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Annette Hackenberg
Annette Hackenberg
University Children`s Hospital - Eleonore Foundation
Verified email at kispi.uzh.ch
Title
Cited by
Cited by
Year
Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2
DE Neilson, MD Adams, CMD Orr, DK Schelling, RM Eiben, DS Kerr, ...
The American Journal of Human Genetics 84 (1), 44-51, 2009
3582009
Monogenic variants in dystonia: an exome-wide sequencing study
M Zech, R Jech, S Boesch, M Škorvánek, S Weber, M Wagner, C Zhao, ...
The Lancet Neurology 19 (11), 908-918, 2020
1722020
Long-term outcome after arterial ischemic stroke in children and young adults
B Goeggel Simonetti, A Cavelti, M Arnold, S Bigi, M Regényi, HP Mattle, ...
Neurology 84 (19), 1941-1947, 2015
1612015
Factors affecting cognitive outcome in early pediatric stroke
M Studer, E Boltshauser, A Capone Mori, A Datta, J Fluss, D Mercati, ...
Neurology 82 (9), 784-792, 2014
1312014
Cerebrospinal fluid findings in patients with myelin oligodendrocyte glycoprotein (MOG) antibodies. Part 2: Results from 108 lumbar punctures in 80 pediatric patients
S Jarius, C Lechner, EM Wendel, M Baumann, M Breu, M Schimmel, ...
Journal of neuroinflammation 17, 1-28, 2020
1162020
Diagnosis and treatment of Guillain-Barré Syndrome in childhood and adolescence: An evidence-and consensus-based guideline
R Korinthenberg, R Trollmann, U Felderhoff-Müser, G Bernert, ...
European Journal of Paediatric Neurology 25, 5-16, 2020
952020
Feasibility, safety, and outcome of recanalization treatment in childhood stroke
S Bigi, A Dulcey, J Gralla, C Bernasconi, A Melliger, AN Datta, M Arnold, ...
Annals of neurology 83 (6), 1125-1132, 2018
852018
Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study
S Groeneweg, FS van Geest, A Abacı, A Alcantud, GP Ambegaonkar, ...
The Lancet Diabetes & Endocrinology 8 (7), 594-605, 2020
722020
The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study
SM Papuc, L Abela, K Steindl, A Begemann, TL Simmons, B Schmitt, ...
European journal of human genetics 27 (3), 408-421, 2019
712019
Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes
A Begemann, MA Acuña, M Zweier, M Vincent, K Steindl, ...
Molecular Medicine 25, 1-15, 2019
492019
Tubulin-related cerebellar dysplasia: definition of a distinct pattern of cerebellar malformation
R Romaniello, F Arrigoni, E Panzeri, A Poretti, A Micalizzi, A Citterio, ...
European radiology 27, 5080-5092, 2017
422017
Inflammatory markers in pediatric stroke: an attempt to better understanding the pathophysiology
SE Buerki, D Grandgirard, AN Datta, A Hackenberg, F Martin, ...
european journal of paediatric neurology 20 (2), 252-260, 2016
382016
Quality of life after paediatric ischaemic stroke
S Kornfeld, M Studer, S Winkelbeiner, M Regényi, E Boltshauser, ...
Developmental Medicine & Child Neurology 59 (1), 45-51, 2017
372017
Infantile epileptic encephalopathy, transient choreoathetotic movements, and hypersomnia due to a De Novo missense mutation in the SCN2A gene
A Hackenberg, A Baumer, H Sticht, B Schmitt, J Kroell-Seger, D Wille, ...
Neuropediatrics 45 (04), 261-264, 2014
372014
High association of MOG-IgG antibodies in children with bilateral optic neuritis
EM Wendel, M Baumann, N Barisic, A Blaschek, EC de Oliveira Koch, ...
European Journal of Paediatric Neurology 27, 86-93, 2020
352020
Temporal dynamics of MOG antibodies in children with acquired demyelinating syndrome
EM Wendel, HS Thonke, A Bertolini, M Baumann, A Blaschek, ...
Neurology: Neuroimmunology & Neuroinflammation 9 (6), e200035, 2022
342022
Severe childhood Guillain‐Barré syndrome associated with Mycoplasma pneumoniae infection: a case series
PM Meyer Sauteur, J Roodbol, A Hackenberg, MCY de Wit, C Vink, ...
Journal of the Peripheral Nervous System 20 (2), 72-78, 2015
322015
Blood DNA methylation provides an accurate biomarker of KMT2B-related dystonia and predicts onset
N Mirza-Schreiber, M Zech, R Wilson, T Brunet, M Wagner, R Jech, ...
Brain 145 (2), 644-654, 2022
312022
Impact of stroke volume on motor outcome in neonatal arterial ischemic stroke
A Wiedemann, M Pastore-Wapp, N Slavova, L Steiner, C Weisstanner, ...
European journal of paediatric neurology 25, 97-105, 2020
302020
Cutis laxa, exocrine pancreatic insufficiency and altered cellular metabolomics as additional symptoms in a new patient with ATP6AP1-CDG
B Dimitrov, N Himmelreich, ALH Ederveen, C Lüchtenborg, JG Okun, ...
Molecular genetics and metabolism 123 (3), 364-374, 2018
302018
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