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New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases.
Mercier S, Dubourg C, Garcelon N, Campillo-Gimenez B, Gicquel I, Belleguic M, Ratié L, Pasquier L, Loget P, Bendavid C, Jaillard S, Rochard L, Quélin C, Dupé V, David V, Odent S. Mercier S, et al. Among authors: garcelon n. J Med Genet. 2011 Nov;48(11):752-60. doi: 10.1136/jmedgenet-2011-100339. Epub 2011 Sep 22. J Med Genet. 2011. PMID: 21940735 Free PMC article.
Risk of Death in Individuals Hospitalized for COVID-19 With and Without Psychiatric Disorders: An Observational Multicenter Study in France.
Hoertel N, Sánchez-Rico M, de la Muela P, Abellán M, Blanco C, Leboyer M, Cougoule C, Gulbins E, Kornhuber J, Carpinteiro A, Becker KA, Vernet R, Beeker N, Neuraz A, Alvarado JM, Herrera-Morueco JJ, Airagnes G, Lemogne C, Limosin F; AP-HP/Université de Paris/Inserm COVID-19 Research Collaboration and the AP-HP COVID CDR Initiative, “Entrepôt de Données de Santé,” AP-HP Consortium. Hoertel N, et al. Biol Psychiatry Glob Open Sci. 2023 Jan;3(1):56-67. doi: 10.1016/j.bpsgos.2021.12.007. Epub 2022 Jan 4. Biol Psychiatry Glob Open Sci. 2023. PMID: 35013734 Free PMC article.
Hyperventilation syndrome in children with asthma.
Beauvais M, Taam RA, Neuraz A, Le Bourgeois M, Delacourt C, Faour H, Garcelon N, Lezmi G. Beauvais M, et al. Among authors: garcelon n. J Asthma. 2023 Nov;60(11):1987-1996. doi: 10.1080/02770903.2023.2206903. Epub 2023 May 31. J Asthma. 2023. PMID: 37092722
Respiratory complications in pediatric epidermal necrolysis: A retrospective study of 22 cases.
Schmartz S, Welfringer-Morin A, Le Bourgeois M, Delacourt C, Berteloot L, Rabia SH, Bellon N, Moulin F, Pouletty M, Garcelon N, Bodemer C, Drummond D. Schmartz S, et al. Among authors: garcelon n. J Am Acad Dermatol. 2023 Oct;89(4):857-859. doi: 10.1016/j.jaad.2023.05.092. Epub 2023 Jun 23. J Am Acad Dermatol. 2023. PMID: 37355226 No abstract available.
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.
Faviez C, Vincent M, Garcelon N, Boyer O, Knebelmann B, Heidet L, Saunier S, Chen X, Burgun A. Faviez C, et al. Among authors: garcelon n. Orphanet J Rare Dis. 2024 Feb 10;19(1):55. doi: 10.1186/s13023-024-03063-7. Orphanet J Rare Dis. 2024. PMID: 38336713 Free PMC article.
103 results