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Paola Mandich

irccs ospedale policlinico san martino
H指数:40
被引数:6,655

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Imaging of Facial Muscles in Facioscapulohumeral Muscular Dystrophy: An Exploratory Study Comparing Magnetic Resonance Imaging and Ultrasound

面肩肱肌营养不良症的面部肌肉成像:一项比较磁共振成像和超声的探索性研究

2026-09-140
OAAI
Compound Heterozygous Structural Variants in Cases with Unsolved PRKN-Associated Parkinson's Disease

PRKN相关帕金森病病例中的复合杂合结构变异

2025-08-300
OAAI
LONG-NEXT: A new accurate and efficient NGS-based method for GBA1 analysis in Parkinson disease

LONG-NEXT:一种用于帕金森病GBA1分析的新型准确且高效的NGS方法

2025-05-010
OAAI
Clinical and metabolic profiles in behavioural frontotemporal dementia: Impact of age at onset
CORTEX
IF3.3
2025-04-010
OAAI
Limbic Network Derangement Mediates Unawareness of Apathy in Mild Cognitive Impairment due to Alzheimer's Disease: Clues from [18F]FDG PET Voxel-Wise Analysis
2025-02-050
PRE
18F-FDG PET findings in Parkinson's disease associated to RAB32 S71R variant
2025-02-010
PRE
Integrating D4Z4 methylation analysis into clinical practice: improvement of FSHD molecular diagnosis through distinct thresholds for 4qA/4qA and 4qA/4qB patients

将D4Z4甲基化分析整合到临床实践中: 通过4qA/4qA和4qA/4qB患者的不同阈值改善FSHD分子诊断

2024-10-221
OAAI
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
The neurological core features of the infantile-onset multisystem neurologic, endocrine, and pancreatic disease: A novel nonsense mutation in an Italian family
2024-06-140
PRE
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
Early Onset Inherited Peripheral Neuropathies: The Experience of a Specialized Referral Center for Genetic Diagnosis Achievement
2024-05-011
PRE
A novel de novo variant in POLR3B gene associated with a primary axonal involvement of the largest nerve fibers
2023-11-132
OAAI
Harmonizing Genetic Testing for Parkinson's Disease: Results of the PARKNET Multicentric Study

协调帕金森病的基因检测: PARKNET多中心研究的结果

2023-09-262
OAAI
The HFE p.H63D (p.His63Asp) Polymorphism Is a Modifier of ALS Outcome in Italian and French Patients with SOD1 Mutations

HFE p.H63D (p.His63Asp) 多态性是意大利和法国SOD1突变患者ALS结果的修饰因子

2023-02-243
OAAI