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Inmaculada Pitarch Castellano

Carlos III Health Institute
H指数:12
被引数:464

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Multimodal characterisation of the SMN locus in SMA: copy number quantification and hybrid gene identification

脊髓性肌萎缩症中SMN基因座的多模态表征:拷贝数定量和嵌合基因鉴定

2026-05-200
OAAI
Long-term clinical and radiological trajectories in ANO5-related myopathies highlight muscle MRI as a predictor of disease progression

ANO5相关肌病长期临床和放射学轨迹凸显肌肉MRI作为疾病进展的预测指标

2026-04-150
OAAI
Recomendaciones para el diagnóstico, tratamiento y seguimiento de la enfermedad de Pompe de inicio tardío

晚期庞贝病的诊断、治疗和随访建议

2025-09-260
OAAI
Real-world data on spinal muscular atrophy in Spain: Insights from over 500 individuals in the CuidAME project

西班牙脊髓性肌萎缩症的真实世界数据:来自CuidAME项目超过500名个体的见解

2025-07-280
PRE
Upper limb motor function in individuals with SMA type 2: natural history and impact of therapies

2型脊髓性肌萎缩症患者上肢运动功能:自然病史及疗法影响

2025-04-090
PRE
Validation of a Set of Instruments to Assess Patient- and Caregiver-Oriented Measurements in Spinal Muscular Atrophy: Results of the SMA-TOOL Study

用于评估脊髓性肌萎缩症患者及照护者相关指标的一组工具的验证:SMA-TOOL研究结果

2022-10-2112
OAAI
Dystrophinopathy Phenotypes and Modifying Factors in DMD Exon 45-55 Deletion
2022-09-0710
OA
A novel TRMT5 mutation causes a complex inherited neuropathy syndrome: The role of nerve pathology in defining a demyelinating neuropathy
2022-04-108
OAAI