Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 454

1.

Interobserver agreement of an electronic von Frey device for measuring mechanical sensory thresholds in normal dogs.

Kerns AT, Cook LB, Kieves N, Moore SA.

Vet J. 2019 Oct;252:105375. doi: 10.1016/j.tvjl.2019.105375. Epub 2019 Sep 4.

PMID:
31554594
2.

Mammary Paget's Disease of the Male Breast: A Rare Case With an Unusual Immunohistochemical Profile.

Moore SA, Notgrass HM, Vandergriff TW, Sahoo S.

Int J Surg Pathol. 2019 Sep 12:1066896919874878. doi: 10.1177/1066896919874878. [Epub ahead of print]

PMID:
31514589
3.

MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement.

Donkervoort S, Sabouny R, Yun P, Gauquelin L, Chao KR, Hu Y, Al Khatib I, Töpf A, Mohassel P, Cummings BB, Kaur R, Saade D, Moore SA, Waddell LB, Farrar MA, Goodrich JK, Uapinyoying P, Chan SHS, Javed A, Leach ME, Karachunski P, Dalton J, Medne L, Harper A, Thompson C, Thiffault I, Specht S, Lamont RE, Saunders C, Racher H, Bernier FP, Mowat D, Witting N, Vissing J, Hanson R, Coffman KA, Hainlen M, Parboosingh JS, Carnevale A, Yoon G, Schnur RE; Care4Rare Canada Consortium, Boycott KM, Mah JK, Straub V, Foley AR, Innes AM, Bönnemann CG, Shutt TE.

Acta Neuropathol. 2019 Aug 29. doi: 10.1007/s00401-019-02059-z. [Epub ahead of print]

PMID:
31463572
4.

Cold-Stored Whole Blood: A Better Method of Trauma Resuscitation?

Hazelton JP, Cannon JW, Zatorski C, Roman JS, Moore SA, Young AJ, Subramanian M, Guzman J, Fogt F, Moran A, Gaughan J, Seamon MJ, Porter J.

J Trauma Acute Care Surg. 2019 Aug 5. doi: 10.1097/TA.0000000000002471. [Epub ahead of print]

PMID:
31389912
5.

Magnetic Resonance Imaging characteristics in case of TOR1AIP1 muscular dystrophy.

Bhatia A, Mobley BC, Cogan J, Koziura ME, Brokamp E, Phillips J, Newman J; Undiagnosed Diseases Network (UDN), Moore SA, Hamid R; Members of the Undiagnosed Diseases Network.

Clin Imaging. 2019 Jun 21;58:108-113. doi: 10.1016/j.clinimag.2019.06.010. [Epub ahead of print]

PMID:
31299614
6.

SMCHD1 mutation spectrum for facioscapulohumeral muscular dystrophy type 2 (FSHD2) and Bosma arhinia microphthalmia syndrome (BAMS) reveals disease-specific localisation of variants in the ATPase domain.

Lemmers RJLF, van der Stoep N, Vliet PJV, Moore SA, San Leon Granado D, Johnson K, Topf A, Straub V, Evangelista T, Mozaffar T, Kimonis V, Shaw ND, Selvatici R, Ferlini A, Voermans N, van Engelen B, Sacconi S, Tawil R, Lamers M, van der Maarel SM.

J Med Genet. 2019 Oct;56(10):693-700. doi: 10.1136/jmedgenet-2019-106168. Epub 2019 Jun 26.

PMID:
31243061
7.

Languishing Students: Linking Complete Mental Health Screening in Schools to Tier II Intervention.

Moore SA, Mayworm AM, Stein R, Sharkey JD, Dowdy E.

J Appl Sch Psychol. 2019;35(3):257-289. doi: 10.1080/15377903.2019.1577780. Epub 2019 Mar 27.

8.

Training Disparities of Our Future Workforce: A Survey of Trauma Fellowship Candidates.

Moore SA, Maduka RC, Tung L, Reilly PM, Morris J, Seamon MJ, Holena DN, Kaplan LJ, Martin ND.

J Surg Res. 2019 Nov;243:198-205. doi: 10.1016/j.jss.2019.04.088. Epub 2019 Jun 8.

PMID:
31185436
9.

Structure of Ddi2, a highly inducible detoxifying metalloenzyme from Saccharomyces cerevisiae.

Li J, Jia Y, Lin A, Hanna M, Chelico L, Xiao W, Moore SA.

J Biol Chem. 2019 Jul 5;294(27):10674-10685. doi: 10.1074/jbc.RA118.006394. Epub 2019 May 31.

