Bonello-Palot N - Search Results

1

[Next-generation DNA sequencing in clinical diagnostics].

Lacoste C, Fabre A, Pécheux C, Lévy N, Krahn M, Malzac P, Bonello-Palot N, Badens C, Bourgeois P. Lacoste C, et al. Arch Pediatr. 2017 Apr;24(4):373-383. doi: 10.1016/j.arcped.2017.01.008. Epub 2017 Feb 24. Arch Pediatr. 2017. PMID: 28242148 Review. French.

2

Clinical and electrophysiological characteristics of women with X-linked Charcot-Marie-Tooth disease.

Barbat du Closel L, Bonello-Palot N, Péréon Y, Echaniz-Laguna A, Camdessanche JP, Nadaj-Pakleza A, Chanson JB, Frachet S, Magy L, Cassereau J, Cintas P, Choumert A, Devic P, Leonard Louis S, Gravier Dumonceau R, Delmont E, Salort-Campana E, Bouhour F, Latour P, Stojkovic T, Attarian S. Barbat du Closel L, et al. Among authors: bonello palot n. Eur J Neurol. 2023 Oct;30(10):3265-3276. doi: 10.1111/ene.15937. Epub 2023 Jul 5. Eur J Neurol. 2023. PMID: 37335503

3

First case of gamma-thalassemia in association with a betaS allele: a pitfall in the neonatal screening for sickle cell disease.

Lacoste C, Bonello-Palot N, Gonnet K, Merono F, Levy N, Thuret I, Badens C. Lacoste C, et al. Haematologica. 2008 Nov;93(11):1754-5. doi: 10.3324/haematol.13262. Epub 2008 Aug 25. Haematologica. 2008. PMID: 18728021 Free article. No abstract available.

4

Relation of body mass index to high on-treatment platelet reactivity and of failed clopidogrel dose adjustment according to platelet reactivity monitoring in patients undergoing percutaneous coronary intervention.

Bonello-Palot N, Armero S, Paganelli F, Mancini J, De Labriolle A, Bonello C, Lévy N, Maillard L, Barragan P, Dignat-George F, Camoin-Jau L, Bonello L. Bonello-Palot N, et al. Am J Cardiol. 2009 Dec 1;104(11):1511-5. doi: 10.1016/j.amjcard.2009.07.015. Am J Cardiol. 2009. PMID: 19932784

5

Analytical evaluation of the Tosoh HLC-723 G8 automated HPLC analyzer for hemoglobin analysis in beta-thalassemia mode.

Merono F, Agouti I, Bonello-Palot N, Paolasso C, Levy N, Badens C. Merono F, et al. Clin Biochem. 2011 Apr;44(5-6):441-3. doi: 10.1016/j.clinbiochem.2010.12.007. Epub 2010 Dec 28. Clin Biochem. 2011. PMID: 21192923

6

Analytical evaluation of the Capillarys 2 Flex piercing for routine haemoglobinopathies diagnosis.

Agouti I, Merono F, Bonello-Palot N, Badens C. Agouti I, et al. Int J Lab Hematol. 2013 Apr;35(2):217-21. doi: 10.1111/ijlh.12000. Epub 2012 Sep 4. Int J Lab Hematol. 2013. PMID: 22943067

7

A novel mutation in FGD4/FRABIN causes Charcot Marie Tooth disease type 4H in patients from a consanguineous Tunisian family.

Boubaker C, Hsairi-Guidara I, Castro C, Ayadi I, Boyer A, Kerkeni E, Courageot J, Abid I, Bernard R, Bonello-Palot N, Kamoun F, Cheikh HB, Lévy N, Triki C, Delague V. Boubaker C, et al. Ann Hum Genet. 2013 Jul;77(4):336-43. doi: 10.1111/ahg.12017. Epub 2013 Apr 2. Ann Hum Genet. 2013. PMID: 23550889

8

Prelamin A accumulation in endothelial cells induces premature senescence and functional impairment.

Bonello-Palot N, Simoncini S, Robert S, Bourgeois P, Sabatier F, Levy N, Dignat-George F, Badens C. Bonello-Palot N, et al. Atherosclerosis. 2014 Nov;237(1):45-52. doi: 10.1016/j.atherosclerosis.2014.08.036. Epub 2014 Aug 28. Atherosclerosis. 2014. PMID: 25200614

9

Clinical and allelic heterogeneity in a pediatric cohort of 11 patients carrying MFN2 mutation.

Di Meglio C, Bonello-Palot N, Boulay C, Milh M, Ovaert C, Levy N, Chabrol B. Di Meglio C, et al. Brain Dev. 2016 May;38(5):498-506. doi: 10.1016/j.braindev.2015.11.006. Epub 2015 Dec 10. Brain Dev. 2016. PMID: 26686600

10

A Heterozygous ZMPSTE24 Mutation Associated with Severe Metabolic Syndrome, Ectopic Fat Accumulation, and Dilated Cardiomyopathy.

Galant D, Gaborit B, Desgrouas C, Abdesselam I, Bernard M, Levy N, Merono F, Coirault C, Roll P, Lagarde A, Bonello-Palot N, Bourgeois P, Dutour A, Badens C. Galant D, et al. Cells. 2016 Apr 25;5(2):21. doi: 10.3390/cells5020021. Cells. 2016. PMID: 27120622 Free PMC article.

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