Found: 13
Select item for more details and to access through your institution.
Mild Lafora disease: Clinical, neurophysiologic, and genetic findings.
- Published in:
- Epilepsia (Series 4), 2014, v. 55, n. 12, p. e129, doi. 10.1111/epi.12806
- By:
- Publication type:
- Article
Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations.
- Published in:
- Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2120, doi. 10.1111/j.1528-1167.2012.03718.x
- By:
- Publication type:
- Article
Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences.
- Published in:
- Epilepsia (Series 4), 2012, v. 53, n. 12, p. e196, doi. 10.1111/epi.12009
- By:
- Publication type:
- Article
A pilot trial of levetiracetam in eyelid myoclonia with absences (Jeavons syndrome).
- Published in:
- Epilepsia (Series 4), 2008, v. 49, n. 3, p. 425, doi. 10.1111/j.1528-1167.2007.01524.x
- By:
- Publication type:
- Article
Impact of Idiopathic Epilepsy on Mothers and Fathers: Strain, Burden of Care, Worries and Perception of Vulnerability.
- Published in:
- Epilepsia (Series 4), 2007, v. 48, n. 9, p. 1810, doi. 10.1111/j.1528-1167.2007.01145.x
- By:
- Publication type:
- Article
Randomized Double-Blind Crossover Study for Evaluating a Probiotic Mixture on Gastrointestinal and Behavioral Symptoms of Autistic Children.
- Published in:
- Journal of Clinical Medicine, 2022, v. 11, n. 18, p. N.PAG, doi. 10.3390/jcm11185263
- By:
- Publication type:
- Article
Long-term applicability of the new ILAE definition of epilepsy. Results from the PRO- LONG study.
- Published in:
- Epilepsia (Series 4), 2017, v. 58, n. 9, p. 1518, doi. 10.1111/epi.13854
- By:
- Publication type:
- Article
Anakinra usage in febrile infection related epilepsy syndrome: an international cohort.
- Published in:
- Annals of Clinical & Translational Neurology, 2020, v. 7, n. 12, p. 2467, doi. 10.1002/acn3.51229
- By:
- Publication type:
- Article
Aromatic L-amino Acid Decarboxylase (AADC) deficiency: results from an Italian modified Delphi consensus.
- Published in:
- Italian Journal of Pediatrics, 2021, v. 47, n. 1, p. 1, doi. 10.1186/s13052-021-00954-4
- By:
- Publication type:
- Article
The Usefulness of a Targeted Next Generation Sequencing Gene Panel in Providing Molecular Diagnosis to Patients With a Broad Spectrum of Neurodevelopmental Disorders.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.875182
- By:
- Publication type:
- Article
Peripheral Markers of the--Aminobutyric Acid (GABA)ergic System in Angelman's Syndrome.
- Published in:
- Journal of Child Neurology, 2003, v. 18, n. 1, p. 21, doi. 10.1177/08830738030180010801
- By:
- Publication type:
- Article
Seizure and EEG Patterns in Angelman's Syndrome.
- Published in:
- Journal of Child Neurology, 1995, v. 10, n. 6, p. 467, doi. 10.1177/088307389501000609
- By:
- Publication type:
- Article
Impact and management of drooling in children with neurological disorders: an Italian Delphi consensus.
- Published in:
- Italian Journal of Pediatrics, 2022, v. 48, n. 1, p. 1, doi. 10.1186/s13052-022-01312-8
- By:
- Publication type:
- Article