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Items: 1 to 50 of 151

1.

Weaning order of vasoactive drugs.

Michels V Jr, Trevisol DJ.

Crit Care. 2019 Mar 13;23(1):90. doi: 10.1186/s13054-018-2218-3. No abstract available.

2.

[Scorbut, historic disease ?]

Schweich M, De VA, Sacré F, Bernard V, Michels V.

Rev Med Liege. 2018 Nov;73(11):541-543. French.

PMID:
30431241
3.

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

Canevello A, Michels V, Hilaire N.

Psychol Trauma. 2016 May;8(3):334-342. doi: 10.1037/tra0000084. Epub 2015 Sep 21.

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.

Hum Mol Genet. 2014 Nov 1;23(21):5793-804. doi: 10.1093/hmg/ddu297. Epub 2014 Jun 11.

5.

Similarity of geleophysic dysplasia and Weill-Marchesani syndrome.

Kochhar A, Kirmani S, Cetta F, Younge B, Hyland JC, Michels V.

Am J Med Genet A. 2013 Dec;161A(12):3130-2. doi: 10.1002/ajmg.a.36147. Epub 2013 Sep 24.

PMID:
24214363
6.

INCASE: accomplishments and challenges.

Michels V.

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

PMID:
24159903
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.

Mol Genet Metab. 2013 Sep-Oct;110(1-2):176-8. doi: 10.1016/j.ymgme.2013.04.004. Epub 2013 Apr 10.

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.

Circ Cardiovasc Genet. 2011 Dec;4(6):585-94. doi: 10.1161/CIRCGENETICS.111.961052. Epub 2011 Sep 30.

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.

J Am Coll Cardiol. 2009 Sep 1;54(10):930-41. doi: 10.1016/j.jacc.2009.05.038.

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.

Clin Genet. 2008 Nov;74(5):445-54. doi: 10.1111/j.1399-0004.2008.01062.x. Epub 2008 Jul 21.

11.

A multicentre, prospective study to evaluate costs of septic patients in Brazilian intensive care units.

Sogayar AM, Machado FR, Rea-Neto A, Dornas A, Grion CM, Lobo SM, Tura BR, Silva CL, Cal RG, Beer I, Michels V, Safi J, Kayath M, Silva E; Costs Study Group - Latin American Sepsis Institute.

Pharmacoeconomics. 2008;26(5):425-34.

PMID:
18429658
12.

[Clinical case of the month. Hepatitis B reactivation in an Ag HBs negative patient].

Michels V, Bastens B, Delforge M, Demoulin JC, Sente JM, Plomteux O, Dupont P, Fontaine F.

Rev Med Liege. 2007 Mar;62(3):135-8. French.

13.

Delineation of the cryptic 1qter deletion phenotype.

Merritt JL 2nd, Zou Y, Jalal SM, Michels VV.

Am J Med Genet A. 2007 Mar 15;143A(6):599-603.

PMID:
17304549
14.

Phase II trial of pirfenidone in adults with neurofibromatosis type 1.

Babovic-Vuksanovic D, Ballman K, Michels V, McGrann P, Lindor N, King B, Camp J, Micic V, Babovic N, Carrero X, Spinner R, O'Neill B.

Neurology. 2006 Nov 28;67(10):1860-2. Epub 2006 Oct 11.

PMID:
17035676
15.

Mosaic ring 20 with no detectable deletion by FISH analysis: Characteristic seizure disorder and literature review.

Zou YS, Van Dyke DL, Thorland EC, Chhabra HS, Michels VV, Keefe JG, Lega MA, Feely MA, Uphoff TS, Jalal SM.

Am J Med Genet A. 2006 Aug 1;140(15):1696-706.

PMID:
16835934
16.

A boy with fever and whorl keratopathy.

Halligan C, Heese BA, Mellor G, Michels VV, Reed A.

J Rheumatol. 2006 Jun;33(6):1210-1. No abstract available.

PMID:
16755678
17.

Does expectancy affect alcohol absorption?

Cole-Harding S, Michels VJ.

Addict Behav. 2007 Jan;32(1):194-8. Epub 2006 May 18.

PMID:
16713125
18.

Usual interstitial pneumonia complicating dyskeratosis congenita.

Utz JP, Ryu JH, Myers JL, Michels VV.

Mayo Clin Proc. 2005 Jun;80(6):817-21.

PMID:
15945534
19.

Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies.

Beauchesne LM, Warnes CA, Connolly HM, Ammash NM, Grogan M, Jalal SM, Michels VV.

J Am Coll Cardiol. 2005 Feb 15;45(4):595-8.

20.

Sodium channel mutations and susceptibility to heart failure and atrial fibrillation.

