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Items: 1 to 50 of 54

1.

mtDNA heteroplasmy level and copy number indicate disease burden in m.3243A>G mitochondrial disease.

Grady JP, Pickett SJ, Ng YS, Alston CL, Blakely EL, Hardy SA, Feeney CL, Bright AA, Schaefer AM, Gorman GS, McNally RJ, Taylor RW, Turnbull DM, McFarland R.

EMBO Mol Med. 2018 May 7. pii: e8262. doi: 10.15252/emmm.201708262. [Epub ahead of print]

2.

MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load.

Ng YS, Lax NZ, Maddison P, Alston CL, Blakely EL, Hepplewhite PD, Riordan G, Meldau S, Chinnery PF, Pierre G, Chronopoulou E, Du A, Hughes I, Morris AA, Kamakari S, Chrousos G, Rodenburg RJ, Saris CGJ, Feeney C, Hardy SA, Sakakibara T, Sudo A, Okazaki Y, Murayama K, Mundy H, Hanna MG, Ohtake A, Schaefer AM, Champion MP, Turnbull DM, Taylor RW, Pitceathly RDS, McFarland R, Gorman GS.

EBioMedicine. 2018 Apr;30:86-93. doi: 10.1016/j.ebiom.2018.02.010. Epub 2018 Feb 24.

3.

Disclosing the functional changes of two genetic alterations in a patient with Chronic Progressive External Ophthalmoplegia: Report of the novel mtDNA m.7486G>A variant.

Bacalhau M, Simões M, Rocha MC, Hardy SA, Vincent AE, Durães J, Macário MC, Santos MJ, Rebelo O, Lopes C, Pratas J, Mendes C, Zuzarte M, Rego AC, Girão H, Wong LC, Taylor RW, Grazina M.

Neuromuscul Disord. 2018 Apr;28(4):350-360. doi: 10.1016/j.nmd.2017.11.006. Epub 2017 Nov 23.

4.

Opening One's Eyes to Mosaicism in Progressive External Ophthalmoplegia.

Sommerville EW, Jones RL, Hardy SA, Blakely EL, Pyle A, Schaefer AM, Chinnery PF, Turnbull DM, Gorman GS, Taylor RW.

Neurol Genet. 2017 Dec 15;3(6):e202. doi: 10.1212/NXG.0000000000000202. eCollection 2017 Dec. No abstract available.

5.

Factor Structure of the Brief Comprehensive Effects of Alcohol Scale in Adolescents.

Ham LS, Zamboanga BL, Meca A, Blumenthal H, Hardy SA, Hurd LE.

Assessment. 2017 Mar 1:1073191117694454. doi: 10.1177/1073191117694454. [Epub ahead of print]

PMID:
29214852
6.

Neurologic Phenotypes Associated With Mutations in RTN4IP1 (OPA10) in Children and Young Adults.

Charif M, Nasca A, Thompson K, Gerber S, Makowski C, Mazaheri N, Bris C, Goudenège D, Legati A, Maroofian R, Shariati G, Lamantea E, Hopton S, Ardissone A, Moroni I, Giannotta M, Siegel C, Strom TM, Prokisch H, Vignal-Clermont C, Derrien S, Zanlonghi X, Kaplan J, Hamel CP, Leruez S, Procaccio V, Bonneau D, Reynier P, White FE, Hardy SA, Barbosa IA, Simpson MA, Vara R, Perdomo Trujillo Y, Galehdari H, Deshpande C, Haack TB, Rozet JM, Taylor RW, Ghezzi D, Amati-Bonneau P, Lenaers G.

JAMA Neurol. 2018 Jan 1;75(1):105-113. doi: 10.1001/jamaneurol.2017.2065.

PMID:
29181510
7.

The Processes and Mechanisms of Cardiac and Pulmonary Fibrosis.

Murtha LA, Schuliga MJ, Mabotuwana NS, Hardy SA, Waters DW, Burgess JK, Knight DA, Boyle AJ.

Front Physiol. 2017 Oct 12;8:777. doi: 10.3389/fphys.2017.00777. eCollection 2017. Review.

8.

Pigmentary retinopathy, rod-cone dysfunction and sensorineural deafness associated with a rare mitochondrial tRNALys (m.8340G>A) gene variant.

