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Efficacy, Retention, and Tolerability of Brivaracetam in Patients With Epileptic Encephalopathies: A Multicenter Cohort Study From Germany.
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- Frontiers in Neurology, 2018, p. N.PAG, doi. 10.3389/fneur.2018.00569
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- Article
Nosological delineation of congenital ocular motor apraxia type Cogan: an observational study.
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- 2016
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- journal article
Neuronal mechanisms of mutations in SCN8A causing epilepsy or intellectual disability.
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- 2019
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- journal article
Rasmussen encephalitis: Incidence and course under randomized therapy with tacrolimus or intravenous immunoglobulins.
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- Epilepsia (Series 4), 2013, v. 54, n. 3, p. 543, doi. 10.1111/epi.12042
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- Article
Febrile infection–related epilepsy syndrome (FIRES): A nonencephalitic encephalopathy in childhood.
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- Epilepsia (Series 4), 2010, v. 51, n. 7, p. 1323, doi. 10.1111/j.1528-1167.2010.02535.x
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- Article
Benign Familial Infantile Convulsions: Linkage to Chromosome 16p12-q12 in 14 Families.
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- Epilepsia (Series 4), 2004, v. 45, n. 6, p. 601, doi. 10.1111/j.0013-9580.2004.48203.x
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- Article
Clinical Research Sulthiame in the Primary Therapy of West Syndrome: A Randomized Double-blind Placebo-controlled Add-on Trial on Baseline Pyridoxine Medication.
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- Epilepsia (Series 4), 2004, v. 45, n. 2, p. 103, doi. 10.1111/j.0013-9580.2004.19003.x
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- Article
Cerebellar Bottom-of-Fissure Dysplasia-a Novel Cerebellar Gray Matter Neuroimaging Pattern.
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- Cerebellum, 2016, v. 15, n. 6, p. 705, doi. 10.1007/s12311-015-0736-y
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- Article
Spontaneous central melatonin secretion and resorption kinetics of exogenous melatonin: a ventricular CSF study.
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- Journal of Pineal Research, 2002, v. 33, n. 4, p. 213, doi. 10.1034/j.1600-079X.2002.02907.x
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- Article
Application of NMR spectroscopy to monitoring MELAS treatment: a case report.
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- 2002
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- journal article
Efficacy, Retention and Tolerability of Everolimus in Patients with Tuberous Sclerosis Complex: A Survey-Based Study on Patients' Perspectives.
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- CNS Drugs, 2021, v. 35, n. 10, p. 1107, doi. 10.1007/s40263-021-00839-4
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- Article
Sleep quality, anxiety, symptoms of depression, and caregiver burden among those caring for patients with Dravet syndrome: a prospective multicenter study in Germany.
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- Orphanet Journal of Rare Diseases, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s13023-023-02697-3
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- Article
Real‐world data on cannabidiol treatment of various epilepsy subtypes: A retrospective, multicenter study.
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- Epilepsia Open, 2023, v. 8, n. 2, p. 360, doi. 10.1002/epi4.12699
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- Article
Direct and indirect costs and cost-driving factors of Tuberous sclerosis complex in children, adolescents, and caregivers: a multicenter cohort study.
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- 2021
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- journal article
Clinical and molecular genetic findings in COLQ-mutant congenital myasthenic syndromes.
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- Brain: A Journal of Neurology, 2008, v. 131, n. 3, p. 747, doi. 10.1093/brain/awm325
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- Article
Critical incidents, nocturnal supervision, and caregiver knowledge on SUDEP in patients with Dravet syndrome: A prospective multicenter study in Germany.
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- Epilepsia (Series 4), 2024, v. 65, n. 1, p. 115, doi. 10.1111/epi.17799
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- Article
Long‐term efficacy, tolerability, and retention of brivaracetam in epilepsy treatment: A longitudinal multicenter study with up to 5 years of follow‐up.
