Igor Nestrasil
Overview
Explore the profile of Igor Nestrasil including associated specialties, affiliations and a list of published articles.
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59
Citations
713
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Recent Articles
1.
Svatkova A, Pasternak O, Eisengart J, Rudser K, Bednarik P, Mueller B, et al.
J Inherit Metab Dis
. 2025 Jan;
48(1):e12830.
PMID: 39761695
Mucopolysaccharidosis type I (MPS I) is an inherited lysosomal storage disorder leading to deleterious brain effects. While animal models suggested that MPS I severely affects white matter (WM), whole-brain diffusion...
2.
Pierpont E, Labounek R, Gupta A, Lund T, Orchard P, Dobyns W, et al.
Neurology
. 2024 Aug;
103(5):e209764.
PMID: 39151102
Background And Objectives: Childhood cerebral adrenoleukodystrophy (C-ALD) is a severe inflammatory demyelinating disease that must be treated at an early stage to prevent permanent brain injury and neurocognitive decline. In...
3.
Kruc R, Osterholm E, Holm T, Nestrasil I, Lanzieri T, Schleiss M
J Pediatric Infect Dis Soc
. 2024 Jun;
13(8):413-420.
PMID: 38847778
Background: Congenital cytomegalovirus (cCMV) is the most common infectious cause of neurodevelopmental deficits in US children. To inform patient management, it is important to define whether central nervous system (CNS)...
4.
Labounek R, Bondy M, Paulson A, Bedard S, Abramovic M, Alonso-Ortiz E, et al.
bioRxiv
. 2024 May;
PMID: 38746371
Clinical research emphasizes the implementation of rigorous and reproducible study designs that rely on between-group matching or controlling for sources of biological variation such as subject's sex and age. However,...
5.
Majovska J, Nestrasil I, Ahmed A, Bondy M, Klempir J, Jahnova H, et al.
J Inherit Metab Dis
. 2023 Dec;
47(2):327-339.
PMID: 38112342
Cerebellar atrophy is a characteristic sign of late-onset Tay-Sachs disease (LOTS). Other structural neuroimaging abnormalities are inconsistently reported. Our study aimed to perform a detailed whole-brain analysis and quantitatively characterize...
6.
Weiss V, Kokosova V, Valenta Z, Dolezalova I, Balaz M, Mangia S, et al.
Neuroimage
. 2023 Dec;
285:120502.
PMID: 38103623
Given the substantial dependence of neurons on continuous supply of energy, the distribution of major cerebral arteries opens a question whether the distance from the main supply arteries constitutes a...
7.
Papez J, Labounek R, Jabandziev P, ceska K, Slaba K, Oslejskova H, et al.
Sci Rep
. 2023 Oct;
13(1):17372.
PMID: 37833343
Our goal was to identify highly accurate empirical models for the prediction of the risk of febrile seizure (FS) and FS recurrence. In a prospective, three-arm, case-control study, we enrolled...
8.
Muschol N, Koehn A, von Cossel K, Okur I, Ezgu F, Harmatz P, et al.
J Clin Invest
. 2022 Nov;
133(2).
PMID: 36413418
BackgroundSanfilippo type B is a mucopolysaccharidosis (MPS) with a major neuronopathic component characterized by heparan sulfate (HS) accumulation due to mutations in the NAGLU gene encoding alfa-N-acetyl-glucosaminidase. Enzyme replacement therapy...
9.
Weiss V, Dolezalova I, Mnuk T, Labounkova I, Herzig R, Nestrasil I
Neurology
. 2022 Jun;
99(7):313-314.
PMID: 35750495
No abstract available.
10.
Ellinwood N, Valentine B, Hess A, Jens J, Snella E, Jamil M, et al.
J Pharmacol Exp Ther
. 2022 Jun;
382(3):277-286.
PMID: 35717448
Mucopolysaccharidosis type IIIB (MPS IIIB; Sanfilippo syndrome B; OMIM #252920) is a lethal, pediatric, neuropathic, autosomal recessive, and lysosomal storage disease with no approved therapy. Patients are deficient in the...