresi, P. (Creator), Servidei, S. (Creator) & Vollono, C. (Creator), figshare, 2021
DOI: 10.6084/m9.figshare.c.5533384.v1, https://springernature.figshare.com/collections/CACNA1A-p_Thr501Met_mutation_associated_with_familial_hemiplegic_migraine_a_family_report/5533384/1
Dataset
-
Isolated light chain deposition disease neuropathy in a patient with multiple myeloma
Romano, A. (Creator), Riso, V. (Creator), Bisogni, G. (Creator), Di Paolantonio, A. (Contributor), Rossi, E. (Creator), Sabatelli, M. (Creator), Servidei, S. (Creator) & Luigetti, M. (Creator), Taylor & Francis, 2019
DOI: 10.6084/m9.figshare.9937802.v1, https://tandf.figshare.com/articles/Isolated_light_chain_deposition_disease_neuropathy_in_a_patient_with_multiple_myeloma/9937802/1
Dataset
-
CACNA1A-p.Thr501Met mutation associated with familial hemiplegic migraine: a family report
Romozzi, M. (Creator), Primiano, G. (Creator), Rollo, E. (Creator), Travaglini, L. (Creator), Calabresi, P. (Creator), Servidei, S. (Creator) & Vollono, C. (Creator), figshare, 2021
DOI: 10.6084/m9.figshare.c.5533384, https://springernature.figshare.com/collections/CACNA1A-p_Thr501Met_mutation_associated_with_familial_hemiplegic_migraine_a_family_report/5533384
Dataset