Conversion of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 to manifest ataxia (RISCA): a longitudinal cohort study.
- DOI
- 10.1016/s1474-4422(20)30235-0
- Published
- 2020 Sep
- Container
- The Lancet. Neurology
- Publisher
- Not recorded
- Open access
- unknown
Credibility signals
limited evidence Score 43/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
Show all credibility signals
- cautionDOI registered: No matching Crossref record was present in this response.
- cautionDOI resolves: No matching Crossref record was present in this response.
- not scoredDirectory of Open Access Journals: No matching DOAJ record was present in this response. No allow-list match; this is not evidence of low credibility.
- not scoredMEDLINE indexed: Not checked or no result supplied; no credibility inference made.
- not scoredOpenAlex core source: Not checked or no result supplied; no credibility inference made.
- not scoredKnown publisher allow-list: Not checked or no result supplied; no credibility inference made.
- not scoredROR affiliation: Not checked or no result supplied; no credibility inference made.
- not scoredRetraction Watch retraction: No retraction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch expression of concern: No expression of concern notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch correction: No correction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch reinstatement: No reinstatement notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredOpen access status: Not checked or no result supplied; no credibility inference made.
- not scoredPublication license: Not checked or no result supplied; no credibility inference made.
- not scoredPublication version: A publication version was supplied but is not scored.
- cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty.
Cite this work
BibTeX
@article{allodium:10.1016/s1474-4422-20-30235-0,
title = {Conversion of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 to manifest ataxia (RISCA): a longitudinal cohort study.},
author = {Jacobi H and du Montcel ST and Romanzetti S and Harmuth F and Mariotti C and Nanetti L and Rakowicz M and Makowicz G and Durr A and Monin ML and Filla A and Roca A and Schöls L and Hengel H and Infante J and Kang JS and Timmann D and Casali C and Masciullo M and Baliko L and Melegh B and Nachbauer W and Bürk-Gergs K and Schulz JB and Riess O and Reetz K and Klockgether T},
year = {2020},
journal = {The Lancet. Neurology},
doi = {10.1016/s1474-4422(20)30235-0},
url = {https://doi.org/10.1016/s1474-4422(20)30235-0}
}RIS
TY - JOUR TI - Conversion of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 to manifest ataxia (RISCA): a longitudinal cohort study. AU - Jacobi H AU - du Montcel ST AU - Romanzetti S AU - Harmuth F AU - Mariotti C AU - Nanetti L AU - Rakowicz M AU - Makowicz G AU - Durr A AU - Monin ML AU - Filla A AU - Roca A AU - Schöls L AU - Hengel H AU - Infante J AU - Kang JS AU - Timmann D AU - Casali C AU - Masciullo M AU - Baliko L AU - Melegh B AU - Nachbauer W AU - Bürk-Gergs K AU - Schulz JB AU - Riess O AU - Reetz K AU - Klockgether T PY - 2020 JO - The Lancet. Neurology DO - 10.1016/s1474-4422(20)30235-0 UR - https://doi.org/10.1016/s1474-4422(20)30235-0 ER -
APA
H, J., ST, D. M., S, R., F, H., C, M., L, N., M, R., G, M., A, D., ML, M., A, F., A, R., L, S., H, H., J, I., JS, K., D, T., C, C., M, M., L, B., B, M., W, N., K, B., JB, S., O, R., K, R., & T, K. (2020). Conversion of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 to manifest ataxia (RISCA): a longitudinal cohort study.. The Lancet. Neurology. https://doi.org/10.1016/s1474-4422(20)30235-0
Source records
- pubmed · retrieved 2026-09-26T04:06:42.567Z