arrow
P

Palma Finelli

Fondazione IRCCS Ca Granda Ospedale Maggiore Policlinico di Milano
H指数:35
被引数:3,648

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

Investigation of plasma-derived extracellular vesicles in hypertrophic cardiomyopathy patients

探究肥厚型心肌病患者的血浆源性外泌体

2026-08-010
PRE
Lithium ameliorates neural differentiation restoring cell death balance in Cornelia de Lange syndrome 2D and 3D models

锂通过恢复细胞死亡平衡来改善Cornelia de Lange综合征的神经分化,在2D和3D模型中均有体现。

2026-03-280
OAAI
Prenatal Exome Sequencing: When Does Diagnostic Yield Meet Clinical Utility?

产前外显子测序:何时诊断率能达到临床实用性?

Genes
IF2.8
2026-01-020
OAAI
Portrait of a Spectrum: Clinical and Genetic Characterization of a Large Cohort of Chromatinopathies—30 Years' Experience From a Third Level Center

《一个谱系的面貌:一个大宗染色质病队列的临床与遗传特征分析——来自一家三级医疗中心30年的经验》

2025-11-020
OAAI
An intragenic duplication in the AFF2 gene associated with Cornelia de Lange syndrome phenotype

与Cornelia de Lange综合征表型相关的AFF2基因内的基因内复制

2024-11-010
OA
DIS3 depletion in multiple myeloma causes extensive perturbation in cell cycle progression and centrosome amplification

多发性骨髓瘤中的DIS3耗竭导致细胞周期进程和中心体扩增的广泛扰动

2023-07-138
OAAI
Exploring by whole exome sequencing patients with initial diagnosis of Rubinstein-Taybi syndrome: the interconnections of epigenetic machinery disorders
2019-02-2629
OAAI
A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes (vol 8, 23, 2016)
2016-04-212
OAAI
A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes
2016-03-0156
OAAI
From Whole Gene Deletion to Point Mutations of EP300-Positive Rubinstein-Taybi Patients: New Insights into the Mutational Spectrum and Peculiar Clinical Hallmarks

从全基因缺失到EP300-Positive rubinstein-taybi患者的点突变: 对突变谱和特殊临床特征的新见解

2015-11-0439
OAAI