Gill JS, Hardy SA, Blakely EL, Hopton S, Nemeth AH, Fratter C, Poulton J, Taylor RW, Downes SM.

Br J Ophthalmol. 2017 Sep;101(9):1298-1302. doi: 10.1136/bjophthalmol-2017-310370. Epub 2017 Jul 20.

9.

Camptocormia and shuffling gait due to a novel MT-TV mutation: Diagnostic pitfalls.

Reimann J, Lehmann D, Hardy SA, Falkous G, Knowles CV, Jones RL, Kunz WS, Taylor RW, Kornblum C.

Neurol Genet. 2017 Apr 5;3(3):e147. doi: 10.1212/NXG.0000000000000147. eCollection 2017 Jun. No abstract available.

10.

Bidirectional relations between different forms of prosocial behaviors and substance use among female college student athletes.

Davis AN, Carlo G, Hardy SA, Olthuis JV, Zamboanga BL.

J Soc Psychol. 2017;157(6):645-657. doi: 10.1080/00224545.2016.1263596. Epub 2016 Dec 2.

PMID:
27911669
11.

Pathogenic variants in HTRA2 cause an early-onset mitochondrial syndrome associated with 3-methylglutaconic aciduria.

Oláhová M, Thompson K, Hardy SA, Barbosa IA, Besse A, Anagnostou ME, White K, Davey T, Simpson MA, Champion M, Enns G, Schelley S, Lightowlers RN, Chrzanowska-Lightowlers ZM, McFarland R, Deshpande C, Bonnen PE, Taylor RW.

J Inherit Metab Dis. 2017 Jan;40(1):121-130. doi: 10.1007/s10545-016-9977-2. Epub 2016 Sep 30.

12.

Clinical features of the pathogenic m.5540G>A mitochondrial transfer RNA tryptophan gene mutation.

Ng YS, Hardy SA, Shrier V, Quaghebeur G, Mole DR, Daniels MJ, Downes SM, Freebody J, Fratter C, Hofer M, Nemeth AH, Poulton J, Taylor RW.

Neuromuscul Disord. 2016 Oct;26(10):702-705. doi: 10.1016/j.nmd.2016.08.009. Epub 2016 Aug 17.

13.

Pathogenic mtDNA mutations causing mitochondrial myopathy: The need for muscle biopsy.

Hardy SA, Blakely EL, Purvis AI, Rocha MC, Ahmed S, Falkous G, Poulton J, Rose MR, O'Mahony O, Bermingham N, Dougan CF, Ng YS, Horvath R, Turnbull DM, Gorman GS, Taylor RW.

Neurol Genet. 2016 Jun 23;2(4):e82. doi: 10.1212/NXG.0000000000000082. eCollection 2016 Aug.

14.

A recurrent mitochondrial p.Trp22Arg NDUFB3 variant causes a distinctive facial appearance, short stature and a mild biochemical and clinical phenotype.

Alston CL, Howard C, Oláhová M, Hardy SA, He L, Murray PG, O'Sullivan S, Doherty G, Shield JP, Hargreaves IP, Monavari AA, Knerr I, McCarthy P, Morris AA, Thorburn DR, Prokisch H, Clayton PE, McFarland R, Hughes J, Crushell E, Taylor RW.

J Med Genet. 2016 Sep;53(9):634-41. doi: 10.1136/jmedgenet-2015-103576. Epub 2016 Apr 18.

15.

LRPPRC mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population.

Oláhová M, Hardy SA, Hall J, Yarham JW, Haack TB, Wilson WC, Alston CL, He L, Aznauryan E, Brown RM, Brown GK, Morris AA, Mundy H, Broomfield A, Barbosa IA, Simpson MA, Deshpande C, Moeslinger D, Koch J, Stettner GM, Bonnen PE, Prokisch H, Lightowlers RN, McFarland R, Chrzanowska-Lightowlers ZM, Taylor RW.

Brain. 2015 Dec;138(Pt 12):3503-19. doi: 10.1093/brain/awv291. Epub 2015 Oct 27.

16.

Youth motivation as a predictor of treatment outcomes in a community mental health system.

Merrill BM, Warren JS, Garcia DJ, Hardy SA.

Psychother Res. 2017 Mar;27(2):215-226. doi: 10.1080/10503307.2015.1090037. Epub 2015 Oct 1.