Olson TM, Michels VV, Ballew JD, Reyna SP, Karst ML, Herron KJ, Horton SC, Rodeheffer RJ, Anderson JL.

JAMA. 2005 Jan 26;293(4):447-54.

21.

Genetic testing: practical, ethical, and counseling considerations.

Ensenauer RE, Michels VV, Reinke SS.

Mayo Clin Proc. 2005 Jan;80(1):63-73. Review.

PMID:
15667031
22.

Mitochondrial causes of renal insufficiency and hearing loss.

Ireland J, Rossetti S, Haugen E, Ireland J, Michels V, Harris P.

Kidney Int. 2004 Jun;65(6):2444-5. No abstract available.

23.

[Clinical case of the month. Adult onset Still's disease: a rare cause of acute febrile hepatitis].

Michels V, Delwaide J, Vermeulen P, Kaye O, Demolin H, Van Severen M, Belaïche J.

Rev Med Liege. 2003 Dec;58(12):729-33. French.

24.

Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients.

Ensenauer RE, Adeyinka A, Flynn HC, Michels VV, Lindor NM, Dawson DB, Thorland EC, Lorentz CP, Goldstein JL, McDonald MT, Smith WE, Simon-Fayard E, Alexander AA, Kulharya AS, Ketterling RP, Clark RD, Jalal SM.

Am J Hum Genet. 2003 Nov;73(5):1027-40. Epub 2003 Oct 2.

25.

Progression of familial and non-familial dilated cardiomyopathy: long term follow up.

Michels VV, Driscoll DJ, Miller FA, Olson TM, Atkinson EJ, Olswold CL, Schaid DJ.

Heart. 2003 Jul;89(7):757-61.

26.

Frequency of development of idiopathic dilated cardiomyopathy among relatives of patients with idiopathic dilated cardiomyopathy.

Michels VV, Olson TM, Miller FA, Ballman KV, Rosales AG, Driscoll DJ.

Am J Cardiol. 2003 Jun 1;91(11):1389-92. No abstract available.

PMID:
12767445
27.

Left ventricular function in the Marfan syndrome without significant valvular regurgitation.

Chatrath R, Beauchesne LM, Connolly HM, Michels VV, Driscoll DJ.

Am J Cardiol. 2003 Apr 1;91(7):914-6. No abstract available.

PMID:
12667591
28.

Utility of subtelomeric fluorescent DNA probes for detection of chromosome anomalies in 425 patients.

Jalal SM, Harwood AR, Sekhon GS, Pham Lorentz C, Ketterling RP, Babovic-Vuksanovic D, Meyer RG, Ensenauer R, Anderson MH Jr, Michels VV.

Genet Med. 2003 Jan-Feb;5(1):28-34.

PMID:
12544473
29.

Familial frontotemporal dementia associated with a novel presenilin-1 mutation.

Tang-Wai D, Lewis P, Boeve B, Hutton M, Golde T, Baker M, Hardy J, Michels V, Ivnik R, Jack C, Petersen R.

Dement Geriatr Cogn Disord. 2002;14(1):13-21.

PMID:
12053127
30.

Pheochromocytomas and paragangliomas in von Hippel-Lindau disease: a role for laparoscopic and cortical-sparing surgery.

Baghai M, Thompson GB, Young WF Jr, Grant CS, Michels VV, van Heerden JA.

Arch Surg. 2002 Jun;137(6):682-8; discussion 688-9.

PMID:
12049539
31.

The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomas.

Cunningham JM, Kim CY, Christensen ER, Tester DJ, Parc Y, Burgart LJ, Halling KC, McDonnell SK, Schaid DJ, Walsh Vockley C, Kubly V, Nelson H, Michels VV, Thibodeau SN.

Am J Hum Genet. 2001 Oct;69(4):780-90. Epub 2001 Aug 24. Erratum in: Am J Hum Genet 2001 Nov;69(5):1160.

32.

Characteristics of two cases with dup(15)(q11.2-q12): one of maternal and one of paternal origin.

Mao R, Jalal SM, Snow K, Michels VV, Szabo SM, Babovic-Vuksanovic D.

Genet Med. 2000 Mar-Apr;2(2):131-5. Review.

PMID:
11397326
33.

Novel mutations and the emergence of a common mutation in the SDHD gene causing familial paraganglioma.

Milunsky JM, Maher TA, Michels VV, Milunsky A.

Am J Med Genet. 2001 May 15;100(4):311-4.

PMID:
11343322
34.

Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy.

Olson TM, Kishimoto NY, Whitby FG, Michels VV.

J Mol Cell Cardiol. 2001 Apr;33(4):723-32.

PMID:
11273725
35.

