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

Hammans

Showing results (61-70 of 87) with videos related to

Pageof 9
Sort By:
Biochimica Et Biophysica Acta|May 24, 1995
Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotypeJ A Morgan-Hughes, M G Sweeney, J M Cooper, et al.
Journal of the Neurological Sciences|January 1, 1992
Evidence for intramitochondrial complementation between deleted and normal mitochondrial DNA in some patients with mitochondrial myopathyS R Hammans, M G Sweeney, I J Holt, et al.
Brain : a Journal of Neurology|June 1, 1993
The mitochondrial DNA transfer RNA(Lys)A-->G(8344) mutation and the syndrome of myoclonic epilepsy with ragged red fibres (MERRF). Relationship of clinical phenotype to proportion of mutant mitochondrial DNAS R Hammans, M G Sweeney, M Brockington, et al.
Biochemical Society Transactions|March 26, 2003
A study of mitochondrial DNA mutations in peripheral lymphocytes in an aging cohortB Zhang, S Ye, A A Sayer, et al.
Brain : a Journal of Neurology|December 21, 2005
Clinical, pathological and genetic characterization of hereditary sensory and autonomic neuropathy type 1 (HSAN I)Henry Houlden, Rosalind King, Julian Blake, et al.
Neuroscience|July 1, 1996
The messenger RNAs for the N-methyl-D-aspartate receptor subunits show region-specific expression of different subunit composition in the human brainM Rigby, B Le Bourdellès, R P Heavens, et al.
Journal of the Neurological Sciences|January 1, 1994
Mitochondrial DNA mutation underlying Leigh's syndrome: clinical, pathological, biochemical, and genetic studies of a patient presenting with progressive myoclonic epilepsyM G Sweeney, S R Hammans, L W Duchen, et al.
European Journal of Human Genetics : EJHG|November 7, 2013
Recessive myosin myopathy with external ophthalmoplegia associated with MYH2 mutationsHoma Tajsharghi, Simon Hammans, Christopher Lindberg, et al.
Muscle & Nerve|October 21, 2017
Chronic pain has a strong impact on quality of life in facioscapulohumeral muscular dystrophyGermán Morís, Libby Wood, Roberto FernáNdez-Torrón, et al.
Bone Marrow Transplantation|May 4, 2010
Allogeneic hematopoietic SCT as treatment option for patients with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a consensus conference proposal for a standardized approachJ Halter, Wmm Schüpbach, C Casali, et al.
Pageof 9

Showing results (61-70 of 87) with videos related to

Sort By:
Pageof 9
Biochimica Et Biophysica Acta|May 24, 1995
Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotypeJ A Morgan-Hughes, M G Sweeney, J M Cooper, et al.
Journal of the Neurological Sciences|January 1, 1992
Evidence for intramitochondrial complementation between deleted and normal mitochondrial DNA in some patients with mitochondrial myopathyS R Hammans, M G Sweeney, I J Holt, et al.
Brain : a Journal of Neurology|June 1, 1993
The mitochondrial DNA transfer RNA(Lys)A-->G(8344) mutation and the syndrome of myoclonic epilepsy with ragged red fibres (MERRF). Relationship of clinical phenotype to proportion of mutant mitochondrial DNAS R Hammans, M G Sweeney, M Brockington, et al.
Biochemical Society Transactions|March 26, 2003
A study of mitochondrial DNA mutations in peripheral lymphocytes in an aging cohortB Zhang, S Ye, A A Sayer, et al.
Brain : a Journal of Neurology|December 21, 2005
Clinical, pathological and genetic characterization of hereditary sensory and autonomic neuropathy type 1 (HSAN I)Henry Houlden, Rosalind King, Julian Blake, et al.
Neuroscience|July 1, 1996
The messenger RNAs for the N-methyl-D-aspartate receptor subunits show region-specific expression of different subunit composition in the human brainM Rigby, B Le Bourdellès, R P Heavens, et al.
Journal of the Neurological Sciences|January 1, 1994
Mitochondrial DNA mutation underlying Leigh's syndrome: clinical, pathological, biochemical, and genetic studies of a patient presenting with progressive myoclonic epilepsyM G Sweeney, S R Hammans, L W Duchen, et al.
European Journal of Human Genetics : EJHG|November 7, 2013
Recessive myosin myopathy with external ophthalmoplegia associated with MYH2 mutationsHoma Tajsharghi, Simon Hammans, Christopher Lindberg, et al.
Muscle & Nerve|October 21, 2017
Chronic pain has a strong impact on quality of life in facioscapulohumeral muscular dystrophyGermán Morís, Libby Wood, Roberto FernáNdez-Torrón, et al.
Bone Marrow Transplantation|May 4, 2010
Allogeneic hematopoietic SCT as treatment option for patients with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a consensus conference proposal for a standardized approachJ Halter, Wmm Schüpbach, C Casali, et al.
Pageof 9