Jutta Becker
Overview
Explore the profile of Jutta Becker including associated specialties, affiliations and a list of published articles.
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19
Citations
870
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Recent Articles
1.
Grass T, Dokuzluoglu Z, Buchner F, Rosignol I, Thomas J, Caldarelli A, et al.
Cell Rep Med
. 2024 Jul;
5(8):101659.
PMID: 39067446
Whether neurodevelopmental defects underlie postnatal neuronal death in neurodegeneration is an intriguing hypothesis only recently explored. Here, we focus on spinal muscular atrophy (SMA), a neuromuscular disorder caused by reduced...
2.
Kirschner J, Becker J, Schorling D, Pechmann A, Wirth B
Neurology
. 2020 Jul;
95(3):145.
PMID: 32690781
No abstract available.
3.
Schorling D, Becker J, Pechmann A, Langer T, Wirth B, Kirschner J
Neurology
. 2019 Jun;
93(6):267-269.
PMID: 31235659
No abstract available.
4.
Kalbe E, Roheger M, Paluszak K, Meyer J, Becker J, Fink G, et al.
Front Aging Neurosci
. 2019 Jan;
10:407.
PMID: 30618714
Combining cognitive training (CT) with physical activity (CPT) has been suggested to be most effective in maintaining cognition in healthy older adults, but data are scarce and inconsistent regarding long-term...
5.
Ventzke A, Feldkotter M, Wei A, Becker J, Beck B, Hoppe B
Pediatr Nephrol
. 2018 Apr;
33(7):1275-1276.
PMID: 29637271
The unit of the HOG-creatinine ratio presented in this article is calculated in μmol/mg creatinine instead of the demonstrated unit of μmol/μmol. This applies to the parameter in the text...
6.
Fazeli W, Herkenrath P, Stiller B, Neugebauer A, Fricke J, Lang-Roth R, et al.
Hum Mol Genet
. 2017 Oct;
26(20):4055-4066.
PMID: 29016863
Congenital cranial dysinnervation disorders (CCDDs) comprise a heterogeneous spectrum of diseases characterized by congenital, non-progressive impairment of eye, eyelid and/or facial movements including Möbius syndrome, Duane retraction syndrome, congenital ptosis,...
7.
Ventzke A, Feldkotter M, Wei A, Becker J, Beck B, Hoppe B
Pediatr Nephrol
. 2017 Jul;
32(12):2263-2271.
PMID: 28711958
Background: There are currently three distinct autosomal recessive inherited types of primary hyperoxaluria (PH: PHI, PHII, and PHIII), all characterized by the endogenous overproduction of oxalate. The PH type is...
8.
Costantini A, Vuorimies I, Makitie R, Mayranpaa M, Becker J, Pekkinen M, et al.
Am J Med Genet A
. 2016 Dec;
173(3):806-808.
PMID: 27901313
No abstract available.
9.
Bogershausen N, Gatinois V, Riehmer V, Kayserili H, Becker J, Thoenes M, et al.
Hum Mutat
. 2016 Jun;
37(9):847-64.
PMID: 27302555
Kabuki syndrome (KS) is a rare but recognizable condition that consists of a characteristic face, short stature, various organ malformations, and a variable degree of intellectual disability. Mutations in KMT2D...
10.
Rahe J, Becker J, Fink G, Kessler J, Kukolja J, Rahn A, et al.
Front Aging Neurosci
. 2015 Nov;
7:187.
PMID: 26528177
Data is inconsistent concerning the question whether cognitive-physical training (CPT) yields stronger cognitive gains than cognitive training (CT). Effects of additional counseling, neurobiological mechanisms, and predictors have scarcely been studied....