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Mafalda Rizzuti

Ca' Granda Ospedale Maggiore Policlinico
H指数:15
被引数:940

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Targeted antisense oligonucleotide treatment rescues developmental alterations in spinal muscular atrophy organoids

靶向反义寡核苷酸治疗可挽救脊髓性肌萎缩症类器官中的发育改变

2025-12-210
OAAI
A Point-of-Care Test for miR-129-5p detection at sub-atto molar concentrations exploiting plasmonic pollen probes combined with complementary DNA

一种利用表面等离振子花粉探针与互补DNA相结合,用于检测亚飞摩尔浓度miR-129-5p的即时检测方法

2025-12-080
OAAI
C9orf72 Repeat Expansion Induces Metabolic Dysfunction in Human iPSC-Derived Microglia and Modulates Glial-Neuronal Crosstalk

C9orf72重复扩展在人类iPSC源性小胶质细胞中诱导代谢功能障碍并调节胶质细胞-神经元相互作用

Glia
IF5.1
2025-09-010
OAAI
Insights into the identification of a molecular signature for amyotrophic lateral sclerosis exploiting integrated microRNA profiling of iPSC-derived motor neurons and exosomes

利用iPSC衍生的运动神经元和外泌体的集成microRNA分析来识别肌萎缩侧索硬化的分子特征

2022-03-1424
OAAI
miR-129-5p: A key factor and therapeutic target in amyotrophic lateral sclerosis

miR-129-5p: 肌萎缩侧索硬化的关键因素和治疗靶点

2020-07-0135
OAAI
A novel homozygous PLA2G6 mutation causes dystonia-parkinsonism

一种新型纯合PLA2G6突变导致肌张力障碍-帕金森综合征

2015-03-0126
PREAI
Lower motor neuron disease with respiratory failure caused by a novel MAPT mutation

由新型MAPT突变引起的下运动神经元疾病伴呼吸衰竭

2014-06-0322
PREAI
Mutations in DNA2 Link Progressive Myopathy to Mitochondrial DNA Instability

DNA2突变将进行性肌病与线粒体DNA不稳定性联系起来

2013-02-01110
OAAI
Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions

下一代测序揭示了线粒体DNA多缺失的成年患者的DGUOK突变

BRAIN
IF11.7
2012-10-0481
OAAI