Found: 20
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Reversible encephalopathy induced by cefoperazone: a case report monitored with EEG.
- Published in:
- Neurological Sciences, 2011, v. 32, n. 3, p. 465, doi. 10.1007/s10072-010-0425-z
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- Publication type:
- Article
Vocal Cord Paralysis and Feeding Difficulties as Early Diagnostic Clues of Congenital Myasthenic Syndrome with Neonatal Onset: A Case Report and Review of Literature.
- Published in:
- Journal of Personalized Medicine, 2023, v. 13, n. 5, p. 798, doi. 10.3390/jpm13050798
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- Publication type:
- Article
De novo p.T362R mutation in MORC2 causes early onset cerebellar ataxia, axonal polyneuropathy and nocturnal hypoventilation.
- Published in:
- 2017
- By:
- Publication type:
- Letter
Reply to: Viability of diffusion tensor imaging for assessing retrochiasmatic involvement in Kearns-Sayre syndrome remains elusive.
- Published in:
- 2020
- By:
- Publication type:
- Letter
Visual pathways evaluation in Kearns Sayre syndrome: a diffusion tensor imaging study.
- Published in:
- Neuroradiology, 2020, v. 62, n. 2, p. 241, doi. 10.1007/s00234-019-02302-0
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- Publication type:
- Article
Case report: A pediatric case of Bickerstaff brainstem encephalitis after COVID-19 vaccination and Mycoplasma pneumoniae infection: Looking for the culprit.
- Published in:
- 2022
- By:
- Publication type:
- Case Study
Corticospinal tract damage in HHH syndrome: a metabolic cause of hereditary spastic paraplegia.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Age‐related sensory neuropathy in patients with spinal muscular atrophy type 1.
- Published in:
- Muscle & Nerve, 2021, v. 64, n. 5, p. 599, doi. 10.1002/mus.27389
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- Publication type:
- Article
Isolated Intracranial Hypertensions as Onset of Myelin Oligodendrocyte Glycoprotein Antibody Disease.
- Published in:
- Journal of Clinical Medicine, 2024, v. 13, n. 15, p. 4468, doi. 10.3390/jcm13154468
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- Publication type:
- Article
Peripheral Nervous System Involvement in Non-Primary Pediatric Cancer: From Neurotoxicity to Possible Etiologies.
- Published in:
- Journal of Clinical Medicine, 2021, v. 10, n. 14, p. 3016, doi. 10.3390/jcm10143016
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- Publication type:
- Article
A New Case of Autosomal-Dominant POLR3B -Related Disorder: Widening Genotypic and Phenotypic Spectrum.
- Published in:
- 2023
- By:
- Publication type:
- Case Study
High Intellectual Potential and High Functioning Autism: Clinical and Neurophysiological Features in a Pediatric Sample.
- Published in:
- Brain Sciences (2076-3425), 2021, v. 11, n. 12, p. 1607, doi. 10.3390/brainsci11121607
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- Publication type:
- Article
Short and Long-Term Toxicity in Pediatric Cancer Treatment: Central Nervous System Damage.
- Published in:
- Cancers, 2022, v. 14, n. 6, p. 1540, doi. 10.3390/cancers14061540
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- Publication type:
- Article
Nonconvulsive status epilepticus induced by acute hypothyroidism in a critically ill patient.
- Published in:
- 2011
- By:
- Publication type:
- Letter
Hereditary spastic paraplegia is a novel phenotype for germline de novo ATP1A1 mutation.
- Published in:
- Clinical Genetics, 2020, v. 97, n. 3, p. 521, doi. 10.1111/cge.13668
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- Publication type:
- Article
Event-Related Potentials in ADHD Associated With Tuberous Sclerosis Complex: A Possible Biomarker of Symptoms Severity?
- Published in:
- Frontiers in Neurology, 2020, v. 11, p. 1, doi. 10.3389/fneur.2020.00546
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- Publication type:
- Article
A cohort study on acute ocular motility disorders in pediatric emergency department.
- Published in:
- Italian Journal of Pediatrics, 2018, v. 44, n. 1, p. N.PAG, doi. 10.1186/s13052-018-0502-0
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- Publication type:
- Article
Brain auditory evoked potentials in pediatric Intensive Care Unit: diagnostic role on encephalopathy and central respiratory failure on infants.
- Published in:
- Minerva Pediatrics, 2024, v. 76, n. 2, p. 197, doi. 10.23736/S2724-5276.21.05931-0
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- Publication type:
- Article
Early electroencephalogram and somatosensory evoked potentials as prognostic bedside tools in the pediatric cardiac intensive care.
- Published in:
- Minerva Pediatrics, 2022, v. 74, n. 6, p. 802, doi. 10.23736/S2724-5276.20.05743-6
- By:
- Publication type:
- Article
Spectrum of ERCC6 -Related Cockayne Syndrome (Type B): From Mild to Severe Forms.
- Published in:
- Genes, 2024, v. 15, n. 4, p. 508, doi. 10.3390/genes15040508
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- Publication type:
- Article