PMC Articles for MedGen (Select 66660) - PMC

Result Filters

Links from MedGen

Items: 1 to 20 of 135

<< First< Prev

Page of 7

Select item 105850431.

Analysis of abnormal posture in patients with Parkinson's disease using a computational model considering muscle tones

Yuichiro Omura, Hiroki Togo, Kohei Kaminishi, Tetsuya Hasegawa, Ryosuke Chiba, Arito Yozu, Kaoru Takakusaki, Mitsunari Abe, Yuji Takahashi, Takashi Hanakawa, Jun Ota

Front Comput Neurosci. 2023; 17: 1218707. Published online 2023 Oct 5. doi: 10.3389/fncom.2023.1218707

PMCID:: PMC10585043

Abstract Article PDF–1.9M

Select item 66340732.

Knee–Hip–Spine Syndrome: Improvement in Preoperative Abnormal Posture following Total Knee Arthroplasty

Yasushi Oshima, Nobuyoshi Watanabe, Norishige Iizawa, Tokifumi Majima, Mitsuhiro Kawata, Shinro Takai

Adv Orthop. 2019; 2019: 8484938. Published online 2019 Jul 1. doi: 10.1155/2019/8484938

PMCID:: PMC6634073

Abstract Article PDF–1.2M

Select item 44834513.

The effects of cervical joint manipulation, based on passive motion analysis, on cervical lordosis, forward head posture, and cervical ROM in university students with abnormal posture of the cervical spine

Wontae Gong

J Phys Ther Sci. 2015 May; 27(5): 1609–1611. Published online 2015 May 26. doi: 10.1589/jpts.27.1609

PMCID:: PMC4483451

Abstract Article PDF–425K

Select item 98424494.

Elective and Emergency Deep Brain Stimulation in Refractory Pediatric Monogenetic Movement Disorders Presenting with Dystonia: Current Practice Illustrated by Two Cases

M. Garofalo, M. Beudel, J.M. Dijk, L.A. Bonouvrié, A.I. Buizer, J. Geytenbeek, R.H.N. Prins, P.R. Schuurman, L.A. van de Pol

Neuropediatrics. 2023 Feb; 54(1): 44–52. Published online 2022 Dec 27. doi: 10.1055/a-1959-9088

PMCID:: PMC9842449

Abstract Article PDF–1.1M

Select item 97436775.

Methylation of the serotonin reuptake transporter gene and non-motor symptoms in dystonia patients

Elze R. Timmers, Torsten Plösch, Marenka Smit, Ingrid H. Hof, Rikst Nynke Verkaik-Schakel, Marina A. J. Tijssen, Tom J. de Koning, Klary E. Niezen-Koning

Clin Epigenetics. 2022; 14: 170. Published online 2022 Dec 11. doi: 10.1186/s13148-022-01384-7

PMCID:: PMC9743677

Abstract Article PDF–898K

Select item 93031496.

Screening of Proliferation-Related Genes and Pathological Changes in Thiram-Induced Tibial Dyschondroplasia

Ali Raza Jahejo, Chen-Liang Zhang, Fazul Nabi, Nazeer Hussain Kalhoro, Qurban Ali Shah, Zohaib Ahmed Bhutto, Jin-Feng Zhao, Jin Yu, Guan-Bao Ning, Ding Zhang, Shu-Ming Chen, Wen-Xia Tian

Biomed Res Int. 2022; 2022: 6209047. Published online 2022 Jul 14. doi: 10.1155/2022/6209047

PMCID:: PMC9303149

Abstract Article PDF–2.1M

Select item 73942007.

Delayed Diagnoses of SGCE Myoclonus-Dystonia

M. Georgeta Varga, Nikita P. Nand, Mark S. LeDoux

Tremor Other Hyperkinet Mov (N Y) 2020; 10: 23. Published online 2020 Jul 28. doi: 10.5334/tohm.334

PMCID:: PMC7394200

Abstract Article PDF–572K

Select item 73893258.

阵发性运动诱发性运动障碍患者的临床表现及基因诊断

朱晓明, 龚育红, 卢思, 程首超, 姚宝珍

Zhongguo Dang Dai Er Ke Za Zhi. 2017 Nov 25; 19(11): 1169–1173. Chinese. doi: 10.7499/j.issn.1008-8830.2017.11.009

PMCID:: PMC7389325

Abstract Article PDF–1.1M

Select item 69790999.

A major facilitator superfamily domain 8 frameshift variant in a cat with suspected neuronal ceroid lipofuscinosis

Julien Guevar, Petra Hug, Felix Giebels, Alexane Durand, Vidhya Jagannathan, Tosso Leeb

J Vet Intern Med. 2020 Jan-Feb; 34(1): 289–293. Published online 2019 Dec 20. doi: 10.1111/jvim.15663

PMCID:: PMC6979099

Abstract Article PDF–515K

Select item 544168610.

