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Dual diagnosis in a child with familial SCN8A-related encephalopathy complicated by a 1p13.2 deletion involving NRAS gene.
- Published in:
- 2021
- By:
- Publication type:
- Letter
Psychiatric features in gelastic epilepsy and hypothalamic hamartoma: long-term psychodiagnostic observations.
- Published in:
- 2014
- By:
- Publication type:
- Letter
Psychiatric features in gelastic epilepsy and hypothalamic hamartoma: long-term psychodiagnostic observations.
- Published in:
- 2014
- By:
- Publication type:
- Case Study
Posterior cortical atrophy with prominent alexia without agraphia in a Tourette syndrome.
- Published in:
- Neurological Sciences, 2011, v. 32, n. 6, p. 1129, doi. 10.1007/s10072-011-0760-8
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- Publication type:
- Article
Temporal lobe epilepsy and anti glutamic acid decarboxylase autoimmunity.
- Published in:
- Neurological Sciences, 2011, v. 32, n. 4, p. 547, doi. 10.1007/s10072-011-0566-8
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- Publication type:
- Article
Sudden death in Unverricht–Lundborg patients: is serotonin the key?
- Published in:
- 2010
- By:
- Publication type:
- Letter
Sudden death in Unverricht-Lundborg patients: is serotonin the key?
- Published in:
- 2010
- By:
- Publication type:
- Letter
In response: DEPDC5 mutations in epilepsy with auditory features.
- Published in:
- Epilepsia (Series 4), 2016, v. 57, n. 2, p. 336, doi. 10.1111/epi.13255
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- Publication type:
- Article
DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy.
- Published in:
- Epilepsia (Series 4), 2015, v. 56, n. 10, p. e168, doi. 10.1111/epi.13094
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- Publication type:
- Article
A prospective study of direct medical costs in a large cohort of consecutively enrolled patients with refractory epilepsy in Italy.
- Published in:
- Epilepsia (Series 4), 2015, v. 56, n. 7, p. 1162, doi. 10.1111/epi.13030
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- Publication type:
- Article
Copy number variations and susceptibility to lateral temporal epilepsy: A study of 21 pedigrees.
- Published in:
- Epilepsia (Series 4), 2014, v. 55, n. 10, p. 1651, doi. 10.1111/epi.12767
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- Publication type:
- Article
Loss-of-function KCNH2 mutation in a family with long QT syndrome, epilepsy, and sudden death.
- Published in:
- Epilepsia (Series 4), 2013, v. 54, n. 8, p. e112, doi. 10.1111/epi.12259
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- Publication type:
- Article
Different electroclinical picture of generalized epilepsy in two families with 15q13.3 microdeletion.
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- Epilepsia (Series 4), 2013, v. 54, n. 5, p. e69, doi. 10.1111/epi.12130
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- Publication type:
- Article
Determinants of health-related quality of life in pharmacoresistant epilepsy: Results from a large multicenter study of consecutively enrolled patients using validated quantitative assessments.
- Published in:
- Epilepsia (Series 4), 2011, v. 52, n. 12, p. 2181, doi. 10.1111/j.1528-1167.2011.03325.x
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- Publication type:
- Article
Natural history and long-term evolution in families with autosomal dominant cortical tremor, myoclonus, and epilepsy.
- Published in:
- Epilepsia (Series 4), 2011, v. 52, n. 7, p. 1245, doi. 10.1111/j.1528-1167.2011.03017.x
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- Publication type:
- Article
Characteristics of a large population of patients with refractory epilepsy attending tertiary referral centers in Italy.
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- Epilepsia (Series 4), 2010, v. 51, n. 5, p. 921, doi. 10.1111/j.1528-1167.2009.02512.x
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- Publication type:
- Article
Hyperhomocysteinemia in epileptic patients on new antiepileptic drugs.
