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Items: 16

1.

Klotho Gene in Human Salt-Sensitive Hypertension.

Citterio L, Delli Carpini S, Lupoli S, Brioni E, Simonini M, Fontana S, Zagato L, Messaggio E, Barlassina C, Cusi D, Manunta P, Lanzani C.

Clin J Am Soc Nephrol. 2020 Jan 28. pii: CJN.08620719. doi: 10.2215/CJN.08620719. [Epub ahead of print]

PMID:
31992575
2.

Hypertension in High School Students: Genetic and Environmental Factors: The HYGEF Study.

Bigazzi R, Zagato L, Lanzani C, Fontana S, Messaggio E, Delli Carpini S, Citterio L, Simonini M, Brioni E, Magnaghi C, Colombo GI, Santini G, Nistri F, Cellai F, Lenti S, Bianchi S, Pertosa GB, Rocchetti MT, Papale M, Mezzolla V, Gesualdo L, Pina Concas M, Campese V, Manunta P.

Hypertension. 2020 Jan;75(1):71-78. doi: 10.1161/HYPERTENSIONAHA.119.13818. Epub 2019 Nov 25.

PMID:
31760884
3.

Lanosterol Synthase Genetic Variants, Endogenous Ouabain, and Both Acute and Chronic Kidney Injury.

Iatrino R, Lanzani C, Bignami E, Casamassima N, Citterio L, Meroni R, Zagato L, Zangrillo A, Alfieri O, Fontana S, Macrina L, Delli Carpini S, Messaggio E, Brioni E, Dell'Antonio G, Manunta P, Hamlyn JM, Simonini M.

Am J Kidney Dis. 2019 Apr;73(4):504-512. doi: 10.1053/j.ajkd.2018.10.012. Epub 2019 Jan 16.

4.

The TRPC6 intronic polymorphism, associated with the risk of neurological disorders in systemic lupus erythematous, influences immune cell function.

Ramirez GA, Coletto LA, Bozzolo EP, Citterio L, Delli Carpini S, Zagato L, Rovere-Querini P, Lanzani C, Manunta P, Manfredi AA, Sciorati C.

J Neuroimmunol. 2018 Dec 15;325:43-53. doi: 10.1016/j.jneuroim.2018.10.010. Epub 2018 Oct 23.

PMID:
30384327
5.

PEAR1 is not a major susceptibility gene for cardiovascular disease in a Flemish population.

Yang WY, Petit T, Cauwenberghs N, Zhang ZY, Sheng CS, Thijs L, Salvi E, Izzi B, Vandenbriele C, Wei FF, Gu YM, Jacobs L, Citterio L, Delli Carpini S, Barlassina C, Cusi D, Hoylaerts MF, Verhamme P, Kuznetsova T, Staessen JA.

BMC Med Genet. 2017 Apr 27;18(1):45. doi: 10.1186/s12881-017-0411-x.

6.

Genetic susceptibility variants for lung cancer: replication study and assessment as expression quantitative trait loci.

Pintarelli G, Cotroneo CE, Noci S, Dugo M, Galvan A, Delli Carpini S, Citterio L, Manunta P, Incarbone M, Tosi D, Santambrogio L, Dragani TA, Colombo F.

Sci Rep. 2017 Feb 9;7:42185. doi: 10.1038/srep42185.

7.

Genetics of ion homeostasis in Ménière's Disease.

Teggi R, Zagato L, Delli Carpini S, Citterio L, Cassandro C, Albera R, Yang WY, Staessen JA, Bussi M, Manunta P, Lanzani C.

Eur Arch Otorhinolaryngol. 2017 Feb;274(2):757-763. doi: 10.1007/s00405-016-4375-9. Epub 2016 Nov 11.

PMID:
27837419
8.

Quantitative proteomics reveals novel therapeutic and diagnostic markers in hypertension.

Matafora V, Zagato L, Ferrandi M, Molinari I, Zerbini G, Casamassima N, Lanzani C, Delli Carpini S, Trepiccione F, Manunta P, Bachi A, Capasso G.

