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Biochemical and Biophysical Research Communications
|
March 15, 2008
Clinical and genetic characterization of Chanarin-Dorfman syndrome
Claudio Bruno, Enrico Bertini, Maja Di Rocco, et al.
Neurology
|
June 27, 2002
Clinicopathological features of genetically confirmed Danon disease
K Sugie, A Yamamoto, K Murayama, et al.
Human Molecular Genetics
|
March 14, 2008
A functionally dominant mitochondrial DNA mutation
Sabrina Sacconi, Leonardo Salviati, Yutaka Nishigaki, et al.
Brain Topography
|
November 1, 2003
A model for frequency dependence of conductivities of the live human skull
M Akhtari, H C Bryant, D Emin, et al.
Human Molecular Genetics
|
October 4, 2017
Defective mitochondrial rRNA methyltransferase MRM2 causes MELAS-like clinical syndrome
Caterina Garone, Aaron R D'Souza, Cristina Dallabona, et al.
Circulation
|
April 7, 2010
Evaluation of a new heparin agent in percutaneous coronary intervention: results of the phase 2 evaluation of M118 IN pErcutaNeous Coronary intErvention (EMINENCE) Trial
Sunil V Rao, Chiara Melloni, Shelley Myles-Dimauro, et al.
Orphanet Journal of Rare Diseases
|
April 21, 2012
Copper and bezafibrate cooperate to rescue cytochrome c oxidase deficiency in cells of patients with SCO2 mutations
Alberto Casarin, Gianpietro Giorgi, Vanessa Pertegato, et al.
International Journal of Molecular Sciences
|
August 29, 2024
Physical Activity and Epigenetic Aging in Breast Cancer Treatment
Chantalle Moulton, Elisa Grazioli, José Santiago Ibáñez-Cabellos, et al.
Annals of Neurology
|
October 3, 2014
A new muscle glycogen storage disease associated with glycogenin-1 deficiency
Edoardo Malfatti, Johanna Nilsson, Carola Hedberg-Oldfors, et al.
Annals of Neurology
|
November 30, 2005
Progressive cavitating leukoencephalopathy: a novel childhood disease
SakkuBai Naidu, Genila Bibat, Doris Lin, et al.
Page
of 95
Search research articles
Search
Showing results (831-840 of 942) with videos related to
Sort By:
Page
of 95
Biochemical and Biophysical Research Communications
|
March 15, 2008
Clinical and genetic characterization of Chanarin-Dorfman syndrome
Claudio Bruno, Enrico Bertini, Maja Di Rocco, et al.
Neurology
|
June 27, 2002
Clinicopathological features of genetically confirmed Danon disease
K Sugie, A Yamamoto, K Murayama, et al.
Human Molecular Genetics
|
March 14, 2008
A functionally dominant mitochondrial DNA mutation
Sabrina Sacconi, Leonardo Salviati, Yutaka Nishigaki, et al.
Brain Topography
|
November 1, 2003
A model for frequency dependence of conductivities of the live human skull
M Akhtari, H C Bryant, D Emin, et al.
Human Molecular Genetics
|
October 4, 2017
Defective mitochondrial rRNA methyltransferase MRM2 causes MELAS-like clinical syndrome
Caterina Garone, Aaron R D'Souza, Cristina Dallabona, et al.
Circulation
|
April 7, 2010
Evaluation of a new heparin agent in percutaneous coronary intervention: results of the phase 2 evaluation of M118 IN pErcutaNeous Coronary intErvention (EMINENCE) Trial
Sunil V Rao, Chiara Melloni, Shelley Myles-Dimauro, et al.
Orphanet Journal of Rare Diseases
|
April 21, 2012
Copper and bezafibrate cooperate to rescue cytochrome c oxidase deficiency in cells of patients with SCO2 mutations
Alberto Casarin, Gianpietro Giorgi, Vanessa Pertegato, et al.
International Journal of Molecular Sciences
|
August 29, 2024
Physical Activity and Epigenetic Aging in Breast Cancer Treatment
Chantalle Moulton, Elisa Grazioli, José Santiago Ibáñez-Cabellos, et al.
Annals of Neurology
|
October 3, 2014
A new muscle glycogen storage disease associated with glycogenin-1 deficiency
Edoardo Malfatti, Johanna Nilsson, Carola Hedberg-Oldfors, et al.
Annals of Neurology
|
November 30, 2005
Progressive cavitating leukoencephalopathy: a novel childhood disease
SakkuBai Naidu, Genila Bibat, Doris Lin, et al.
Page
of 95