Dorian Pustina
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Explore the profile of Dorian Pustina including associated specialties, affiliations and a list of published articles.
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28
Citations
514
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Recent Articles
1.
Halchenko Y, Meyer K, Poldrack B, Solanky D, Wagner A, Gors J, et al.
J Open Source Softw
. 2024 Oct;
6(63).
PMID: 39469147
DataLad is a Python-based tool for the joint management of code, data, and their relationship, built on top of a versatile system for data logistics (git-annex) and the most popular...
2.
Vasilkovska T, Verschuuren M, Pustina D, van den Berg M, Van Audekerke J, Pintelon I, et al.
Clin Transl Med
. 2024 Oct;
14(10):e70055.
PMID: 39422700
Background: Huntington's disease (HD) is marked by irreversible loss of neuronal function for which currently no availability for disease-modifying treatment exists. Advances in the understanding of disease progression can aid...
3.
Vasilkovska T, Salajeghe S, Vanreusel V, Van Audekerke J, Verschuuren M, Hirschler L, et al.
J Biomed Sci
. 2024 Apr;
31(1):37.
PMID: 38627751
Background: Huntington's disease (HD) is marked by a CAG-repeat expansion in the huntingtin gene that causes neuronal dysfunction and loss, affecting mainly the striatum and the cortex. Alterations in the...
4.
Vidas-Guscic N, van Rijswijk J, Van Audekerke J, Jeurissen B, Nnah I, Tang H, et al.
Neurobiol Dis
. 2024 Feb;
193:106438.
PMID: 38365045
Huntington's disease (HD) is a progressive neurodegenerative disease affecting motor and cognitive abilities. Multiple studies have found white matter anomalies in HD-affected humans and animal models of HD. The identification...
5.
Wijeratne P, Eshaghi A, Scotton W, Kohli M, Aksman L, Oxtoby N, et al.
Imaging Neurosci (Camb)
. 2023 Sep;
1:1-19.
PMID: 37719837
Timelines of events, such as symptom appearance or a change in biomarker value, provide powerful signatures that characterise progressive diseases. Understanding and predicting the timing of events is important for...
6.
Adhikari M, Vasilkovska T, Cachope R, Tang H, Liu L, Keliris G, et al.
Sci Rep
. 2023 Jun;
13(1):10194.
PMID: 37353500
Huntington's disease (HD) is a neurodegenerative disorder caused by expanded (≥ 40) glutamine-encoding CAG repeats in the huntingtin gene, which leads to dysfunction and death of predominantly striatal and cortical...
7.
Pre-surgical features of intrinsic brain networks predict single and joint epilepsy surgery outcomes
Hinds W, Modi S, Ankeeta Ankeeta , Sperling M, Pustina D, Tracy J
Neuroimage Clin
. 2023 Apr;
38:103387.
PMID: 37023491
Despite the effectiveness of surgical interventions for the treatment of intractable focal temporal lobe epilepsy (TLE), the substrates that support good outcomes are poorly understood. While algorithms have been developed...
8.
Vasilkovska T, Adhikari M, Van Audekerke J, Salajeghe S, Pustina D, Cachope R, et al.
Neurobiol Dis
. 2023 Mar;
181:106095.
PMID: 36963694
Huntington's disease is an autosomal, dominantly inherited neurodegenerative disease caused by an expansion of the CAG repeats in exon 1 of the huntingtin gene. Neuronal degeneration and dysfunction that precedes...
9.
Castro E, Polosecki P, Pustina D, Wood A, Sampaio C, Cecchi G
Mov Disord
. 2022 Sep;
37(12):2407-2416.
PMID: 36173150
Background: Atrophy in the striatum is a hallmark of Huntington's disease (HD), including the period before clinical motor diagnosis (before-CMD), but it extends to other subcortical structures. The study of...
10.
Medaglia J, Erickson B, Pustina D, Kelkar A, DeMarco A, Dickens J, et al.
J Neurosci
. 2022 May;
42(24):4913-4926.
PMID: 35545436
Aphasia is a prevalent cognitive syndrome caused by stroke. The rarity of premorbid imaging and heterogeneity of lesion obscures the links between the local effects of the lesion, global anatomic...