BBA Clin. 2014 Oct 22;2:79-87. doi: 10.1016/j.bbacli.2014.10.001. eCollection 2014 Dec.

9.

Lanosterol Synthase Gene Polymorphisms and Changes in Endogenous Ouabain in the Response to Low Sodium Intake.

Lanzani C, Gatti G, Citterio L, Messaggio E, Delli Carpini S, Simonini M, Casamassima N, Zagato L, Brioni E, Hamlyn JM, Manunta P.

Hypertension. 2016 Feb;67(2):342-8. doi: 10.1161/HYPERTENSIONAHA.115.06415. Epub 2015 Dec 14.

10.

Coronary risk in relation to genetic variation in MEOX2 and TCF15 in a Flemish population.

Yang WY, Petit T, Thijs L, Zhang ZY, Jacobs L, Hara A, Wei FF, Salvi E, Citterio L, Delli Carpini S, Gu YM, Knez J, Cauwenberghs N, Barcella M, Barlassina C, Manunta P, Coppiello G, Aranguren XL, Kuznetsova T, Cusi D, Verhamme P, Luttun A, Staessen JA.

BMC Genet. 2015 Oct 1;16:116. doi: 10.1186/s12863-015-0272-2.

11.

Left ventricular radial function associated with genetic variation in the cGMP-dependent protein kinase.

Kuznetsova T, Citterio L, Zagato L, Delli Carpini S, Thijs L, Casamassima N, D'hooge J, Bianchi G, Manunta P, Staessen JA.

Hypertension. 2013 Dec;62(6):1034-9. doi: 10.1161/HYPERTENSIONAHA.113.01630. Epub 2013 Sep 23.

PMID:
24060898
12.

cGMP-dependent protein kinase 1 polymorphisms underlie renal sodium handling impairment.

Citterio L, Ferrandi M, Delli Carpini S, Simonini M, Kuznetsova T, Molinari I, Dell' Antonio G, Lanzani C, Merlino L, Brioni E, Staessen JA, Bianchi G, Manunta P.

Hypertension. 2013 Dec;62(6):1027-33. doi: 10.1161/HYPERTENSIONAHA.113.01628. Epub 2013 Sep 23.

PMID:
24060892
13.

Genes involved in vasoconstriction and vasodilation system affect salt-sensitive hypertension.

Citterio L, Simonini M, Zagato L, Salvi E, Delli Carpini S, Lanzani C, Messaggio E, Casamassima N, Frau F, D'Avila F, Cusi D, Barlassina C, Manunta P.

PLoS One. 2011 May 9;6(5):e19620. doi: 10.1371/journal.pone.0019620.

14.

Endogenous ouabain in Ménière's disease.

Teggi R, Zagato L, Delli Carpini S, Messaggio E, Casamassima N, Lanzani C, Manunta P, Bussi M.

Otol Neurotol. 2010 Jan;31(1):153-6. doi: 10.1097/MAO.0b013e3181c0eaba.

PMID:
19887986
15.

Gly460Trp alpha-adducin mutation as a possible mechanism leading to endolymphatic hydrops in Ménière's syndrome.

Teggi R, Lanzani C, Zagato L, Delli Carpini S, Manunta P, Bianchi G, Bussi M.

Otol Neurotol. 2008 Sep;29(6):824-8. doi: 10.1097/MAO.0b013e318180a4b1.

PMID:
18667944
16.

Physiological interaction between alpha-adducin and WNK1-NEDD4L pathways on sodium-related blood pressure regulation.

Manunta P, Lavery G, Lanzani C, Braund PS, Simonini M, Bodycote C, Zagato L, Delli Carpini S, Tantardini C, Brioni E, Bianchi G, Samani NJ.

Hypertension. 2008 Aug;52(2):366-72. doi: 10.1161/HYPERTENSIONAHA.108.113977. Epub 2008 Jun 30.

PMID:
18591455

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