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Results 1 - 10 of 17 for Ackerman syndrome
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  1. Ankyrin-B syndrome 
    ... 2014 Sep 30. Citation on PubMed Tester DJ, Ackerman MJ. Genetics of long QT syndrome. Methodist Debakey Cardiovasc J. 2014 Jan-Mar;10( ...
    https://medlineplus.gov/genetics/condition/ankyrin-b-syndrome - Genetics
  2. Romano-Ward syndrome 
    ... or Free article on PubMed Central Tester DJ, Ackerman MJ. Genetics of long QT syndrome. Methodist Debakey Cardiovasc J. 2014 Jan-Mar;10( ...
    https://medlineplus.gov/genetics/condition/romano-ward-syndrome - Genetics
  3. ANK2 gene 
    ... article on PubMed Central Sherman J, Tester DJ, Ackerman MJ. Targeted mutational analysis of ankyrin-B in 541 consecutive, unrelated patients referred for long QT syndrome genetic testing and 200 healthy subjects. Heart Rhythm. ...
    https://medlineplus.gov/genetics/gene/ank2 - Genetics
  4. RAF1 gene 
    ... Torrente I, Marino B, Digilio MC, Zampino G, Ackerman MJ, Dallapiccola B, Tartaglia M, Gelb BD. Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy. Nat Genet. 2007 Aug;39( ...
    https://medlineplus.gov/genetics/gene/raf1 - Genetics
  5. SCN5A gene 
    ... Guicheney P, Wilde AA, Brugada R, Schott JJ, Ackerman MJ. An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing. Heart Rhythm. 2010 Jan;7(1): ...
    https://medlineplus.gov/genetics/gene/scn5a - Genetics
  6. Brugada syndrome 
    ... Simone S, Will ML, Dagradi F, Schwartz PJ, Ackerman MJ. Spectrum and prevalence of mutations involving BrS1- through BrS12-susceptibility genes in a cohort of unrelated patients referred for Brugada syndrome genetic testing: implications for genetic testing. J Am ...
    https://medlineplus.gov/genetics/condition/brugada-syndrome - Genetics
  7. CAV3 gene 
    ... or Free article on PubMed Central Vatta M, Ackerman MJ, Ye ... is associated with long-QT syndrome. Circulation. 2006 Nov 14;114(20):2104-12. ...
    https://medlineplus.gov/genetics/gene/cav3 - Genetics
  8. Familial dilated cardiomyopathy 
    ... DILATED, 1II; CMD1II CARDIOMYOPATHY, DILATED, 1BB; CMD1BB PubMed Ackerman MJ, Priori SG, Willems S, Berul C, Brugada ... M, Di Lenarda A, Sinagra G, Bos JM, Ackerman MJ, Mitchell RN, Murry CE, Lakdawala NK, Ho ...
    https://medlineplus.gov/.../familial-dilated-cardiomyopathy - Genetics
  9. GJA1 gene 
    ... Srinivas M, Tester DJ, Saffitz JE, Duffy HS, Ackerman MJ. Connexin43 mutation causes heterogeneous gap junction loss ... as a cause of keratoderma-hypotrichosis-leukonychia totalis syndrome. Hum Mol Genet. 2015 Jan 1;24(1): ...
    https://medlineplus.gov/genetics/gene/gja1 - Genetics
  10. NOTCH1 gene 
    ... McKellar SH, Tester DJ, Yagubyan M, Majumdar R, Ackerman MJ, Sundt TM 3rd. Novel NOTCH1 mutations in ... NOTCH1 Receptor as a Cause of Adams-Oliver Syndrome With Variable Cardiac Anomalies. Circ Cardiovasc Genet. 2015 ...
    https://medlineplus.gov/genetics/gene/notch1 - Genetics
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