Deletion of 2.7 kb near HOXD3 in an Arabian horse with occipitoatlantoaxial malformation

MH Bordbari, MCT Penedo, M. Aleman, SJ Valberg, J. Mickelson, CJ Finno

Anim Genet. Author manuscript; available in PMC 2018 Jun 1.

Published in final edited form as: Anim Genet. 2017 Jun; 48(3): 287–294. Published online 2017 Jan 23. doi: 10.1111/age.12531

PMCID:: PMC5441686

Abstract Article PDF–610K

Select item 504868711.

Tor1a+/- mice develop dystonia-like movements via a striatal dopaminergic dysregulation triggered by peripheral nerve injury

Chi Wang Ip, Ioannis U. Isaias, Burak B. Kusche-Tekin, Dennis Klein, Janos Groh, Aet O’Leary, Susanne Knorr, Takahiro Higuchi, James B. Koprich, Jonathan M. Brotchie, Klaus V. Toyka, Andreas Reif, Jens Volkmann

Acta Neuropathol Commun. 2016; 4: 108. Published online 2016 Oct 3. doi: 10.1186/s40478-016-0375-7

PMCID:: PMC5048687

Abstract Article PDF–1.8M

Select item 400746212.

The BiP Molecular Chaperone Plays Multiple Roles during the Biogenesis of TorsinA, an AAA⁺ ATPase Associated with the Neurological Disease Early-onset Torsion Dystonia

Lucía F. Zacchi, Hui-Chuan Wu, Samantha L. Bell, Linda Millen, Adrienne W. Paton, James C. Paton, Philip J. Thomas, Michal Zolkiewski, Jeffrey L. Brodsky

J Biol Chem. 2014 May 2; 289(18): 12727–12747. Published online 2014 Mar 13. doi: 10.1074/jbc.M113.529123

PMCID:: PMC4007462

Abstract Article PDF–2.4M

Select item 349862813.

Functional Analysis of Dopaminergic Systems in a DYT1 Knock-in Mouse Model of Dystonia

Chang-Hyun Song, Xueliang Fan, Cicely J. Exeter, Ellen J. Hess, H. A. Jinnah

Neurobiol Dis. Author manuscript; available in PMC 2013 Oct 1.

Published in final edited form as: Neurobiol Dis. 2012 Oct; 48(1): 66–78. Published online 2012 May 31. doi: 10.1016/j.nbd.2012.05.009

PMCID:: PMC3498628

Abstract Article PDF–966K

Select item 325729214.

Parallel Mapping and Simultaneous Sequencing Reveals Deletions in BCAN and FAM83H Associated with Discrete Inherited Disorders in a Domestic Dog Breed

Oliver P. Forman, Jacques Penderis, Claudia Hartley, Louisa J. Hayward, Sally L. Ricketts, Cathryn S. Mellersh

PLoS Genet. 2012 Jan; 8(1): e1002462. Published online 2012 Jan 12. doi: 10.1371/journal.pgen.1002462

PMCID:: PMC3257292

Abstract Article PDF–764K

Select item 309899915.

A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy

Yusuke Sakiyama, Yuji Okamoto, Itsuro Higuchi, Yukie Inamori, Yoko Sangatsuda, Kumiko Michizono, Osamu Watanabe, Hideyuki Hatakeyama, Yu-ichi Goto, Kimiyoshi Arimura, Hiroshi Takashima

Acta Neuropathol. 2011; 121(6): 775–783. Published online 2011 Mar 22. doi: 10.1007/s00401-011-0818-y

PMCID:: PMC3098999

Abstract Article PDF–738K

Select item 262645016.

Severe Mandibuloacral Dysplasia-Associated Lipodystrophy and Progeria in a Young Girl with a Novel Homozygous Arg527Cys LMNA Mutation

Anil K. Agarwal, Irina Kazachkova, Svetlana Ten, Abhimanyu Garg

J Clin Endocrinol Metab. 2008 Dec; 93(12): 4617–4623. Published online 2008 Sep 16. doi: 10.1210/jc.2008-0123

PMCID:: PMC2626450

Abstract Article

Select item 257574117.

Hypertonia-associated Protein Trak1 is a Novel Regulator of Endosome-to-Lysosome Trafficking

Elizabeth Webber, Lian Li, Lih-Shen Chin

J Mol Biol. Author manuscript; available in PMC 2009 Oct 10.

Published in final edited form as: J Mol Biol. 2008 Oct 10; 382(3): 638–651. Published online 2008 Jul 25. doi: 10.1016/j.jmb.2008.07.045

PMCID:: PMC2575741

Abstract Article PDF–2.8M

Select item 239378618.

P-Rex2 regulates Purkinje cell dendrite morphology and motor coordination

Sarah Donald, Trevor Humby, Ian Fyfe, Anne Segonds-Pichon, Simon A. Walker, Simon R. Andrews, W. John Coadwell, Piers Emson, Lawrence S. Wilkinson, Heidi C. E. Welch

Proc Natl Acad Sci U S A. 2008 Mar 18; 105(11): 4483–4488. Published online 2008 Mar 11. doi: 10.1073/pnas.0712324105