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Items: 5

1.

Histological, biochemical, and genetic characterization of early-onset fulminating sialidosis type 2 in a Korean neonate with hydrops fetalis.

Lee BH, Kim YM, Kim JH, Kim GH, Lee BS, Kim CJ, Yoo HJ, Yoo HW.

Brain Dev. 2014 Feb;36(2):171-5. doi: 10.1016/j.braindev.2013.01.012. Epub 2013 Feb 19.

PMID:
23433491
2.

[Sialidosis type 2].

Suzuki Y.

Ryoikibetsu Shokogun Shirizu. 1999;(27 Pt 2):169-70. Review. Japanese. No abstract available.

PMID:
10434621
3.

Electrophysiological studies of myoclonus in sialidosis type 2.

Tobimatsu S, Fukui R, Shibasaki H, Kato M, Kuroiwa Y.

Electroencephalogr Clin Neurophysiol. 1985 Jan;60(1):16-22.

PMID:
2578348
4.

Sialidosis type 2 in Japan. Clinical study in two siblings' cases and review of literature.

Matsuo T, Egawa I, Okada S, Suetsugu M, Yamamoto K, Watanabe M.

J Neurol Sci. 1983 Jan;58(1):45-55.

PMID:
6405017
5.

Sialidosis type 2 (acid neuraminidase deficiency): clinical and biochemical features of a further case.

Winter RM, Swallow DM, Baraitser M, Purkiss P.

Clin Genet. 1980 Sep;18(3):203-10.

PMID:
6777097

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