Isolated supravalvular aortic stenosis: functional haploinsufficiency of the elastin gene as a result of nonsense-mediated decay.

Urbán Z, Michels VV, Thibodeau SN, Davis EC, Bonnefont JP, Munnich A, Eyskens B, Gewillig M, Devriendt K, Boyd CD.

Hum Genet. 2000 Jun;106(6):577-88.

PMID:
10942104
36.

von Hippel-Lindau disease.

Couch V, Lindor NM, Karnes PS, Michels VV.

Mayo Clin Proc. 2000 Mar;75(3):265-72. Review.

PMID:
10725953
37.

Inherited interstitial deletion of chromosomes 5p and 16q without apparent phenotypic effect: further confirmation.

Hand JL, Michels VV, Marinello MJ, Ketterling RP, Jalal SM.

Prenat Diagn. 2000 Feb;20(2):144-8; discussion 149-51.

PMID:
10694687
38.

Severe hypoglycemia as a presenting symptom of carbohydrate-deficient glycoprotein syndrome.

Babovic-Vuksanovic D, Patterson MC, Schwenk WF, O'Brien JF, Vockley J, Freeze HH, Mehta DP, Michels VV.

J Pediatr. 1999 Dec;135(6):775-81.

PMID:
10586187
39.

Refined gene localization for MRX7.

Tackels D, Schwartz CE, Thibodeau SN, Michels VV.

Am J Med Genet. 1999 Jul 30;85(3):288-9. No abstract available.

PMID:
10398245
40.

Guidelines for buccal smear collection in breast-fed infants.

Babovic-Vuksanovic D, Michels VV, Law ME, Bailey R, Wyatt WA, Lindor NM, Jalal SM.

Am J Med Genet. 1999 Jun 4;84(4):357-60.

PMID:
10340651
41.

Supravalvular aortic stenosis: a splice site mutation within the elastin gene results in reduced expression of two aberrantly spliced transcripts.

Urbán Z, Michels VV, Thibodeau SN, Donis-Keller H, Csiszár K, Boyd CD.

Hum Genet. 1999 Feb;104(2):135-42.

PMID:
10190324
42.

Childhood-onset schizophrenia associated with parkinsonism in a patient with a microdeletion of chromosome 22.

Krahn LE, Maraganore DM, Michels VV.

Mayo Clin Proc. 1998 Oct;73(10):956-9.

PMID:
9787744
43.

Spinocerebellar ataxia type 2 (SCA 2) in an infant with extreme CAG repeat expansion.

Babovic-Vuksanovic D, Snow K, Patterson MC, Michels VV.

Am J Med Genet. 1998 Oct 12;79(5):383-7.

PMID:
9779806
44.

A novel mutation in KVLQT1 is the molecular basis of inherited long QT syndrome in a near-drowning patient's family.

Ackerman MJ, Schroeder JJ, Berry R, Schaid DJ, Porter CJ, Michels VV, Thibodeau SN.

Pediatr Res. 1998 Aug;44(2):148-53.

PMID:
9702906
45.

Maternal cell contamination of buccal smear samples in nursing neonates.

Babovic-Vuksanovic D, Michels VV, Law ME, Lindor NM, Jalal SM.

Clin Genet. 1998 Feb;53(2):114-8.

PMID:
9611071
46.

Actin mutations in dilated cardiomyopathy, a heritable form of heart failure.

Olson TM, Michels VV, Thibodeau SN, Tai YS, Keating MT.

Science. 1998 May 1;280(5364):750-2.

47.

Heritable connective tissue disorders in cervical artery dissections: a prospective study.

Schievink WI, Wijdicks EF, Michels VV, Vockley J, Godfrey M.

Neurology. 1998 Apr;50(4):1166-9.

PMID:
9566419
48.

Microsatellite instability in colorectal cancer: different mutator phenotypes and the principal involvement of hMLH1.

Thibodeau SN, French AJ, Cunningham JM, Tester D, Burgart LJ, Roche PC, McDonnell SK, Schaid DJ, Vockley CW, Michels VV, Farr GH Jr, O'Connell MJ.

Cancer Res. 1998 Apr 15;58(8):1713-8.

49.

Intracranial aneurysms in Marfan's syndrome: an autopsy study.

Schievink WI, Parisi JE, Piepgras DG, Michels VV.

Neurosurgery. 1997 Oct;41(4):866-70; discussion 871.

PMID:
9316048
50.

Familial paragangliomas: linkage to chromosome 11q23 and clinical implications.

Milunsky J, DeStefano AL, Huang XL, Baldwin CT, Michels VV, Jako G, Milunsky A.

Am J Med Genet. 1997 Oct 3;72(1):66-70.

PMID:
9295078

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