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Brain : a Journal of Neurology
|
September 24, 2002
Progression of nigrostriatal dysfunction in a parkin kindred: an [18F]dopa PET and clinical study
Naheed L Khan, David J Brooks, Nicola Pavese, et al.
The Journal of Antimicrobial Chemotherapy
|
October 31, 2002
Vancomycin therapeutic drug monitoring: is there a consensus view? The results of a UK National External Quality Assessment Scheme (UK NEQAS) for Antibiotic Assays questionnaire
C M Tobin, J M Darville, A H Thomson, et al.
Diabetologia
|
April 1, 1994
Mitochondrial gene defects in patients with NIDDM
J C Alcolado, A Majid, M Brockington, et al.
Annals of the New York Academy of Sciences
|
November 1, 2017
A Family with Friedreich Ataxia and Onion-Bulb Formations at Sural Nerve Biopsy
A A Barreira, W Marques, M G Sweeney, et al.
Scientific Reports
|
July 2, 2017
Heart Failure and MEF2 Transcriptome Dynamics in Response to β-Blockers
S W Tobin, S Hashemi, K Dadson, et al.
Lancet (London, England)
|
December 5, 1992
Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA
W Reardon, R J Ross, M G Sweeney, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 15, 2005
Parkinsonism and nigrostriatal dysfunction are associated with spinocerebellar ataxia type 6 (SCA6)
Naheed L Khan, Paola Giunti, Mary G Sweeney, et al.
American Journal of Human Genetics
|
May 1, 1995
Congenital encephalomyopathy and adult-onset myopathy and diabetes mellitus: different phenotypic associations of a new heteroplasmic mtDNA tRNA glutamic acid mutation
M G Hanna, I Nelson, M G Sweeney, et al.
The British Journal of Ophthalmology
|
April 29, 2008
Characterisation of the macular dystrophy in patients with the A3243G mitochondrial DNA point mutation with fundus autofluorescence
P P Rath, S Jenkins, M Michaelides, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 23, 2005
Spinocerebellar ataxia type 17: extension of phenotype with putaminal rim hyperintensity on magnetic resonance imaging
Clement T Loy, Mary G Sweeney, Mary B Davis, et al.
Page
of 22
Search research articles
Search
Showing results (131-140 of 220) with videos related to
Sort By:
Page
of 22
Brain : a Journal of Neurology
|
September 24, 2002
Progression of nigrostriatal dysfunction in a parkin kindred: an [18F]dopa PET and clinical study
Naheed L Khan, David J Brooks, Nicola Pavese, et al.
The Journal of Antimicrobial Chemotherapy
|
October 31, 2002
Vancomycin therapeutic drug monitoring: is there a consensus view? The results of a UK National External Quality Assessment Scheme (UK NEQAS) for Antibiotic Assays questionnaire
C M Tobin, J M Darville, A H Thomson, et al.
Diabetologia
|
April 1, 1994
Mitochondrial gene defects in patients with NIDDM
J C Alcolado, A Majid, M Brockington, et al.
Annals of the New York Academy of Sciences
|
November 1, 2017
A Family with Friedreich Ataxia and Onion-Bulb Formations at Sural Nerve Biopsy
A A Barreira, W Marques, M G Sweeney, et al.
Scientific Reports
|
July 2, 2017
Heart Failure and MEF2 Transcriptome Dynamics in Response to β-Blockers
S W Tobin, S Hashemi, K Dadson, et al.
Lancet (London, England)
|
December 5, 1992
Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA
W Reardon, R J Ross, M G Sweeney, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 15, 2005
Parkinsonism and nigrostriatal dysfunction are associated with spinocerebellar ataxia type 6 (SCA6)
Naheed L Khan, Paola Giunti, Mary G Sweeney, et al.
American Journal of Human Genetics
|
May 1, 1995
Congenital encephalomyopathy and adult-onset myopathy and diabetes mellitus: different phenotypic associations of a new heteroplasmic mtDNA tRNA glutamic acid mutation
M G Hanna, I Nelson, M G Sweeney, et al.
The British Journal of Ophthalmology
|
April 29, 2008
Characterisation of the macular dystrophy in patients with the A3243G mitochondrial DNA point mutation with fundus autofluorescence
P P Rath, S Jenkins, M Michaelides, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 23, 2005
Spinocerebellar ataxia type 17: extension of phenotype with putaminal rim hyperintensity on magnetic resonance imaging
Clement T Loy, Mary G Sweeney, Mary B Davis, et al.
Page
of 22