Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Lorenzo Figà-Talamanca"'
Autor:
Alessia Guarnera, Francesca Bottino, Antonio Napolitano, Giorgia Sforza, Marco Cappa, Laura Chioma, Luca Pasquini, Maria Camilla Rossi-Espagnet, Giulia Lucignani, Lorenzo Figà-Talamanca, Chiara Carducci, Claudia Ruscitto, Massimiliano Valeriani, Daniela Longo, Laura Papetti
Publikováno v:
The Journal of Headache and Pain, Vol 22, Iss 1, Pp 1-13 (2021)
Abstract Background Migraine is the most common neurological disease, with high social-economical burden. Although there is growing evidence of brain structural and functional abnormalities in patients with migraine, few studies have been conducted o
Externí odkaz:
https://doaj.org/article/ae93271034f74fa1b729f87bffcfd266
Autor:
Giulia Lucignani, Leonardo Vattermoli, Maria Camilla Rossi-Espagnet, Alessia Guarnera, Antonio Napolitano, Lorenzo Figà-Talamanca, Francesca Campi, Sara Ronci, Carlo Dionisi Vici, Diego Martinelli, Carlo Gandolfo, Daniela Longo
Publikováno v:
Children, Vol 10, Iss 6, p 1072 (2023)
Molybdenum cofactor deficiency (MoCD) is a rare and severe autosomal recessive in-born error of metabolism caused by the mutation in MOCS1, MOCS2, MOCS3 or GEPH genes, with an incidence ranging between 1 in 100,000 and 200,000 live births. The clinic
Externí odkaz:
https://doaj.org/article/f649484808de4006813b96602bb4fe85
Autor:
Francesca Bottino, Martina Lucignani, Luca Pasquini, Michele Mastrogiovanni, Simone Gazzellini, Matteo Ritrovato, Daniela Longo, Lorenzo Figà-Talamanca, Maria Camilla Rossi Espagnet, Antonio Napolitano
Publikováno v:
Frontiers in Neuroscience, Vol 15 (2022)
There is growing interest in studying human brain connectivity and in modelling the brain functional structure as a network. Brain network creation requires parcellation of the cerebral cortex to define nodes. Parcellation might be affected by possib
Externí odkaz:
https://doaj.org/article/276104dd759c4a7bab1c887b2eb96641
Autor:
Lorenza Romani, Peter Richard Williamson, Silvia Di Cesare, Gigliola Di Matteo, Maia De Luca, Rita Carsetti, Lorenzo Figà-Talamanca, Caterina Cancrini, Paolo Rossi, Andrea Finocchi
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
The hyper IgM syndromes are a rare group of primary immunodeficiency. The X-linked Hyper IgM syndrome (HIGM), due to a gene defect in CD40L, is the commonest variant; it is characterized by an increased susceptibility to a narrow spectrum of opportun
Externí odkaz:
https://doaj.org/article/91811472d57747bd81e888e4abb6ea01
Autor:
Andrea Diociaiuti, Claudia Carnevale, Eulalia Baselga Torres, Christine Léauté-Labrèze, Iria Neri, Roberta Rotunno, Lorenzo Figà-Talamanca, May El Hachem
Publikováno v:
Acta Dermato-Venereologica, Vol 100, Iss 16, p adv00255 (2020)
Infantile haemangiomas are very common benign tumours in the first months of life. They are mostly cutaneous; however, extracutaneous lesions are possible, and occur in very rare cases in the central nervous system. A European multicentre observation
Externí odkaz:
https://doaj.org/article/d751108caa34446094c6f90775fa44dd
Autor:
Giulia Lucignani, Alessia Guarnera, Maria Camilla Rossi-Espagnet, Giulia Moltoni, Amanda Antonelli, Lorenzo Figà Talamanca, Chiara Carducci, Francesca Ippolita Calo Carducci, Antonio Napolitano, Carlo Gandolfo, Francesca Campi, Cinzia Auriti, Cecilia Parazzini, Daniela Longo
Publikováno v:
Children, Vol 9, Iss 8, p 1210 (2022)
Congenital infections represent a challenging and varied clinical scenario in which the brain is frequently involved. Therefore, fetal and neonatal neuro-imaging plays a pivotal role in reaching an accurate diagnosis and in predicting the clinical ou
Externí odkaz:
https://doaj.org/article/98977f6c6781490d8f93d162883adc49
Autor:
Michela Ada Noris Ferilli, Roberto Paparella, Ilaria Morandini, Laura Papetti, Lorenzo Figà Talamanca, Claudia Ruscitto, Fabiana Ursitti, Romina Moavero, Giorgia Sforza, Samuela Tarantino, Martina Proietti Checchi, Federico Vigevano, Massimiliano Valeriani
Publikováno v:
Life, Vol 12, Iss 1, p 19 (2021)
Neuromyelitis Optica Spectrum Disorder (NMOSD) is a central nervous system (CNS) inflammatory demyelinating disease characterized by recurrent inflammatory events that primarily involve optic nerves and the spinal cord, but also affect other regions
Externí odkaz:
https://doaj.org/article/4a07d26b197f45558a0774500365c616
Autor:
Laura Papetti, Lorenzo Figà Talamanca, Alberto Spalice, Federico Vigevano, Diego Centonze, Massimiliano Valeriani
Publikováno v:
Frontiers in Neurology, Vol 9 (2019)
Background/Objective: The aim of the study was to estimate the rate of evolution or for multiple sclerosis (MS), after a first acute demyelinating event (ADE) in pediatric patients, and to investigate the variables that predict this evolution.Methods
Externí odkaz:
https://doaj.org/article/cb2bc95ff4f9478bb08ce71150156dd9
Autor:
Giorgia Sforza, Gabriele Monte, Alessandra Voci, Lorenzo Figà Talamanca, Laura Papetti, Michela Ada Noris Ferilli, Martina Proietti Checchi, Massimiliano Valeriani, Romina Moavero
Publikováno v:
Sforza, G, Monte, G, Voci, A, Figà Talamanca, L, Papetti, L, Ferilli, M A N, Proietti Checchi, M, Valeriani, M & Moavero, R 2023, ' A Case Report of Pediatric Patient with Tuberous Sclerosis and Radiologically Isolated Syndrome ', Journal of Clinical Medicine, vol. 12, no. 9, 3284 . https://doi.org/10.3390/jcm12093284
INTRODUCTION: Tuberous sclerosis complex (TSC) is an autosomal dominant neurocutaneous disease with central nervous system (CNS) involvement. Multiple sclerosis (MS) is a chronic inflammatory demyelinating disease of the CNS characterized by symptoma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::404ba2b10ef32ec6e92146f998e68b33
https://vbn.aau.dk/ws/files/528828702/jcm_12_03284.pdf
https://vbn.aau.dk/ws/files/528828702/jcm_12_03284.pdf
Autor:
Alessandro De Benedictis, Andrea Pietrobattista, Lorenzo Figà Talamanca, Lidia Monti, Guglielmo Paolantonio, Gian Luigi Natali, Antonella Bua, Alessandra Savioli, Eng Alessandra Marasi, Franco Randi, Andrea Carai, Marco Spada, Carlo Efisio Marras
Publikováno v:
Clinical neurology and neurosurgery. 217
De novo arterio-venous malformations (AVMs) of the brain have been rarely previously reported, especially in the pediatric population. Although AVMs have possible connections with other diseases, the association with congenital portosystemic shunt (C