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Items: 1 to 20 of 2045

1.
Treatment for speech disorder in Friedreich ataxia and other hereditary ataxia syndromes
Adam P Vogel, Joanne Folker, Matthew L Poole, Cochrane Neuromuscular Group
Cochrane Database Syst Rev. 2014 Oct; 2014(10): CD008953. Published online 2014 Oct 28. doi: 10.1002/14651858.CD008953.pub2
PMCID:
PMC11214034
AbstractArticlePDF–730K
2.
Risk factors for mortality in post-myocardial infarction patients: insights from the improve SCA bridge study
Dileep Kumar, Fawaz Bardooli, Wen-Jone Chen, Dejia Huang, Mullasari Ajit Sankardas, Waqar Habib Ahmed, Houng-Bang Liew, Hyeon-Cheol Gwon, Brian Van Dorn, Thomas Holmes, Amy Thompson, Shu Zhang
Egypt Heart J. 2024 Dec; 76: 72. Published online 2024 Jun 7. doi: 10.1186/s43044-024-00505-2
PMCID:
PMC11161447
AbstractArticlePDF–1.4M
3.
Effect of a Home‐Base Core Stability Exercises in Hereditary Ataxia. A Randomized Controlled Trial. A Pilot Randomized Controlled Trial
Rosa Cabanas‐Valdés, Helena Fernández‐Lago, Selma Peláez‐Hervás, Laura Serra‐Rusiñol, Carlos López‐de‐Celis, Maria Masbernat‐Almenara
Mov Disord Clin Pract. 2024 Jun; 11(6): 666–675. Published online 2024 Apr 2. doi: 10.1002/mdc3.14036
PMCID:
PMC11145153
AbstractArticlePDF–1.7M
4.
Quantitative Oculomotor Assessment in Hereditary Ataxia: Systematic Review and Consensus by the Ataxia Global Initiative Working Group on Digital-motor Biomarkers
Pilar Garces, Chrystalina A. Antoniades, Anna Sobanska, Norbert Kovacs, Sarah H. Ying, Anoopum S. Gupta, Susan Perlman, David J. Szmulewicz, Chiara Pane, Andrea H. Németh, Laura B. Jardim, Giulia Coarelli, Michaela Dankova, Andreas Traschütz, Alexander A. Tarnutzer
Cerebellum. 2024; 23(3): 896–911. Published online 2023 Apr 28. doi: 10.1007/s12311-023-01559-9
PMCID:
PMC11102387
AbstractArticlePDF–909K
5.
The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous population
Nejat Mahdieh, Morteza Heidari, Zahra Rezaei, Ali Reza Tavasoli, Sareh Hosseinpour, Maryam Rasulinejad, Ali Zare Dehnavi, Masoud Ghahvechi Akbari, Reza Shervin Badv, Elahe Vafaei, Ali Mohebbi, Pouria Mohammadi, Seyyed Mohammad Mahdi Hosseiny, Reza Azizimalamiri, Ali Nikkhah, Elham Pourbakhtyaran, Mohammad Rohani, Narges Khanbanha, Sedigheh Nikbakht, Mojtaba Movahedinia, Parviz Karimi, Homa Ghabeli, Seyed Ahmad Hosseini, Fatemeh Sadat Rashidi, Masoud Garshasbi, Morteza Rezvani Kashani, Noor M. Ghiasvand, Stephan Zuchner, Matthis Synofzik, Mahmoud Reza Ashrafi
Hum Genomics. 2024; 18: 35. Published online 2024 Apr 3. doi: 10.1186/s40246-024-00598-5
PMCID:
PMC10988936
AbstractArticlePDF–2.4M
6.
