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Items: 1 to 20 of 106

1.

Early postnatal behavioral, cellular, and molecular changes in models of Huntington disease are reversible by HDAC inhibition.

Siebzehnrübl FA, Raber KA, Urbach YK, Schulze-Krebs A, Canneva F, Moceri S, Habermeyer J, Achoui D, Gupta B, Steindler DA, Stephan M, Nguyen HP, Bonin M, Riess O, Bauer A, Aigner L, Couillard-Despres S, Paucar MA, Svenningsson P, Osmand A, Andreew A, Zabel C, Weiss A, Kuhn R, Moussaoui S, Blockx I, Van der Linden A, Cheong RY, Roybon L, Petersén Å, von Hörsten S.

Proc Natl Acad Sci U S A. 2018 Sep 11;115(37):E8765-E8774. doi: 10.1073/pnas.1807962115. Epub 2018 Aug 27.

2.

Brain-Derived Neurotrophic Factor (BDNF) and Serotonin Transporter (SERT) in Platelets of Patients with Mild Huntington's Disease: Relationships with Social Cognition Symptoms.

Betti L, Palego L, Unti E, Mazzucchi S, Kiferle L, Palermo G, Bonuccelli U, Giannaccini G, Ceravolo R.

Arch Ital Biol. 2018 Jul 1;156(1-2):27-39. doi: 10.12871/00039829201813.

PMID:
30039833
3.

Human cellular models of medium spiny neuron development and Huntington disease.

Golas MM.

Life Sci. 2018 Sep 15;209:179-196. doi: 10.1016/j.lfs.2018.07.030. Epub 2018 Jul 18. Review.

PMID:
30031060
4.

String Grammar Unsupervised Possibilistic Fuzzy C-Medians for Gait Pattern Classification in Patients with Neurodegenerative Diseases.

Klomsae A, Auephanwiriyakul S, Theera-Umpon N.

Comput Intell Neurosci. 2018 Jun 13;2018:1869565. doi: 10.1155/2018/1869565. eCollection 2018.

5.

Sexual behavior and testis morphology in the BACHD rat model.

Novati A, Yu-Taeger L, Gonzalez Menendez I, Quintanilla Martinez L, Nguyen HP.

PLoS One. 2018 Jun 8;13(6):e0198338. doi: 10.1371/journal.pone.0198338. eCollection 2018.

6.

Large-scale transcriptomic analysis reveals that pridopidine reverses aberrant gene expression and activates neuroprotective pathways in the YAC128 HD mouse.

Kusko R, Dreymann J, Ross J, Cha Y, Escalante-Chong R, Garcia-Miralles M, Tan LJ, Burczynski ME, Zeskind B, Laifenfeld D, Pouladi M, Geva M, Grossman I, Hayden MR.

Mol Neurodegener. 2018 May 21;13(1):25. doi: 10.1186/s13024-018-0259-3.

7.

Agreement between clinician-rated versus patient-reported outcomes in Huntington disease.

Carlozzi NE, Boileau NR, Perlmutter JS, Chou KL, Stout JC, Paulsen JS, McCormack MK, Cella D, Nance MA, Lai JS, Dayalu P.

J Neurol. 2018 Jun;265(6):1443-1453. doi: 10.1007/s00415-018-8852-5. Epub 2018 Apr 23.

PMID:
29687215
8.

Objective assessment of gait and posture in premanifest and manifest Huntington disease - A multi-center study.

Beckmann H, Bohlen S, Saft C, Hoffmann R, Gerss J, Muratori L, Ringelstein EB, Landwehrmeyer GB, Reilmann R.

Gait Posture. 2018 May;62:451-457. doi: 10.1016/j.gaitpost.2018.03.039. Epub 2018 Apr 7.

PMID:
29660633
9.

Long-term predictors for psychological outcome of pre-symptomatic testing for late-onset neurological diseases.

Lêdo S, Ramires A, Leite Â, Dinis MAP, Sequeiros J.

Eur J Med Genet. 2018 Oct;61(10):575-580. doi: 10.1016/j.ejmg.2018.03.010. Epub 2018 Mar 23.

PMID:
29581083
10.

