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N

Nardo Nardocci

pediatric neurosciences
H指数:47
被引数:9,118

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Transition to adulthood in Duchenne Muscular Dystrophy: a systematic review with narrative synthesis on health systems; policies; and the role of health care providers

杜氏肌营养不良症中的成年过渡：一项关于卫生系统、政策和医疗保健提供者作用的系统综述与叙事综合

Frontiers in Public Health
IF3.4
2026-05-300
OAAI
SF Sebastian Friedrich; JW Jana Willems; SR Sunil Rodger; JP Jo-Anne Petropoulos; DR Delaney Ringer; EW Ellen Wang; JF Julia Frei; KP Kinga Pozniak; AS Anna Swain; EG Erika Guastafierro; AM Alessia Marcassoli; GT Giulia Trucco; AM Angelica Mazzilli; GR Gudrun Reeskau; FD Fernanda De Angelis; HO Homira Osman; AF Anne Fournier; RG Rocio Giselle Gutierrez Rojas; JW Jan Willem Gorter; IM Isabella Moroni; ML Matilde Leonardi; NN Nardo Nardocci; OK Olaf Kraus de Camargo; TL Thorsten Langer
Genetic complexity in pediatric onset epilepsy-movement disorder syndromes: Insights from a cohort of 97 subjects

儿科起病癫痫-运动障碍综合征的遗传复杂性：来自97例受试者队列的见解

Epilepsia
IF6.6
2025-10-240
OAAI
Davide Caputo; Roberta Solazzi; Barbara Castellotti; Celeste Panteghini; Francesca Luisa Sciacca; Elisa Visani; Elena Freri; Francesca Ragona; Laura Canafoglia; Federica Zibordi; Giovanna Zorzi; Shari Gandelli; Cinzia Gellera; Silvana Franceschetti; Nardo Nardocci; Tiziana Granata
Correction: Open-label evaluation of oral trehalose in patients with neuronal ceroid lipofuscinoses

更正：奥普仑（open-label）评价口服海藻糖在神经元蜡样脂褐质沉积症患者中的应用

Journal of Neurology
IF4.6
2025-10-150
PRE
Stefania Della Vecchia; Nicola Gammaldi; Ivana Ricca; Serena Mero; Stefano Doccini; Anna Ardissone; Silvia Bagnoli; Roberta Battini; Elisa Colombi; Jacopo Favaro; Roberto Furlan; Lucio Giordano; Assunta Ingannato; Alessandra Mandelli; Francesca Maria Paola Manzoni; Giuseppe Milito; Isabella Moroni; Benedetta Nacmias; Nardo Nardocci; Lucio Parmeggiani; Francesco Pezzini; Nicola Pietrafusa; Stefano Sartori; Nicola Specchio; Marina Trivisano; A.-N. C. L. ETS; Alessandro Simonati; Filippo Maria Santorelli
Gaps and challenges in the transition of care in Neuromuscular Disorders with a focus on Duchenne Muscular Dystrophy

