Author Rosewich, Hendrik
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2023 | Journal Article
Association of Overweight and Obesity With Bell Palsy in Children
Breitling, V.; Leha, A.; Schiller, S.; Kruizenga, M.; Gärtner, J. & Rosewich, H. (2023)
Pediatric Neurology, 139 pp. 43-48. DOI: https://doi.org/10.1016/j.pediatrneurol.2022.11.007
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2022 | Journal Article
How to Detect Isolated PEX10-Related Cerebellar Ataxia?
Nava, E.; Hartmann, B.; Boxheimer, L.; Capone Mori, A.; Nuoffer, J.-M.; Sargsyan, Y. & Thoms, S. et al. (2022)
Neuropediatrics,. DOI: https://doi.org/10.1055/s-0041-1741383
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2022 | Journal Article
Clinical presentation and basic defect of the CFTR genotype p.Phe508del / p.Arg117His in a mother and her monozygous twin daughters
Lex, C.; Minso, R.; Alfeis, N.; Rosewich, H.; Schucht, S. & Tümmler, B. (2022)
Journal of Cystic Fibrosis, 21(2) pp. 375-377. DOI: https://doi.org/10.1016/j.jcf.2021.08.018
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2021 | Journal Article | Research Paper |
Targeted metabolomics revealed changes in phospholipids during the development of neuroinflammation in Abcd1 tm1Kds mice and X‐linked adrenoleukodystrophy patients
Kettwig, M.; Klemp, H.; Nessler, S.; Streit, F.; Krätzner, R.; Rosewich, H. & Gärtner, J. (2021)
Journal of Inherited Metabolic Disease, 44(5) pp. 1174-1185. DOI: https://doi.org/10.1002/jimd.12389
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2018 | Journal Article | Erratum
Correction to: The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management
Tranebjærg, L.; Strenzke, N. ; Lindholm, S.; Rendtorff, N. D.; Poulsen, H.; Khandelia, H. & Kopec, W. et al. (2018)
Human Genetics (Berlin), 137(3) pp. 279-280. DOI: https://doi.org/10.1007/s00439-018-1870-7
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2016 | Journal Article
Absence of biochemical evidence at an early age delays diagnosis in a patient with a clinically severe peroxisomal biogenesis disorder
Luesebrink, N.; Porto, L.; Waterham, H. R.; Ferdinandusse, S.; Rosewich, H.; Kurlemann, G. & Kieslich, M. (2016)
European Journal of Paediatric Neurology, 20(2) pp. 331-335. DOI: https://doi.org/10.1016/j.ejpn.2015.11.008
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2015 | Journal Article |
Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype
Jaffer, F.; Avbersek, A.; Vavassori, R.; Fons, C.; Campistol, J.; Stagnaro, M. & De Grandis, E. et al. (2015)
Brain, 138 pp. 2859-2874. DOI: https://doi.org/10.1093/brain/awv243
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2014 | Journal Article | Letter Note
Biopsy findings of symptomatic cerebral X-linked adrenoleucodystrophy and histological differentiation from multiple sclerosis
Pfeifenbring, S.; von Baumgarten, L.; Schueller, U.; Rosewich, H.; Thal, D. R.; Wirtz, C. R. & Hecht, M.-L. et al. (2014)
Neuropathology and Applied Neurobiology, 40(5) pp. 658-661. DOI: https://doi.org/10.1111/nan.12089
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2005 | Journal Article
Prosaposin deficiency - A rarely diagnosed, rapidly progressing, neonatal neurovisceral lipid storage disease. Report of a further patient
Elleder, M.; Jerabkova, M.; Befekadu, A.; Hrebicek, M.; Berna, L.; Ledvinova, J. & Hulkova, H. et al. (2005)
Neuropediatrics, 36(3) pp. 171-180. DOI: https://doi.org/10.1055/s-2005-865608
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