IL-27-induced PD-L1highSca-1+ innate lymphoid cells suppress contact hypersensitivity in an IL-10-dependent manner
Keun Young Min, Do-Kyun Kim, Min Geun Jo, min Yeong Choi, Dajeong Lee, Jeong Won Park, Young-Jun Park, Yeonseok Chung, Young Mi Kim, Yeong-Min Park, Hyuk Soon Kim, Wahn Soo Choi
Exp Mol Med. 2024 Mar; 56(3): 616–629. Published online 2024 Mar 1. doi: 10.1038/s12276-024-01187-1
PMCID:
PMC10984996
AbstractArticlePDF–6.6M
7.
Staged stent-assisted, transcirculatory coiling of partially-thrombosed, mixed saccular and fusiform SCA aneurysm
Kunal P Raygor, M Travis Caton, Daniel A Tonetti, Amanda Baker, Todd B Dubnicoff, Adib A Abla
Interv Neuroradiol. 2024 Feb; 30(1): 126. Published online 2022 Jul 19. doi: 10.1177/15910199221108312
PMCID:
PMC10956447
AbstractArticle
8.
Hereditary Ataxias: From Bench to Clinic, Where Do We Stand?
Federica Pilotto, Andrea Del Bondio, Hélène Puccio
Cells. 2024 Feb; 13(4): 319. Published online 2024 Feb 9. doi: 10.3390/cells13040319
PMCID:
PMC10886822
AbstractArticlePDF–1.2M
9.
Patients’ Perspective in Hereditary Ataxia
Sorina Gorcenco, Christin Karremo, Andreas Puschmann
Cerebellum. 2024; 23(1): 82–91. Published online 2022 Dec 16. doi: 10.1007/s12311-022-01505-1
PMCID:
PMC10864479
AbstractArticlePDF–1.0M
10.
Quantitative Oculomotor Assessment in Hereditary Ataxia: Discriminatory Power, Correlation with Severity Measures, and Recommended Parameters for Specific Genotypes
Pilar Garces, Chrystalina A. Antoniades, Anna Sobanska, Norbert Kovacs, Sarah H. Ying, Anoopum S. Gupta, Susan Perlman, David J. Szmulewicz, Chiara Pane, Andrea H. Németh, Laura B. Jardim, Giulia Coarelli, Michaela Dankova, Andreas Traschütz, Alexander A. Tarnutzer
Cerebellum. 2024; 23(1): 121–135. Published online 2023 Jan 14. doi: 10.1007/s12311-023-01514-8
PMCID:
PMC10864420
AbstractArticlePDF–1.0M
11.
Risk assessment for commercial crime and legal protection based on modularity-optimized LM and SCA-optimized CNN
YunZhe Wang, FengLan Su
PeerJ Comput Sci. 2023; 9: e1683. Published online 2023 Nov 16. doi: 10.7717/peerj-cs.1683
PMCID:
PMC10703012
AbstractArticlePDF–1.3M
12.
Tumor-Infiltrating iNKT Cells Activated through c-Kit/Sca-1 Are Induced by Pentoxifylline, Norcantharidin, and Their Mixtures for Killing Murine Melanoma Cells
Maximiliano V. M. Correa-Lara, Israel Lara-Vega, Minerva Nájera-Martínez, María Lilia Domínguez-López, Elba Reyes-Maldonado, Armando Vega-López
Pharmaceuticals (Basel) 2023 Oct; 16(10): 1472. Published online 2023 Oct 16. doi: 10.3390/ph16101472
PMCID:
PMC10610189
AbstractArticlePDF–4.6M
13.
The Association Between Educational Attainment and SCA 3 Age of Onset and Disease Course
Katherine Iannuzzelli, Rosa Shi, Reece Carter, Rachel Huynh, Owen Morgan, Sheng-Han Kuo, Jee Bang, Kelly A. Mills, Kristin Baranano, David S. Zee, Emile Moukheiber, Ricardo Roda, Ankur Butala, Cherie Marvel, Michelle Joyce, Ximin Li, Jiangxia Wang, Liana S. Rosenthal
Parkinsonism Relat Disord. Author manuscript; available in PMC 2023 Sep 13.
Published in final edited form as: Parkinsonism Relat Disord. 2022 May; 98: 99–102. Published online 2022 Mar 10. doi: 10.1016/j.parkreldis.2022.02.025
PMCID:
PMC10498785
AbstractArticlePDF–259K
14.
