Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Jun Goto

Showing results (81-90 of 171) with videos related to

Pageof 18
Sort By:
Internal Medicine (Tokyo, Japan)|August 6, 2010
A case of atypical amyloid polyneuropathy with predominant upper-limb involvement with the diagnosis unexpectedly found at lung operationYuichiro Shirota, Atsushi Iwata, Hiroyuki Ishiura, et al.
Gan to Kagaku Ryoho. Cancer & Chemotherapy|December 28, 2012
[A new attempt to promote home medical care in Kashiwa city-usefulness of information and communication technology with seamless multidisciplinary cooperation]Katsuya Iijima, Satoru Yoshie, Mari Kimata, et al.
Neurobiology of Disease|February 21, 2012
DRPLA transgenic mouse substrains carrying single copy of full-length mutant human DRPLA gene with variable sizes of expanded CAG repeats exhibit CAG repeat length- and age-dependent changes in behavioral abnormalities and gene expression profilesKazushi Suzuki, Jiayi Zhou, Toshiya Sato, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 1, 2009
TRPM7 is not associated with amyotrophic lateral sclerosis-parkinsonism dementia complex in the Kii peninsula of JapanKenju Hara, Yasumasa Kokubo, Hiroyuki Ishiura, et al.
Neurogenetics|July 28, 2010
Identification of novel SNPs of ABCD1, ABCD2, ABCD3, and ABCD4 genes in patients with X-linked adrenoleukodystrophy (ALD) based on comprehensive resequencing and association studies with ALD phenotypesTakashi Matsukawa, Muriel Asheuer, Yuji Takahashi, et al.
Internal Medicine (Tokyo, Japan)|June 11, 2019
Prominent Spasticity and Hyperreflexia of the Legs in a Nepalese Patient with Friedreich AtaxiaHiroya Naruse, Yuji Takahashi, Hiroyuki Ishiura, et al.
The American Journal of Gastroenterology|January 13, 2006
Usefulness of contrast-enhanced endoscopic ultrasonography in the differentiation between malignant and benign lymphadenopathyAkira Kanamori, Yoshiki Hirooka, Akihiro Itoh, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|June 20, 2012
Mutational analysis of familial and sporadic amyotrophic lateral sclerosis with OPTN mutations in Japanese populationHiroya Naruse, Yuji Takahashi, Tameko Kihira, et al.
Journal of Human Genetics|September 13, 2020
Loss-of-function variants in NEK1 are associated with an increased risk of sporadic ALS in the Japanese populationHiroya Naruse, Hiroyuki Ishiura, Jun Mitsui, et al.
Cerebellum (London, England)|December 28, 2024
A Japanese Family with a Novel Pathogenic Variant in KIF1A Presenting with Spastic Paraparesis, Cerebellar Ataxia, and Intellectual DisabilityAkihiko Mitsutake, Mizuho Kawai, Kenta Orimo, et al.
Pageof 18

Showing results (81-90 of 171) with videos related to

Sort By:
Pageof 18
Internal Medicine (Tokyo, Japan)|August 6, 2010
A case of atypical amyloid polyneuropathy with predominant upper-limb involvement with the diagnosis unexpectedly found at lung operationYuichiro Shirota, Atsushi Iwata, Hiroyuki Ishiura, et al.
Gan to Kagaku Ryoho. Cancer & Chemotherapy|December 28, 2012
[A new attempt to promote home medical care in Kashiwa city-usefulness of information and communication technology with seamless multidisciplinary cooperation]Katsuya Iijima, Satoru Yoshie, Mari Kimata, et al.
Neurobiology of Disease|February 21, 2012
DRPLA transgenic mouse substrains carrying single copy of full-length mutant human DRPLA gene with variable sizes of expanded CAG repeats exhibit CAG repeat length- and age-dependent changes in behavioral abnormalities and gene expression profilesKazushi Suzuki, Jiayi Zhou, Toshiya Sato, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 1, 2009
TRPM7 is not associated with amyotrophic lateral sclerosis-parkinsonism dementia complex in the Kii peninsula of JapanKenju Hara, Yasumasa Kokubo, Hiroyuki Ishiura, et al.
Neurogenetics|July 28, 2010
Identification of novel SNPs of ABCD1, ABCD2, ABCD3, and ABCD4 genes in patients with X-linked adrenoleukodystrophy (ALD) based on comprehensive resequencing and association studies with ALD phenotypesTakashi Matsukawa, Muriel Asheuer, Yuji Takahashi, et al.
Internal Medicine (Tokyo, Japan)|June 11, 2019
Prominent Spasticity and Hyperreflexia of the Legs in a Nepalese Patient with Friedreich AtaxiaHiroya Naruse, Yuji Takahashi, Hiroyuki Ishiura, et al.
The American Journal of Gastroenterology|January 13, 2006
Usefulness of contrast-enhanced endoscopic ultrasonography in the differentiation between malignant and benign lymphadenopathyAkira Kanamori, Yoshiki Hirooka, Akihiro Itoh, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|June 20, 2012
Mutational analysis of familial and sporadic amyotrophic lateral sclerosis with OPTN mutations in Japanese populationHiroya Naruse, Yuji Takahashi, Tameko Kihira, et al.
Journal of Human Genetics|September 13, 2020
Loss-of-function variants in NEK1 are associated with an increased risk of sporadic ALS in the Japanese populationHiroya Naruse, Hiroyuki Ishiura, Jun Mitsui, et al.
Cerebellum (London, England)|December 28, 2024
A Japanese Family with a Novel Pathogenic Variant in KIF1A Presenting with Spastic Paraparesis, Cerebellar Ataxia, and Intellectual DisabilityAkihiko Mitsutake, Mizuho Kawai, Kenta Orimo, et al.
Pageof 18