White matter changes in GM1 gangliosidosis-Reference-Cited by-同舟云学术

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White matter changes in GM1 gangliosidosis

Published:2015-02 Issue:2 Volume:52 Page:155-156
ISSN:0019-6061
Container-title:Indian Pediatrics
language:en
Short-container-title:Indian Pediatr

Author:

Tuteja Moni,Bidchol Abdul Mueed,Girisha Katta Mohan,Phadke Shubha R.

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s13312-015-0593-2.pdf

Reference7 articles.

1. Sperb F, Vairo F, Burin M, Mayer FQ, Matte U, Giugliani R. Genotypic and phenotypic characterization of Brazilian patients with GM1 gangliosidosis. Gene. 2013;512:113–6.

2. Gururaj A, Sztriha L, Hertecant J, Johansen JG, Georgiou T, Campos Y, et al. Magnetic resonance imaging findings and novel mutations in GM1 gangliosidosis. J Child Neurol. 2005;20:57–60.

3. Kobayashi, Takashima S. Thalamic hyperdensity on CT in infantile GM1-gangliosidosis. Brain Dev. 1994;16:472–4.

4. Grandis E De, Rocco MD, Pessagno A, Venesseli E, Rossi A. MR Imaging Findings in 2 Cases of Late Infantile GM1 Gangliosidosis. Am J Neuroradiol. 2009;30:1325–7.

5. Fei P, Qin M, Hu T. Ocular manifestations of patients with gangliosidosis. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1994;16:285–9.

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4. Clinical and genetic spectrum of 104 Indian families with central nervous system white matter abnormalities;Clinical Genetics;2021-07-30

5. The juvenile gangliosidoses: A timeline of clinical change;Molecular Genetics and Metabolism Reports;2020-12

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