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 (251-260 of 1,071) with videos related to

Pageof 108
Sort By:
Muscle & Nerve. Supplement|January 1, 1995
Molecular genetic studies in muscle phosphoglycerate mutase (PGAM-M) deficiencyS Tsujino, S Shanske, S Sakoda, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Skin fibroblast carnitine uptake in secondary carnitine deficiency disordersI Tein, D C De Vivo, D Ranucci, et al.
Journal of Traumatic Stress|July 27, 2016
Perceived Support From Multiple Sources: Associations With PTSD SymptomsJennifer DiMauro, Keith D Renshaw, Brian N Smith, et al.
Science (New York, N.Y.)|June 24, 2006
Silk genes support the single origin of orb websJessica E Garb, Teresa Dimauro, Victoria Vo, et al.
Archives of Neurology|June 24, 2004
Association of mutations in SCO2, a cytochrome c oxidase assembly gene, with early fetal lethalityStacey K H Tay, Sara Shanske, Paige Kaplan, et al.
Neuromuscular Disorders : NMD|February 13, 2010
A novel mutation in the tRNAIle gene (MTTI) affecting the variable loop in a patient with chronic progressive external ophthalmoplegia (CPEO)Andres Berardo, Jorida Coku, Bulent Kurt, et al.
Archives of Neurology|March 1, 1973
Serum carnitine. An index of muscle destruction in manS DiMauro, C Scott, A S Penn, et al.
Biology|September 28, 2024
Exploring the Impact of Exercise-Derived Extracellular Vesicles in Cancer BiologyMonica Silvestri, Elisa Grazioli, Guglielmo Duranti, et al.
Diagnostic Cytopathology|January 1, 1992
Postoperative spindle-cell nodule of urinary bladder with unusual intracytoplasmic inclusionsJ W Lo, C H Fung, T Yonan, et al.
Neurology|February 1, 1975
Hereditary carnitine deficiency of muscleD H VanDyke, R C Griggs, W Markesbery, et al.
Pageof 108

Showing results (251-260 of 1,071) with videos related to

Sort By:
Pageof 108
Muscle & Nerve. Supplement|January 1, 1995
Molecular genetic studies in muscle phosphoglycerate mutase (PGAM-M) deficiencyS Tsujino, S Shanske, S Sakoda, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Skin fibroblast carnitine uptake in secondary carnitine deficiency disordersI Tein, D C De Vivo, D Ranucci, et al.
Journal of Traumatic Stress|July 27, 2016
Perceived Support From Multiple Sources: Associations With PTSD SymptomsJennifer DiMauro, Keith D Renshaw, Brian N Smith, et al.
Science (New York, N.Y.)|June 24, 2006
Silk genes support the single origin of orb websJessica E Garb, Teresa Dimauro, Victoria Vo, et al.
Archives of Neurology|June 24, 2004
Association of mutations in SCO2, a cytochrome c oxidase assembly gene, with early fetal lethalityStacey K H Tay, Sara Shanske, Paige Kaplan, et al.
Neuromuscular Disorders : NMD|February 13, 2010
A novel mutation in the tRNAIle gene (MTTI) affecting the variable loop in a patient with chronic progressive external ophthalmoplegia (CPEO)Andres Berardo, Jorida Coku, Bulent Kurt, et al.
Archives of Neurology|March 1, 1973
Serum carnitine. An index of muscle destruction in manS DiMauro, C Scott, A S Penn, et al.
Biology|September 28, 2024
Exploring the Impact of Exercise-Derived Extracellular Vesicles in Cancer BiologyMonica Silvestri, Elisa Grazioli, Guglielmo Duranti, et al.
Diagnostic Cytopathology|January 1, 1992
Postoperative spindle-cell nodule of urinary bladder with unusual intracytoplasmic inclusionsJ W Lo, C H Fung, T Yonan, et al.
Neurology|February 1, 1975
Hereditary carnitine deficiency of muscleD H VanDyke, R C Griggs, W Markesbery, et al.
Pageof 108