arrow
G

Guja Astrea

irccs fondazione stella maris
H指数:29
被引数:2,581

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

Late-onset Pompe’s disease in pediatrics: results from an Italian national survey on 38 patients and proposal of a targeted diagnostic algorithm

儿科迟发性庞贝病:来自一项意大利全国性调查的38例患者的结果及针对性诊断算法的提出

2025-11-280
OAAI
HPDL Biallelic Variants in Cerebral Palsy and Childhood-Onset Hereditary Spastic Paraplegia: Human and Zebrafish Insights

HPDL 双等位基因变异在脑瘫和儿童期发病的遗传性痉挛性截瘫中的研究:人类的斑马鱼研究洞察

2025-07-280
PRE
Association between Reported Sleep Disorders and Behavioral Issues in Children with Myotonic Dystrophy Type 1-Results from a Retrospective Analysis in Italy

1型强直性肌营养不良儿童报告的睡眠障碍与行为问题之间的关联-意大利回顾性分析的结果

2024-09-140
OAAI
Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillary and Distal Myopathies Experience From the Italian Network
2024-08-271
PRE
The IAAM LTBP4 Haplotype is Protective Against Dystrophin-Deficient Cardiomyopathy
2024-02-162
OAAI
Deep phenotyping of the neuroimaging and skeletal features in KBG syndrome: a study of 53 patients and review of the literature
2023-08-167
OAAI
Epilepsy Course and Developmental Trajectories in STXBP1-DEE
2022-06-0125
OAAI
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study

扩大具有核心和微型核心的RYR1-related先天性肌病的临床病理和遗传谱: 一项意大利人口研究

2022-04-1510
OAAI
Genotype-phenotype correlations in recessive titinopathies

隐性titinopathies的基因型-表型相关性

2020-12-0140
OAAI
Genetic modifiers of respiratory function in Duchenne muscular dystrophy

Duchenne肌营养不良症呼吸功能的遗传修饰

2020-04-2834
OA
Next-generation sequencing approach to hyperCKemia A 2-year cohort study
2019-10-0133
OAAI
Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study
2018-09-2630
OAAI