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

Late-onset Leber's hereditary optic neuropathy and antiandrogens for prostate cancer: is there a causative link?

晚发性莱伯氏遗传性视神经病变与前列腺癌抗雄激素治疗:二者之间是否存在因果关系?

Amore, Giulia; Carbonelli, Michele; D'Angeli, Diego; Bonan, Luigi; Faustini-Fustini, Marco; Maresca, Alessandra; Carelli, Valerio; La Morgia, Chiara

Expanding the Clinical Spectrum of SPG26: A Case Report and Review of B4GALNT1-Associated Hereditary Spastic Paraplegia

拓展SPG26的临床谱:B4GALNT1相关遗传性痉挛性截瘫病例报告及综述

Giacomozzi, Sebastiano; Bonan, Luigi; La Morgia, Chiara; Carbonelli, Michele; Santucci, Margherita; Isidori, Federica; Pippucci, Tommaso; Liguori, Rocco; Rizzo, Giovanni

Machine Learning Applied to Visual Fields of Dominant Optic Atrophy Patients

机器学习在优势视神经萎缩患者视野中的应用

Coutinho, Catarina P; Zanchetta, Ferdinando; Carbonelli, Michele; Battista, Marco; Galzignato, Alice; La Morgia, Chiara; Amore, Giulia; Romagnoli, Martina; Savini, Giacomo; Brotto, Luigi; Nucci, Paolo; Caporali, Leonardo; Bandello, Francesco; Carelli, Valerio; Cascavilla, Maria Lucia; Fioresi, Rita; Barboni, Piero

An exploration of trauma-informed care curricula in chiropractic programs: A scoping document analysis protocol

对脊椎按摩疗法课程中创伤知情护理课程的探索:范围界定文件分析方案

Bensel, Victoria A; Cupler, Zachary; Poppen, Olivia; Joyce, Jane; Allgeier, Mike; Wiles, Michael; Driscoll, Mary; Carbonelli-Cloutier, Kristy; Coleman, Brian C

A Case of Late-Onset Leber's Hereditary Optic Neuropathy in Association with Heteroplasmic m.11778G>A/ND4 Mutation

一例伴有异质性m.11778G>A/ND4突变的迟发性Leber遗传性视神经病变

Portaro, Giacomo; Cavallieri, Francesco; Amore, Giulia; Carbonelli, Michele; Pelloni, Simone; Cavallieri, Giuseppe; Carelli, Valerio; Valzania, Franco; Morgia, Chiara La

A comparative audit of chiropractic geriatric courses taught at 17 English-speaking accredited chiropractic educational programs worldwide

对全球17个英语授课的认证脊椎按摩教育机构开设的脊椎按摩老年课程进行比较审计

Gleberzon, Brian J; Carbonelli-Cloutier, Kristy; de Luca, Katie

Medical Nutrition Therapy in Dermatological Diseases: A Joint Consensus Statement of the Italian Association of Dietetics and Clinical Nutrition (ADI), the Italian Society of Dermatology and Sexually Transmitted Diseases (SIDeMaST), the Italian Society of Nutraceuticals (SINut), Club Ketodiets and Nutraceuticals "KetoNut-SINut" and the Italian Society of Endocrinology (SIE), Club Nutrition, Hormones and Metabolism

皮肤病医学营养治疗:意大利营养与临床营养学会 (ADI)、意大利皮肤病与性传播疾病学会 (SIDeMaST)、意大利营养保健品学会 (SINut)、生酮饮食与营养保健品俱乐部“KetoNut-SINut”以及意大利内分泌学会 (SIE)、营养、激素与代谢俱乐部联合共识声明

Barrea, Luigi; Verde, Ludovica; Annunziata, Giuseppe; Antiga, Emiliano; Camajani, Elisabetta; Caprio, Massimiliano; Carbonelli, Maria Grazia; Carducci, Augusto; Cava, Edda; Di Marco, Giorgia; Grassi, Davide; Guida, Stefania; Martinelli, Barbara; Marzano, Angelo Valerio; Moltrasio, Chiara; Petrelli, Massimiliano; Prignano, Francesca; Rongioletti, Franco; Savastano, Silvia; Paolini, Barbara; Bagnato, Carmela; Argenziano, Giuseppe; Cicero, Arrigo Francesco Giuseppe; Colao, Annamaria; Ferone, Diego; Aimaretti, Gianluca; Muscogiuri, Giovanna

Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy

影响 NQO1 蛋白水平的基因变异会影响艾地苯醌治疗莱伯遗传性视神经病变的疗效。

Serena Jasmine Aleo ,Valentina Del Dotto ,Martina Romagnoli ,Claudio Fiorini ,Giada Capirossi ,Camille Peron ,Alessandra Maresca ,Leonardo Caporali ,Mariantonietta Capristo ,Concetta Valentina Tropeano ,Claudia Zanna ,Fred N Ross-Cisneros ,Alfredo A Sadun ,Maria Gemma Pignataro ,Carla Giordano ,Chiara Fasano ,Andrea Cavaliere ,Anna Maria Porcelli ,Gaia Tioli ,Francesco Musiani ,Alessia Catania ,Costanza Lamperti ,Stefania Bianchi Marzoli ,Annamaria De Negri ,Maria Lucia Cascavilla ,Marco Battista ,Piero Barboni ,Michele Carbonelli ,Giulia Amore ,Chiara La Morgia ,Dmitrii Smirnov ,Catalina Vasilescu ,Aiman Farzeen ,Beryll Blickhaeuser ,Holger Prokisch ,Claudia Priglinger ,Bettina Livonius ,Claudia B Catarino ,Thomas Klopstock ,Valeria Tiranti ,Valerio Carelli ,Anna Maria Ghelli

Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy

影响 NQO1 蛋白水平的基因变异会影响艾地苯醌治疗莱伯遗传性视神经病变的疗效。

Serena Jasmine Aleo,Valentina Del Dotto,Martina Romagnoli,Claudio Fiorini,Giada Capirossi,Camille Peron,Alessandra Maresca,Leonardo Caporali,Mariantonietta Capristo,Concetta Valentina Tropeano,Claudia Zanna,Fred N Ross-Cisneros,Alfredo A Sadun,Maria Gemma Pignataro,Carla Giordano,Chiara Fasano,Andrea Cavaliere,Anna Maria Porcelli,Gaia Tioli,Francesco Musiani,Alessia Catania,Costanza Lamperti,Stefania Bianchi Marzoli,Annamaria De Negri,Maria Lucia Cascavilla,Marco Battista,Piero Barboni,Michele Carbonelli,Giulia Amore,Chiara La Morgia,Dmitrii Smirnov,Catalina Vasilescu,Aiman Farzeen,Beryll Blickhaeuser,Holger Prokisch,Claudia Priglinger,Bettina Livonius,Claudia B Catarino,Thomas Klopstock,Valeria Tiranti,Valerio Carelli,Anna Maria Ghelli

Co-occurrence of glial fibrillary acidic protein astrocytopathy in a patient with Leber's hereditary optic neuropathy due to DNAJC30 mutations

DNAJC30 突变引起的 Leber 遗传性视神经病变患者合并胶质纤维酸性蛋白星形胶质细胞病

Giannoccaro, Maria Pia; Morelli, Luana; Ricciardiello, Fortuna; Donadio, Vincenzo; Bartiromo, Fiorina; Tonon, Caterina; Carbonelli, Michele; Amore, Giulia; Carelli, Valerio; Liguori, Rocco; La Morgia, Chiara