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

DiMauro

Showing results (821-830 of 942) with videos related to

Pageof 95
Sort By:
American Journal of Human Genetics|August 16, 2006
Navajo neurohepatopathy is caused by a mutation in the MPV17 geneCharalampos L Karadimas, Tuan H Vu, Stephen A Holve, et al.
Annals of Neurology|May 11, 2000
Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2C M Sue, C Karadimas, N Checcarelli, et al.
Prenatal Diagnosis|July 29, 2006
Prenatal diagnosis of glycogen storage disease type IVH Orhan Akman, Charalampos Karadimas, Yolanda Gyftodimou, et al.
Plos One|September 18, 2015
Inhibition of Inactive States of Tetrodotoxin-Sensitive Sodium Channels Reduces Spontaneous Firing of C-Fiber Nociceptors and Produces Analgesia in Formalin and Complete Freund's Adjuvant Models of PainDavid J Matson, Darryl T Hamamoto, Howard Bregman, et al.
Physical Review Letters|February 7, 2013
Scaling of the low-energy structure in above-threshold ionization in the tunneling regime: theory and experimentL Guo, S S Han, X Liu, et al.
Brain : a Journal of Neurology|April 7, 2007
The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) geneKlaus Gempel, Haluk Topaloglu, Beril Talim, et al.
Annals of Neurology|September 3, 2002
Mitochondrial DNA depletion and dGK gene mutationsLeonardo Salviati, Sabrina Sacconi, Michelangelo Mancuso, et al.
Brain Topography|May 11, 2002
Conductivities of three-layer live human skullM Akhtari, H C Bryant, A N Mamelak, et al.
Journal of the American College of Cardiology|May 28, 2003
A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathyRobert W Taylor, Carla Giordano, Mercy M Davidson, et al.
Archives of Neurology|April 12, 2012
Loss of myelin-associated glycoprotein in kearns-sayre syndromeNichola Z Lax, Graham R Campbell, Amy K Reeve, et al.
Pageof 95

Showing results (821-830 of 942) with videos related to

Sort By:
Pageof 95
American Journal of Human Genetics|August 16, 2006
Navajo neurohepatopathy is caused by a mutation in the MPV17 geneCharalampos L Karadimas, Tuan H Vu, Stephen A Holve, et al.
Annals of Neurology|May 11, 2000
Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2C M Sue, C Karadimas, N Checcarelli, et al.
Prenatal Diagnosis|July 29, 2006
Prenatal diagnosis of glycogen storage disease type IVH Orhan Akman, Charalampos Karadimas, Yolanda Gyftodimou, et al.
Plos One|September 18, 2015
Inhibition of Inactive States of Tetrodotoxin-Sensitive Sodium Channels Reduces Spontaneous Firing of C-Fiber Nociceptors and Produces Analgesia in Formalin and Complete Freund's Adjuvant Models of PainDavid J Matson, Darryl T Hamamoto, Howard Bregman, et al.
Physical Review Letters|February 7, 2013
Scaling of the low-energy structure in above-threshold ionization in the tunneling regime: theory and experimentL Guo, S S Han, X Liu, et al.
Brain : a Journal of Neurology|April 7, 2007
The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) geneKlaus Gempel, Haluk Topaloglu, Beril Talim, et al.
Annals of Neurology|September 3, 2002
Mitochondrial DNA depletion and dGK gene mutationsLeonardo Salviati, Sabrina Sacconi, Michelangelo Mancuso, et al.
Brain Topography|May 11, 2002
Conductivities of three-layer live human skullM Akhtari, H C Bryant, A N Mamelak, et al.
Journal of the American College of Cardiology|May 28, 2003
A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathyRobert W Taylor, Carla Giordano, Mercy M Davidson, et al.
Archives of Neurology|April 12, 2012
Loss of myelin-associated glycoprotein in kearns-sayre syndromeNichola Z Lax, Graham R Campbell, Amy K Reeve, et al.
Pageof 95