Human Umbilical Cord Matrix Stem Cells Reverse Oxidative Stress-Induced Cell Death and Ameliorate Motor Function and Striatal Atrophy in Rat Model of Huntington Disease.

Ebrahimi MJ, Aliaghaei A, Boroujeni ME, Khodagholi F, Meftahi G, Abdollahifar MA, Ahmadi H, Danyali S, Daftari M, Sadeghi Y.

Neurotox Res. 2018 Aug;34(2):273-284. doi: 10.1007/s12640-018-9884-4. Epub 2018 Mar 8.

PMID:
29520722
11.

Preventing mutant huntingtin proteolysis and intermittent fasting promote autophagy in models of Huntington disease.

Ehrnhoefer DE, Martin DDO, Schmidt ME, Qiu X, Ladha S, Caron NS, Skotte NH, Nguyen YTN, Vaid K, Southwell AL, Engemann S, Franciosi S, Hayden MR.

Acta Neuropathol Commun. 2018 Mar 6;6(1):16. doi: 10.1186/s40478-018-0518-0.

12.

Genetic Rodent Models of Huntington Disease.

Stricker-Shaver J, Novati A, Yu-Taeger L, Nguyen HP.

Adv Exp Med Biol. 2018;1049:29-57. doi: 10.1007/978-3-319-71779-1_2. Review.

PMID:
29427097
13.

Calpastatin ablation aggravates the molecular phenotype in cell and animal models of Huntington disease.

Weber JJ, Kloock SJ, Nagel M, Ortiz-Rios MM, Hofmann J, Riess O, Nguyen HP.

Neuropharmacology. 2018 May 1;133:94-106. doi: 10.1016/j.neuropharm.2018.01.022.

PMID:
29355642
14.

Evaluating the current state of the art of Huntington disease research: a scientometric analysis.

Barboza LA, Ghisi NC.

Braz J Med Biol Res. 2018 Jan 11;51(3):e6299. doi: 10.1590/1414-431X20176299. Review.

15.

Alteration in Fluidity of Cell Plasma Membrane in Huntington Disease Revealed by Spectral Phasor Analysis.

Sameni S, Malacrida L, Tan Z, Digman MA.

Sci Rep. 2018 Jan 15;8(1):734. doi: 10.1038/s41598-018-19160-0. Erratum in: Sci Rep. 2018 Apr 11;8(1):6060.

16.

Huntington disease.

Ghosh R, Tabrizi SJ.

Handb Clin Neurol. 2018;147:255-278. doi: 10.1016/B978-0-444-63233-3.00017-8. Review.

PMID:
29325616
17.

Effects of endurance training on skeletal muscle mitochondrial function in Huntington disease patients.

Mueller SM, Gehrig SM, Petersen JA, Frese S, Mihaylova V, Ligon-Auer M, Khmara N, Nuoffer JM, Schaller A, Lundby C, Toigo M, Jung HH.

Orphanet J Rare Dis. 2017 Dec 19;12(1):184. doi: 10.1186/s13023-017-0740-z.

18.

Evaluating cognition in individuals with Huntington disease: Neuro-QoL cognitive functioning measures.

Lai JS, Goodnight S, Downing NR, Ready RE, Paulsen JS, Kratz AL, Stout JC, McCormack MK, Cella D, Ross C, Russell J, Carlozzi NE.

Qual Life Res. 2018 Mar;27(3):811-822. doi: 10.1007/s11136-017-1755-6. Epub 2017 Dec 8.

PMID:
29222609
19.

Understanding the need for assistance with survey completion in people with Huntington disease.

Hahn EA, Downing NR, Stout JC, Paulsen JS, Ready B, Goodnight S, Lai JS, Miner JA, Carlozzi NE.

Qual Life Res. 2018 Mar;27(3):801-810. doi: 10.1007/s11136-017-1747-6. Epub 2017 Dec 6.

PMID:
29214414
20.

Mutant huntingtin protein expression and blood-spinal cord barrier dysfunction in huntington disease.

Sciacca G, Cicchetti F.

Ann Neurol. 2017 Dec;82(6):981-994. doi: 10.1002/ana.25107. Epub 2017 Dec 12.

PMID:
29171910

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