4.6 Review

Amyotrophic lateral sclerosis and motor neuron syndromes in Asia

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。
Article Public, Environmental & Occupational Health

Clinical and demographic factors and outcome of amyotrophic lateral sclerosis in relation to population ancestral origin

Benoit Marin et al.

EUROPEAN JOURNAL OF EPIDEMIOLOGY (2016)

Letter Clinical Neurology

The distinctive genetic architecture of ALS in mainland China

Zhang-Yu Zou et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2016)

Article Clinical Neurology

Association of the functional SNP rs2275294 in ZNF512B with risk of amyotrophic lateral sclerosis and Parkinson's disease in Han Chinese

Xinglong Yang et al.

AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION (2016)

Article Clinical Neurology

A rapid functional decline type of amyotrophic lateral sclerosis is linked to low expression of TTN

Hazuki Watanabe et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2016)

Article Geriatrics & Gerontology

Next-generation sequencing of 28 ALS-related genes in a Japanese ALS cohort

Ryoichi Nakamura et al.

NEUROBIOLOGY OF AGING (2016)

Editorial Material Clinical Neurology

A unique account of ALS in China: exploring ethnic heterogeneity

William Huynh et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2015)

Review Clinical Neurology

Natural history and clinical features of sporadic amyotrophic lateral sclerosis in China

Lu Chen et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2015)

Article Medicine, General & Internal

Incidence, prevalence, and medical expenditures of classical amyotrophic lateral sclerosis in Taiwan, 1999-2008

Ching-Piao Tsai et al.

JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION (2015)

Article Geriatrics & Gerontology

C9orf72 hexanucleotide repeat expansions in Chinese sporadic amyotrophic lateral sclerosis

Ji He et al.

NEUROBIOLOGY OF AGING (2015)

Article Clinical Neurology

Amyotrophic lateral sclerosis progression: Iran-ALS clinical registry, a multicentre study

Hosein Shamshiri et al.

AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION (2015)

Article Clinical Neurology

A single blind randomized controlled clinical trial of mexiletine in amyotrophic lateral sclerosis: Efficacy and safety of sodium channel blocker phase II trial

Kazumoto Shibuya et al.

AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION (2015)

Article Clinical Neurology

The predictors of survival in Chinese amyotrophic lateral sclerosis patients

Qianqian Wei et al.

AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION (2015)

Article Clinical Neurology

Optineurin mutations in patients with sporadic amyotrophic lateral sclerosis in China

Chengyu Li et al.

AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION (2015)

Article Clinical Neurology

Six SQSTM1 mutations in a Chinese amyotrophic lateral sclerosis cohort

Yi Yang et al.

AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION (2015)

Article Clinical Neurology

Factors affecting longitudinal functional decline and survival in amyotrophic lateral sclerosis patients

Hazuki Watanabe et al.

AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION (2015)

Article Clinical Neurology

Age at onset of amyotrophic lateral sclerosis in China

M. S. Liu et al.

ACTA NEUROLOGICA SCANDINAVICA (2014)

Article Clinical Neurology

Epidemiological characteristics of motor neuron disease in Chinese patients

F. Cui et al.

ACTA NEUROLOGICA SCANDINAVICA (2014)

Article Clinical Neurology

Searching for Grendel: origin and global spread of the C9ORF72 repeat expansion

Hannah A. Pliner et al.

ACTA NEUROPATHOLOGICA (2014)

Article Public, Environmental & Occupational Health

Prevalence and Incidence of Amyotrophic Lateral Sclerosis in Japan

Yuriko Doi et al.

JOURNAL OF EPIDEMIOLOGY (2014)

Article Geriatrics & Gerontology

SQSTM1 mutations in Han Chinese populations with sporadic amyotrophic lateral sclerosis

YongPing Chen et al.

NEUROBIOLOGY OF AGING (2014)

Article Geriatrics & Gerontology

Extensive molecular genetic survey of Taiwanese patients with amyotrophic lateral sclerosis

Bing-Wen Soong et al.

NEUROBIOLOGY OF AGING (2014)

Article Geriatrics & Gerontology

Identify mutation in amyotrophic lateral sclerosis cases using HaloPlex target enrichment system

Zhi-Jun Liu et al.

NEUROBIOLOGY OF AGING (2014)

Article Clinical Neurology

Monomelic amyotrophy: Clinical profile and natural history of 279 cases seen over 35 years (1976-2010)

Atchayaram Nalini et al.

AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION (2014)

Article Clinical Neurology

Japanese amyotrophic lateral sclerosis patients with GGGGCC hexanucleotide repeat expansion in C9ORF72

Takuya Konno et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2013)

Article Clinical Neurology

Pathophysiological insights into ALS with C9ORF72 expansions

Kelly L. Williams et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2013)

Article Clinical Neurology

Neck weakness is a potent prognostic factor in sporadic amyotrophic lateral sclerosis patients

Ryoichi Nakamura et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2013)

Article Cell Biology

Mitochondrial DNA variations in Madras motor neuron disease

Periyasamy Govindaraj et al.

MITOCHONDRION (2013)

Review Clinical Neurology

The epidemiology of ALS: a conspiracy of genes, environment and time

Ammar Al-Chalabi et al.

NATURE REVIEWS NEUROLOGY (2013)

Article Geriatrics & Gerontology

Screening for C9orf72 repeat expansions in Chinese amyotrophic lateral sclerosis patients

Zhang-Yu Zou et al.

