Identification ofGFAP gene mutation in hereditary adult-onset Alexander's disease-Reference-Cited by-同舟云学术

Identification ofGFAP gene mutation in hereditary adult-onset Alexander's disease

Published:2002-11-23 Issue:6 Volume:52 Page:779-785
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Namekawa Michito,Takiyama Yoshihisa,Aoki Yoko,Takayashiki Norio,Sakoe Kumi,Shimazaki Haruo,Taguchi Tomohiro,Tanaka Yasufumi,Nishizawa Masatoyo,Saito Ken,Matsubara Yoichi,Nakano Imaharu

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference36 articles.

1. PROGRESSIVE FIBRINOID DEGENERATION OF FIBRILLARY ASTROCYTES ASSOCIATED WITH MENTAL RETARDATION IN A HYDROCEPHALIC INFANT

2. ALEXANDER'S DISEASE

3. BULBAR PALSY WITH ROSENTHAL FIBER FORMATION IN THE MEDULLA OF A 15-YEAR-OLD GIRL. LOCALIZED FORM OF ALEXANDER'S DISEASE?

4. Multiple Sklerose mit Rosenthalschen Fasern

5. Alexander's Disease in an Adult

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