Detalhe da pesquisa
1.
Critical incidents, nocturnal supervision, and caregiver knowledge on SUDEP in patients with Dravet syndrome: A prospective multicenter study in Germany.
Epilepsia
; 65(1): 115-126, 2024 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-37846648
2.
Spectrum, Evolution, and Clinical Relationship of Magnetic Resonance Imaging in 31 Children with Febrile Infection-Related Epilepsy Syndrome.
Neuropediatrics
; 55(1): 9-15, 2024 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-37798920
3.
Biallelic variants in PIGN cause Fryns syndrome, multiple congenital anomalies-hypotonia-seizures syndrome, and neurologic phenotypes: A genotype-phenotype correlation study.
Genet Med
; 25(1): 37-48, 2023 01.
Artigo
Inglês
| MEDLINE | ID: mdl-36322149
4.
Sex-based electroclinical differences and prognostic factors in epilepsy with eyelid myoclonia.
Epilepsia
; 64(6): e105-e111, 2023 06.
Artigo
Inglês
| MEDLINE | ID: mdl-37021337
5.
Perampanel as precision therapy in rare genetic epilepsies.
Epilepsia
; 64(4): 866-874, 2023 04.
Artigo
Inglês
| MEDLINE | ID: mdl-36734057
6.
Autoimmune Encephalitis with Autoantibodies to NMDAR1 following Herpes Encephalitis in Children and Adolescents.
Neuropediatrics
; 54(1): 14-19, 2023 02.
Artigo
Inglês
| MEDLINE | ID: mdl-36543183
7.
The spectrum of epilepsy with eyelid myoclonia: delineation of disease subtypes from a large multicenter study.
Epilepsia
; 2022 Oct 28.
Artigo
Inglês
| MEDLINE | ID: mdl-36307934
8.
PIGN encephalopathy: Characterizing the epileptology.
Epilepsia
; 63(4): 974-991, 2022 04.
Artigo
Inglês
| MEDLINE | ID: mdl-35179230
9.
Efficacy, tolerability, and retention of fenfluramine for the treatment of seizures in patients with Dravet syndrome: Compassionate use program in Germany.
Epilepsia
; 62(10): 2518-2527, 2021 10.
Artigo
Inglês
| MEDLINE | ID: mdl-34378197
10.
Epilepsy in Nicolaides-Baraitser Syndrome: Review of Literature and Report of 25 Patients Focusing on Treatment Aspects.
Neuropediatrics
; 52(2): 109-122, 2021 04.
Artigo
Inglês
| MEDLINE | ID: mdl-33578439
11.
Safety and efficacy of rufinamide in children and adults with Lennox-Gastaut syndrome: A post hoc analysis from Study 022.
Epilepsy Behav
; 124: 108275, 2021 Sep 09.
Artigo
Inglês
| MEDLINE | ID: mdl-34509883
12.
Stability of 0.5% Glucose-Containing Balanced Electrolyte Solutions for Patients on Ketogenic Diets: A Laboratory Study.
Neuropediatrics
; 51(6): 397-400, 2020 12.
Artigo
Inglês
| MEDLINE | ID: mdl-32842160
13.
Cooccurrence of Two Different Genetic Diseases: A Case of Valproic Acid Hepatotoxicity in Nicolaides-Baraitser Syndrome (SMARCA2 Mutation)-Due to a POLG1-Related Effect?
Neuropediatrics
; 51(1): 49-52, 2020 02.
Artigo
Inglês
| MEDLINE | ID: mdl-31541998
14.
Dog-Assisted Therapy in Neurorehabilitation of Children with Severe Neurological Impairment: An Explorative Study.
Neuropediatrics
; 51(4): 267-274, 2020 08.
Artigo
Inglês
| MEDLINE | ID: mdl-32176927
15.
Generalized myoclonic epilepsy with photosensitivity in juvenile dogs caused by a defective DIRAS family GTPase 1.
Proc Natl Acad Sci U S A
; 114(10): 2669-2674, 2017 03 07.
Artigo
Inglês
| MEDLINE | ID: mdl-28223533
16.
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.
Epilepsia
; 60(8): 1697-1710, 2019 08.
Artigo
Inglês
| MEDLINE | ID: mdl-31247127
17.
Unresponsive Wakefulness Syndrome in Children after Near-Drowning: Long-Term Outcome and Impact on the Families.
Neuropediatrics
; 50(2): 71-79, 2019 04.
Artigo
Inglês
| MEDLINE | ID: mdl-30572371
18.
Seizure management and prescription patterns of anticonvulsants in Dravet syndrome: A multicenter cohort study from Germany and review of literature.
Epilepsy Behav
; 98(Pt A): 88-95, 2019 09.
Artigo
Inglês
| MEDLINE | ID: mdl-31301455
19.
FOXG1 syndrome: genotype-phenotype association in 83 patients with FOXG1 variants.
Genet Med
; 20(1): 98-108, 2018 01.
Artigo
Inglês
| MEDLINE | ID: mdl-28661489
20.
Seizure Freedom in Patients with Dravet Syndrome with Contraceptives: A Case Report with Two Patients.
Neuropediatrics
; 49(4): 276-278, 2018 08.
Artigo
Inglês
| MEDLINE | ID: mdl-29571173