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Fiore Manganelli

university federico ii
H指数:44
被引数:7,147

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Refining Electrophysiological Criteria in CIDP and MMN: Toward a Unified Definition of Motor Conduction Block and Proximal Temporal Dispersion

在慢性炎性脱髓鞘性多发性神经病和运动神经病中优化电生理标准:迈向运动传导阻滞和近端时间离散的统一定义

2026-09-030
OAAI
Distinct sensory and autonomic involvement in hypermobile Ehlers–Danlos syndrome compared with idiopathic small fiber neuropathy: a multimodal study

与特发性小纤维神经病相比,高弹性埃勒斯-当洛斯综合征中感觉和自主神经的差异性参与:一项多模式研究

2026-07-030
OA
A Quantitative Assessment of Upper Limb Motor Function Across Disease Stages in Hereditary Transthyretin Amyloidosis

遗传性甲状腺素转运蛋白淀粉样变性不同疾病阶段上肢运动功能的定量评估

2026-06-050
OAAI
Deep Phenotyping of F64L Mutation in a Multicentric Cohort of Patisiran-Treated Hereditary Transthyretin Amyloidosis Patients (Patisiranitaly)

对Patisiranitaly研究中Patisiran治疗的家族性转甲状腺素蛋白淀粉样变性患者多中心队列中F64L突变的深度表型分析

2026-06-010
OA
Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency (MADD): Clinical Features, Diagnostic Challenges, and the Role of Oxidative Stress in Pathophysiology

迟发型多酰基辅酶A脱氢酶缺乏症(MADD):临床特征、诊断挑战以及氧化应激在病理生理学中的作用

2025-11-260
OAAI
A Comprehensive Description of the Roadmap to Identify and Validate a Myelin Biomarker

《识别和验证髓鞘生物标志物的路线图全面描述》

2025-07-060
OA
Clinical and genetic features of CMT2T in Italian patients confirm the importance of MME pathogenic variants in idiopathic, late-onset axonal neuropathies
2024-09-090
OAAI
Nerve ultrasound in CANVAS-spectrum disease: Reduced nerve size distinguishes genetically confirmed CANVAS from other axonal polyneuropathies

CANVAS频谱疾病中的神经超声: 减少的神经大小将遗传证实的CANVAS与其他轴突多神经病区分开来

2024-09-022
OA
Phenotypic spectrum of myelin protein zero-related neuropathies: a large cohort study from five mutation clusters across Italy

髓磷脂蛋白零相关神经病的表型谱: 来自意大利五个突变簇的大型队列研究

2024-06-050
OAAI
Multiple Phenotypes of Chronic Coronary Syndromes Identified by ABCDE Stress Echocardiography
2024-05-016
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