- Published in:
- Epilepsia (Series 4), 2010, v. 51, n. 2, p. 274, doi. 10.1111/j.1528-1167.2009.02303.x
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- Publication type:
- Article
Comment on “Factors influencing clinical features of absence seizures”.
- Published in:
- 2009
- By:
- Publication type:
- Letter
<sup>1</sup>H-MR spectroscopy indicates prominent cerebellar dysfunction in benign adult familial myoclonic epilepsy.
- Published in:
- Epilepsia (Series 4), 2009, v. 50, n. 6, p. 1491, doi. 10.1111/j.1528-1167.2008.01900.x
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- Publication type:
- Article
Eyelid fluttering, typical EEG pattern, and impaired intellectual function: A homogeneous epileptic condition among the patients presenting with eyelid myoclonia.
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- Epilepsia (Series 4), 2009, v. 50, n. 6, p. 1536, doi. 10.1111/j.1528-1167.2008.02002.x
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- Publication type:
- Article
Transient epileptic amnesia: An emerging late-onset epileptic syndrome.
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- Epilepsia (Series 4), 2009, v. 50, p. 58, doi. 10.1111/j.1528-1167.2009.02124.x
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- Publication type:
- Article
Introduction.
- Published in:
- Epilepsia (Series 4), 2009, v. 50, p. 1, doi. 10.1111/j.1528-1167.2009.02111.x
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- Publication type:
- Article
Eyelid myoclonia with absences (Jeavons syndrome): A well-defined idiopathic generalized epilepsy syndrome or a spectrum of photosensitive conditions?
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- Epilepsia (Series 4), 2009, v. 50, p. 15, doi. 10.1111/j.1528-1167.2009.02114.x
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- Publication type:
- Article
The syndrome gelastic seizures–hypothalamic hamartoma: Severe, potentially reversible encephalopathy.
- Published in:
- Epilepsia (Series 4), 2009, v. 50, p. 62, doi. 10.1111/j.1528-1167.2009.02125.x
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- 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
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- Publication type:
- Article
Antiepileptic Drugs and MTHFR Polymorphisms Influence Hyper-Homocysteinemia Recurrence in Epileptic Patients.
- Published in:
- Epilepsia (Series 4), 2007, v. 48, n. 10, p. 1990, doi. 10.1111/j.1528-1167.2007.01164.x
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- Publication type:
- Article
Life-Threatening Status Epilepticus Following Gabapentin Administration in a Patient with Benign Adult Familial Myoclonic Epilepsy.
- Published in:
- Epilepsia (Series 4), 2007, v. 48, n. 10, p. 1995, doi. 10.1111/j.1528-1167.2007.01198.x
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- Publication type:
- Article
Lateralizing Value of the Auditory Aura in Partial Seizures.
- Published in:
- Epilepsia (Series 4), 2006, v. 47, p. 68, doi. 10.1111/j.1528-1167.2006.00881.x
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- Publication type:
- Article
6q Terminal Deletion Syndrome Associated with a Distinctive EEG and Clinical Pattern: A Report of Five Cases.
- Published in:
- Epilepsia (Series 4), 2006, v. 47, n. 5, p. 830, doi. 10.1111/j.1528-1167.2006.00522.x
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- Publication type:
- Article
Clinical and Genetic Findings in 26 Italian Patients with Lafora Disease.
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- Epilepsia (Series 4), 2006, v. 47, n. 3, p. 640, doi. 10.1111/j.1528-1167.2006.00479.x
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- Publication type:
- Article
Epileptogenesis due to Peripheral Injury as a Cause of Focal Epilepsy.
- Published in:
- 2006
- By:
- Publication type:
- Letter
Insulinoma Presenting as Refractory Late-onset Epilepsy.
- Published in:
- 2006
- By:
- Publication type:
- Letter
Electroclinical and Genetic Findings in a Family with Cortical Tremor, Myoclonus, and Epilepsy.
