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Nicolas Garcelon

universite paris cite
H指数:23
被引数:2,232
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Proceedings of the Second Artificial Intelligence in Primary Immunodeficiencies (AIPI) Meeting

第二届人工智能在原发性免疫缺陷中的应用(AIPI)会议论文集

2025-09-170
OAAI
Hospitalization for child physical abuse before hospitalization for osteogenesis imperfecta or severe hemophilia: A nationwide cohort study in France

因儿童躯体虐待住院先于因成骨不全症或重度血友病住院:一项在法国进行的国家队列研究

2025-07-080
OA
Corrigendum to “Genotype-Phenotype Correlations in Denys-Drash Syndrome in Children” [Kidney International Reports Volume 10, Issue 4, April 2025, Pages 1205-1212]

勘误:“儿童德尼-德拉斯综合征的基因型-表型相关性” [《国际肾脏报告》第10卷第4期,2025年4月,第1205-1212页]

2025-05-040
OA
Dupilumab in atopic-dermatitis-like eczema associated with inborn errors of immunity: A nationwide study
2025-01-010
PRE
Genotype-Phenotype Correlations in Denys-Drash Syndrome in Children

儿童Denys-Drash综合征中的基因型-表型相关性

2025-01-011
OAAI
Charting a course for global progress in PIDs by 2030-proceedings from the IPOPI global multi-stakeholders' summit (September 2023)
2024-06-271
OAAI
Objectivizing issues in the diagnosis of complex rare diseases: lessons learned from testing existing diagnosis support systems on ciliopathies

复杂罕见疾病诊断中的客观化问题: 从测试现有纤毛病诊断支持系统中学到的经验教训

2024-05-241
OAAI
Histological characterization of liver involvement in systemic mastocytosis

系统性肥大细胞增多症肝脏受累的组织学表征

2024-03-301
OAAI
Performance and clinical utility of a new supervised machine-learning pipeline in detecting rare ciliopathy patients based on deep phenotyping from electronic health records and semantic similarity

基于电子健康记录和语义相似性的深度表型检测罕见纤毛病患者的新监督机器学习管道的性能和临床效用

2024-02-103
OAAI
Next generation phenotyping for diagnosis and phenotype-genotype correlations in Kabuki syndrome
2024-01-286
OAAI
Pathophysiologic implications of elevated prevalence of hereditary alpha-tryptasemia in all mastocytosis subtypes

所有肥大细胞增多症亚型中遗传性 α-胰蛋白酶血症患病率升高的病理生理意义

2024-01-019
OA