Garcelon N - Search Results

1

Induction therapy for pediatric onset class IV lupus nephritis: Mycophenolate Mofetil versus Cyclophosphamide.

Chbihi M, Eveillard LA, Riller Q, Brousse R, Berthaud R, Quartier P, Salomon R, Charbit M, Avramescu M, Biebuyck N, Dehoux L, Garcelon N, Duong-Van-Huyen JP, Bader-Meunier B, Boyer O. Chbihi M, et al. Among authors: garcelon n. J Nephrol. 2023 Apr;36(3):829-839. doi: 10.1007/s40620-022-01438-2. Epub 2022 Oct 8. J Nephrol. 2023. PMID: 36208405

2

Improving a full-text search engine: the importance of negation detection and family history context to identify cases in a biomedical data warehouse.

Garcelon N, Neuraz A, Benoit V, Salomon R, Burgun A. Garcelon N, et al. J Am Med Inform Assoc. 2017 May 1;24(3):607-613. doi: 10.1093/jamia/ocw144. J Am Med Inform Assoc. 2017. PMID: 28339516 Free PMC article.

3

Finding patients using similarity measures in a rare diseases-oriented clinical data warehouse: Dr. Warehouse and the needle in the needle stack.

Garcelon N, Neuraz A, Benoit V, Salomon R, Kracker S, Suarez F, Bahi-Buisson N, Hadj-Rabia S, Fischer A, Munnich A, Burgun A. Garcelon N, et al. J Biomed Inform. 2017 Sep;73:51-61. doi: 10.1016/j.jbi.2017.07.016. Epub 2017 Jul 25. J Biomed Inform. 2017. PMID: 28754522 Free article.

4

A clinician friendly data warehouse oriented toward narrative reports: Dr. Warehouse.

Garcelon N, Neuraz A, Salomon R, Faour H, Benoit V, Delapalme A, Munnich A, Burgun A, Rance B. Garcelon N, et al. J Biomed Inform. 2018 Apr;80:52-63. doi: 10.1016/j.jbi.2018.02.019. Epub 2018 Mar 1. J Biomed Inform. 2018. PMID: 29501921 Free article.

5

Next generation phenotyping using narrative reports in a rare disease clinical data warehouse.

Garcelon N, Neuraz A, Salomon R, Bahi-Buisson N, Amiel J, Picard C, Mahlaoui N, Benoit V, Burgun A, Rance B. Garcelon N, et al. Orphanet J Rare Dis. 2018 May 31;13(1):85. doi: 10.1186/s13023-018-0830-6. Orphanet J Rare Dis. 2018. PMID: 29855327 Free PMC article.

6

The "salt and pepper" pattern on renal ultrasound in a group of children with molecular-proven diagnosis of ciliopathy-related renal diseases.

Iorio P, Heidet L, Rutten C, Garcelon N, Audrézet MP, Morinière V, Boddaert N, Salomon R, Berteloot L. Iorio P, et al. Among authors: garcelon n. Pediatr Nephrol. 2020 Jun;35(6):1033-1040. doi: 10.1007/s00467-020-04480-z. Epub 2020 Feb 10. Pediatr Nephrol. 2020. PMID: 32040628

7

Electronic health records for the diagnosis of rare diseases.

Garcelon N, Burgun A, Salomon R, Neuraz A. Garcelon N, et al. Kidney Int. 2020 Apr;97(4):676-686. doi: 10.1016/j.kint.2019.11.037. Epub 2020 Jan 14. Kidney Int. 2020. PMID: 32111372 Free article. Review.

8

Diagnosis support systems for rare diseases: a scoping review.

Faviez C, Chen X, Garcelon N, Neuraz A, Knebelmann B, Salomon R, Lyonnet S, Saunier S, Burgun A. Faviez C, et al. Among authors: garcelon n. Orphanet J Rare Dis. 2020 Apr 16;15(1):94. doi: 10.1186/s13023-020-01374-z. Orphanet J Rare Dis. 2020. PMID: 32299466 Free PMC article. Review.

9

Association between 25(OH) vitamin D and graft survival in renal transplanted children.

Mosca M, Lion-Lambert M, Bienaimé F, Berthaud R, Dorval G, Garcelon N, Dehoux L, Krid S, Charbit M, Rabant M, Niaudet P, Salomon R, Bacchetta J, Boyer O. Mosca M, et al. Among authors: garcelon n. Pediatr Transplant. 2020 Nov;24(7):e13809. doi: 10.1111/petr.13809. Epub 2020 Aug 26. Pediatr Transplant. 2020. PMID: 32845557

10

Long-term kidney and liver outcome in 50 children with autosomal recessive polycystic kidney disease.

Dorval G, Boyer O, Couderc A, Delbet JD, Heidet L, Debray D, Krug P, Girard M, Llanas B, Charbit M, Krid S, Biebuyck N, Fila M, Courivaud C, Tilley F, Garcelon N, Blanc T, Chardot C, Salomon R, Lacaille F. Dorval G, et al. Among authors: garcelon n. Pediatr Nephrol. 2021 May;36(5):1165-1173. doi: 10.1007/s00467-020-04808-9. Epub 2020 Nov 9. Pediatr Nephrol. 2021. PMID: 33165639

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