A clinicopathological and genetic study of sporadic diffuse leukoencephalopathy with spheroids: a report of two cases (Q37601370)

21 August 2017

6 references

25 April 2019

12 September 2019

23 July 2020

10 September 2020

24 November 2020

29 April 2021

A clinicopathological and genetic study of sporadic diffuse leukoencephalopathy with spheroids: a report of two cases (English)

1 reference

genetic predisposition to disease

21 August 2017

1 reference

12 September 2019

3 references

23 July 2020

24 November 2020

29 April 2021

2 references

23 July 2020

10 September 2020

1 reference

29 April 2021

T Kimura

1

1 reference

21 August 2017

K Ishizawa

2

1 reference

21 August 2017

T Mitsufuji

3

1 reference

21 August 2017

T Abe

4

1 reference

21 August 2017

Y Nakazato

5

1 reference

21 August 2017

K Yoshida

6

1 reference

21 August 2017

A Sasaki

7

1 reference

21 August 2017

N Araki

8

1 reference

21 August 2017

1 December 2013

6 references

Neuropathology and Applied Neurobiology

21 August 2017

25 April 2019

12 September 2019

23 July 2020

24 November 2020

29 April 2021

7 references

21 August 2017

25 April 2019

12 September 2019

23 July 2020

10 September 2020

24 November 2020

29 April 2021

39

1 reference

21 August 2017

7

1 reference

21 August 2017

837-843

1 reference

Creative Commons Attribution 3.0 Unported

21 August 2017

6 references

25 April 2019

12 September 2019

23 July 2020

10 September 2020

24 November 2020

Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids

29 April 2021

0 references

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): a misdiagnosed disease entity

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

Rapid onset frontal leukodystrophy with decreased diffusion coefficient and neuroaxonal spheroids

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

Insights into the dynamics of hereditary diffuse leukoencephalopathy with axonal spheroids

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

Sporadic adult-onset leukoencephalopathy with neuroaxonal spheroids mimicking cerebral MS.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

Adult onset leukodystrophy with neuroaxonal spheroids and pigmented glia: report of a family, historical perspective, and review of the literature

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

Hereditary diffuse leucoencephalopathy with spheroids

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

Mutations in two genes encoding different subunits of a receptor signaling complex result in an identical disease phenotype

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

Loss-of-function mutations in TYROBP (DAP12) result in a presenile dementia with bone cysts.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia can present as frontotemporal dementia syndrome

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

Leucoencephalopathy with neuroaxonal spheroids (LENAS) presenting as the cerebellar subtype of multiple system atrophy

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

Hereditary diffuse leukoencephalopathy with axonal spheroids caused by R782H mutation in CSF1R: case report.

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

Nasu-Hakola disease with a splicing mutation of TREM2 in a Japanese family.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

Adult-onset leukodystrophy with axonal spheroids

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

Neurological picture. Hereditary diffuse leukoencephalopathy with neuroaxonal spheroids: novel imaging findings

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

Sporadic leucodystrophy with neuroaxonal spheroids: persistence of DWI changes and neurocognitive profiles: a case study.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

Leukoencephalopathy with neuroaxonal spheroids presenting as frontotemporal dementia.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

CT and MR imaging of neuroaxonal leukodystrophy presenting as early-onset frontal dementia.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

Hereditary diffuse leukoencephalopathy with spheroids: clinical, pathologic and genetic studies of a new kindred.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

An autopsy case of hereditary diffuse leukoencephalopathy with spheroids, clinically suspected of Alzheimer's disease.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

Late-onset neuroaxonal leucoencephalopathy with spheroids and vascular amyloid.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

Accumulation of phosphorylated alpha-synuclein in aging human brain.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

Neuroaxonal leukoencephalopathy with axonal spheroids.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

Autosomal dominant diffuse leukoencephalopathy with neuroaxonal spheroids.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933763

Two cases of LENAS: diagnosis by MRI and biopsy

1 September 2018

1 reference

12 December 2020

Nasu-Hakola's disease (membranous lipodystrophy)

1 reference

12 December 2020

Hereditary diffuse leucoencephalopathy with spheroids

1 reference

12 December 2020

Adult onset leucodystrophy with neuroaxonal spheroids and pigmented glia (ALSP): report of a new kindred

1 reference

12 December 2020

Identifiers

DOI

10.1111/NAN.12046

1 reference

21 August 2017

1 reference

21 August 2017

PubMed publication ID

23521113

1 reference