CSF1R related leukoencephalopathy - Rare childhood presentation of an autosomal dominant microgliopathy!
Main Authors: | Neeharika Sriram, Hansashree Padmanabha, Sadanandavalli R Chandra, Rohan Mahale, Bevinahalli Nandeesh, Maya D Bhat, Rita Christopher, Manisha Gupta, Gautham A Udupi, Pooja Mailankody, Pavagada S Mathuranath |
---|---|
Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2022-01-01
|
Series: | Annals of Indian Academy of Neurology |
Online Access: | http://www.annalsofian.org/article.asp?issn=0972-2327;year=2022;volume=25;issue=2;spage=311;epage=314;aulast=Sriram |
Similar Items
-
Autosomal dominant cerebral small vessel disease in HTRA1 gene mutation
by: Rohan R Mahale, et al.
Published: (2021-01-01) -
CSF1R ⁃ related leukoencephalopathy: from hereditary diffuse leukoencephalopathy with spheroids to primary microgliopathy
by: Yan⁃qiu WEI, et al.
Published: (2020-01-01) -
Neuro-Bechet’s disease: a case series from India
by: Rohan R. Mahale, et al.
Published: (2022-12-01) -
Spastic ataxia with sensory neuropathy sans cerebral leukodystrophy in probable adult polyglucosan body disease
by: Rohan Mahale, et al.
Published: (2023-01-01) -
Granulomatous panuveitis in multiple sclerosis: A rare occurrence
by: Rutul Shah, et al.
Published: (2022-01-01)