- Published in:
- 2005
- By:
- Publication type:
- Letter
A t(4;9)(q34;p22) Translocation Associated with Partial Epilepsy, Mental Retardation, and Dysmorphism.
- Published in:
- 2005
- By:
- Publication type:
- Letter
Original Letter A New Benign Adult Familial Myoclonic Epilepsy (BAFME) Pedigree Suggesting Linkage to Chromosome 2p11.1-q12.2.
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- Epilepsia (Series 4), 2004, v. 45, n. 2, p. 190, doi. 10.1111/j.0013-9580.2004.39903.x
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- Publication type:
- Article
Severe epilepsy in an adult with partial trisomy 18q.
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- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 12, p. 3148, doi. 10.1002/ajmg.a.36743
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- Publication type:
- Article
Characterization of Reproductive Endocrine Disorders in Women with Epilepsy.
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- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 2, p. 2950
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- Publication type:
- Article
Characterization of Reproductive Endocrine Disorders in Women with Epilepsy.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 7, p. 2950, doi. 10.1210/jcem.86.7.7633
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- Publication type:
- Article
Familial mesial temporal lobe epilepsy (FMTLE).
- Published in:
- Journal of Neurology, 2008, v. 255, n. 1, p. 16, doi. 10.1007/s00415-007-0653-1
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- Publication type:
- Article
A novel mutation in GCH-1 gene in a case of dopa-responsive dystonia.
- Published in:
- Journal of Neurology, 2007, v. 254, n. 8, p. 1133, doi. 10.1007/s00415-006-0475-6
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- Publication type:
- Article
Unfavourable outcome of Hashimoto encephalopathy due to status epilepticus.
- Published in:
- Journal of Neurology, 2006, v. 253, n. 2, p. 248, doi. 10.1007/s00415-005-0925-6
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- Publication type:
- Article
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation.
- Published in:
- Journal of Neurology, 2005, v. 252, n. 8, p. 897, doi. 10.1007/s00415-005-0766-3
- By:
- Publication type:
- Article
Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case series.
- Published in:
- International Journal of Legal Medicine, 2015, v. 129, n. 3, p. 495, doi. 10.1007/s00414-014-1063-4
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- Publication type:
- Article
Diagnosis and Management of Type 1 Sialidosis: Clinical Insights from Long-Term Care of Four Unrelated Patients.
- Published in:
- Brain Sciences (2076-3425), 2020, v. 10, n. 8, p. 506, doi. 10.3390/brainsci10080506
- By:
- Publication type:
- Article
Off-Label Prescribing of Antiepileptic Drugs in Pharmacoresistant Epilepsy: A Cross-Sectional Drug Utilization Study of Tertiary Care Centers in Italy.
- Published in:
- CNS Drugs, 2014, v. 28, n. 10, p. 939, doi. 10.1007/s40263-014-0189-8
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- Publication type:
- Article
Posterior reversible encephalopathy syndrome in intensive care medicine.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Autosomal recessive epilepsy associated with contactin 2 mutation is different from familial cortical tremor, myoclonus and epilepsy.
- Published in:
- Brain: A Journal of Neurology, 2013, v. 136, n. 10, p. e253, doi. 10.1093/brain/awt140
- By:
- Publication type:
- Article
Familial adult myoclonus epilepsy: Clinical findings, disease course, and comorbidities.
- Published in:
- Epilepsia (Series 4), 2023, v. 64, p. S9, doi. 10.1111/epi.17595
- By:
- Publication type:
- Article
Clinical features and evolution of the gelastic seizures-hypothalamic hamartoma syndrome.
- Published in:
- Epilepsia (Series 4), 2017, v. 58, p. 12, doi. 10.1111/epi.13753
- By:
- Publication type:
- Article
Safety of Overnight Switch from Brand-Name to Generic Levetiracetam.
- Published in:
- Clinical Drug Investigation, 2016, v. 36, n. 1, p. 87, doi. 10.1007/s40261-015-0351-1
- By:
- Publication type:
- Article