Cargando…

Pathologic basis of the preferential thinning of thecorpus callosum in adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP)

BACKGROUND: Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) is an early onset dementia characterized by axonal loss in the cerebral white matter with swollen axons (spheroids). It had been reported that the preferential thinning and “focal lesions” of the corpus callo...

Descripción completa

Detalles Bibliográficos
Autores principales:	Kinoshita, Michiaki, Oyanagi, Kiyomitsu, Kondo, Yasufumi, Ishizawa, Keisuke, Ishihara, Kenji, Yoshida, Mari, Inoue, Teruhiko, Mitsuyama, Yoshio, Yoshida, Kunihiro, Yamada, Mitsunori, Sekijima, Yoshiki, Ikeda, Shu-ichi
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2021
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844436/ https://www.ncbi.nlm.nih.gov/pubmed/33553700 http://dx.doi.org/10.1016/j.ensci.2021.100310

Ejemplares similares

Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia (ALSP) in an Indian Man
por: Rao, Tejaswi, et al.
Publicado: (2022)

Adult-onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia (ALSP) Masquerading Primary Progressive Aphasia
por: Goyal, Sheetal, et al.
Publicado: (2022)

A case of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) with a high antinuclear antibody titer
por: Zheng, Shitan, et al.
Publicado: (2021)

An Autopsy Proven Case of CSF1R-mutant Adult-onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia (ALSP) with Premature Ovarian Failure
por: Kim, Seong-Ik, et al.
Publicado: (2019)

Minocycline protects against microgliopathy in a Csf1r haplo-insufficient mouse model of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP)
por: Li, Xin, et al.
Publicado: (2023)

Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia: A case report
por: Kang, Seongsu, et al.
Publicado: (2019)

Chitotriosidase is a biomarker for adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia
por: Hayer, Stefanie N., et al.
Publicado: (2022)

Clinical and genetic characterization of adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutation
por: Konno, T., et al.
Publicado: (2016)

A clinicopathological and genetic study of sporadic diffuse leukoencephalopathy with spheroids: a report of two cases
por: Kimura, T, et al.
Publicado: (2013)

An AARS1 variant identified to cause adult-onset leukoencephalopathy with neuroaxonal spheroids and pigmented glia
por: Wu, Jingying, et al.
Publicado: (2023)

A Unique Radiological Correlate of CSF1R Mutation: “Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia - Sine Leukoencephalopathy“
por: Das, Shambaditya, et al.
Publicado: (2022)

Adult-Onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia: Review of Clinical Manifestations as Foundations for Therapeutic Development
por: Papapetropoulos, Spyros, et al.
Publicado: (2022)

A case of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia presenting with alien hand syndrome
por: Chung, Bora, et al.
Publicado: (2022)

Teaching case 1-2020: Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia – An unusual cause of dementia
por: Klotz, Sigrid, et al.
Publicado: (2020)

Redefining the phenotype of ALSP and AARS2 mutation–related leukodystrophy
por: Lakshmanan, Rahul, et al.
Publicado: (2017)

Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia Caused by a Novel R782G Mutation in CSF1R
por: Foulds, Nicola, et al.
Publicado: (2015)

Adult-onset diffuse leukoencephalopathy with axonal spheroids and pigmented glia presenting with acute stroke-like symptoms: A rare clinical scenario
por: Purohit, Bela, et al.
Publicado: (2020)

Factors predictive of the presence of a CSF1R mutation in patients with leukoencephalopathy
por: Kondo, Y., et al.
Publicado: (2019)

Adult-Onset Leukoencephalopathy with Axonal Spheroid and Pigmented Glia: Different Histological Spectrums Presented in Autopsy Cases of Siblings and a Surgical Case of Stereotactic Biopsy
por: Kwon, Hee Jung, et al.
Publicado: (2023)

Suspected Perinatal Depression Revealed to be Hereditary Diffuse Leukoencephalopathy with Spheroids
por: Blume, Josefine, et al.
Publicado: (2017)

Identification and functional characterization of novel mutations including frameshift mutation in exon 4 of CSF1R in patients with adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
por: Miura, Takeshi, et al.
Publicado: (2018)

Teaching case 1-2020 – ADDENDUM: Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia due to a novel CSF1R mutation – An unusual cause of dementia
por: Klotz, Sigrid, et al.
Publicado: (2022)

CSF1R mutations in hereditary diffuse leukoencephalopathy with spheroids are loss of function
por: Pridans, Clare, et al.
Publicado: (2013)

An AARS variant as the likely cause of Swedish type hereditary diffuse leukoencephalopathy with spheroids
por: Sundal, Christina, et al.
Publicado: (2019)

Toxic leukoencephalopathy with axonal spheroids caused by chemotherapeutic drugs other than methotrexate
por: Lim, Ka Young, et al.
Publicado: (2022)

A novel A792D mutation in the CSF1R gene causes hereditary diffuse leukoencephalopathy with axonal spheroids characterized by slow progression
por: Ueda, Sakiho, et al.
Publicado: (2015)

Nonsynaptic junctions on myelinating glia promote preferential myelination of electrically active axons
por: Wake, Hiroaki, et al.
Publicado: (2015)

Brain abnormalities, neurodegeneration, and dysosteosclerosis (BANDDOS): new cases, systematic literature review, and associations with CSF1R-ALSP
por: Dulski, Jarosław, et al.
Publicado: (2023)

Distinctive features of degenerating Purkinje cells in spinocerebellar ataxia type 31
por: Yoshida, Kunihiro, et al.
Publicado: (2014)

Involvement of the optic nerve in mutated CSF1R-induced hereditary diffuse leukoencephalopathy with axonal spheroids
por: Shu, Yaqing, et al.
Publicado: (2016)

Functional characterization of a novel CSF1R mutation causing hereditary diffuse leukoencephalopathy with spheroids
por: Kraya, Torsten, et al.
Publicado: (2019)

Hereditary Diffuse Leukoencephalopathy with Spheroids: Diffusion Restriction on Magnetic Resonance Imaging and Novel Mutation in an Indian Patient
por: Manjunath, Varun, et al.
Publicado: (2022)

Temporary focal cerebral ischemia results in swollen astrocytic end-feet that compress microvessels and lead to focal cortical infarction
por: Ito, Umeo, et al.
Publicado: (2011)

Mannitol infusion immediately after reperfusion suppresses the development of focal cortical infarction after temporary cerebral ischemia in gerbils
por: Ito, Umeo, et al.
Publicado: (2014)

Evidence for Altered Metabolism of Sphingosine-1-Phosphate in the Corpus Callosum of Patients with Schizophrenia
por: Esaki, Kayoko, et al.
Publicado: (2020)

Reversible Leukoencephalopathy in a Man with Childhood-onset Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome
por: Hoshino, Yumi, et al.
Publicado: (2021)

Mutations in the colony stimulating factor 1 receptor (CSF1R) cause hereditary diffuse leukoencephalopathy with spheroids
por: Rademakers, Rosa, et al.
Publicado: (2011)

Dysfunction of Protein Quality Control in Parkinsonism–Dementia Complex of Guam
por: Verheijen, Bert M., et al.
Publicado: (2018)

Hereditary leukoencephalopathy with axonal spheroids: a spectrum of phenotypes from CNS vasculitis to parkinsonism in an adult onset leukodystrophy series
por: Lynch, David S, et al.
Publicado: (2016)

MR Spectroscopy in Patients with Hereditary Diffuse Leukoencephalopathy with Spheroids and Asymptomatic Carriers of Colony-stimulating Factor 1 Receptor Mutation
por: Abe, Takashi, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_chg2nl362b90ar7s919g3njptr