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Items: 1 to 20 of 70

1.
Loss of microRNA-15a/16-1 function promotes neuropathological and functional recovery in experimental traumatic brain injury
Chao Zhou, Shun Li, Na Qiu, Ping Sun, Milton H. Hamblin, C. Edward Dixon, Jun Chen, Ke-Jie Yin
JCI Insight. 2024 Jun 24; 9(12): e178650. Published online 2024 Jun 24. doi: 10.1172/jci.insight.178650
PMCID:
PMC11383186
ArticlePDF–26M
2.
Differential Expression of PACAP/VIP Receptors in the Post-Mortem CNS White Matter of Multiple Sclerosis Donors
Margo Iris Jansen, Giuseppe Musumeci, Alessandro Castorina
Int J Mol Sci. 2024 Aug; 25(16): 8850. Published online 2024 Aug 14. doi: 10.3390/ijms25168850
PMCID:
PMC11354662
ArticlePDF–16M
3.
Canavan’s spongiform leukodystrophy (Aspartoacylase deficiency) with emphasis on sonographic features in infancy: description of a case report and review of the literature
Leon Rossler, Stefan Lemburg, Almut Weitkämper, Charlotte Thiels, Sabine Hoffjan, Huu Phuc Nguyen, Thomas Lücke, Christoph M. Heyer
J Ultrasound. 2023 Dec; 26(4): 757–764. Published online 2022 Feb 20. doi: 10.1007/s40477-022-00667-2
PMCID:
PMC10632335
ArticlePDF–1.6M
4.
Detection and verification of neurodegeneration after traumatic brain injury in the mouse: Immunohistochemical staining for amyloid precursor protein
Guoxiang Xiong, Hannah Metheny, Kaitlin Hood, Ian Jean, Anthony M. Farrugia, Brian N. Johnson, Shanti R. Tummala, Noam A. Cohen, Akiva S. Cohen
Brain Pathol. 2023 Nov; 33(6): e13163. Published online 2023 May 8. doi: 10.1111/bpa.13163
PMCID:
PMC10580020
ArticlePDF–7.1M
5.
Neuronal tau pathology worsens late-phase white matter degeneration after traumatic brain injury in transgenic mice
Fengshan Yu, Diego Iacono, Daniel P. Perl, Chen Lai, Jessica Gill, Tuan Q. Le, Patricia Lee, Gauthaman Sukumar, Regina C. Armstrong
Acta Neuropathol. 2023; 146(4): 585–610. Published online 2023 Aug 14. doi: 10.1007/s00401-023-02622-9
PMCID:
PMC10499978
ArticlePDF–30M
6.
Variants in the zinc transporter TMEM163 cause a hypomyelinating leukodystrophy
Michelle C do Rosario, Guillermo Rodriguez Bey, Bruce Nmezi, Fang Liu, Talia Oranburg, Ana S A Cohen, Keith A Coffman, Maya R Brown, Kirill Kiselyov, Quinten Waisfisz, Myrthe T Flohil, Shahyan Siddiqui, Jill A Rosenfeld, Alejandro Iglesias, Katta Mohan Girisha, Nicole I Wolf, Quasar Saleem Padiath, Anju Shukla
Brain. 2022 Dec; 145(12): 4202–4209. Published online 2022 Aug 12. doi: 10.1093/brain/awac295
PMCID:
PMC10200305
ArticlePDF–1006K
7.
DNA methylation changes in glial cells of the normal-appearing white matter in Multiple Sclerosis patients
Lara Kular, Ewoud Ewing, Maria Needhamsen, Majid Pahlevan Kakhki, Ruxandra Covacu, David Gomez-Cabrero, Lou Brundin, Maja Jagodic
Epigenetics. 2022; 17(11): 1311–1330. Published online 2022 Jan 30. doi: 10.1080/15592294.2021.2020436
PMCID:
PMC9586622
ArticlePDF–4.6M
8.
Radiological manifestation of familial acute necrotizing encephalopathy with RANBP2 mutation in a Far-East Asian family: Case report
Yu-Jung Park, Jae-Yeon Hwang, Yong-Woo Kim, Yun-Jin Lee, Ara Ko
Medicine (Baltimore) 2021 Mar 26; 100(12): e25171. Published online 2021 Mar 26. doi: 10.1097/MD.0000000000025171
PMCID:
PMC9282079
ArticlePDF–383K
9.
The Primary Microglial Leukodystrophies: A Review
Isidro Ferrer
Int J Mol Sci. 2022 Jun; 23(11): 6341. Published online 2022 Jun 6. doi: 10.3390/ijms23116341
PMCID:
PMC9181167
ArticlePDF–1.4M
10.
White matter microstructural differences in children and genetic risk for multiple sclerosis: A population-based study
C Louk de Mol, Rinze F Neuteboom, Philip R Jansen, Tonya White
Mult Scler. 2022 Apr; 28(5): 730–741. Published online 2021 Aug 11. doi: 10.1177/13524585211034826
PMCID:
PMC8978478
ArticlePDF–3.1M
11.