PMID:
26429772
17.

The perplexing issue of severe mental illness, physical health screening and primary care in England.

Hardy SA.

J Psychiatr Ment Health Nurs. 2015 Oct;22(8):647-52. doi: 10.1111/jpm.12236. No abstract available.

PMID:
26337596
18.

Corrigendum: Long-term survival in a child with severe encephalopathy, multiple respiratory chain deficiency and GFM1 mutations.

Brito S, Thompson K, Campistol J, Colomer J, Hardy SA, He L, Fernández-Marmiesse A, Palacios L, Jou C, Jiménez-Mallebrera C, Armstrong J, Montero R, Artuch R, Tischner C, Wenz T, McFarland R, Taylor RW.

Front Genet. 2015 Jul 28;6:254. doi: 10.3389/fgene.2015.00254. eCollection 2015.

19.

Sudden adult death syndrome in m.3243A>G-related mitochondrial disease: an unrecognized clinical entity in young, asymptomatic adults.

Ng YS, Grady JP, Lax NZ, Bourke JP, Alston CL, Hardy SA, Falkous G, Schaefer AG, Radunovic A, Mohiddin SA, Ralph M, Alhakim A, Taylor RW, McFarland R, Turnbull DM, Gorman GS.

Eur Heart J. 2016 Aug 21;37(32):2552-9. doi: 10.1093/eurheartj/ehv306. Epub 2015 Jul 17.

20.

Religiousness and Levels of Hazardous Alcohol Use: A Latent Profile Analysis.

Jankowski PJ, Hardy SA, Zamboanga BL, Ham LS, Schwartz SJ, Kim SY, Forthun LF, Bersamin MM, Donovan RA, Whitbourne SK, Hurley EA, Cano MÁ.

J Youth Adolesc. 2015 Oct;44(10):1968-83. doi: 10.1007/s10964-015-0302-4. Epub 2015 May 15.

PMID:
25976527
21.

Clinical, biochemical, and genetic spectrum of seven patients with NFU1 deficiency.

Ahting U, Mayr JA, Vanlander AV, Hardy SA, Santra S, Makowski C, Alston CL, Zimmermann FA, Abela L, Plecko B, Rohrbach M, Spranger S, Seneca S, Rolinski B, Hagendorff A, Hempel M, Sperl W, Meitinger T, Smet J, Taylor RW, Van Coster R, Freisinger P, Prokisch H, Haack TB.

Front Genet. 2015 Apr 13;6:123. doi: 10.3389/fgene.2015.00123. eCollection 2015.

22.

Pathogenic mitochondrial mt-tRNA(Ala) variants are uniquely associated with isolated myopathy.

Lehmann D, Schubert K, Joshi PR, Hardy SA, Tuppen HA, Baty K, Blakely EL, Bamberg C, Zierz S, Deschauer M, Taylor RW.

Eur J Hum Genet. 2015 Dec;23(12):1735-8. doi: 10.1038/ejhg.2015.73. Epub 2015 Apr 15.

23.

Mental health nurses can increase capability and capacity in primary care by educating practice nurses: an evaluation of an education programme in England.

Hardy SA, Kingsnorth R.

J Psychiatr Ment Health Nurs. 2015 May;22(4):270-7. doi: 10.1111/jpm.12208. Epub 2015 Apr 8.

PMID:
25858036
24.

Long-term survival in a child with severe encephalopathy, multiple respiratory chain deficiency and GFM1 mutations.

Brito S, Thompson K, Campistol J, Colomer J, Hardy SA, He L, Fernández-Marmiesse A, Palacios L, Jou C, Jiménez-Mallebrera C, Armstrong J, Montero R, Artuch R, Tischner C, Wenz T, McFarland R, Taylor RW.

Front Genet. 2015 Mar 23;6:102. doi: 10.3389/fgene.2015.00102. eCollection 2015. Erratum in: Front Genet. 2015;6:254.

25.

Moral Identity and Adolescent Prosocial and Antisocial Behaviors: Interactions with Moral Disengagement and Self-regulation.

Hardy SA, Bean DS, Olsen JA.

J Youth Adolesc. 2015 Aug;44(8):1542-54. doi: 10.1007/s10964-014-0172-1. Epub 2014 Aug 22.

