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Items: 4

1.

Copper deficiency presenting as metabolic bone disease in extremely low birth weight, short-gut infants.

Marquardt ML, Done SL, Sandrock M, Berdon WE, Feldman KW.

Pediatrics. 2012 Sep;130(3):e695-8. doi: 10.1542/peds.2011-1295. Epub 2012 Aug 6.

PMID:
22869833
2.

Electrocardiographic changes and arrhythmias following percutaneous atrial septal defect and patent foramen ovale device closure.

Johnson JN, Marquardt ML, Ackerman MJ, Asirvatham SJ, Reeder GS, Cabalka AK, Cetta F, Hagler DJ.

Catheter Cardiovasc Interv. 2011 Aug 1;78(2):254-61. doi: 10.1002/ccd.23028. Epub 2011 May 11.

PMID:
21563292
3.

Molecular and functional characterization of novel hypertrophic cardiomyopathy susceptibility mutations in TNNC1-encoded troponin C.

Landstrom AP, Parvatiyar MS, Pinto JR, Marquardt ML, Bos JM, Tester DJ, Ommen SR, Potter JD, Ackerman MJ.

J Mol Cell Cardiol. 2008 Aug;45(2):281-8. doi: 10.1016/j.yjmcc.2008.05.003. Epub 2008 May 11.

4.

Mutation of an A-kinase-anchoring protein causes long-QT syndrome.

Chen L, Marquardt ML, Tester DJ, Sampson KJ, Ackerman MJ, Kass RS.

Proc Natl Acad Sci U S A. 2007 Dec 26;104(52):20990-5. Epub 2007 Dec 19.

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