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American Journal of Human Genetics
|
August 16, 2006
Navajo neurohepatopathy is caused by a mutation in the MPV17 gene
Charalampos 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 SCO2
C M Sue, C Karadimas, N Checcarelli, et al.
Prenatal Diagnosis
|
July 29, 2006
Prenatal diagnosis of glycogen storage disease type IV
H 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 Pain
David 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 experiment
L 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) gene
Klaus Gempel, Haluk Topaloglu, Beril Talim, et al.
Annals of Neurology
|
September 3, 2002
Mitochondrial DNA depletion and dGK gene mutations
Leonardo Salviati, Sabrina Sacconi, Michelangelo Mancuso, et al.
Brain Topography
|
May 11, 2002
Conductivities of three-layer live human skull
M 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 cardiomyopathy
Robert W Taylor, Carla Giordano, Mercy M Davidson, et al.
Archives of Neurology
|
April 12, 2012
Loss of myelin-associated glycoprotein in kearns-sayre syndrome
Nichola Z Lax, Graham R Campbell, Amy K Reeve, et al.
Page
of 95
Search research articles
Search
Showing results (821-830 of 942) with videos related to
Sort By:
Page
of 95
American Journal of Human Genetics
|
August 16, 2006
Navajo neurohepatopathy is caused by a mutation in the MPV17 gene
Charalampos 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 SCO2
C M Sue, C Karadimas, N Checcarelli, et al.
Prenatal Diagnosis
|
July 29, 2006
Prenatal diagnosis of glycogen storage disease type IV
H 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 Pain
David 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 experiment
L 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) gene
Klaus Gempel, Haluk Topaloglu, Beril Talim, et al.
Annals of Neurology
|
September 3, 2002
Mitochondrial DNA depletion and dGK gene mutations
Leonardo Salviati, Sabrina Sacconi, Michelangelo Mancuso, et al.
Brain Topography
|
May 11, 2002
Conductivities of three-layer live human skull
M 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 cardiomyopathy
Robert W Taylor, Carla Giordano, Mercy M Davidson, et al.
Archives of Neurology
|
April 12, 2012
Loss of myelin-associated glycoprotein in kearns-sayre syndrome
Nichola Z Lax, Graham R Campbell, Amy K Reeve, et al.
Page
of 95