SCA: recovering single-cell heterogeneity through information-based dimensionality reduction
Benjamin DeMeo, Bonnie Berger
Genome Biol. 2023; 24: 195. Published online 2023 Aug 25. doi: 10.1186/s13059-023-02998-7
PMCID:
PMC10464206
AbstractArticlePDF–3.5M
15.
SCA-NGS: Secure compression algorithm for next generation sequencing data using genetic operators and block sorting
Muhammad Sardaraz, Muhammad Tahir
Sci Prog. 2021 Apr-Jun; 104(2): 00368504211023276. Published online 2021 Jun 18. doi: 10.1177/00368504211023276
PMCID:
PMC10454964
AbstractArticlePDF–1.1M
16.
Is Social Training Delivered with a Head-Mounted Display Suitable for Patients with Hereditary Ataxia?
Giorgia Malerba, Silvia Bellazzecca, Cosimo Urgesi, Niccolò Butti, Maria Grazia D’Angelo, Eleonora Diella, Emilia Biffi
Brain Sci. 2023 Jul; 13(7): 1017. Published online 2023 Jun 30. doi: 10.3390/brainsci13071017
PMCID:
PMC10376992
AbstractArticlePDF–3.0M
17.
Phenotypic and genetic aspects of hereditary ataxia in dogs
Kimberley Stee, Mario Van Poucke, Mark Lowrie, Luc Van Ham, Luc Peelman, Natasha Olby, Sofie F.M. Bhatti
J Vet Intern Med. 2023 Jul-Aug; 37(4): 1306–1322. Published online 2023 Jun 21. doi: 10.1111/jvim.16742
PMCID:
PMC10365067
AbstractArticlePDF–3.7M
18.
ATP purinergic receptor signalling promotes Sca-1+ cell proliferation and migration for vascular remodelling
Yiqin Cui, Chunshu Li, Xinyi Zeng, Xiaoyu Wei, Pengyun Li, Jun Cheng, Qingbo Xu, Yan Yang
Cell Commun Signal. 2023; 21: 173. Published online 2023 Jul 10. doi: 10.1186/s12964-023-01185-2
Correction in:
Cell Commun Signal. 2023; 21: 174.
PMCID:
PMC10332060
AbstractArticlePDF–6.5M
19.
Functional genomics provide key insights to improve the diagnostic yield of hereditary ataxia
Zhongbo Chen, Arianna Tucci, Valentina Cipriani, Emil K Gustavsson, Kristina Ibañez, Regina H Reynolds, David Zhang, Letizia Vestito, Alejandro Cisterna García, Siddharth Sethi, Jonathan W Brenton, Sonia García-Ruiz, Aine Fairbrother-Browne, Ana-Luisa Gil-Martinez, Genomics England Research Consortium , Nick Wood, John A Hardy, Damian Smedley, Henry Houlden, Juan Botía, Mina Ryten
Brain. 2023 Jul; 146(7): 2869–2884. Published online 2023 Jan 10. doi: 10.1093/brain/awad009
PMCID:
PMC10316781
AbstractArticlePDF–1.2M
20.
Spinocerebellar Ataxia 36 is a Frequent Cause of Hereditary Ataxia in Eastern Spain
Raquel Baviera‐Muñoz, Lidón Carretero‐Vilarroig, Nuria Muelas, Rafael Sivera, Pablo Sopena‐Novales, Begoña Martínez‐Sanchis, Isabel Sastre‐Bataller, Marina Campins‐Romeu, Irene Martínez‐Torres, Jose Manuel García‐Verdugo, Jose M. Millán, Teresa Jaijo, Elena Aller, Luis Bataller
Mov Disord Clin Pract. 2023 Jun; 10(6): 992–997. Published online 2023 May 5. doi: 10.1002/mdc3.13740
PMCID:
PMC10272893
AbstractArticlePDF–860K

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