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Coffee consumption and mortality in Japan with 18 years of follow-up: the Jichi Medical School Cohort Study

Public health (London), 2021-02, Vol.191, p.23-30

2021

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SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years

Neurology, 2006-01, Vol.66 (1), p.112-114

2006

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Status of the ITER remote experimentation centre

Fusion engineering and design, 2018-03, Vol.128, p.158-162

2018

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Mutations in the SPG3A gene encoding the GTPase atlastin interfere with vesicle trafficking in the ER/Golgi interface and Golgi morphogenesis

Molecular and cellular neuroscience, 2007-05, Vol.35 (1), p.1-13

2007

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16q-linked autosomal dominant cerebellar ataxia: A clinical and genetic study

Journal of the neurological sciences, 2006-09, Vol.247 (2), p.180-186

2006

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Identification of a SACS gene missense mutation in ARSACS

Neurology, 2004-01, Vol.62 (1), p.107-109

2004

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Early-onset ataxia with ocular motor apraxia and hypoalbuminemia: the aprataxin gene mutations

Neurology, 2002-08, Vol.59 (4), p.590-595

2002

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Efficacy and safety of levetiracetam in patients with epileptic seizures

Journal of the neurological sciences, 2017-10, Vol.381, p.341-341

2017

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Efficacy and safety of leuprorelin in patients with spinal and bulbar muscular atrophy (JASMITT study): a multicentre, randomised, double-blind, placebo-controlled trial

Lancet neurology, 2010-09, Vol.9 (9), p.875-884

2010

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Autosomal-recessive complicated spastic paraplegia with a novel lysosomal trafficking regulator gene mutation

Journal of neurology, neurosurgery and psychiatry, 2014-09, Vol.85 (9), p.1024-1028

2014

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Clinical characteristics and detailed haplotype analysis of patients with SCA36 in Japan

Journal of the neurological sciences, 2017-10, Vol.381, p.383-384

2017

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A case of sporadic adult Alexander disease presenting with acute onset, remission and relapse

Journal of neurology, neurosurgery and psychiatry, 2010-11, Vol.81 (11), p.1292-1293

2010

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Single Sperm Analysis of the CAG Repeats in the Gene for Machado-Joseph Disease (MJD1): Evidence for Non-Mendelian Transmission of the MJD1 Gene and for the Effect of the Intragenic CGG/GGG Polymorphism on the Intergenerational Instability

Human molecular genetics, 1997-07, Vol.6 (7), p.1063-1068

1997

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Clinical predictors of prolonged postresection hypotension after laparoscopic adrenalectomy for pheochromocytoma

Surgery, 2016-03, Vol.159 (3), p.763-770

2016

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A Japanese SPG4 family with a novel missense mutation of the SPG4 gene: intrafamilial variability in age at onset and clinical severity

Acta neurologica Scandinavica, 2002-12, Vol.106 (6), p.387-391

2002

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

Annals of neurology, 2002-12, Vol.52 (6), p.779-785

2002

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Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28)

Annals of neurology, 2005-04, Vol.57 (4), p.567-571

2005

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His-Purkinje system-related incessant ventricular tachycardia arising from the left coronary cusp

Journal of arrhythmia, 2014-08, Vol.30 (4), p.323-326

2014

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Neuromuscular sarcoidosis: A retrospective study of 12 cases

Journal of the neurological sciences, 2013-10, Vol.333, p.e440-e440

2013

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Sonographic detection of diffuse peripheral nerve hypertrophy in chronic inflammatory demyelinating polyradiculoneuropathy

Journal of clinical ultrasound, 2000-11, Vol.28 (9), p.488-491

2000

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Response to commentary on: The necessary preoperative dose of alpha-blockers reflects higher tumor activity in pheochromocytoma

Surgery, 2016

2016

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Favorable outcomes of patients with vasospastic angina associated with cardiac arrest

Journal of cardiology, 2014-01, Vol.63 (1), p.41-45

2014

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A founder effect and mutational hot spots may contribute to the most frequent mutations in the SPG3A gene

Neurogenetics, 2006-05, Vol.7 (2), p.131-132

2006

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Ventricular fibrillation caused by coronary artery spasm during mild therapeutic hypothermia after resuscitation

The American journal of emergency medicine, 2013-02, Vol.31 (2), p.453.e5-453.e8

2013

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A large Japanese SPG4 family with a novel insertion mutation of the SPG4 gene: a clinical and genetic study

Journal of the neurological sciences, 2001-03, Vol.185 (1), p.63-68

2001

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Coffee consumption and mortality in Japan with 18 years of follow-up: the Jichi Medical School Cohort Study

SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years

Status of the ITER remote experimentation centre

Mutations in the SPG3A gene encoding the GTPase atlastin interfere with vesicle trafficking in the ER/Golgi interface and Golgi morphogenesis

16q-linked autosomal dominant cerebellar ataxia: A clinical and genetic study

Identification of a SACS gene missense mutation in ARSACS

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia: the aprataxin gene mutations

Efficacy and safety of levetiracetam in patients with epileptic seizures

Efficacy and safety of leuprorelin in patients with spinal and bulbar muscular atrophy (JASMITT study): a multicentre, randomised, double-blind, placebo-controlled trial

Autosomal-recessive complicated spastic paraplegia with a novel lysosomal trafficking regulator gene mutation

Clinical characteristics and detailed haplotype analysis of patients with SCA36 in Japan

A case of sporadic adult Alexander disease presenting with acute onset, remission and relapse

Single Sperm Analysis of the CAG Repeats in the Gene for Machado-Joseph Disease (MJD1): Evidence for Non-Mendelian Transmission of the MJD1 Gene and for the Effect of the Intragenic CGG/GGG Polymorphism on the Intergenerational Instability

Clinical predictors of prolonged postresection hypotension after laparoscopic adrenalectomy for pheochromocytoma

A Japanese SPG4 family with a novel missense mutation of the SPG4 gene: intrafamilial variability in age at onset and clinical severity

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

Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28)

His-Purkinje system-related incessant ventricular tachycardia arising from the left coronary cusp

Neuromuscular sarcoidosis: A retrospective study of 12 cases

Sonographic detection of diffuse peripheral nerve hypertrophy in chronic inflammatory demyelinating polyradiculoneuropathy

Response to commentary on: The necessary preoperative dose of alpha-blockers reflects higher tumor activity in pheochromocytoma

Favorable outcomes of patients with vasospastic angina associated with cardiac arrest

A founder effect and mutational hot spots may contribute to the most frequent mutations in the SPG3A gene

Ventricular fibrillation caused by coronary artery spasm during mild therapeutic hypothermia after resuscitation

A large Japanese SPG4 family with a novel insertion mutation of the SPG4 gene: a clinical and genetic study

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