PMID:
31152065
10.

Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease.

Gonorazky HD, Naumenko S, Ramani AK, Nelakuditi V, Mashouri P, Wang P, Kao D, Ohri K, Viththiyapaskaran S, Tarnopolsky MA, Mathews KD, Moore SA, Osorio AN, Villanova D, Kemaladewi DU, Cohn RD, Brudno M, Dowling JJ.

Am J Hum Genet. 2019 May 2;104(5):1007. doi: 10.1016/j.ajhg.2019.04.004. No abstract available.

11.

Clinical, genetic, and pathologic characterization of FKRP Mexican founder mutation c.1387A>G.

Lee AJ, Jones KA, Butterfield RJ, Cox MO, Konersman CG, Grosmann C, Abdenur JE, Boyer M, Beson B, Wang C, Dowling JJ, Gibbons MA, Ballard A, Janas JS, Leshner RT, Donkervoort S, Bönnemann CG, Malicki DM, Weiss RB, Moore SA, Mathews KD.

Neurol Genet. 2019 Mar 1;5(2):e315. doi: 10.1212/NXG.0000000000000315. eCollection 2019 Apr.

12.

Identifying factors associated with sedentary time after stroke. Secondary analysis of pooled data from nine primary studies.

Hendrickx W, Riveros C, Askim T, Bussmann JBJ, Callisaya ML, Chastin SFM, Dean CM, Ezeugwu VE, Jones TM, Kuys SS, Mahendran N, Manns TJ, Mead G, Moore SA, Paul L, Pisters MF, Saunders DH, Simpson DB, Tieges Z, Verschuren O, English C.

Top Stroke Rehabil. 2019 Jul;26(5):327-334. doi: 10.1080/10749357.2019.1601419. Epub 2019 Apr 26.

PMID:
31025908
13.

Biomarkers in Motor Neuron Disease: A State of the Art Review.

Verber NS, Shepheard SR, Sassani M, McDonough HE, Moore SA, Alix JJP, Wilkinson ID, Jenkins TM, Shaw PJ.

Front Neurol. 2019 Apr 3;10:291. doi: 10.3389/fneur.2019.00291. eCollection 2019. Review.

14.

ACTA1-myopathy with prominent finger flexor weakness and rimmed vacuoles.

Liewluck T, Niu Z, Moore SA, Alsharabati M, Milone M.

Neuromuscul Disord. 2019 May;29(5):388-391. doi: 10.1016/j.nmd.2019.02.012. Epub 2019 Mar 2.

PMID:
30987788
15.

A latent transition analysis of the longitudinal stability of dual-factor mental health in adolescence.

Moore SA, Dowdy E, Nylund-Gibson K, Furlong MJ.

J Sch Psychol. 2019 Apr;73:56-73. doi: 10.1016/j.jsp.2019.03.003. Epub 2019 Mar 15.

PMID:
30961881
16.

Diagnosis-Related Group in Colon Surgery: Identifying Areas of Improvement to Drive High-Value Care.

Hughes BD, Moore SA, Mehta HB, Shan Y, Senagore AJ.

Am Surg. 2019 Mar 1;85(3):256-260.

PMID:
30947770
17.

Aberrant regulation of epigenetic modifiers contributes to the pathogenesis in patients with selenoprotein N-related myopathies.

Bachmann C, Noreen F, Voermans NC, Schär PL, Vissing J, Fock JM, Bulk S, Kusters B, Moore SA, Beggs AH, Mathews KD, Meyer M, Genetti CA, Meola G, Cardani R, Mathews E, Jungbluth H, Muntoni F, Zorzato F, Treves S.

Hum Mutat. 2019 Jul;40(7):962-974. doi: 10.1002/humu.23745. Epub 2019 Apr 1.

PMID:
30932294
18.

Wristband Accelerometers to motiVate arm Exercises after Stroke (WAVES): a pilot randomized controlled trial.

Da-Silva RH, Moore SA, Rodgers H, Shaw L, Sutcliffe L, van Wijck F, Price CI.

Clin Rehabil. 2019 Aug;33(8):1391-1403. doi: 10.1177/0269215519834720. Epub 2019 Mar 7.

PMID:
30845829
19.

Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease.

Gonorazky HD, Naumenko S, Ramani AK, Nelakuditi V, Mashouri P, Wang P, Kao D, Ohri K, Viththiyapaskaran S, Tarnopolsky MA, Mathews KD, Moore SA, Osorio AN, Villanova D, Kemaladewi DU, Cohn RD, Brudno M, Dowling JJ.

