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Brain : a Journal of Neurology
|
August 1, 1994
The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias
P Giunti, M G Sweeney, M Spadaro, et al.
Journal of Clinical Gastroenterology
|
August 1, 1991
Hypertrophic gastropathy symptoms responsive to prednisone. A case report and a review of the literature
G E Davis, M C O'Rourke, J R Metz, et al.
Molecular Biology and Evolution
|
March 24, 2017
Convergent Balancing Selection on the Mu-Opioid Receptor in Primates
Carolyn G Sweeney, Juliette M Rando, Helen N Panas, et al.
Brain : a Journal of Neurology
|
June 1, 1995
The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic study
S R Hammans, M G Sweeney, M G Hanna, et al.
Neuromuscular Disorders : NMD
|
August 28, 2012
Stiffness as a presenting symptom of an odd clinical condition caused by multiple sclerosis and myotonia congenita
Simona Portaro, Olimpia Musumeci, Vincenzo Rizzo, et al.
Brain : a Journal of Neurology
|
April 1, 1995
The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation
P Riordan-Eva, M D Sanders, G G Govan, et al.
Cell Reports
|
May 11, 2025
Reliable sensory processing of superficial cortical interneurons is modulated by behavioral state
Carolyn G Sweeney, Maryse E Thomas, Christine Junhui Liu, et al.
The Journal of Biological Chemistry
|
October 13, 2001
Differential effects of phosphatidylinositol 3-kinase inhibition on intracellular signals regulating GLUT4 translocation and glucose transport
R Somwar, W Niu, D Y Kim, et al.
The British Journal of Ophthalmology
|
September 1, 1992
Late onset Leber's optic neuropathy: a case confused with ischaemic optic neuropathy
F X Borruat, W T Green, E M Graham, et al.
Neurology
|
December 31, 1997
Multiple-system atrophy is genetically distinct from identified inherited causes of spinocerebellar degeneration
O Bandmann, M G Sweeney, S E Daniel, et al.
Page
of 22
Search research articles
Search
Showing results (121-130 of 220) with videos related to
Sort By:
Page
of 22
Brain : a Journal of Neurology
|
August 1, 1994
The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias
P Giunti, M G Sweeney, M Spadaro, et al.
Journal of Clinical Gastroenterology
|
August 1, 1991
Hypertrophic gastropathy symptoms responsive to prednisone. A case report and a review of the literature
G E Davis, M C O'Rourke, J R Metz, et al.
Molecular Biology and Evolution
|
March 24, 2017
Convergent Balancing Selection on the Mu-Opioid Receptor in Primates
Carolyn G Sweeney, Juliette M Rando, Helen N Panas, et al.
Brain : a Journal of Neurology
|
June 1, 1995
The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic study
S R Hammans, M G Sweeney, M G Hanna, et al.
Neuromuscular Disorders : NMD
|
August 28, 2012
Stiffness as a presenting symptom of an odd clinical condition caused by multiple sclerosis and myotonia congenita
Simona Portaro, Olimpia Musumeci, Vincenzo Rizzo, et al.
Brain : a Journal of Neurology
|
April 1, 1995
The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation
P Riordan-Eva, M D Sanders, G G Govan, et al.
Cell Reports
|
May 11, 2025
Reliable sensory processing of superficial cortical interneurons is modulated by behavioral state
Carolyn G Sweeney, Maryse E Thomas, Christine Junhui Liu, et al.
The Journal of Biological Chemistry
|
October 13, 2001
Differential effects of phosphatidylinositol 3-kinase inhibition on intracellular signals regulating GLUT4 translocation and glucose transport
R Somwar, W Niu, D Y Kim, et al.
The British Journal of Ophthalmology
|
September 1, 1992
Late onset Leber's optic neuropathy: a case confused with ischaemic optic neuropathy
F X Borruat, W T Green, E M Graham, et al.
Neurology
|
December 31, 1997
Multiple-system atrophy is genetically distinct from identified inherited causes of spinocerebellar degeneration
O Bandmann, M G Sweeney, S E Daniel, et al.
Page
of 22