日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Cardiovascular autonomic failure correlates with cutaneous autonomic denervation in PD and MSA

帕金森病和多系统萎缩症患者的心血管自主神经功能衰竭与皮肤自主神经支配丧失相关。

Koay, Shiwen; Provitera, Vincenzo; Vichayanrat, Ekawat; Caporaso, Giuseppe; Valerio, Fernanda; Stancanelli, Annamaria; Borreca, Ilaria; Manganelli, Fiore; Santoro, Lucio; Nolano, Maria; Iodice, Valeria

Autonomic dysfunction is associated with disease progression and survival in amyotrophic lateral sclerosis: a prospective longitudinal cohort study

自主神经功能障碍与肌萎缩侧索硬化症的疾病进展和生存率相关:一项前瞻性纵向队列研究

Dubbioso, Raffaele; Provitera, Vincenzo; Pacella, Daniela; Santoro, Lucio; Manganelli, Fiore; Nolano, Maria

Postganglionic Sudomotor Assessment in Early Stage of Multiple System Atrophy and Parkinson Disease: A Morpho-functional Study

多系统萎缩和帕金森病早期节后汗腺运动功能评估:一项形态功能研究

Provitera, Vincenzo; Iodice, Valeria; Manganelli, Fiore; Mozzillo, Stefania; Caporaso, Giuseppe; Stancanelli, Annamaria; Borreca, Ilaria; Esposito, Marcello; Dubbioso, Raffaele; Iodice, Rosa; Vitale, Floriana; Koay, Shiwen; Vichayanrat, Ekawat; Valerio, Fernanda; Santoro, Lucio; Nolano, Maria

Quantitative Sensory Testing in Late-Onset ATTRv Presymptomatic Subjects: A Single Center Experience

对晚发型 ATTRv 无症状患者进行定量感觉测试:单中心经验

Tozza, Stefano; Severi, Daniele; Palumbo, Giovanni; Provitera, Vincenzo; Ruggiero, Lucia; Dubbioso, Raffaele; Iodice, Rosa; Nolano, Maria; Manganelli, Fiore

Serpinin in the Skin.

皮肤中的丝氨酸蛋白酶抑制剂

Fraquelli Cristina, Hauzinger Jasmine, Humpel Christian, Nolano Maria, Provitera Vincenzo, Sharma Vinay Kumar, Loh Peng, Pidsudko Zenon, Blatsios Georgios, Troger Josef

Impaired Vagal Activity in Long-COVID-19 Patients

新冠后遗症患者迷走神经活动受损

Acanfora, Domenico; Nolano, Maria; Acanfora, Chiara; Colella, Camillo; Provitera, Vincenzo; Caporaso, Giuseppe; Rodolico, Gabriele Rosario; Bortone, Alessandro Santo; Galasso, Gennaro; Casucci, Gerardo

Contribution of Skin Biopsy in Peripheral Neuropathies

皮肤活检在周围神经病变中的作用

Nolano, Maria; Tozza, Stefano; Caporaso, Giuseppe; Provitera, Vincenzo

Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination

神经纤维蛋白基因的双等位基因突变会导致神经发育障碍和周围神经脱髓鞘。

Efthymiou, Stephanie; Salpietro, Vincenzo; Malintan, Nancy; Poncelet, Mallory; Kriouile, Yamna; Fortuna, Sara; De Zorzi, Rita; Payne, Katelyn; Henderson, Lindsay B; Cortese, Andrea; Maddirevula, Sateesh; Alhashmi, Nadia; Wiethoff, Sarah; Ryten, Mina; Botia, Juan A; Provitera, Vincenzo; Schuelke, Markus; Vandrovcova, Jana; Walsh, Laurence; Torti, Erin; Iodice, Valeria; Najafi, Maryam; Karimiani, Ehsan Ghayoor; Maroofian, Reza; Siquier-Pernet, Karine; Boddaert, Nathalie; De Lonlay, Pascale; Cantagrel, Vincent; Aguennouz, Mhammed; El Khorassani, Mohamed; Schmidts, Miriam; Alkuraya, Fowzan S; Edvardson, Simon; Nolano, Maria; Devaux, Jérôme; Houlden, Henry

A novel SCN9A splicing mutation in a compound heterozygous girl with congenital insensitivity to pain, hyposmia and hypogeusia.

一名患有先天性痛觉缺失、嗅觉减退和味觉减退的复合杂合子女孩,其 SCN9A 剪接突变是一种新型突变

Marchi Margherita, Provitera Vincenzo, Nolano Maria, Romano Marcello, Maccora Simona, D'Amato Ilaria, Salvi Erika, Gerrits Monique, Santoro Lucio, Lauria Giuseppe

Charcot-Marie-Tooth disease: New insights from skin biopsy

夏科-马里-图斯病:皮肤活检的新发现

Manganelli, Fiore; Nolano, Maria; Pisciotta, Chiara; Provitera, Vincenzo; Fabrizi, Gian M; Cavallaro, Tiziana; Stancanelli, Annamaria; Caporaso, Giuseppe; Shy, Michael E; Santoro, Lucio