Type 3 GM I gangliosidosis: clinical and neuroradiological findings in an 11-year-old girl-Reference-Cited by-同舟云学术

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Type 3 GM I gangliosidosis: clinical and neuroradiological findings in an 11-year-old girl

Published:1995 Issue:5 Volume:242 Page:299-303
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Tanaka Rieko,Momoi Toru,Yoshida Akira,Okumura Mitsuyoshi,Yamakura Shinji,Takasaki Yoshinori,Kiyomasu Takahiro,Yamanaka Chutaro

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,Neurology

Link

http://link.springer.com/content/pdf/10.1007/BF00878872.pdf

Reference21 articles.

1. Angelini L, Nardocci N, Rumi V, Zorzi C, Strada L, Savoiardo M (1992) Hallervorden-Spatz disease: clinical and MRI study of 11 cases diagnosed in life. J Neurol 239:417?425

2. Ben-Yoseph Y, Momoi T, Baylerian MS, Nadler HL (1982) Km defect in neuraminidase of dysmorphic type sialidosis with and without ?-galactosidase deficiency. Clin Chim Acta 123:233?240

3. Drayer B, Burger P, Darwin R, Riederer S, Herfkens R, Johnson GA (1986) Magnetic resonance imaging of brain iron. AJNR 7:373?380

4. Drayer BP, Olanow W, Burger P, Johnson GA, Herfkens R, Riederer S (1986) Parkinson plus syndrome: diagnosis using high field MR imaging of brain iron. Radiology 159:493?498

5. Goldman JE, Katz D, Rapin I, Purpura DP, Suzuki K (1981) Chronic GMI gangliosidosis presenting as dystonia. 1. Clinical and pathological features. Ann Neurol 9:465?475

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