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Items: 1 to 20 of 31

1.

Mitochondrial Dysfunction in Aging and Diseases of Aging.

Haas RH.

Biology (Basel). 2019 Jun 17;8(2). pii: E48. doi: 10.3390/biology8020048.

2.

CoQ10 and Aging.

Barcelos IP, Haas RH.

Biology (Basel). 2019 May 11;8(2). pii: E28. doi: 10.3390/biology8020028. Review.

3.

Paroxysmal motor disorders: expanding phenotypes lead to coalescing genotypes.

Zima L, Ceulemans S, Reiner G, Galosi S, Chen D, Sahagian M, Haas RH, Hyland K, Friedman J.

Ann Clin Transl Neurol. 2018 Jul 17;5(8):996-1010. doi: 10.1002/acn3.597. eCollection 2018 Aug. Review.

4.

Endocrine Disorders in Primary Mitochondrial Disease.

Al-Gadi IS, Haas RH, Falk MJ, Goldstein A, McCormack SE.

J Endocr Soc. 2018 Feb 19;2(4):361-373. doi: 10.1210/js.2017-00434. eCollection 2018 Apr 1.

5.

Microwave ablation of focal hepatic malignancies regardless of size: A 9-year retrospective study of 64 patients.

Alexander ES, Wolf FJ, Machan JT, Charpentier KP, Beland MD, Iannuccilli JD, Haas RH, Dupuy DE.

Eur J Radiol. 2015 Jun;84(6):1083-90. doi: 10.1016/j.ejrad.2015.02.027. Epub 2015 Mar 14.

PMID:
25818732
6.

Platelet mitochondrial activity and pesticide exposure in early Parkinson's disease.

Bronstein JM, Paul K, Yang L, Haas RH, Shults CW, Le T, Ritz B.

Mov Disord. 2015 May;30(6):862-6. doi: 10.1002/mds.26164. Epub 2015 Mar 11.

7.

Assessing bioenergetic compromise in autism spectrum disorder with 31P magnetic resonance spectroscopy: preliminary report.

Golomb BA, Erickson LC, Scott-Van Zeeland AA, Koperski S, Haas RH, Wallace DC, Naviaux RK, Lincoln AJ, Reiner GE, Hamilton G.

J Child Neurol. 2014 Feb;29(2):187-93. doi: 10.1177/0883073813498466. Epub 2013 Oct 18.

8.

Orthostatic tremor, progressive external ophthalmoplegia, and Twinkle.

Milone M, Klassen BT, Landsverk ML, Haas RH, Wong LJ.

JAMA Neurol. 2013 Nov;70(11):1429-31. doi: 10.1001/jamaneurol.2013.3521.

PMID:
24061067
9.

Automated methods for the analysis of skeletal muscle fiber size and metabolic type.

Kostrominova TY, Reiner DS, Haas RH, Ingermanson R, McDonough PM.

Int Rev Cell Mol Biol. 2013;306:275-332. doi: 10.1016/B978-0-12-407694-5.00007-9. Review.

PMID:
24016528
10.

A seven-day study of the pharmacokinetics of intravenous levetiracetam in neonates: marked changes in pharmacokinetics occur during the first week of life.

Sharpe CM, Capparelli EV, Mower A, Farrell MJ, Soldin SJ, Haas RH.

Pediatr Res. 2012 Jul;72(1):43-9. doi: 10.1038/pr.2012.51. Epub 2012 Apr 11.

PMID:
22495532
11.

Effects of endotracheal intubation and surfactant on a 3-channel neonatal electroencephalogram.

Shangle CE, Haas RH, Vaida F, Rich WD, Finer NN.

J Pediatr. 2012 Aug;161(2):252-7. doi: 10.1016/j.jpeds.2012.02.014. Epub 2012 Mar 16.

12.

Quality improvement of mitochondrial respiratory chain complex enzyme assays using Caenorhabditis elegans.

Chen X, Thorburn DR, Wong LJ, Vladutiu GD, Haas RH, Le T, Hoppel C, Sedensky M, Morgan P, Hahn SH.

Genet Med. 2011 Sep;13(9):794-9. doi: 10.1097/GIM.0b013e31821afca5.

PMID:
21633293
13.

Fibroblast immuno-diagnosis of cytochrome oxidase (COX) deficiency in mitochondrial disease.

Du A, Naviaux RK, Le T, Xu C, Sommer SS, Haas RH.

Mitochondrion. 2011 May;11(3):430-6. doi: 10.1016/j.mito.2010.12.014. Epub 2010 Dec 25.

PMID:
21187165
14.

Platelet mitochondrial complex I and I+III activities do not correlate with cerebral mitochondrial oxidative metabolism.

Powers WJ, Haas RH, Le T, Videen TO, Markham J, Perlmutter JS.

J Cereb Blood Flow Metab. 2011 Jan;31(1):e1-5. doi: 10.1038/jcbfm.2010.179. Epub 2010 Oct 20.

15.

Autism and mitochondrial disease.

Haas RH.

Dev Disabil Res Rev. 2010;16(2):144-53. doi: 10.1002/ddrr.112. Review.

PMID:
20818729
16.

Determination of DNA mutation load in human tissues using denaturing HPLC-based heteroduplex analysis.

Lim KS, Naviaux RK, Haas RH.

Methods Mol Biol. 2009;554:287-99. doi: 10.1007/978-1-59745-521-3_18.

PMID:
19513681
17.

'Succinic semialdehyde dehydrogenase deficiency: phenotype evolution in an adolescent patient at 20-year follow-up'.

Crutchfield SR, Haas RH, Nyhan WL, Gibson KM.

Dev Med Child Neurol. 2008 Nov;50(11):880-1. doi: 10.1111/j.1469-8749.2008.03116.x. Epub 2008 Sep 20. No abstract available.

18.

Statin myopathy as a metabolic muscle disease.

Phillips PS, Haas RH.

Expert Rev Cardiovasc Ther. 2008 Aug;6(7):971-8. doi: 10.1586/14779072.6.7.971. Review.

PMID:
18666847
19.

Impact of nucleoside reverse transcriptase inhibitors on mitochondrial DNA and RNA in human skeletal muscle cells.

Saitoh A, Haas RH, Naviaux RK, Salva NG, Wong JK, Spector SA.

Antimicrob Agents Chemother. 2008 Aug;52(8):2825-30. doi: 10.1128/AAC.00434-08. Epub 2008 Jun 9.

20.

The in-depth evaluation of suspected mitochondrial disease.

Mitochondrial Medicine Society's Committee on Diagnosis, Haas RH, Parikh S, Falk MJ, Saneto RP, Wolf NI, Darin N, Wong LJ, Cohen BH, Naviaux RK.

Mol Genet Metab. 2008 May;94(1):16-37. doi: 10.1016/j.ymgme.2007.11.018. Epub 2008 Feb 1. Review.

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