Found: 13
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Erdheim‐Chester disease of brain parenchyma without any systemic involvement: A case report and review of literature.
- Published in:
- Neuropathology, 2024, v. 44, n. 1, p. 59, doi. 10.1111/neup.12930
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- Publication type:
- Article
Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype.
- Published in:
- Rheumatology, 2023, v. 62, n. 9, p. 3188, doi. 10.1093/rheumatology/kead044
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- Publication type:
- Article
Çocuk romatolojisinde genetiğin yeri.
- Published in:
- Türk Pediatri Arşivi, 2017, v. 52, n. 3, p. 113, doi. 10.5152/TurkPediatriArs.2017.4953
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- Publication type:
- Article
Prospective outcome analysis of multiple sclerosis cases reveals candidate prognostic cerebrospinal fluid markers.
- Published in:
- PLoS ONE, 2023, v. 17, n. 6, p. 1, doi. 10.1371/journal.pone.0287463
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- Publication type:
- Article
Investigation of multiple sclerosis-related pathways through the integration of genomic and proteomic data.
- Published in:
- PeerJ, 2021, p. 1, doi. 10.7717/peerj.11922
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- Publication type:
- Article
A Case of Coexistent Spinocerebellar Ataxia Type 2 and Primary Progressive Multiple Sclerosis—Coincidental or Associated?
- Published in:
- 2024
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- Publication type:
- Case Study
Identification of multiple sclerosis-related pathways by integration of genomic and proteomic data.
- Published in:
- 2018
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- Publication type:
- Abstract
Gene Defects in Familial Form of Juvenile Arthritis.
- Published in:
- 2018
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- Publication type:
- letter
Investigating the role of common and rare variants in multiplex multiple sclerosis families reveals an increased burden of common risk variation.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-21484-x
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- Publication type:
- Article
Correction to: Diagnostic utility of a targeted next-generation sequencing gene panel in the clinical suspicion of systemic autoinflammatory diseases: a multi-center study.
- Published in:
- 2019
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- Publication type:
- Correction Notice
Diagnostic utility of a targeted next-generation sequencing gene panel in the clinical suspicion of systemic autoinflammatory diseases: a multi-center study.
- Published in:
- Rheumatology International, 2019, v. 39, n. 5, p. 911, doi. 10.1007/s00296-019-04252-5
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- Publication type:
- Article
MYO1H is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia.
- Published in:
- Molecular Genetics & Genomics, 2022, v. 297, n. 4, p. 1141, doi. 10.1007/s00438-022-01910-5
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- Publication type:
- Article
Comparison of multiple sclerosis patients with or without rebound activity after fingolimod cessation: Five‐year clinical outcomes.
- Published in:
- European Journal of Neurology, 2023, v. 30, n. 9, p. 2745, doi. 10.1111/ene.15913
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- Publication type:
- Article