Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

24 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Classical osseous lesions leading to an unsuspected diagnosis.
Almes M, Fayard C, Gonzales E, Hermeziu B, Bellesme C, Jacquemin E, Koné-Paut I, Adamsbaum C, Dusser P. Almes M, et al. Among authors: bellesme c. Arch Pediatr. 2017 Dec;24(12):1278-1280. doi: 10.1016/j.arcped.2017.09.004. Epub 2017 Nov 16. Arch Pediatr. 2017. PMID: 29153906 No abstract available.
Unusual osseous presentation of Wilson disease in a child.
Almes M, Fayard C, Gonzales E, Hermeziu B, Bellesme C, Jacquemin E, Koné-Paut I, Adamsbaum C, Dusser P. Almes M, et al. Among authors: bellesme c. Arch Pediatr. 2017 Dec;24(12):1324-1327. doi: 10.1016/j.arcped.2017.09.005. Epub 2017 Nov 16. Arch Pediatr. 2017. PMID: 29153911 No abstract available.
[Medical care of brain malformative vascular diseases discovered during the pre- or neonatal period].
Sachet M, Tardieu M, Durand P, Ozanne A, Soubrier F, Tissières P, Chevret L, Husson B, Adamsbaum C, Bellesme C, Senat MV, Ducreux D, Saliou G; Centre de référence des maladies neurovasculaires malformatives de l'enfant. Sachet M, et al. Among authors: bellesme c. Arch Pediatr. 2013 Jan;20(1):74-81. doi: 10.1016/j.arcped.2012.10.019. Epub 2012 Dec 21. Arch Pediatr. 2013. PMID: 23266172 French.
Acute ischemic stroke in adolescents.
Rambaud T, Legris N, Bejot Y, Bellesme C, Lapergue B, Jouvent E, Pico F, Smadja D, Zuber M, Crozier S, Lamy C, Spelle L, Tuppin P, Kossorotoff M, Denier C. Rambaud T, et al. Among authors: bellesme c. Neurology. 2020 Jan 14;94(2):e158-e169. doi: 10.1212/WNL.0000000000008783. Epub 2019 Dec 12. Neurology. 2020. PMID: 31831601
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita.
Laquerriere A, Jaber D, Abiusi E, Maluenda J, Mejlachowicz D, Vivanti A, Dieterich K, Stoeva R, Quevarec L, Nolent F, Biancalana V, Latour P, Sternberg D, Capri Y, Verloes A, Bessieres B, Loeuillet L, Attie-Bitach T, Martinovic J, Blesson S, Petit F, Beneteau C, Whalen S, Marguet F, Bouligand J, Héron D, Viot G, Amiel J, Amram D, Bellesme C, Bucourt M, Faivre L, Jouk PS, Khung S, Sigaudy S, Delezoide AL, Goldenberg A, Jacquemont ML, Lambert L, Layet V, Lyonnet S, Munnich A, Van Maldergem L, Piard J, Guimiot F, Landrieu P, Letard P, Pelluard F, Perrin L, Saint-Frison MH, Topaloglu H, Trestard L, Vincent-Delorme C, Amthor H, Barnerias C, Benachi A, Bieth E, Boucher E, Cormier-Daire V, Delahaye-Duriez A, Desguerre I, Eymard B, Francannet C, Grotto S, Lacombe D, Laffargue F, Legendre M, Martin-Coignard D, Mégarbané A, Mercier S, Nizon M, Rigonnot L, Prieur F, Quélin C, Ranjatoelina-Randrianaivo H, Resta N, Toutain A, Verhelst H, Vincent M, Colin E, Fallet-Bianco C, Granier M, Grigorescu R, Saada J, Gonzales M, Guiochon-Mantel A, Bessereau JL, Tawk M, Gut I, Gitiaux C, Melki J. Laquerriere A, et al. Among authors: bellesme c. J Med Genet. 2022 Jun;59(6):559-567. doi: 10.1136/jmedgenet-2020-107595. Epub 2021 Apr 5. J Med Genet. 2022. PMID: 33820833 Free PMC article.
24 results