相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Genetics of amyotrophic lateral sclerosis: A review
Stephane Mathis et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2019)
Familial amyotrophic lateral sclerosis with an I104F mutation in the SOD1 gene: Multisystem degeneration with neurofilamentous aggregates and SOD1 inclusions
Haishan Jiang et al.
NEUROPATHOLOGY (2017)
A Japanese familial ALS patient with autonomic failure and a p. Cys146Arg mutation in the gene for SOD1 (SOD1)
Kentaro Hayashi et al.
NEUROPATHOLOGY (2016)
An autopsy case of sporadic amyotrophic lateral sclerosis associated with the I113T SOD1 mutation
Seika Nakamura et al.
NEUROPATHOLOGY (2014)
Clinico-Pathological Correlation in Progressive Ataxia and Palatal Tremor: A Novel Tauopathy
Zoltan Mari et al.
MOVEMENT DISORDERS CLINICAL PRACTICE (2014)
The genetics and neuropathology of amyotrophic lateral sclerosis
Ammar Al-Chalabi et al.
ACTA NEUROPATHOLOGICA (2012)
Distinctive clinicopathological features of 2 large families with amyotrophic lateral sclerosis having L106V mutation in SOD1 gene
Akiyo Hineno et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2012)
FALS with Gly72Ser mutation in SOD1 gene: Report of a family including the first autopsy case
Zen Kobayashi et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2011)
Pathological study of pseudohypertrophy of the inferior olivary nucleus
Katsuhiko Ogawa et al.
NEUROPATHOLOGY (2010)
Familial amyotrophic lateral sclerosis with Gly93Ser mutation in Cu/Zn superoxide dismutase: A clinical and neuropathological study
Megumi Suzuki et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2008)
Amyotrophic lateral sclerosis
J. D. Mitchell et al.
LANCET (2007)
Increased neuronal expression of alpha B-crystallin in human olivary hypertrophy
Kazuko Fukushima et al.
NEUROPATHOLOGY (2006)
Familial amyotrophic lateral sclerosis with bulbar onset and a novel Asp101Tyr Cu/Zn superoxide dismutase gene mutation
CF Tan et al.
ACTA NEUROPATHOLOGICA (2004)
A novel SOD1 gene mutation in familial ALS with low penetrance in females
T Murakami et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2001)
Familial amyotrophic lateral sclerosis with a novel Leu126Ser mutation in the copper/zinc superoxide dismutase gene showing mild clinical features and Lewy body-like hyaline inclusions
Y Takehisa et al.
ARCHIVES OF NEUROLOGY (2001)