Nadia Moulin Nathan

机构：Hôpital Necker-Enfants Malades, Inserm, Sorbonne Université, Hôpital Armand-Trousseau, Assistance Publique – Hôpitaux de Paris, Expression Génétique Microbienne, Maladies génétiques d’expression pédiatrique

发表论文 9 篇 · 总被引 5 次 · h-index 2

代表论文

Biallelic LAMP3 variants in 5 families with interstitial lung disease: Evidence of a disease-gene association (2026 · Genetics in Medicine · 被引 3)
Management and Long-Term Outcomes of Persistent Tachypnea of Infancy/Neuroendocrine Cell Hyperplasia of Infancy (2026 · CHEST Journal · 被引 2)
Management and Long-Term Outcomes of Persistent Tachypnea of Infancy/Neuroendocrine Cell Hyperplasia of Infancy: A European Multicenter Retrospective Study. (2026 · Open Access CRIS of the University of Bern)
Hémoptysie et hémorragie pulmonaire de l’enfant (2026 · Perfectionnement en Pédiatrie)
Determinants of Clinical Severity in Children with Sickle Cell Disease and Confirmed Asthma (2026 · medRxiv)
Reply to “Familial Segregation Highlights Challenges in Rare SFTPA2 Variant Classification” (2026 · Respirology)