Found: 11
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Post-Stroke Asymmetric Prurigo Nodularis Responding to Dupilumab Treatment: A Case Report.
- Published in:
- Brain Sciences (2076-3425), 2022, v. 12, n. 5, p. 605, doi. 10.3390/brainsci12050605
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- Publication type:
- Article
Personality disorders in individuals with functional seizures: a systematic review.
- Published in:
- Frontiers in Psychiatry, 2024, p. 1, doi. 10.3389/fpsyt.2024.1411189
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- Publication type:
- Article
Non-Coding RNAs: New Biomarkers and Therapeutic Targets for Temporal Lobe Epilepsy.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 6, p. 3063, doi. 10.3390/ijms23063063
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- Article
Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia.
- Published in:
- 2024
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- Publication type:
- Case Study
Enlarging the clinical spectrum of chorea-acanthocytosis.
- Published in:
- 2022
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- Publication type:
- Letter
Value of Multimodal Imaging Approach to Diagnosis of Neurosarcoidosis.
- Published in:
- Brain Sciences (2076-3425), 2019, v. 9, n. 10, p. 243, doi. 10.3390/brainsci9100243
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- Publication type:
- Article
Idiopathic generalized epilepsy in a family with SCN4A‐related myotonia.
- Published in:
- Epilepsia Open, 2024, v. 9, n. 3, p. 951, doi. 10.1002/epi4.12920
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- Publication type:
- Article
May anti‐seizure medications alter brain structure in temporal lobe epilepsy? A prospective study.
- Published in:
- Epilepsia Open, 2024, v. 9, n. 3, p. 1076, doi. 10.1002/epi4.12912
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- Publication type:
- Article
Neuropsychiatric profile in average intelligent individuals with coexisting epilepsy and psychogenic non‐epileptic seizures.
- Published in:
- Epilepsia Open, 2023, v. 8, n. 2, p. 678, doi. 10.1002/epi4.12731
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- Publication type:
- Article
Looking for indicative magnetic resonance imaging signs of hippocampal developmental abnormalities in patients with mesial temporal lobe epilepsy and healthy controls.
- Published in:
- Epilepsia (Series 4), 2020, v. 61, n. 8, p. 1714, doi. 10.1111/epi.16608
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- Publication type:
- Article
Glucose transporter‐1 deficiency syndrome with extreme phenotypic variability in a five‐generation family carrying a novel SLC2A1 variant.
- Published in:
- European Journal of Neurology, 2024, v. 31, n. 8, p. 1, doi. 10.1111/ene.16325
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- Publication type:
- Article