Top

Published in:

01-01-2000 | Case Report

Juvenile-onset generalized neuroaxonal dystrophy (Hallervorden-Spatz disease) with diffuse neurofibrillary and Lewy body pathology

Authors: K. Wakabayashi, T. Fukushima, R. Koide, Y. Horikawa, M. Hasegawa, Y. Watanabe, T. Noda, I. Eguchi, T. Morita, M. Yoshimoto, T. Iwatsubo, H. Takahashi

Published in: Acta Neuropathologica | Issue 3/2000

Title: Juvenile-onset generalized neuroaxonal dystrophy (Hallervorden-Spatz disease) with diffuse neurofibrillary and Lewy body pathology
Authors: K. Wakabayashi
T. Fukushima
R. Koide
Y. Horikawa
M. Hasegawa
Y. Watanabe
T. Noda
I. Eguchi
T. Morita
M. Yoshimoto
T. Iwatsubo
H. Takahashi
Publication date: 01-01-2000
Publisher: Springer-Verlag
Published in: Acta Neuropathologica / Issue 3/2000
Print ISSN: 0001-6322
Electronic ISSN: 1432-0533
DOI: https://doi.org/10.1007/s004010050049

At a glance: The STEP trials

Springer Medicine

Juvenile-onset generalized neuroaxonal dystrophy (Hallervorden-Spatz disease) with diffuse neurofibrillary and Lewy body pathology

At a glance: The STEP trials

Springer Medicine

Please log in to get access to this content

Other articles of this Issue 3/2000

Hypoglycaemic neuropathy: occurrence of axon terminals in plantar skin and plantar muscle of diabetic BB/Wor rats treated with insulin implants

Dejerine-Sottas disease with a novel de novo dominant mutation, Ser 149 Arg, of the peripheral myelin protein 22

Apoptosis of perineurial cells in sensory perineuritis

Spontaneous and ethyl-nitrosourea-induced medullomyoblastomas in cerebellar vermis defect (CVD) mutant rats

Glial pathology in development of cerebellar dysplasia in the hereditary cerebellar vermis defect (CVD) rat

Hepatitis C virus infection and myositis: a polymerase chain reaction study