Mathilde Bostelmann
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Explore the profile of Mathilde Bostelmann including associated specialties, affiliations and a list of published articles.
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9
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82
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Recent Articles
1.
Maeder J, Bostelmann M, Schneider M, Bortolin K, Kliegel M, Eliez S
Front Psychiatry
. 2021 Jul;
12:597681.
PMID: 34220562
Previous studies on possible memory deficits in 22q11DS often focused on quantifying the information memorized, whereas learning processes have been mostly overlooked. Furthermore, methodological differences in task design have made...
2.
Bostelmann M, Ruggeri P, Circelli A, Costanzo F, Menghini D, Vicari S, et al.
Front Psychol
. 2020 Dec;
11:571394.
PMID: 33362636
Williams (WS) and Down (DS) syndromes are neurodevelopmental disorders with distinct genetic origins and different spatial memory profiles. In real-world spatial memory tasks, where spatial information derived from all sensory...
3.
Bostelmann M, Lavenex P, Banta Lavenex P
Cogn Psychol
. 2020 May;
121:101307.
PMID: 32445986
Although spatial navigation competence improves greatly from birth to adulthood, different spatial memory capacities emerge at different ages. Here, we characterized the capacity of 5-9-year-old children to use path integration...
4.
Maeder J, Sandini C, Zoller D, Schneider M, Bostelmann M, Pouillard V, et al.
Child Neuropsychol
. 2019 Aug;
26(3):289-311.
PMID: 31460828
Chromosome 22q11.2 deletion syndrome (22q11.2DS) is a genetic disease associated with an increased risk for schizophrenia and a specific cognitive profile. In this paper, we challenge the current view of...
5.
Bostelmann M, Costanzo F, Martorana L, Menghini D, Vicari S, Banta Lavenex P, et al.
Front Psychol
. 2018 Nov;
9:2049.
PMID: 30416470
Down syndrome (DS), the most common genetic cause of intellectual disability, results from the partial or complete triplication of chromosome 21. Individuals with DS are impaired at using a high-resolution,...
6.
Bostelmann M, Fragniere E, Costanzo F, Di Vara S, Menghini D, Vicari S, et al.
Hippocampus
. 2017 Jul;
27(11):1192-1203.
PMID: 28710800
Williams syndrome (WS), a genetic deletion syndrome, is characterized by severe visuospatial deficits affecting performance on both tabletop spatial tasks and on tasks which assess orientation and navigation. Nevertheless, previous...
7.
Bostelmann M, Schneider M, Padula M, Maeder J, Schaer M, Scariati E, et al.
J Neurodev Disord
. 2016 Nov;
8:41.
PMID: 27843501
Background: Children affected by the 22q11.2 deletion syndrome (22q11.2DS) have a specific neuropsychological profile with strengths and weaknesses in several cognitive domains. Specifically, previous evidence has shown that patients with...
8.
Maeder J, Schneider M, Bostelmann M, Debbane M, Glaser B, Menghetti S, et al.
J Neurodev Disord
. 2016 Mar;
8:10.
PMID: 27018204
Background: 22q11.2 deletion syndrome (22q11.2DS) is a genetic disorder associated with a specific cognitive profile. Higher-order cognitive skills like executive functions (EF) are reported as a relative weakness in this...
9.
Banta Lavenex P, Bostelmann M, Brandner C, Costanzo F, Fragniere E, Klencklen G, et al.
Front Psychol
. 2015 Mar;
6:62.
PMID: 25762946
Studies have shown that persons with Down syndrome (DS) exhibit relatively poor language capacities, and impaired verbal and visuoperceptual memory, whereas their visuospatial memory capacities appear comparatively spared. Individuals with...