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10 years of CEMARA database in the AnDDI-Rares network: a unique resource facilitating research and epidemiology in developmental disorders in France.
Messiaen C, Racine C, Khatim A, Soussand L, Odent S, Lacombe D, Manouvrier S, Edery P, Sigaudy S, Geneviève D, Thauvin-Robinet C, Pasquier L, Petit F, Rossi M, Willems M, Attié-Bitach T, Roux-Levy PH, Demougeot L, Slama LB, Landais P; AnDDI-Rares network; Jannot AS, Binquet C, Sandrin A, Verloes A, Faivre L. Messiaen C, et al. Among authors: jannot as. Orphanet J Rare Dis. 2021 Aug 4;16(1):345. doi: 10.1186/s13023-021-01957-4. Orphanet J Rare Dis. 2021. PMID: 34348744 Free PMC article.
Machine-learning-derived sepsis bundle of care.
Kalimouttou A, Lerner I, Cheurfa C, Jannot AS, Pirracchio R. Kalimouttou A, et al. Among authors: jannot as. Intensive Care Med. 2023 Jan;49(1):26-36. doi: 10.1007/s00134-022-06928-2. Epub 2022 Nov 29. Intensive Care Med. 2023. PMID: 36446854
Overview of patients' cohorts in the French National rare disease registry.
Pichon T, Messiaen C, Soussand L, Angin C, Sandrin A, Elarouci N, Jannot AS; BNDMR infrastructure team. Pichon T, et al. Among authors: jannot as. Orphanet J Rare Dis. 2023 Jul 3;18(1):176. doi: 10.1186/s13023-023-02725-2. Orphanet J Rare Dis. 2023. PMID: 37400917 Free PMC article.
Diagnostic Impasse and Wandering in Patients With Rare Neuromuscular Diseases: Insights Into Patient Characteristics From the French National Network for Rare Neuromuscular Diseases (FILNEMUS) and the French National Rare Disease Database (BNDMR).
Dumas R, Jannot AS, Elarouci N, Salort-Campana E, Pisella L, Tard C, Sacconi S, Bouhour F, Sarrazin E, Spinazzi M, Laforet P, Pereon Y, Nadaj-Pakleza A, Echaniz-Laguna A, Choumert A, Magy L, Feasson L, Esselin F, Cances C, Espile C, Desguerre I, Rouzier C, Cintas P, Stojkovic T, Solé G, Attarian S; FILNEMUS Study Group. Dumas R, et al. Among authors: jannot as. Eur J Neurol. 2025 Sep;32(9):e70347. doi: 10.1111/ene.70347. Eur J Neurol. 2025. PMID: 40905397 Free PMC article.
154 results