Clinicopathological study of familial late infantile Hallervorden-Spatz disease: a particular form of neuroacanthocytosis-Reference-Cited by-同舟云学术

Clinicopathological study of familial late infantile Hallervorden-Spatz disease: a particular form of neuroacanthocytosis

Published:1996-03 Issue:3 Volume:12 Page:155-160
ISSN:0256-7040
Container-title:Child's Nervous System
language:en
Short-container-title:Child's Nerv Syst

Author:

Malandrini Alessandro,Fabrizi Gian Maria,Bartalucci Paola,Salvadori Claudio,Berti Gianna,Guazzi Gian Carlo,Sab� Claudio

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,General Medicine,Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/BF00266820.pdf

Reference26 articles.

1. Aicardi J, Castelein P (1979) Infantile neuroaxonal dystrophy. Brain 102: 727?748

2. 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

3. Brin MF (1993) Acanthocytosis. In: Goetz CG, Tanner CM, Aminoff MJ (eds) Handbook of clinical neurology, vol 19. (63). Elsevier, Amsterdam, pp 271?299

4. Bruyn GW (1986) Chorea-acanthocytoisis. In: Vinken PJ, Bruyn GW, Klawans HL (eds) Handbook of clinicai neurology, vol 5 (49). Elsevier, Amsterdam, pp 327?334

5. Dooling EC, Schoene WC, Richardson EP (1974). Hallervorden-Spatz syndrone. Arch Neurol 30:70?83

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