arrow
A

Anna Ardissone

Fondazione IRCCS Istituto Neurologico Carlo Besta
H指数:27
被引数:2,148

个人简介

暂无内容

教育背景

暂无内容

工作经历

暂无内容

荣誉奖项

暂无内容

A prospective, longitudinal, natural history study of neurological disease trajectory in children with late-infantile or juvenile-onset GM1 gangliosidosis or GM2 gangliosidoses: the PRONTO study

一项前瞻性、纵向、自然病史研究:探究儿童晚期婴儿型或青少年型GM1神经节苷脂贮积症或GM2神经节苷脂贮积症中的神经疾病轨迹——PRONTO研究

2026-10-070
OAAI
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

2025-10-150
PRE
Fourteen New Pediatric Cases of Shapiro Syndrome

十四例新的希普森综合征儿科病例

2025-07-170
OA
Natural history of Becker muscular dystrophy: DMD gene mutations predict clinical severity

贝克肌营养不良的自然史:DMD基因突变预测临床严重程度

BRAIN
IF11.7
2024-11-050
PRE
A natural history study of late-infantile and juvenile GM1 and GM2 gangliosidoses (PRONTO): Baseline clinical data
2024-02-010
PRE
A natural history study of late-infantile and juvenile GM1 and GM2 gangliosidosis (PRONTO): Evaluation of different assessments
2024-02-010
PRE
A natural history study of late-infantile and juvenile GM1 and GM2 gangliosidoses (PRONTO): Patients' and caregivers' assessments
2024-02-010
PRE
Antibody Deficiency in Patients with Biallelic KARS1 Mutations (Sept, 10.1007/s10875-023-01584-7, 2023)

双等位基因KARS1突变患者的抗体缺乏 (2023,10.1007/s10875-023-01584-7,9月)

2023-11-030
OA
Antibody Deficiency in Patients with Biallelic KARS1 Mutations
2023-09-282
PRE