Am J Hum Genet. 2019 Mar 7;104(3):466-483. doi: 10.1016/j.ajhg.2019.01.012. Epub 2019 Feb 28. Erratum in: Am J Hum Genet. 2019 May 2;104(5):1007.

20.

The effect of malondialdehyde is modified by simian virus 40 transformation in human lung fibroblast cells.

Yates SA, Murphy MF, Moore SA.

Toxicology. 2019 Mar 1;415:1-9. doi: 10.1016/j.tox.2019.01.009. Epub 2019 Jan 15.

PMID:
30658077
21.

Insight into the PTEN - p85α interaction and lipid binding properties of the p85α BH domain.

Marshall JDS, Mellor P, Ruan X, Whitecross DE, Moore SA, Anderson DH.

Oncotarget. 2018 Dec 11;9(97):36975-36992. doi: 10.18632/oncotarget.26432. eCollection 2018 Dec 11.

22.

How should long-term free-living physical activity be targeted after stroke? A systematic review and narrative synthesis.

Moore SA, Hrisos N, Flynn D, Errington L, Price C, Avery L.

Int J Behav Nutr Phys Act. 2018 Oct 17;15(1):100. doi: 10.1186/s12966-018-0730-0.

23.

Suppression of myopathic lamin mutations by muscle-specific activation of AMPK and modulation of downstream signaling.

Chandran S, Suggs JA, Wang BJ, Han A, Bhide S, Cryderman DE, Moore SA, Bernstein SI, Wallrath LL, Melkani GC.

Hum Mol Genet. 2019 Feb 1;28(3):351-371. doi: 10.1093/hmg/ddy332.

PMID:
30239736
24.

Read All About It: Health Literacy and Veterinary Client Educational Materials.

Moore SA.

Top Companion Anim Med. 2018 Jun;33(2):A2. doi: 10.1053/j.tcam.2018.06.002. No abstract available.

PMID:
30223988
25.

Validation of a Muscle-Specific Tissue Image Analysis Tool for Quantitative Assessment of Dystrophin Staining in Frozen Muscle Biopsies.

Aeffner F, Faelan C, Moore SA, Moody A, Black JC, Charleston JS, Frank DE, Dworzak J, Piper JK, Ranjitkar M, Wilson K, Kanaly S, Rudmann DG, Lange H, Young GD, Milici AJ.

Arch Pathol Lab Med. 2019 Feb;143(2):197-205. doi: 10.5858/arpa.2017-0536-OA. Epub 2018 Aug 31.

PMID:
30168727
26.

FSHD type 2 and Bosma arhinia microphthalmia syndrome: Two faces of the same mutation.

Mul K, Lemmers RJLF, Kriek M, van der Vliet PJ, van den Boogaard ML, Badrising UA, Graham JM Jr, Lin AE, Brand H, Moore SA, Johnson K, Evangelista T, Töpf A, Straub V, Kapetanovic García S, Sacconi S, Tawil R, Tapscott SJ, Voermans NC, van Engelen BGM, Horlings CGC, Shaw ND, van der Maarel SM.

Neurology. 2018 Aug 7;91(6):e562-e570. doi: 10.1212/WNL.0000000000005958. Epub 2018 Jul 6.

27.

Absence of Axoglial Paranodal Junctions in a Child With CNTNAP1 Mutations, Hypomyelination, and Arthrogryposis.

Conant A, Curiel J, Pizzino A, Sabetrasekh P, Murphy J, Bloom M, Evans SH, Helman G, Taft RJ, Simons C, Whitehead MT, Moore SA, Vanderver A.

J Child Neurol. 2018 Sep;33(10):642-650. doi: 10.1177/0883073818776157. Epub 2018 Jun 8.

PMID:
29882456
28.

TRAPPC11 and GOSR2 mutations associate with hypoglycosylation of α-dystroglycan and muscular dystrophy.

Larson AA, Baker PR 2nd, Milev MP, Press CA, Sokol RJ, Cox MO, Lekostaj JK, Stence AA, Bossler AD, Mueller JM, Prematilake K, Tadjo TF, Williams CA, Sacher M, Moore SA.

Skelet Muscle. 2018 May 31;8(1):17. doi: 10.1186/s13395-018-0163-0.

29.

Development of an International Canine Spinal Cord Injury observational registry: a collaborative data-sharing network to optimize translational studies of SCI.

Moore SA, Zidan N, Spitzbarth I, Nout-Lomas YS, Granger N, da Costa RC, Levine JM, Jeffery ND, Stein VM, Tipold A, Olby NJ.

