Michels V - Search Results

1

Michels V Jr, Trevisol DJ. Michels V Jr, et al. Crit Care. 2019 Mar 13;23(1):90. doi: 10.1186/s13054-018-2218-3. Crit Care. 2019. PMID: 30867012 Free PMC article. No abstract available.

2

[Scorbut, historic disease ?].

Schweich M, De VA, Sacré F, Bernard V, Michels V. Schweich M, et al. Among authors: michels v. Rev Med Liege. 2018 Nov;73(11):541-543. Rev Med Liege. 2018. PMID: 30431241 Free article. French.

3

Supporting close others' growth after trauma: The role of responsiveness in romantic partners' mutual posttraumatic growth.

Canevello A, Michels V, Hilaire N. Canevello A, et al. Among authors: michels v. Psychol Trauma. 2016 May;8(3):334-342. doi: 10.1037/tra0000084. Epub 2015 Sep 21. Psychol Trauma. 2016. PMID: 26390112

4

TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy.

Theis JL, Zimmermann MT, Larsen BT, Rybakova IN, Long PA, Evans JM, Middha S, de Andrade M, Moss RL, Wieben ED, Michels VV, Olson TM. Theis JL, et al. Among authors: michels vv. Hum Mol Genet. 2014 Nov 1;23(21):5793-804. doi: 10.1093/hmg/ddu297. Epub 2014 Jun 11. Hum Mol Genet. 2014. PMID: 24925317 Free PMC article.

5

Similarity of geleophysic dysplasia and Weill-Marchesani syndrome.

Kochhar A, Kirmani S, Cetta F, Younge B, Hyland JC, Michels V. Kochhar A, et al. Among authors: michels v. Am J Med Genet A. 2013 Dec;161A(12):3130-2. doi: 10.1002/ajmg.a.36147. Epub 2013 Sep 24. Am J Med Genet A. 2013. PMID: 24214363

6

INCASE: accomplishments and challenges.

Michels V. Michels V. Subst Abus. 2013;34(4):342-3. doi: 10.1080/08897077.2013.826615. Subst Abus. 2013. PMID: 24159903 No abstract available.

7

Aripiprazole and trazodone cause elevations of 7-dehydrocholesterol in the absence of Smith-Lemli-Opitz Syndrome.

Hall P, Michels V, Gavrilov D, Matern D, Oglesbee D, Raymond K, Rinaldo P, Tortorelli S. Hall P, et al. Among authors: michels v. Mol Genet Metab. 2013 Sep-Oct;110(1-2):176-8. doi: 10.1016/j.ymgme.2013.04.004. Epub 2013 Apr 10. Mol Genet Metab. 2013. PMID: 23628460

8

Homozygosity mapping and exome sequencing reveal GATAD1 mutation in autosomal recessive dilated cardiomyopathy.

Theis JL, Sharpe KM, Matsumoto ME, Chai HS, Nair AA, Theis JD, de Andrade M, Wieben ED, Michels VV, Olson TM. Theis JL, et al. Among authors: michels vv. Circ Cardiovasc Genet. 2011 Dec;4(6):585-94. doi: 10.1161/CIRCGENETICS.111.961052. Epub 2011 Sep 30. Circ Cardiovasc Genet. 2011. PMID: 21965549 Free PMC article.

9

Mutations in ribonucleic acid binding protein gene cause familial dilated cardiomyopathy.

Brauch KM, Karst ML, Herron KJ, de Andrade M, Pellikka PA, Rodeheffer RJ, Michels VV, Olson TM. Brauch KM, et al. Among authors: michels vv. J Am Coll Cardiol. 2009 Sep 1;54(10):930-41. doi: 10.1016/j.jacc.2009.05.038. J Am Coll Cardiol. 2009. PMID: 19712804 Free PMC article.

10

Cardiac troponin T mutation in familial cardiomyopathy with variable remodeling and restrictive physiology.

Menon SC, Michels VV, Pellikka PA, Ballew JD, Karst ML, Herron KJ, Nelson SM, Rodeheffer RJ, Olson TM. Menon SC, et al. Among authors: michels vv. Clin Genet. 2008 Nov;74(5):445-54. doi: 10.1111/j.1399-0004.2008.01062.x. Epub 2008 Jul 21. Clin Genet. 2008. PMID: 18651846 Free PMC article.

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