Understanding microstructure of the brain by comparison of neurite orientation dispersion and density imaging (NODDI) with transparent mouse brain
K Sato, A Kerever, K Kamagata… - Acta radiologica …, 2017 - journals.sagepub.com
Background Neurite orientation dispersion and density imaging (NODDI) is a diffusion
magnetic resonance imaging (MRI) technique with the potential to visualize the …
magnetic resonance imaging (MRI) technique with the potential to visualize the …
[HTML][HTML] Altered local cerebellar and brainstem development in preterm infants
Y Wu, C Stoodley, M Brossard-Racine, K Kapse… - Neuroimage, 2020 - Elsevier
Background Premature birth is associated with high prevalence of neurodevelopmental
impairments in surviving infants. The putative role of cerebellar and brainstem dysfunction …
impairments in surviving infants. The putative role of cerebellar and brainstem dysfunction …
Simple and clear differentiation of spinocerebellar degenerations: Overview of macroscopic and low‐power view findings
K Iwabuchi, S Koyano, S Yagishita - Neuropathology, 2022 - Wiley Online Library
Spinocerebellar degenerations (SCDs) are a diverse group of rare and slowly progressive
neurological diseases that include spinocerebellar ataxia type 1 (SCA1), SCA2, SCA3 …
neurological diseases that include spinocerebellar ataxia type 1 (SCA1), SCA2, SCA3 …
Hindbrain regional growth in preterm newborns and its impairment in relation to brain injury
Premature birth globally affects about 11.1% of all newborns and is a risk factor for
neurodevelopmental disability in surviving infants. Histology has suggested that hindbrain …
neurodevelopmental disability in surviving infants. Histology has suggested that hindbrain …
Degenerative Ataxias: challenges in clinical research
SH Subramony - Annals of Clinical and Translational …, 2017 - Wiley Online Library
The degenerative ataxias are a very heterogeneous group of disorders that include
numerous genetic diseases as well as apparently “sporadic” entities. There has been an …
numerous genetic diseases as well as apparently “sporadic” entities. There has been an …
Sensory and motor cortex function contributes to symptom severity in spinocerebellar ataxia type 6
Abstract Spinocerebellar ataxia type 6 (SCA6) is a genetic disease that causes
degeneration of Purkinje cells, and recent evidence points to degeneration of Betz cells in …
degeneration of Purkinje cells, and recent evidence points to degeneration of Betz cells in …
Ataksje zwyrodnieniowe: wyzwania w badaniach klinicznych
SH Subramony - Neurologia Praktyczna, 2017 - journals.czelej.com.pl
Ataksje zwyrodnieniowe są bardzo niejednorodną grupą schorzeń, do której należą liczne
choroby dziedziczne, a także jednostki chorobowe wyraźnie „sporadyczne”. Eksplozja …
choroby dziedziczne, a także jednostki chorobowe wyraźnie „sporadyczne”. Eksplozja …
