Found: 15
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White matter integrity changes and neurocognitive functioning in adult-late onset DM1: a follow-up DTI study.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-07820-1
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- Publication type:
- Article
Age‐related cognitive decline in myotonic dystrophy type 1: An 11‐year longitudinal follow‐up study.
- Published in:
- Journal of Neuropsychology, 2020, v. 14, n. 1, p. 121, doi. 10.1111/jnp.12192
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- Publication type:
- Article
Nonsense mutations in alpha-II spectrin in three families with juvenile onset hereditary motor neuropathy.
- Published in:
- 2019
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- Publication type:
- journal article
Blood Markers in Healthy-Aged Nonagenarians: A Combination of High Telomere Length and Low Amyloidβ Are Strongly Associated With Healthy Aging in the Oldest Old.
- Published in:
- Frontiers in Aging Neuroscience, 2018, p. N.PAG, doi. 10.3389/fnagi.2018.00380
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- Publication type:
- Article
Neurodegeneration trajectory in pediatric and adult/late DM1: A follow‐up MRI study across a decade.
- Published in:
- Annals of Clinical & Translational Neurology, 2020, v. 7, n. 10, p. 1802, doi. 10.1002/acn3.51163
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- Publication type:
- Article
A deep intronic splice variant advises reexamination of presumably dominant SPG7 Cases.
- Published in:
- Annals of Clinical & Translational Neurology, 2020, v. 7, n. 1, p. 105, doi. 10.1002/acn3.50967
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- Publication type:
- Article
Leukocyte telomere length in patients with myotonic dystrophy type I: a pilot study.
- Published in:
- Annals of Clinical & Translational Neurology, 2020, v. 7, n. 1, p. 126, doi. 10.1002/acn3.50954
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- Publication type:
- Article
Shedding light on motor premanifest myotonic dystrophy type 1: A molecular, muscular and central nervous system follow‐up study.
- Published in:
- European Journal of Neurology, 2023, v. 30, n. 1, p. 215, doi. 10.1111/ene.15604
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- Publication type:
- Article
Six Serum miRNAs Fail to Validate as Myotonic Dystrophy Type 1 Biomarkers.
- Published in:
- PLoS ONE, 2016, v. 11, n. 2, p. 1, doi. 10.1371/journal.pone.0150501
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- Publication type:
- Article
Reply to: "Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion".
- Published in:
- 2019
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- Publication type:
- Letter
Parkinsonism and spastic paraplegia type 7: Expanding the spectrum of mitochondrial Parkinsonism.
- Published in:
- 2019
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- Publication type:
- journal article
Dysregulated FOXO1 activity drives skeletal muscle intrinsic dysfunction in amyotrophic lateral sclerosis.
- Published in:
- Acta Neuropathologica, 2024, v. 148, n. 1, p. 1, doi. 10.1007/s00401-024-02794-y
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- Publication type:
- Article
Targeted Next-Generation Sequencing in a Large Cohort of Genetically Undiagnosed Patients with Neuromuscular Disorders in Spain.
- Published in:
- Genes, 2020, v. 11, n. 5, p. 539, doi. 10.3390/genes11050539
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- Publication type:
- Article
Social cognition in myotonic dystrophy type 1: Specific or secondary impairment?
- Published in:
- PLoS ONE, 2018, v. 13, n. 9, p. 1, doi. 10.1371/journal.pone.0204227
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- Publication type:
- Article
The unexpected co-occurrence of GRN and MAPT p.A152T in Basque families: Clinical and pathological characteristics.
- Published in:
- PLoS ONE, 2017, v. 12, n. 6, p. 1, doi. 10.1371/journal.pone.0178093
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- Publication type:
- Article