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

K Sahashi

Showing results (81-90 of 96) with videos related to

Pageof 10
Sort By:
Biochimica Et Biophysica Acta|August 27, 1991
Direct DNA sequencing from colony: analysis of multiple deletions of mitochondrial genomeK Ohno, M Tanaka, H Ino, et al.
Journal of the Neurological Sciences|November 1, 1990
Cytoplasmic body and mitochondrial DNA deletionK Sahashi, K Ohno, M Tanaka, et al.
Annals of the New York Academy of Sciences|January 1, 1981
Recently recognized congenital myasthenic syndromes: (a) end-plate acetylcholine (ACh) esterase deficiency (b) putative abnormality of the ACh induced ion channel (c) putative defect of ACh resynthesis or mobilization - clinical features, ultrastructure and cytochemistryA G Engel, E H Lambert, D M Mulder, et al.
Nihon Naika Gakkai Zasshi. the Journal of the Japanese Society of Internal Medicine|July 10, 1991
[A case of myasthenia gravis complicated with severe aplastic anemia]I Aizawa, K Sahashi, H Kaneko, et al.
Lancet (London, England)|January 12, 1985
Presymptomatic diagnosis of heterozygosity for familial amyloidotic polyneuropathy by recombinant DNA techniquesH Sasaki, Y Sakaki, Y Takagi, et al.
Neurology|December 1, 1992
Strong correlation between the number of CAG repeats in androgen receptor genes and the clinical onset of features of spinal and bulbar muscular atrophyS Igarashi, Y Tanno, O Onodera, et al.
Annals of Neurology|June 1, 1982
A newly recognized congenital myasthenic syndrome attributed to a prolonged open time of the acetylcholine-induced ion channelA G Engel, E H Lambert, D M Mulder, et al.
The American Journal of the Medical Sciences|March 1, 1986
Thyrotropin releasing hormone levels in human cerebrospinal fluid in various neurologic diseasesT Mitsuma, T Nogimori, K Sahashi, et al.
Nihon Kyobu Shikkan Gakkai Zasshi|February 1, 1990
[A case of pigeon breeder's disease]S Ito, K Shima, K Sahashi, et al.
Nihon Kyobu Shikkan Gakkai Zasshi|January 1, 1994
[Clinical study of anti-phospholipid antibody in patients with sarcoidosis]S Ito, Y Ina, H Hashiba, et al.
Pageof 10

Showing results (81-90 of 96) with videos related to

Sort By:
Pageof 10
Biochimica Et Biophysica Acta|August 27, 1991
Direct DNA sequencing from colony: analysis of multiple deletions of mitochondrial genomeK Ohno, M Tanaka, H Ino, et al.
Journal of the Neurological Sciences|November 1, 1990
Cytoplasmic body and mitochondrial DNA deletionK Sahashi, K Ohno, M Tanaka, et al.
Annals of the New York Academy of Sciences|January 1, 1981
Recently recognized congenital myasthenic syndromes: (a) end-plate acetylcholine (ACh) esterase deficiency (b) putative abnormality of the ACh induced ion channel (c) putative defect of ACh resynthesis or mobilization - clinical features, ultrastructure and cytochemistryA G Engel, E H Lambert, D M Mulder, et al.
Nihon Naika Gakkai Zasshi. the Journal of the Japanese Society of Internal Medicine|July 10, 1991
[A case of myasthenia gravis complicated with severe aplastic anemia]I Aizawa, K Sahashi, H Kaneko, et al.
Lancet (London, England)|January 12, 1985
Presymptomatic diagnosis of heterozygosity for familial amyloidotic polyneuropathy by recombinant DNA techniquesH Sasaki, Y Sakaki, Y Takagi, et al.
Neurology|December 1, 1992
Strong correlation between the number of CAG repeats in androgen receptor genes and the clinical onset of features of spinal and bulbar muscular atrophyS Igarashi, Y Tanno, O Onodera, et al.
Annals of Neurology|June 1, 1982
A newly recognized congenital myasthenic syndrome attributed to a prolonged open time of the acetylcholine-induced ion channelA G Engel, E H Lambert, D M Mulder, et al.
The American Journal of the Medical Sciences|March 1, 1986
Thyrotropin releasing hormone levels in human cerebrospinal fluid in various neurologic diseasesT Mitsuma, T Nogimori, K Sahashi, et al.
Nihon Kyobu Shikkan Gakkai Zasshi|February 1, 1990
[A case of pigeon breeder's disease]S Ito, K Shima, K Sahashi, et al.
Nihon Kyobu Shikkan Gakkai Zasshi|January 1, 1994
[Clinical study of anti-phospholipid antibody in patients with sarcoidosis]S Ito, Y Ina, H Hashiba, et al.
Pageof 10