PMID:
25146465
26.

Adolescent Motivations to Engage in Pro-Social Behaviors and Abstain From Health-Risk Behaviors: A Self-Determination Theory Approach.

Hardy SA, Dollahite DC, Johnson N, Christensen JB.

J Pers. 2015 Oct;83(5):479-90. doi: 10.1111/jopy.12123. Epub 2014 Oct 13.

PMID:
25130713
27.

Cisplatin-induced haemolytic uraemic syndrome associated with a novel intronic mutation of CD46 treated with eculizumab.

Gilbert RD, Stanley LK, Fowler DJ, Angus EM, Hardy SA, Goodship TH.

Clin Kidney J. 2013 Aug;6(4):421-425.

28.

Pilot of BRAF mutation analysis in indeterminate, suspicious and malignant thyroid FNA cytology.

Johnson SJ, Hardy SA, Roberts C, Bourn D, Mallick U, Perros P.

Cytopathology. 2014 Jun;25(3):146-54. doi: 10.1111/cyt.12125. Epub 2014 Jan 12.

PMID:
24417615
29.

Screening for metabolic risk among patients with severe mental illness and diabetes: a national comparison.

Mitchell AJ, Hardy SA.

Psychiatr Serv. 2013 Oct;64(10):1060-3. doi: 10.1176/appi.ps.201200514.

PMID:
24081407
30.

Moral identity as moral ideal self: links to adolescent outcomes.

Hardy SA, Walker LJ, Olsen JA, Woodbury RD, Hickman JR.

Dev Psychol. 2014 Jan;50(1):45-57. doi: 10.1037/a0033598. Epub 2013 Jul 29.

PMID:
23895167
31.

Religiousness and hazardous alcohol use: a conditional indirect effects model.

Jankowski PJ, Hardy SA, Zamboanga BL, Ham LS.

J Adolesc. 2013 Aug;36(4):747-58. doi: 10.1016/j.adolescence.2013.06.001. Epub 2013 Jul 2.

PMID:
23849669
32.

Eculizumab therapy for atypical haemolytic uraemic syndrome due to a gain-of-function mutation of complement factor B.

Gilbert RD, Fowler DJ, Angus E, Hardy SA, Stanley L, Goodship TH.

Pediatr Nephrol. 2013 Aug;28(8):1315-8. doi: 10.1007/s00467-013-2492-x. Epub 2013 Apr 28.

PMID:
23624872
33.

Adolescent-parent attachment as a mediator of relations between parenting and adolescent social behavior and wellbeing in China.

Cai M, Hardy SA, Olsen JA, Nelson DA, Yamawaki N.

Int J Psychol. 2013;48(6):1185-90. doi: 10.1080/00207594.2013.774091. Epub 2013 Mar 20.

PMID:
23509911
34.

Titin founder mutation is a common cause of myofibrillar myopathy with early respiratory failure.

Pfeffer G, Barresi R, Wilson IJ, Hardy SA, Griffin H, Hudson J, Elliott HR, Ramesh AV, Radunovic A, Winer JB, Vaidya S, Raman A, Busby M, Farrugia ME, Ming A, Everett C, Emsley HC, Horvath R, Straub V, Bushby K, Lochmüller H, Chinnery PF, Sarkozy A.

J Neurol Neurosurg Psychiatry. 2014 Mar;85(3):331-8. doi: 10.1136/jnnp-2012-304728. Epub 2013 Mar 13.

PMID:
23486992
35.

Meaning in Life in Emerging Adulthood: A Person-Oriented Approach.

Dezutter J, Waterman AS, Schwartz SJ, Luyckx K, Beyers W, Meca A, Kim SY, Whitbourne SK, Zamboanga BL, Lee RM, Hardy SA, Forthun LF, Ritchie RA, Weisskirch RS, Brown EJ, Caraway SJ.

J Pers. 2014 Feb;82(1):57-68. doi: 10.1111/jopy.12033. Epub 2013 Apr 8.

PMID:
23437779
36.

Identity dimensions and related processes in emerging adulthood: helpful or harmful?

Ritchie RA, Meca A, Madrazo VL, Schwartz SJ, Hardy SA, Zamboanga BL, Weisskirch RS, Kim SY, Whitbourne SK, Ham LS, Lee RM.

