Detalhe da pesquisa
1.
Olfactory function after mild traumatic brain injury in children-a longitudinal case control study.
Cereb Cortex
; 34(4)2024 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38629798
2.
[Gender-specific results of the Dresden children and adolescents headache program DreKiP]. / Geschlechtsspezifische Ergebnisse des Dresdner Kinder- und Jugendkopfschmerzprogrammes DreKiP.
Schmerz
; 38(2): 107-117, 2024 Apr.
Artigo
em Alemão
| MEDLINE | ID: mdl-37737282
3.
Feedback-Based Learning of Timing in Attention-Deficit/Hyperactivity Disorder and Neurofibromatosis Type 1.
J Int Neuropsychol Soc
; 28(1): 12-21, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33573707
4.
Effect of Different Corticosteroid Dosing Regimens on Clinical Outcomes in Boys With Duchenne Muscular Dystrophy: A Randomized Clinical Trial.
JAMA
; 327(15): 1456-1468, 2022 04 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-35381069
5.
Functional improvement in children and adolescents with primary headache after an interdisciplinary multimodal therapy program: the DreKiP study.
J Headache Pain
; 23(1): 109, 2022 Aug 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-36008766
6.
The clinical-phenotype continuum in DYNC1H1-related disorders-genomic profiling and proposal for a novel classification.
J Hum Genet
; 65(11): 1003-1017, 2020 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-32788638
7.
Just Expect It: Compound Heterozygous Variants of POMT1 in a Consanguineous Family-The Role of Next Generation Sequencing in Neuromuscular Disorders.
Neuropediatrics
; 51(1): 72-75, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31627234
8.
[Recommendations for gene therapy of spinal muscular atrophy with onasemnogene abeparvovec-AVXS-101 : Consensus paper of the German representatives of the Society for Pediatric Neurology (GNP) and the German treatment centers with collaboration of the medical scientific advisory board of the German Society for Muscular Diseases (DGM)]. / Handlungsempfehlungen zur Gentherapie der spinalen Muskelatrophie mit Onasemnogene Abeparvovec AVXS-101 : Konsensuspapier der deutschen Vertretung der Gesellschaft für Neuropädiatrie (GNP) und der deutschen Behandlungszentren unter Mitwirkung des Medizinisch-Wissenschaftlichen Beirates der Deutschen Gesellschaft für Muskelkranke (DGM) e.â¯V.
Nervenarzt
; 91(6): 518-529, 2020 Jun.
Artigo
em Alemão
| MEDLINE | ID: mdl-32394004
9.
The prevalence of headache in German pupils of different ages and school types.
Cephalalgia
; 39(8): 1030-1040, 2019 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-30884960
10.
Influence of chronic diseases on the olfactory function in children.
Eur J Pediatr
; 178(8): 1185-1193, 2019 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-31144163
11.
Deep Brain Stimulation in a Patient with TSPOAP1-Biallelic Variant of Autosomal-Recessive Dystonia.
Mov Disord
; 38(11): 2139-2140, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37850637
12.
Acquired Olfactory Dysfunction in Children and Adolescents: A Systematic Review of the Literature.
Chem Senses
; 43(8): 571-581, 2018 09 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-30020456
13.
Novel VPS33B mutation in a patient with autosomal recessive keratoderma-ichthyosis-deafness syndrome.
Am J Med Genet A
; 176(12): 2862-2866, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30561130
14.
Childhood primary large vessel CNS vasculitis: single-centre experience and review of the literature.
Clin Exp Rheumatol
; 35 Suppl 103(1): 213-220, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28375836
15.
Genomic profiling in neuronal dyneinopathies and updated classifications.
Am J Med Genet A
; 185(8): 2607-2610, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33991169
16.
Novel Mutation in the DKC1 Gene: Neonatal Hoyeraal-Hreidarsson Syndrome As a Rare Differential Diagnosis in Pontocerebellar Hypoplasia, Primary Microcephaly, and Progressive Bone Marrow Failure.
Neuropediatrics
; 47(3): 182-6, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26951492
17.
Dysferlinopathy in Switzerland: clinical phenotypes and potential founder effects.
BMC Neurol
; 15: 182, 2015 Oct 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26444858
18.
A five year-old child with clear cell petro-clival meningioma: case report with clinical and histopathological long-term follow-up.
Childs Nerv Syst
; 31(11): 2193-8, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26077595
19.
Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defect.
Am J Hum Genet
; 88(2): 162-72, 2011 Feb 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-21310273
20.
Novel deletion of lysine 7 expands the clinical, histopathological and genetic spectrum of TPM2-related myopathies.
Brain
; 136(Pt 2): 508-21, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23413262