Congenital CLN disease in two siblings-Reference-Cited by-同舟云学术

Congenital CLN disease in two siblings

Published:2015-05 Issue:9-10 Volume:165 Page:210-213
ISSN:0043-5341
Container-title:Wiener Medizinische Wochenschrift
language:en
Short-container-title:Wien Med Wochenschr

Author:

Meyer Sascha,Yilmaz Umut,Kim Yoo-Jin,Steinfeld Robert,Meyberg-Solomayer Gabriele,Oehl-Jaschkowitz Barbara,Tzschach Andreas,Gortner Ludwig,Igel Julia,Schofer Otto

Publisher

Springer Science and Business Media LLC

Subject

General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s10354-015-0359-4.pdf

Reference8 articles.

1. Barohn RJ, Dowd DC, Kagan-Hallet KS. Congenital ceroid-lipofuscinosis. Pediatr Neurol. 1992;8:54–9.

2. Cotman SL, Karaa A, Staropoli JF, Sims KB. Neuronal ceroid lipofuscinosis: impact of recent genetic advances and expansion of the clinicopathologic spectrum. Clin Neurol Neurosci Rep. 2013;13:366.

3. Kohlschütter A, Schulz A. Towards understanding the neuronal ceroid lipofuscinoses. Brain Dev. 2009;31:499–502.

4. Mink JW, Augustine EF, Adams HR, Marshall FJ, Kwon JM. Classification and natural history of the neuronal ceroid lipofuscinoses. J Child Neurol. 2013;28:1101–5.

5. Mole SE, Williams RE, Goebel HH, eds. The neuronal ceroid lipofusinoses. 2nd ed. Oxford: Oxford University Press; 2011.

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