神经肌肉疾病照护过渡中的差距与挑战：以杜氏肌营养不良症为重点

Pediatric Neurology
IF2.1
2025-10-130
PRE
A. Marcassoli; N. Rajapakse; E. Guastafierro; J.A. Petropoulos; G. Trucco; A. Mazzilli; S. Friedrich; S. Rodger; J. Willems; D. Ringer; J. Frei; A. Swain; M. Leonardi; N. Nardocci; T. Langer; O. Kraus De Camargo; J.W. Gorter; K. Pozniak; A. Fournier; R. Gutierrez; F. De Angelis; H. Osman; G. Reeskau; D. McCauley; E. Wang; B. Brigliadori; I. Moroni
Molecular and clinical spectrum of epilepsy-dyskinesia syndromes: a cross-sectional study of 609 patients
Brain
IF11.7
2025-08-140
PRE
Vicente Quiroz; Julian E Alecu; Umar Zubair; Katerina Bernardi; Zainab Zaman; Joshua Rong; Amy Tam; Avaneesh Kunta; Habibah A P Agianda; Nicole Battaglia; Henri J D Schmidt; Dario Resch; Noah Wyman; Lindsey M Vogt; Wafa Bani Uraba; Leonie F Becker; Kavitha Kothur; Deepak Gill; Bernardita Suarez; Javiera I Jofre; Carolina Arias; Claudia Castiglioni; Patricia Dumke da Silva Möller; Andre Felipe Pinto Duarte; Alexander Eggers-Lisboa; Loreto Ríos-Pohl; Magdalena Gonzalez-Ubilla; Chinmay Chaudhari; Ainara Salazar-Villacorta; Xiaojuan Tian; Lifang Dai; Changhong Ding; Mina Zamani; Pardis Nourbakhsh; Gholamreza Shariati; Tamara Pringsheim; Wei Kang Lim; Emanuele Bartolini; Maria Stamelou; Poonam Bhatia; Michael C Kruer; Soaham Desai; Mary Iype; Ján Necpál; David Crosiers; Hannah F Jones; Javier Ricardo Perez-Sanchez; Esra Demir Unal; Nuria Lopez-Ariztegui; Sruthi Kola; Wei-Sheng Lin; Alia Hassan Mansour; Chahnez Charfi Triki; Emilio Fernandez-Alvarez; Emmanuel Roze; Jitendra Kumar Sahu; Asif Doja; Nardo Nardocci; Davide Caputo; Anne Koy; Sanjay Bhate; Marios Kaliakatsos; Robert Robinson; Jane Hassell; Roser Pons; Alexander Munchau; Luca Soliani; Alonso Zea-Vera; Laura Tochen; Hugo Morales-Briceño; Russell C Dale; Alissa D’Gama; Tobias Loddenkemper; Phillip L Pearl; Shekeeb S Mohammad; Manju A Kurian; Carolina Gorodetsky; Juan Darío Ortigoza-Escobar; Luca Schierbaum; Kathryn Yang; Darius Ebrahimi-Fakhari
GLUT1-DS Italian registry: past, present, and future: a useful tool for rare disorders
ORPHANET JOURNAL OF RARE DISEASES
IF3.5
2023-03-213
OAAI
Varesio, Costanza; De Giorgis, Valentina; Veggiotti, Pierangelo; Nardocci, Nardo; Granata, Tiziana; Ragona, Francesca; Pasca, Ludovica; Mensi, Martina Maria; Borgatti, Renato; Olivotto, Sara; Previtali, Roberto; Riva, Antonella; Mancardi, Maria Margherita; Striano, Pasquale; Cavallin, Mara; Guerrini, Renzo; Operto, Francesca Felicia; Pizzolato, Alice; Di Maulo, Ruggero; Martino, Fabiola; Lodi, Andrea; Marini, Carla
Variants in ATP5F1B are associated with dominantly inherited dystonia
BRAIN
IF11.7
2023-03-017
OAAI
Nasca, Alessia; Mencacci, Niccolo E.; Invernizzi, Federica; Zech, Michael; Sarmiento, Ignacio J. Keller; Legati, Andrea; Frascarelli, Chiara; Bustos, Bernabe, I; Romito, Luigi M.; Krainc, Dimitri; Winkelmann, Juliane; Carecchio, Miryam; Nardocci, Nardo; Zorzi, Giovanna; Prokisch, Holger; Lubbe, Steven J.; Garavaglia, Barbara; Ghezzi, Daniele
Recurrent, founder and hypomorphic variants contribute to the genetic landscape of Joubert syndrome