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- Epilepsia (Series 4), 2021, v. 62, n. 12, p. 2994, doi. 10.1111/epi.17087
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- Article
Efficacy, tolerability, and retention of fenfluramine for the treatment of seizures in patients with Dravet syndrome: Compassionate use program in Germany.
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- Epilepsia (Series 4), 2021, v. 62, n. 10, p. 2518, doi. 10.1111/epi.17034
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- Article
A multicenter, matched case‐control analysis comparing burden‐of‐illness in Dravet syndrome to refractory epilepsy and seizure remission in patients and caregivers in Germany.
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- Epilepsia (Series 4), 2019, v. 60, n. 8, p. 1697, doi. 10.1111/epi.16099
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- Article
Use of brivaracetam in genetic generalized epilepsies and for acute, intravenous treatment of absence status epilepticus.
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- Epilepsia (Series 4), 2018, v. 59, n. 8, p. 1549, doi. 10.1111/epi.14476
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- Article
Postmarketing experience with brivaracetam in the treatment of epilepsies: A multicenter cohort study from Germany.
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- Epilepsia (Series 4), 2017, v. 58, n. 7, p. 1208, doi. 10.1111/epi.13768
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- Article
Predictors of and attitudes toward counseling about SUDEP and other epilepsy risk factors among Austrian, German, and Swiss neurologists and neuropediatricians.
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- Epilepsia (Series 4), 2016, v. 57, n. 4, p. 612, doi. 10.1111/epi.13337
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- Article
CD8<sup>+</sup> T-cell pathogenicity in Rasmussen encephalitis elucidated by large-scale T-cell receptor sequencing.
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- Nature Communications, 2016, v. 7, n. 4, p. 11153, doi. 10.1038/ncomms11153
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- Article
Direct and indirect costs and cost-driving factors in adults with tuberous sclerosis complex: a multicenter cohort study and a review of the literature.
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- 2021
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- Publication type:
- journal article
Germline and somatic FGFR1 abnormalities in dysembryoplastic neuroepithelial tumors.
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- Acta Neuropathologica, 2016, v. 131, n. 6, p. 847, doi. 10.1007/s00401-016-1549-x
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- Article
A multicenter, matched case–control analysis comparing burden of illness among patients with tuberous sclerosis complex related epilepsy, generalized idiopathic epilepsy, and focal epilepsy in Germany.
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- Neurological Research & Practice, 2024, v. 6, n. 1, p. 1, doi. 10.1186/s42466-024-00323-6
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- Article
Exploring the relationships between composite scores of disease severity, seizure-freedom and quality of life in Dravet syndrome.
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- Neurological Research & Practice, 2022, v. 4, n. 1, p. 1, doi. 10.1186/s42466-022-00186-9
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- Publication type:
- Article
Exploring the relationships between composite scores of disease severity, seizure-freedom and quality of life in Dravet syndrome.
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- Neurological Research & Practice, 2022, v. 4, n. 1, p. 1, doi. 10.1186/s42466-022-00186-9
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- Article
Brain Tumors in Children: Initial Symptoms and Their Influence on the Time Span Between Symptom Onset and Diagnosis.
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- Journal of Child Neurology, 2008, v. 23, n. 2, p. 178, doi. 10.1177/0883073807308692
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- Article
Adult Height and Target Height in 111 Boys and 98 Girls Treated for Epilepsy During Childhood.
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- Journal of Child Neurology, 1997, v. 12, n. 8, p. 513, doi. 10.1177/088307389701200810
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- Article
PRRT2 Mutations are the major cause of benign familial infantile seizures.
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- Human Mutation, 2012, v. 33, n. 10, p. 1439, doi. 10.1002/humu.22126
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- Article
Cerebral arterial stenoses and stroke: novel features of Aicardi-Goutières syndrome caused by the Arg164X mutation in SAMHD1 are associated with altered cytokine expression.
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- Human Mutation, 2010, v. 31, n. 11, p. E1836, doi. 10.1002/humu.21357
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- Article