Found: 6
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Tetraparesis and sensorimotor axonal polyneuropathy due to co-occurrence of Pompe disease and hereditary ATTR amyloidosis.
- Published in:
- Neurological Sciences, 2021, v. 42, n. 4, p. 1523, doi. 10.1007/s10072-020-04896-3
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- Publication type:
- Article
CERA Attenuates Kidney Fibrogenesis in the db/db Mouse by Influencing the Renal Myofibroblast Generation.
- Published in:
- Journal of Clinical Medicine, 2018, v. 7, n. 2, p. 15, doi. 10.3390/jcm7020015
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- Publication type:
- Article
Expansion of the phenotypic and molecular spectrum of CWF19L1‐related disorder.
- Published in:
- Clinical Genetics, 2023, v. 103, n. 5, p. 566, doi. 10.1111/cge.14275
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- Publication type:
- Article
Bi-Allelic COQ4 Variants Cause Adult-Onset Ataxia-Spasticity Spectrum Disease.
- Published in:
- 2022
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- Publication type:
- journal article
Adult‐Onset Neurodegeneration in Nucleotide Excision Repair Disorders (NERD<sub>ND</sub>): Time to Move Beyond the Skin.
- Published in:
- Movement Disorders, 2022, v. 37, n. 8, p. 1707, doi. 10.1002/mds.29071
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- Publication type:
- Article
A Novel NPTX1 de novo Variant in a Late‐Onset Ataxia Patient.
- Published in:
- Movement Disorders, 2022, v. 37, n. 6, p. 1319, doi. 10.1002/mds.28985
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- Publication type:
- Article