NEUROBIOLOGY OF AGING (2013)

Article Neurosciences

Chin fasciculations in Madras motor neuron disease: A new clinical feature

Mandaville Gourie-Devi et al.

NEUROLOGY INDIA (2013)

Article Clinical Neurology

Tracheostomy with invasive ventilation for ALS patients: Neurologists' roles in the US and Japan

Judith Rabkin et al.

AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION (2013)

Article Clinical Neurology

C9orf72 repeat expansions are not detected in Chinese patients with familial ALS

Rong Liu et al.

AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION (2013)

Article Clinical Neurology

C9ORF72 Repeat Expansion in Amyotrophic Lateral Sclerosis in the Kii Peninsula of Japan

Hiroyuki Ishiura et al.

ARCHIVES OF NEUROLOGY (2012)

Article Medicine, General & Internal

Oral Solubilized Ursodeoxycholic Acid Therapy in Amyotrophic Lateral Sclerosis: A Randomized Cross-Over Trial

Ju-Hong Min et al.

JOURNAL OF KOREAN MEDICAL SCIENCE (2012)

Letter Clinical Neurology

Optineurin mutations in Japanese amyotrophic lateral sclerosis

Sinead M. Murphy et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2012)

Article Geriatrics & Gerontology

Large-scale screening of TARDBP mutation in amyotrophic lateral sclerosis in Japanese

Aritoshi Iida et al.

NEUROBIOLOGY OF AGING (2012)

Article Geriatrics & Gerontology

Analysis of C9orf72 repeat expansion in 563 Japanese patients with amyotrophic lateral sclerosis

Kotaro Ogaki et al.

NEUROBIOLOGY OF AGING (2012)

Article Geriatrics & Gerontology

TARDBP gene mutations among Chinese patients with sporadic amyotrophic lateral sclerosis

Rui Huang et al.

NEUROBIOLOGY OF AGING (2012)

Article Clinical Neurology

Survival and prognostic factors of motor neuron disease in a multi-ethnic Asian population

Khean-Jin Goh et al.

AMYOTROPHIC LATERAL SCLEROSIS (2011)

Article Biochemistry & Molecular Biology

A functional variant in ZNF512B is associated with susceptibility to amyotrophic lateral sclerosis in Japanese

Aritoshi Iida et al.

HUMAN MOLECULAR GENETICS (2011)

Article Clinical Neurology

Behavioral changes in early ALS correlate with voxel-based morphometry and diffusion tensor imaging

Masashi Tsujimoto et al.

JOURNAL OF THE NEUROLOGICAL SCIENCES (2011)

Article Medicine, General & Internal

Amyotrophic lateral sclerosis

Matthew C. Kiernan et al.

LANCET (2011)

Article Clinical Neurology

Clinical features of Hirayama disease in mainland China

Bo Zhou et al.

AMYOTROPHIC LATERAL SCLEROSIS (2010)

Article Genetics & Heredity

Association between novel TARDBP mutations and Chinese patients with amyotrophic lateral sclerosis

Hui-Ling Xiong et al.

BMC MEDICAL GENETICS (2010)

Article Medicine, General & Internal

Effects of Gender in Amyotrophic Lateral Sclerosis

Pamela A. McCombe et al.

GENDER MEDICINE (2010)

Article Multidisciplinary Sciences

Mutations of optineurin in amyotrophic lateral sclerosis

Hirofumi Maruyama et al.

NATURE (2010)

Article Clinical Neurology

Age at onset influences on wide-ranged clinical features of sporadic amyotrophic lateral sclerosis

Naoki Atsuta et al.

JOURNAL OF THE NEUROLOGICAL SCIENCES (2009)

Article Clinical Neurology

Reduced frequency of ALS in an ethnically mixed population

T. Zaldivar et al.

NEUROLOGY (2009)

Article Clinical Neurology

A clinical study of Hirayama disease in Taiwan

Ying-Chih Huang et al.

MUSCLE & NERVE (2008)

Review Clinical Neurology

The ALS/PDC syndrome of Guam and the cycad hypothesis

John C. Steele et al.

NEUROLOGY (2008)

Article Clinical Neurology

Increasing incidence of ALS in Canterbury, New Zealand A 22-year study

M. Murphy et al.

NEUROLOGY (2008)

Review Clinical Neurology

Ethnic variation in the incidence of ALS - A systematic review

Simon Cronin et al.

NEUROLOGY (2007)

Article Clinical Neurology

Nationwide survey of juvenile muscular atrophy of distal upper extremity (Hirayama disease) in Japan

K Tashiro et al.

AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS (2006)

Article Clinical Neurology

Changes in the incidence of amyotrophic lateral sclerosis in Wakayama, Japan

T Kihira et al.

AMYOTROPHIC LATERAL SCLEROSIS (2005)

Article Clinical Neurology

Prevalence and patterns of cognitive impairment in sporadic ALS

GM Ringholz et al.

NEUROLOGY (2005)

Article Clinical Neurology

Parkinsonism-dementia complex of Guam

JC Steele

MOVEMENT DISORDERS (2005)

Article Clinical Neurology

Madras motor neuron disease variant, clinical features of seven patients

M Gourie-Devi et al.

JOURNAL OF THE NEUROLOGICAL SCIENCES (2003)

Article Clinical Neurology

Long-term follow-up of 44 patients with brachial monomelic amyotrophy

M Gourie-Devi et al.

ACTA NEUROLOGICA SCANDINAVICA (2003)

Review Medicine, General & Internal

Juvenile muscular atrophy of distal upper extremity (Hirayama disease)

K Hirayama

INTERNAL MEDICINE (2000)