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    Results: 1 to 20 of 27

    1.

    Polyuric-polydipsic syndrome in a pediatric case of non-glucocorticoid remediable familial hyperaldosteronism.

    Mussa A, Camilla R, Monticone S, Porta F, Tessaris D, Verna F, Mulatero P, Einaudi S.

    Endocr J. 2012 Jun 30;59(6):497-502. Epub 2012 Mar 11.

    PMID:
    22447138
    [PubMed - indexed for MEDLINE]
    Free Article
    2.

    The genetic basis of primary aldosteronism.

    Funder JW.

    Curr Hypertens Rep. 2012 Apr;14(2):120-4. doi: 10.1007/s11906-012-0255-x. Review.

    PMID:
    22359160
    [PubMed - indexed for MEDLINE]
    3.

    The prevalence of familial hyperaldosteronism in apparently sporadic primary aldosteronism in Germany: a single center experience.

    Pallauf A, Schirpenbach C, Zwermann O, Fischer E, Morak M, Holinski-Feder E, Hofbauer L, Beuschlein F, Reincke M.

    Horm Metab Res. 2012 Mar;44(3):215-20. doi: 10.1055/s-0031-1299730. Epub 2012 Jan 24.

    PMID:
    22274719
    [PubMed - indexed for MEDLINE]
    4.

    KCNJ5 mutations in European families with nonglucocorticoid remediable familial hyperaldosteronism.

    Mulatero P, Tauber P, Zennaro MC, Monticone S, Lang K, Beuschlein F, Fischer E, Tizzani D, Pallauf A, Viola A, Amar L, Williams TA, Strom TM, Graf E, Bandulik S, Penton D, Plouin PF, Warth R, Allolio B, Jeunemaitre X, Veglio F, Reincke M.

    Hypertension. 2012 Feb;59(2):235-40. doi: 10.1161/HYPERTENSIONAHA.111.183996. Epub 2011 Dec 27.

    PMID:
    22203740
    [PubMed - indexed for MEDLINE]
    Free Article
    5.

    A new presentation of the chimeric CYP11B1/CYP11B2 gene with low prevalence of primary aldosteronism and atypical gene segregation pattern.

    Carvajal CA, Campino C, Martinez-Aguayo A, Tichauer JE, Bancalari R, Valdivia C, Trejo P, Aglony M, Baudrand R, Lagos CF, Mellado C, Garcia H, Fardella CE.

    Hypertension. 2012 Jan;59(1):85-91. doi: 10.1161/HYPERTENSIONAHA.111.180513. Epub 2011 Nov 14.

    PMID:
    22083159
    [PubMed - indexed for MEDLINE]
    Free Article
    6.

    Prevalence and characteristics of familial hyperaldosteronism: the PATOGEN study (Primary Aldosteronism in TOrino-GENetic forms).

    Mulatero P, Tizzani D, Viola A, Bertello C, Monticone S, Mengozzi G, Schiavone D, Williams TA, Einaudi S, La Grotta A, Rabbia F, Veglio F.

    Hypertension. 2011 Nov;58(5):797-803. doi: 10.1161/HYPERTENSIONAHA.111.175083. Epub 2011 Aug 29.

    PMID:
    21876069
    [PubMed - indexed for MEDLINE]
    Free Article
    7.

    Familial or genetic primary aldosteronism and Gordon syndrome.

    Stowasser M, Pimenta E, Gordon RD.

    Endocrinol Metab Clin North Am. 2011 Jun;40(2):343-68, viii. doi: 10.1016/j.ecl.2011.01.007.

    PMID:
    21565671
    [PubMed - indexed for MEDLINE]
    8.

    Is familial hyperaldosteronism underdiagnosed in hypertensive children?

    Mulatero P, Williams TA, Monticone S, Veglio F.

    Hypertension. 2011 Jun;57(6):1053-5. doi: 10.1161/HYPERTENSIONAHA.111.172916. Epub 2011 Apr 18. No abstract available.

    PMID:
    21502569
    [PubMed - indexed for MEDLINE]
    Free Article
    9.

    Frequency of familial hyperaldosteronism type 1 in a hypertensive pediatric population: clinical and biochemical presentation.

    Aglony M, Martínez-Aguayo A, Carvajal CA, Campino C, García H, Bancalari R, Bolte L, Avalos C, Loureiro C, Trejo P, Brinkmann K, Giadrosich V, Mericq V, Rocha A, Avila A, Perez V, Inostroza A, Fardella CE.

    Hypertension. 2011 Jun;57(6):1117-21. doi: 10.1161/HYPERTENSIONAHA.110.168740. Epub 2011 Apr 18.