J Clin Psychol. 2013 Apr;69(4):415-32. doi: 10.1002/jclp.21960. Epub 2013 Jan 24.

PMID:
23348360
37.

The roles of identity formation and moral identity in college student mental health, health-risk behaviors, and psychological well-being.

Hardy SA, Francis SW, Zamboanga BL, Kim SY, Anderson SG, Forthun LF.

J Clin Psychol. 2013 Apr;69(4):364-82. doi: 10.1002/jclp.21913. Epub 2012 Oct 8. Review.

PMID:
23044630
38.

Role of mesenchymal stem cells in neurogenesis and nervous system repair.

Maltman DJ, Hardy SA, Przyborski SA.

Neurochem Int. 2011 Sep;59(3):347-56. doi: 10.1016/j.neuint.2011.06.008. Epub 2011 Jun 21. Review.

PMID:
21718735
39.

Relational and social-cognitive correlates of early adolescents' forgiveness of parents.

Christensen KJ, Padilla-Walker LM, Busby DM, Hardy SA, Day RD.

J Adolesc. 2011 Oct;34(5):903-13. doi: 10.1016/j.adolescence.2011.01.001. Epub 2011 Feb 5.

PMID:
21296401
40.

Examining the light and dark sides of emerging adults' identity: a study of identity status differences in positive and negative psychosocial functioning.

Schwartz SJ, Beyers W, Luyckx K, Soenens B, Zamboanga BL, Forthun LF, Hardy SA, Vazsonyi AT, Ham LS, Kim SY, Whitbourne SK, Waterman AS.

J Youth Adolesc. 2011 Jul;40(7):839-59. doi: 10.1007/s10964-010-9606-6. Epub 2010 Nov 19.

PMID:
21088875
41.

Links between adolescents' expected parental reactions and prosocial behavioral tendencies: the mediating role of prosocial values.

Hardy SA, Carlo G, Roesch SC.

J Youth Adolesc. 2010 Jan;39(1):84-95. doi: 10.1007/s10964-008-9383-7. Epub 2009 Jan 7.

PMID:
20091219
42.

Moral identity and psychological distance: the case of adolescent parental socialization.

Hardy SA, Bhattacharjee A, Reed Ii A, Aquino K.

J Adolesc. 2010 Feb;33(1):111-23. doi: 10.1016/j.adolescence.2009.04.008. Epub 2009 Jul 1.

PMID:
19570572
43.

Mesenchymal stem cells as mediators of neural differentiation.

Hardy SA, Maltman DJ, Przyborski SA.

Curr Stem Cell Res Ther. 2008 Jan;3(1):43-52. Review.

PMID:
18220922
44.

Development and confirmatory factor analysis of the community norms of child neglect scale.

Goodvin R, Johnson DR, Hardy SA, Graef MI, Chambers JM.

Child Maltreat. 2007 Feb;12(1):68-85.

PMID:
17218649
45.

The efficacy and safety of lower doses of aripiprazole for the treatment of patients with acute exacerbation of schizophrenia.

Cutler AJ, Marcus RN, Hardy SA, O'Donnell A, Carson WH, McQuade RD.

CNS Spectr. 2006 Sep;11(9):691-702; quiz 719.

PMID:
16946694
46.

Valency of antibody binding to virions and its determination by surface plasmon resonance.

Dimmock NJ, Hardy SA.

Rev Med Virol. 2004 Mar-Apr;14(2):123-35. Review.

PMID:
15027004
47.

Adolescent religiosity and sexuality: an investigation of reciprocal influences.

Hardy SA, Raffaelli M.

J Adolesc. 2003 Dec;26(6):731-9.

PMID:
14643743
48.
49.

Comparison of five clustering algorithms to classify phytoplankton from flow cytometry data.

Wilkins MF, Hardy SA, Boddy L, Morris CW.

Cytometry. 2001 Jul 1;44(3):210-7.

PMID:
11429771
50.

A double-blind, placebo-controlled trial of nefazodone in the treatment of patients hospitalized for major depression.

Feighner J, Targum SD, Bennett ME, Roberts DL, Kensler TT, D'Amico MF, Hardy SA.

J Clin Psychiatry. 1998 May;59(5):246-53.

PMID:
9632036

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