Benammar N - Search Results

1

A novel mutation in SCN5A, delQKP 1507-1509, causing long QT syndrome: role of Q1507 residue in sodium channel inactivation.

Keller DI, Acharfi S, Delacrétaz E, Benammar N, Rotter M, Pfammatter JP, Fressart V, Guicheney P, Chahine M. Keller DI, et al. Among authors: benammar n. J Mol Cell Cardiol. 2003 Dec;35(12):1513-21. doi: 10.1016/j.yjmcc.2003.08.007. J Mol Cell Cardiol. 2003. PMID: 14654377

2

The occurrence of Brugada syndrome and isolated cardiac conductive disease in the same family could be due to a single SCN5A mutation or to the accidental association of both diseases.

Six I, Hermida JS, Huang H, Gouas L, Fressart V, Benammar N, Hainque B, Denjoy I, Chahine M, Guicheney P. Six I, et al. Among authors: benammar n. Europace. 2008 Jan;10(1):79-85. doi: 10.1093/europace/eum271. Epub 2007 Dec 21. Europace. 2008. PMID: 18156160

3

Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations.

Lupoglazoff JM, Denjoy I, Villain E, Fressart V, Simon F, Bozio A, Berthet M, Benammar N, Hainque B, Guicheney P. Lupoglazoff JM, et al. Among authors: benammar n. J Am Coll Cardiol. 2004 Mar 3;43(5):826-30. doi: 10.1016/j.jacc.2003.09.049. J Am Coll Cardiol. 2004. PMID: 14998624 Free article.

4

Brugada syndrome and fever: genetic and molecular characterization of patients carrying SCN5A mutations.

Keller DI, Rougier JS, Kucera JP, Benammar N, Fressart V, Guicheney P, Madle A, Fromer M, Schläpfer J, Abriel H. Keller DI, et al. Among authors: benammar n. Cardiovasc Res. 2005 Aug 15;67(3):510-9. doi: 10.1016/j.cardiores.2005.03.024. Cardiovasc Res. 2005. PMID: 15890323 Free article.

5

[Neonatal forms of congenital long QT syndrome].

Lupoglazoff JM, Denjoy I, Villain E, Fressart V, Legall-Petit I, Bozio A, Berthet M, Benammar N, Hainque B, Guicheney P. Lupoglazoff JM, et al. Among authors: benammar n. Arch Mal Coeur Vaiss. 2004 May;97(5):479-83. Arch Mal Coeur Vaiss. 2004. PMID: 15214551 French.

6

Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?

Charles P, Camuzat A, Benammar N, Sellal F, Destée A, Bonnet AM, Lesage S, Le Ber I, Stevanin G, Dürr A, Brice A; French Parkinson's Disease Genetic Study Group. Charles P, et al. Among authors: benammar n. Neurology. 2007 Nov 20;69(21):1970-5. doi: 10.1212/01.wnl.0000269323.21969.db. Epub 2007 Jun 13. Neurology. 2007. PMID: 17568014

7

Spinocerebellar ataxia with mental retardation (SCA13).

Stevanin G, Durr A, Benammar N, Brice A. Stevanin G, et al. Among authors: benammar n. Cerebellum. 2005;4(1):43-6. doi: 10.1080/14734220510007923. Cerebellum. 2005. PMID: 15895558 Review.

8

Transient CD4 cell recovery after hepatitis C virus cure in HIV/hepatitis C virus coinfected patients (ANRS CO13 HEPAVIH cohort).

Barré T, Ramier C, Ory K, Sogni P, Aumaitre H, Saidi T, Carrieri P, Marcellin F; ANRS CO13 HEPAVIH Study Group. Barré T, et al. HIV Med. 2024 Dec 11. doi: 10.1111/hiv.13752. Online ahead of print. HIV Med. 2024. PMID: 39663177 No abstract available.

9

Immunovirological status in people with perinatal and adult-acquired HIV-1 infection: a multi-cohort analysis from France.

Seng R, Frange P, Faye A, Dollfus C, le Chenadec J, Boufassa F, Essat A, Goetghebuer T, Arezes E, Avettand-Fènoël V, Bigna JJ, Blanche S, Goujard C, Meyer L, Warszawski J, Viard JP; ANRS EPF; COVERTE; PRIMO; SEROPRI; COPANA study groups. Seng R, et al. Lancet Reg Health Eur. 2024 Apr 1;40:100885. doi: 10.1016/j.lanepe.2024.100885. eCollection 2024 May. Lancet Reg Health Eur. 2024. PMID: 38576825 Free PMC article.

10

Substance use and CD4/CD8 ratio in HIV/HCV co-infected people receiving direct-acting antiviral treatment (ANRS CO13 HEPAVIH).

Barré T, Zucman D, Marcellin F, Ramier C, Protopopescu C, Tardieu R, Ory K, Salmon-Céron D, Carrieri P; ANRS CO13 HEPAVIH Study Group. Barré T, et al. J Viral Hepat. 2023 Nov;30(11):897-900. doi: 10.1111/jvh.13865. Epub 2023 Jun 26. J Viral Hepat. 2023. PMID: 37357886 No abstract available.

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