    PMID:
    21502562
    [PubMed - indexed for MEDLINE]
    Free Article
    10.

    Further study of chromosome 7p22 to identify the molecular basis of familial hyperaldosteronism type II.

    Carss KJ, Stowasser M, Gordon RD, O'Shaughnessy KM.

    J Hum Hypertens. 2011 Sep;25(9):560-4. doi: 10.1038/jhh.2010.93. Epub 2010 Oct 7.

    PMID:
    20927129
    [PubMed - indexed for MEDLINE]
    11.

    A mother/daughter case of familial hyperaldosteronism.

    Somekh NN, Finkielstein D.

    Clin Cardiol. 2010 Dec;33(12):E68-9. doi: 10.1002/clc.20654. Epub 2010 Sep 23. No abstract available.

    PMID:
    20865750
    [PubMed - indexed for MEDLINE]
    12.

    A de novo unequal cross-over mutation between CYP11B1 and CYP11B2 genes causes familial hyperaldosteronism type I.

    Carvajal CA, Stehr CB, González PA, Riquelme EM, Montero T, Santos MJ, Kalergis AM, Fardella CE.

    J Endocrinol Invest. 2011 Feb;34(2):140-4. doi: 10.3275/7171. Epub 2010 Jul 13.

    PMID:
    20634641
    [PubMed - indexed for MEDLINE]
    13.

    Familial hyperaldosteronism I-III.

    Quack I, Vonend O, Rump LC.

    Horm Metab Res. 2010 Jun;42(6):424-8. doi: 10.1055/s-0029-1246187. Epub 2010 Feb 3. Review.

    PMID:
    20131203
    [PubMed - indexed for MEDLINE]
    14.

    Familial hyperaldosteronism type 1 in pregnancy.

    Hamilton E, O'Callaghan C, O'Brien RM, Stowasser M, Gordon R, Zajac J, Grossmann M.

    Intern Med J. 2009 Feb;39(2):135-6. doi: 10.1111/j.1445-5994.2008.01869.x. No abstract available.

    PMID:
    19356193
    [PubMed - indexed for MEDLINE]
    15.

    Elevated serum interleukin 6 levels in normotensive individuals with familial hyperaldosteronism type 1.

    Staermose S, Marwick TH, Gordon RD, Cowley D, Dowling A, Stowasser M.

    Hypertension. 2009 Apr;53(4):e31-2. doi: 10.1161/HYPERTENSIONAHA.108.128512. Epub 2009 Feb 16. No abstract available.

    PMID:
    19221206
    [PubMed - indexed for MEDLINE]
    Free Article
    16.

    A new form of hereditary primary aldosteronism: familial hyperaldosteronism type III.

    Mulatero P.

    J Clin Endocrinol Metab. 2008 Aug;93(8):2972-4. doi: 10.1210/jc.2008-1241. No abstract available.

    PMID:
    18685118
    [PubMed - indexed for MEDLINE]
    Free Article
    17.

    Further evidence for linkage of familial hyperaldosteronism type II at chromosome 7p22 in Italian as well as Australian and South American families.

    Sukor N, Mulatero P, Gordon RD, So A, Duffy D, Bertello C, Kelemen L, Jeske Y, Veglio F, Stowasser M.

    J Hypertens. 2008 Aug;26(8):1577-82. doi: 10.1097/HJH.0b013e3283028352.

    PMID:
    18622235
    [PubMed - indexed for MEDLINE]
    18.

    Examination of chromosome 7p22 candidate genes RBaK, PMS2 and GNA12 in familial hyperaldosteronism type II.

    Jeske YW, So A, Kelemen L, Sukor N, Willys C, Bulmer B, Gordon RD, Duffy D, Stowasser M.

    Clin Exp Pharmacol Physiol. 2008 Apr;35(4):380-5. doi: 10.1111/j.1440-1681.2008.04882.x.

    PMID:
    18307725
    [PubMed - indexed for MEDLINE]
    19.

    Detecting and treating primary aldosteronism: primary aldosteronism.

    Mantero F, Mattarello MJ, Albiger NM.

    Exp Clin Endocrinol Diabetes. 2007 Mar;115(3):171-4. Review.

    PMID:
    17427105
    [PubMed - indexed for MEDLINE]
    20.

    No evidence for coding region mutations in the retinoblastoma-associated Kruppel-associated box protein gene (RBaK) causing familial hyperaldosteronism type II.

    So A, Jeske YW, Gordon RD, Duffy D, Kelemen L, Stowasser M.

    Clin Endocrinol (Oxf). 2006 Dec;65(6):829-31. No abstract available.

    PMID:
    17121540
    [PubMed - indexed for MEDLINE]

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