Spinal Cord. 2018 Jul;56(7):656-665. doi: 10.1038/s41393-018-0145-4. Epub 2018 May 23.

30.

Understanding and Treating Chiari-like Malformation and Syringomyelia in Dogs.

Hechler AC, Moore SA.

Top Companion Anim Med. 2018 Mar;33(1):1-11. doi: 10.1053/j.tcam.2018.03.002. Epub 2018 Mar 15. Review.

PMID:
29793722
31.

Uniparental disomy unveils a novel recessive mutation in POMT2.

Brun BN, Willer T, Darbro BW, Gonorazky HD, Naumenko S, Dowling JJ, Campbell KP, Moore SA, Mathews KD.

Neuromuscul Disord. 2018 Jul;28(7):592-596. doi: 10.1016/j.nmd.2018.04.003. Epub 2018 Apr 10.

32.

Self-directed therapy programmes for arm rehabilitation after stroke: a systematic review.

Da-Silva RH, Moore SA, Price CI.

Clin Rehabil. 2018 Aug;32(8):1022-1036. doi: 10.1177/0269215518775170. Epub 2018 May 13.

PMID:
29756513
33.

Patient-derived mutations within the N-terminal domains of p85α impact PTEN or Rab5 binding and regulation.

Mellor P, Marshall JDS, Ruan X, Whitecross DE, Ross RL, Knowles MA, Moore SA, Anderson DH.

Sci Rep. 2018 May 8;8(1):7108. doi: 10.1038/s41598-018-25487-5.

34.

A novel CAPN3 mutation in late-onset limb-girdle muscular dystrophy with early respiratory insufficiency.

Martinez-Thompson JM, Moore SA, Liewluck T.

J Clin Neurosci. 2018 Jul;53:229-231. doi: 10.1016/j.jocn.2018.04.025. Epub 2018 Apr 21.

35.

Clinical features and short-term outcome of presumptive intracranial complications associated with otitis media/interna: a multi-center retrospective study of 19 cats (2009-2017).

Moore SA, Bentley RT, Carrera-Justiz S, Foss KD, da Costa RC, Cook LB.

J Feline Med Surg. 2019 Feb;21(2):148-155. doi: 10.1177/1098612X18764582. Epub 2018 Apr 18.

PMID:
29667535
36.

A novel ANO5 splicing variant in a LGMD2L patient leads to production of a truncated aggregation-prone Ano5 peptide.

Xu J, Xu L, Lau YS, Gao Y, Moore SA, Han R.

J Pathol Clin Res. 2018 Apr;4(2):135-145. doi: 10.1002/cjp2.92. Epub 2018 Mar 1.

37.

Extranodal non-B, non-T-cell lymphoma with bilateral tympanic bulla involvement in a cat.

Kerns AT, Brakel KA, Premanandan C, Saffire A, Moore SA.

JFMS Open Rep. 2018 Feb 19;4(1):2055116918756724. doi: 10.1177/2055116918756724. eCollection 2018 Jan-Jun.

38.

Hydrothermal Growth of ZnO Nanowires on UV-Nanoimprinted Polymer Structures.

Park S, Moore SA, Lee J, Song IH, Farshchian B, Kim N.

J Nanosci Nanotechnol. 2018 May 1;18(5):3686-3692. doi: 10.1166/jnn.2018.14668.

PMID:
29442884
39.

Dystrophinopathy muscle biopsies in the genetic testing ERA: One center's data.

Carlson CR, Moore SA, Mathews KD.

Muscle Nerve. 2018 Jan 24. doi: 10.1002/mus.26083. [Epub ahead of print]

40.

The h-index for associate and full professors of dermatology in the United States: an epidemiologic study of scholastic production.

Yuan JT, Aires DJ, DaCunha M, Funk K, Habashi-Daniel A, Moore SA, Heimes A, Sawaf H, Fraga GR.

Cutis. 2017 Dec;100(6):395-398.

PMID:
29360887
41.

Social and Contextual Influences on Mental Health Following an Episode of Mass Violence.

Felix ED, Moore SA, Meskunas H, Terzieva A.

J Interpers Violence. 2017 Nov 1:886260517742915. doi: 10.1177/0886260517742915. [Epub ahead of print]

PMID:
29294998
42.

Comprehensive measurement of stroke gait characteristics with a single accelerometer in the laboratory and community: a feasibility, validity and reliability study.

Moore SA, Hickey A, Lord S, Del Din S, Godfrey A, Rochester L.

