Cerebral white matter: neuroanatomy, clinical neurology, and neurobehavioral correlates
JD Schmahmann, EE Smith, FS Eichler… - Annals of the New …, 2008 - Wiley Online Library
Lesions of the cerebral white matter (WM) result in focal neurobehavioral syndromes,
neuropsychiatric phenomena, and dementia. The cerebral WM contains fiber pathways that …
neuropsychiatric phenomena, and dementia. The cerebral WM contains fiber pathways that …
[HTML][HTML] Magnetic resonance imaging of myelin
The ability to measure myelin in vivo has great consequences for furthering our knowledge
of normal development, as well as for understanding a wide range of neurological disorders …
of normal development, as well as for understanding a wide range of neurological disorders …
[HTML][HTML] The splenium of the corpus callosum: embryology, anatomy, function and imaging with pathophysiological hypothesis
J Blaauw, LC Meiners - Neuroradiology, 2020 - Springer
Background and purpose The splenium of the corpus callosum is the most posterior part of
the corpus callosum. Its embryological development, anatomy, vascularization, function …
the corpus callosum. Its embryological development, anatomy, vascularization, function …
Adult leukodystrophies: a step-by-step diagnostic approach
LL Resende, ARB de Paiva, F Kok, C da Costa Leite… - Radiographics, 2019 - pubs.rsna.org
Leukodystrophies usually affect children, but in the last several decades, many instances of
adult leukodystrophies have been reported in the medical literature. Because the clinical …
adult leukodystrophies have been reported in the medical literature. Because the clinical …
RETRACTED: Inhibition of Notch1 reverses EMT and chemoresistance to cisplatin via direct downregulation of MCAM in triple‐negative breast cancer cells
D Zeng, YK Liang, YS Xiao, XL Wei… - … Journal of Cancer, 2020 - Wiley Online Library
Resistance to chemotherapy continues to be a critical issue in the clinical therapy of triple‐
negative breast cancer (TNBC). Epithelial–mesenchymal transition (EMT) is thought to …
negative breast cancer (TNBC). Epithelial–mesenchymal transition (EMT) is thought to …
[HTML][HTML] Quantitative MRI in leukodystrophies
MD Stellingwerff, PJW Pouwels, SD Roosendaal… - NeuroImage: Clinical, 2023 - Elsevier
Leukodystrophies constitute a large and heterogeneous group of genetic diseases primarily
affecting the white matter of the central nervous system. Different disorders target different …
affecting the white matter of the central nervous system. Different disorders target different …
Krabbe disease in adults: phenotypic and genotypic update from a series of 11 cases and a review
R Debs, R Froissart, P Aubourg… - Journal of Inherited …, 2013 - Wiley Online Library
Krabbe disease usually presents as a severe leukodystrophy in early infancy and childhood.
From a series of 11 patients and 30 cases previously reported in the literature we describe …
From a series of 11 patients and 30 cases previously reported in the literature we describe …
A practical approach to diagnosing adult onset leukodystrophies
RM Ahmed, E Murphy, I Davagnanam… - Journal of Neurology …, 2014 - jnnp.bmj.com
The term leukodystrophy refers to a group of conditions that are inherited and involve the
progressive destruction or loss of previously acquired myelin. 1 The most commonly …
progressive destruction or loss of previously acquired myelin. 1 The most commonly …
Later onset phenotypes of Krabbe disease: results of the world-wide registry
PK Duffner, A Barczykowski, DM Kay, K Jalal, L Yan… - Pediatric …, 2012 - Elsevier
The majority of newborns screening positive for Krabbe disease have not exhibited the
expected early infantile phenotype, with most clinically normal despite low …
expected early infantile phenotype, with most clinically normal despite low …
Can MR imaging diagnose adult-onset Alexander disease?
L Farina, D Pareyson, L Minati… - American journal …, 2008 - Am Soc Neuroradiology
BACKGROUND AND PURPOSE: In recent years, the discovery that mutations in the glial
fibrillary acidic protein gene (GFAP) were responsible for Alexander disease (AD) brought …
fibrillary acidic protein gene (GFAP) were responsible for Alexander disease (AD) brought …