反复发作，创始人和拟态变异有助于Joubert综合征的遗传景观

JOURNAL OF MEDICAL GENETICS
IF3.7
2023-02-146
OAAI
Serpieri, Valentina; Mortarini, Giulia; Loucks, Hailey; Biagini, Tommaso; Micalizzi, Alessia; Palmieri, Ilaria; Dempsey, Jennifer C.; D'Abrusco, Fulvio; Mazzotta, Concetta; Battini, Roberta; Bertini, Enrico Silvio; Boltshauser, Eugen; Borgatti, Renato; Brockmann, Knut; D'Arrigo, Stefano; Nardocci, Nardo; Fischetto, Rita; Agolini, Emanuele; Novelli, Antonio; Romano, Alfonso; Romaniello, Romina; Stanzial, Franco; Signorini, Sabrina; Strisciuglio, Pietro; Gana, Simone; Mazza, Tommaso; Doherty, Dan; Valente, Enza Maria
Early Immunotherapy and Longer Corticosteroid Treatment Are Associated With Lower Risk of Relapsing Disease Course in Pediatric MOGAD
NEUROLOGY-NEUROIMMUNOLOGY & NEUROINFLAMMATION
IF7.5
2023-01-0128
OAAI
Nosadini, Margherita; Eyre, Michael; Giacomini, Thea; Valeriani, Massimiliano; Della Corte, Marida; Pratico, Andrea D.; Annovazzi, Pietro; Cordani, Ramona; Cordelli, Duccio Maria; Crichiutti, Giovanni; Di Rosa, Gabriella; Dolcemascolo, Valentina; Fetta, Anna; Freri, Elena; Gallo, Paolo; Gastaldi, Matteo; Granata, Tiziana; Grazian, Luisa; Iorio, Raffaele; Lombardini, Martina; Margoni, Monica; Mariotto, Sara; Matricardi, Sara; Melani, Federico; Nardocci, Nardo; Papetti, Laura; Passarini, Alice; Pisani, Francesco; Po, Chiara; Puthenparampil, Marco; Ragona, Francesca; Savasta, Salvatore; Siliquini, Sabrina; Toldo, Irene; Tozzo, Alessandra; Turco, Emanuela Claudia; Varone, Antonio; Vogrig, Alberto; Zuliani, Luigi; Bugin, Samuela; Rossato, Sara; Orsini, Alessandro; Cantalupo, Gaetano; Mancardi, Maria Margherita; Ferilli, Michela Ada Noris; Foiadelli, Thomas; Sartori, Stefano
Refining the mutational spectrum and gene-phenotype correlates in pontocerebellar hypoplasia: results of a multicentric study
JOURNAL OF MEDICAL GENETICS
IF3.7
2021-03-0516
PRE
Nuovo, Sara; Micalizzi, Alessia; Romaniello, Romina; Arrigoni, Filippo; Ginevrino, Monia; Casella, Antonella; Serpieri, Valentina; D'Arrigo, Stefano; Briguglio, Marilena; Salerno, Grazia Gabriella; Rossato, Sara; Sartori, Stefano; Leuzzi, Vincenzo; Battini, Roberta; Ben-Zeev, Bruria; Graziano, Claudio; Mirabelli Badenier, Marisol; Brankovic, Vesna; Nardocci, Nardo; Spiegel, Ronen; Petkovic Ramadza, Danijela; Vento, Giovanni; Marti, Itxaso; Simonati, Alessandro; Dipresa, Savina; Freri, Elena; Mazza, Tommaso; Bassi, Maria Teresa; Bosco, Luca; Travaglini, Lorena; Zanni, Ginevra; Bertini, Enrico Silvio; Vanacore, Nicola; Borgatti, Renato; Valente, Enza Maria

研究方向

暂未获取到该数据
G
Giovanna Zorzi
H 指数:41论文数:192被引数:6,240
B
Barbara Garavaglia
H 指数:0论文数:1被引数:18
B
Barbara Garavaglia
H 指数:50论文数:353被引数:8,555
T
Tiziana Granata
H 指数:56论文数:310被引数:1.2万
F
Federica Zibordi
H 指数:28论文数:123被引数:2,248
E
Enrico Bertini
H 指数:113论文数:1,266被引数:5.5万
L
Lucia Angelini
H 指数:26论文数:109被引数:1,879
L
Luisa Chiapparini
H 指数:42论文数:243被引数:5,858
C
Celeste Panteghini
H 指数:20论文数:73被引数:1,047
F
Federica Invernizzi
H 指数:35论文数:121被引数:4,544