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

126 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Determinants of adherence and consequences of the transition from adolescence to adulthood among young people with severe haemophilia (TRANSHEMO): A multicentric French national observational cross-sectional study based on the FranceCoag registry.
Nguyen NAT, Auquier P, Beltran Anzola A, Harroche A, Castet S, Huguenin Y, Meunier S, Repesse Y, D'Oiron R, Rauch A, Desprez D, Spiegel A, Chamouni P, Schneider P, Baumstarck K, Boucekine M, Tabele C, Viprey M, Leroy T, Roques MA, Sannie T, Giraud N, Chambost H, Resseguier N; TRANSHEMO Study group. Nguyen NAT, et al. Among authors: d oiron r. Haemophilia. 2023 Sep;29(5):1202-1218. doi: 10.1111/hae.14841. Epub 2023 Aug 12. Haemophilia. 2023. PMID: 37572328
Dangerous fluoroquinolones: The urologist's dilemma.
Nickel JC, Doiron RC. Nickel JC, et al. Can Urol Assoc J. 2020 Apr;14(4):85-86. doi: 10.5489/cuaj.6498. Epub 2020 Apr 1. Can Urol Assoc J. 2020. PMID: 32254009 Free PMC article. No abstract available.
[Erythrocyte indices and iron stores in cord blood].
Diagne I, Archambeaud MP, Diallo D, d'Oiron R, Yvart J, Tchernia G. Diagne I, et al. Arch Pediatr. 1995 Mar;2(3):208-14. doi: 10.1016/0929-693x(96)81129-8. Arch Pediatr. 1995. PMID: 7742903 French.
Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes.
Neerman-Arbez M, de Moerloose P, Honsberger A, Parlier G, Arnuti B, Biron C, Borg JY, Eber S, Meili E, Peter-Salonen K, Ripoll L, Vervel C, d'Oiron R, Staeger P, Antonarakis SE, Morris MA. Neerman-Arbez M, et al. Hum Genet. 2001 Mar;108(3):237-40. doi: 10.1007/s004390100469. Hum Genet. 2001. PMID: 11354637
126 results