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Biochimica Et Biophysica Acta
|
May 24, 1995
Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotype
J 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 myopathy
S 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 DNA
S 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 cohort
B 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 brain
M 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 epilepsy
M 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 mutations
Homa 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 dystrophy
Germán 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 approach
J Halter, Wmm Schüpbach, C Casali, et al.
Page
of 9
Search research articles
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Showing results (61-70 of 87) with videos related to
Sort By:
Page
of 9
Biochimica Et Biophysica Acta
|
May 24, 1995
Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotype
J 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 myopathy
S 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 DNA
S 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 cohort
B 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 brain
M 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 epilepsy
M 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 mutations
Homa 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 dystrophy
Germán 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 approach
J Halter, Wmm Schüpbach, C Casali, et al.
Page
of 9