Found: 10
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Influence of isolated low‐grade intracranial haemorrhages on the neurodevelopmental outcome of infants born very low birthweight.
- Published in:
- Developmental Medicine & Child Neurology, 2023, v. 65, n. 10, p. 1366, doi. 10.1111/dmcn.15559
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- Publication type:
- Article
Long‐term effectiveness of add‐on perampanel in patients with Lennox–Gastaut syndrome: A multicenter retrospective study.
- Published in:
- Epilepsia (Series 4), 2023, v. 64, n. 6, p. e98, doi. 10.1111/epi.17601
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- Publication type:
- Article
Comparison of Qualitative and Quantitative Analyses of MR-Arterial Spin Labeling Perfusion Data for the Assessment of Pediatric Patients with Focal Epilepsies.
- Published in:
- Diagnostics (2075-4418), 2022, v. 12, n. 4, p. 811, doi. 10.3390/diagnostics12040811
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- Publication type:
- Article
Symptomatic eating epilepsy: two novel pediatric patients and review of literature.
- Published in:
- Italian Journal of Pediatrics, 2021, v. 47, n. 1, p. 1, doi. 10.1186/s13052-021-01051-2
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- Publication type:
- Article
Prevention of human rabies: a challenge for the European Union and the European Economic Area.
- Published in:
- Eurosurveillance (15607917), 2020, v. 25, n. 38, p. 16, doi. 10.2807/1560-7917.ES.2020.25.38.2000158
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- Publication type:
- Article
Targeted re-sequencing for early diagnosis of genetic causes of childhood epilepsy: the Italian experience from the 'beyond epilepsy' project.
- Published in:
- Italian Journal of Pediatrics, 2020, v. 46, n. 1, p. 1, doi. 10.1186/s13052-020-00860-1
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- Publication type:
- Article
Predicción temprana de deserción mediante aprendizaje automático en cursos profesionales en línea.
- Published in:
- RIED: Revista Iberoamericana de Educación a Distancia, 2020, v. 23, n. 2, p. 147, doi. 10.5944/ried.23.2.26356
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- Publication type:
- Article
New molecular tools for meningitis diagnostics in Ethiopia - a necessary step towards improving antimicrobial prescription.
- Published in:
- 2018
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- Publication type:
- journal article
Combined early treatment in hemiplegic attacks related to CACNA1A encephalopathy with brain oedema: Blocking the cascade?
- Published in:
- 2017
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- Publication type:
- journal article
A novel homozygous splicing mutation in PSAP gene causes metachromatic leukodystrophy in two Moroccan brothers.
- Published in:
- Neurogenetics, 2014, v. 15, n. 2, p. 101, doi. 10.1007/s10048-014-0390-4
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- Publication type:
- Article