J Neuroeng Rehabil. 2017 Dec 29;14(1):130. doi: 10.1186/s12984-017-0341-z.

43.

Duchenne and Becker Muscular Dystrophies: A Review of Animal Models, Clinical End Points, and Biomarker Quantification.

Wilson K, Faelan C, Patterson-Kane JC, Rudmann DG, Moore SA, Frank D, Charleston J, Tinsley J, Young GD, Milici AJ.

Toxicol Pathol. 2017 Oct;45(7):961-976. doi: 10.1177/0192623317734823. Epub 2017 Oct 3. Review.

44.

Autosomal dominant calpainopathy due to heterozygous CAPN3 C.643_663del21.

Martinez-Thompson JM, Niu Z, Tracy JA, Moore SA, Swenson A, Wieben ED, Milone M.

Muscle Nerve. 2018 Apr;57(4):679-683. doi: 10.1002/mus.25970. Epub 2017 Sep 30.

45.

Pathophysiology of exercise intolerance in chronic diseases: the role of diminished cardiac performance in mitochondrial and heart failure patients.

McCoy J, Bates M, Eggett C, Siervo M, Cassidy S, Newman J, Moore SA, Gorman G, Trenell MI, Velicki L, Seferovic PM, Cleland JGF, MacGowan GA, Turnbull DM, Jakovljevic DG.

Open Heart. 2017 Jul 28;4(2):e000632. doi: 10.1136/openhrt-2017-000632. eCollection 2017.

46.

Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome.

Shaw ND, Brand H, Kupchinsky ZA, Bengani H, Plummer L, Jones TI, Erdin S, Williamson KA, Rainger J, Stortchevoi A, Samocha K, Currall BB, Dunican DS, Collins RL, Willer JR, Lek A, Lek M, Nassan M, Pereira S, Kammin T, Lucente D, Silva A, Seabra CM, Chiang C, An Y, Ansari M, Rainger JK, Joss S, Smith JC, Lippincott MF, Singh SS, Patel N, Jing JW, Law JR, Ferraro N, Verloes A, Rauch A, Steindl K, Zweier M, Scheer I, Sato D, Okamoto N, Jacobsen C, Tryggestad J, Chernausek S, Schimmenti LA, Brasseur B, Cesaretti C, García-Ortiz JE, Buitrago TP, Silva OP, Hoffman JD, Mühlbauer W, Ruprecht KW, Loeys BL, Shino M, Kaindl AM, Cho CH, Morton CC, Meehan RR, van Heyningen V, Liao EC, Balasubramanian R, Hall JE, Seminara SB, Macarthur D, Moore SA, Yoshiura KI, Gusella JF, Marsh JA, Graham JM Jr, Lin AE, Katsanis N, Jones PL, Crowley WF Jr, Davis EE, FitzPatrick DR, Talkowski ME.

Nat Genet. 2017 May 26;49(6):969. doi: 10.1038/ng0617-969c. No abstract available.

PMID:
28546579
47.

Child Neurology: LAMA2 muscular dystrophy without contractures.

Dean M, Rashid S, Kupsky W, Moore SA, Jiang H.

Neurology. 2017 May 23;88(21):e199-e203. doi: 10.1212/WNL.0000000000003958. No abstract available.

48.

Identifying conflict potential in a coastal and marine environment using participatory mapping.

Moore SA, Brown G, Kobryn H, Strickland-Munro J.

J Environ Manage. 2017 Jul 15;197:706-718. doi: 10.1016/j.jenvman.2016.12.026. Epub 2017 Apr 24.

PMID:
28448808
49.

Cytoplasmic body pathology in severe ACTA1-related myopathy in the absence of typical nemaline rods.

Donkervoort S, Chan SHS, Hayes LH, Bradley N, Nguyen D, Leach ME, Mohassel P, Hu Y, Thangarajh M, Bharucha-Goebel D, Kan A, Ho RSL, Reyes CA, Nance J, Moore SA, Foley AR, Bönnemann CG.

Neuromuscul Disord. 2017 Jun;27(6):531-536. doi: 10.1016/j.nmd.2017.02.012. Epub 2017 Mar 2.

50.

Evaluation of osseous-associated cervical spondylomyelopathy in dogs using kinematic magnetic resonance imaging.

Provencher M, Habing A, Moore SA, Cook L, Phillips G, da Costa RC.

Vet Radiol Ultrasound. 2017 Jul;58(4):411-421. doi: 10.1111/vru.12495. Epub 2017 Apr 12.

PMID:
28402031

Supplemental Content

Loading ...
Support Center