Leukoencephalopathy with brain calcifications and cysts (Labrune syndrome) case report: diagnosis and management of a rare neurological disease
Michelle Paff, Nardin Samuel, Noor Alsafwani, Darcia Paul, Phedias Diamandis, Seth A. Climans, Walter Kucharczyk, Mandy Yi Rong Ding, Andrew F. Gao, Andres M. Lozano
BMC Neurol. 2022; 22: 10. Published online 2022 Jan 5. doi: 10.1186/s12883-021-02531-y
PMCID:
PMC8729138
ArticlePDF–1.4M
12.
Opposing white matter microstructure abnormalities in 22q11.2 deletion and duplication carriers
Johanna Seitz-Holland, Monica Lyons, Leila Kushan, Amy Lin, Julio E. Villalon-Reina, Kang Ik Kevin Cho, Fan Zhang, Tashrif Billah, Sylvain Bouix, Marek Kubicki, Carrie E. Bearden, Ofer Pasternak
Transl Psychiatry. 2021; 11: 580. Published online 2021 Nov 10. doi: 10.1038/s41398-021-01703-1
PMCID:
PMC8581007
ArticlePDF–3.4M
13.
MR imaging of the brain in five members of a family with Pelizaeus-Merzbacher disease.
A M Silverstein, D K Hirsh, J D Trobe, S S Gebarski
AJNR Am J Neuroradiol. 1990 May; 11(3): 495-9.
PMCID:
PMC8367490
SummaryPDF–2.6M
14.
MR findings in adult-onset adrenoleukodystrophy.
A J Kumar, W Köhler, B Kruse, S Naidu, A Bergin, D Edwin, H W Moser
AJNR Am J Neuroradiol. 1995 Jun-Jul; 16(6): 1227-37.
PMCID:
PMC8337821
SummaryPDF–1.0M
15.
White matter changes associated with deletions of the long arm of chromosome 18 (18q- syndrome): a dysmyelinating disorder?
L A Loevner, R M Shapiro, R I Grossman, J Overhauser, J Kamholz
AJNR Am J Neuroradiol. 1996 Nov-Dec; 17(10): 1843-8.
PMCID:
PMC8337541
SummaryPDF–292K
16.
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: MR findings.
S J Skehan, M Hutchinson, D P MacErlaine
AJNR Am J Neuroradiol. 1995 Nov-Dec; 16(10): 2115-9.
PMCID:
PMC8337226
SummaryPDF–378K
17.
Further Delineation of the Clinical and Pathologic Features of HIKESHI-Related Hypomyelinating Leukodystrophy
Guy Helman, Ayelet Zerem, Akshata Almad, Julia L. Hacker, Sarah Woidill, Sunetra Sase, Alexandra N. LeFevre, Josef Ekstein, Martin M. Johansson, Chloe A. Stutterd, Ryan J. Taft, Cas Simons, Judith B. Grinspan, Amy Pizzino, Johanna L. Schmidt, Brian Harding, Yoel Hirsch, Angela N. Viaene, Aviva Fattal-Valevski, Adeline Vanderver
Pediatr Neurol. Author manuscript; available in PMC 2022 Aug 1.
Published in final edited form as: Pediatr Neurol. 2021 Aug; 121: 11–19. Published online 2021 May 14. doi: 10.1016/j.pediatrneurol.2021.04.014
PMCID:
PMC8327280
ArticlePDF–1.3M
18.
Multiple sclerosis and subclinical neuropathology in healthy individuals with familial risk: A scoping review of MRI studies
Matin Mortazavi, Öznur Hizarci, Lisa Ann Gerdes, Joachim Havla, Tania Kümpfel, Reinhard Hohlfeld, Sophia Stöcklein, Daniel Keeser, Birgit Ertl-Wagner
Neuroimage Clin. 2021; 31: 102734. Published online 2021 Jun 18. doi: 10.1016/j.nicl.2021.102734
PMCID:
PMC8234346
ArticlePDF–791K
19.
Genetic inactivation of SARM1 axon degeneration pathway improves outcome trajectory after experimental traumatic brain injury based on pathological, radiological, and functional measures
Donald V. Bradshaw, Jr., Andrew K. Knutsen, Alexandru Korotcov, Genevieve M. Sullivan, Kryslaine L. Radomski, Bernard J. Dardzinski, Xiaomei Zi, Dennis P. McDaniel, Regina C. Armstrong
Acta Neuropathol Commun. 2021; 9: 89. Published online 2021 May 17. doi: 10.1186/s40478-021-01193-8
PMCID:
PMC8130449
ArticlePDF–11M
20.
Waning efficacy in a long-term AAV-mediated gene therapy study in the murine model of Krabbe disease
Gregory J. Heller, Michael S. Marshall, Yazan Issa, Jeffrey N. Marshall, Duc Nguyen, Emily Rue, Koralege C. Pathmasiri, Miriam S. Domowicz, Richard B. van Breemen, Leon M. Tai, Stephanie M. Cologna, Stephen J. Crocker, Maria I. Givogri, Mark S. Sands, Ernesto R. Bongarzone
Mol Ther. 2021 May 5; 29(5): 1883–1902. Published online 2021 Jan 26. doi: 10.1016/j.ymthe.2021.01.026
PMCID:
PMC8116612
ArticlePDF–9.9M

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