Found: 11
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Novel heterozygous mutation in ANO3 responsible for craniocervical dystonia.
- Published in:
- 2016
- By:
- Publication type:
- letter
Singular DYT6 phenotypes in association with new THAP1 frameshift mutations.
- Published in:
- Movement Disorders, 2011, v. 26, n. 9, p. 1774, doi. 10.1002/mds.23641
- By:
- Publication type:
- Article
The p.Asp216His TOR1A allele effect is not found in the French population.
- Published in:
- Movement Disorders, 2009, v. 24, n. 6, p. 919, doi. 10.1002/mds.22407
- By:
- Publication type:
- Article
Volume Analysis to Predict the Long-Term Evolution of Residual Aortic Dissection after Type A Repair.
- Published in:
- Journal of Cardiovascular Development & Disease (JCDD), 2022, v. 9, n. 10, p. 349, doi. 10.3390/jcdd9100349
- By:
- Publication type:
- Article
ATTACHMENT BONDS FOR HUMAN-LIKE ROBOTS.
- Published in:
- International Journal of Humanoid Robotics, 2006, v. 3, n. 3, p. 301, doi. 10.1142/S0219843606000771
- By:
- Publication type:
- Article
Results of a prospective follow-up study after type A aortic dissection repair: a high rate of distal aneurysmal evolution and reinterventions.
- Published in:
- European Journal of Cardio-Thoracic Surgery, 2022, v. 61, n. 1, p. 152, doi. 10.1093/ejcts/ezab317
- By:
- Publication type:
- Article
A 10-Year Aortic Center Experience with Hybrid Repair of Chronic "Residual" Aortic Dissection After Type A Repair.
- Published in:
- Cardiovascular Drugs & Therapy, 2022, v. 36, n. 2, p. 285, doi. 10.1007/s10557-021-07150-w
- By:
- Publication type:
- Article
Actionable Genes, Core Databases, and Locus-Specific Databases.
- Published in:
- Human Mutation, 2016, v. 37, n. 12, p. 1299, doi. 10.1002/humu.23112
- By:
- Publication type:
- Article
UMD-Predictor: A High-Throughput Sequencing Compliant System for Pathogenicity Prediction of any Human cDNA Substitution.
- Published in:
- Human Mutation, 2016, v. 37, n. 5, p. 439, doi. 10.1002/humu.22965
- By:
- Publication type:
- Article
DYT6 dystonia: Review of the literature and creation of the UMD locus-specific database (LSDB) for mutations in the THAP1 gene.
- Published in:
- Human Mutation, 2011, v. 32, n. 11, p. 1213, doi. 10.1002/humu.21564
- By:
- Publication type:
- Article
Primary Non-Aortic Lesions Are Not Rare in Marfan Syndrome and Are Associated with Aortic Dissection Independently of Age.
- Published in:
- Journal of Clinical Medicine, 2023, v. 12, n. 8, p. 2902, doi. 10.3390/jcm12082902
- By:
- Publication type:
- Article