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Movement Disorders : Official Journal of the Movement Disorder Society
|
June 1, 2012
Brain metabolite alterations and cognitive dysfunction in early Huntington's disease
Paul G Unschuld, Richard A E Edden, Aaron Carass, et al.
Psychiatry Research
|
September 15, 2012
Depressive symptoms in prodromal Huntington's Disease correlate with Stroop-interference related functional connectivity in the ventromedial prefrontal cortex
Paul G Unschuld, Suresh E Joel, James J Pekar, et al.
Molecular Psychiatry
|
April 4, 2025
Protein aggregation identified in olfactory neuronal cells is associated with cognitive impairments in a subset of living schizophrenia patients
Leslie G Nucifora, Koko Ishizuka, Nagat El Demerdash, et al.
Schizophrenia Bulletin
|
August 20, 2016
Abnormal Grey Matter Arteriolar Cerebral Blood Volume in Schizophrenia Measured With 3D Inflow-Based Vascular-Space-Occupancy MRI at 7T
Jun Hua, Allison S Brandt, SeungWook Lee, et al.
The American Journal of Psychiatry
|
May 7, 2019
Increased Protein Insolubility in Brains From a Subset of Patients With Schizophrenia
Leslie G Nucifora, Matthew L MacDonald, Brian J Lee, et al.
Human Mutation
|
August 21, 2010
Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias
Claudia Cagnoli, Giovanni Stevanin, Alessandro Brussino, et al.
Nature Reviews. Neurology
|
March 12, 2014
Huntington disease: natural history, biomarkers and prospects for therapeutics
Christopher A Ross, Elizabeth H Aylward, Edward J Wild, et al.
Annals of Neurology
|
July 12, 2002
Trinucleotide repeat expansions in the junctophilin-3 gene are not found in Caucasian patients with a Huntington's disease-like phenotype
Ingrid Bauer, Martin Gencik, Franco Laccone, et al.
Psychiatric Genetics
|
August 13, 2009
Long tandem repeats as a form of genomic copy number variation: structure and length polymorphism of a chromosome 5p repeat in control and schizophrenia populations
Heather A Bruce, Nancy Sachs, Dobrila D Rudnicki, et al.
Nature Communications
|
March 4, 2021
Pharmacological rescue in patient iPSC and mouse models with a rare DISC1 mutation
Nam-Shik Kim, Zhexing Wen, Jing Liu, et al.
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of 13
Search research articles
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Showing results (101-110 of 127) with videos related to
Sort By:
Page
of 13
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 1, 2012
Brain metabolite alterations and cognitive dysfunction in early Huntington's disease
Paul G Unschuld, Richard A E Edden, Aaron Carass, et al.
Psychiatry Research
|
September 15, 2012
Depressive symptoms in prodromal Huntington's Disease correlate with Stroop-interference related functional connectivity in the ventromedial prefrontal cortex
Paul G Unschuld, Suresh E Joel, James J Pekar, et al.
Molecular Psychiatry
|
April 4, 2025
Protein aggregation identified in olfactory neuronal cells is associated with cognitive impairments in a subset of living schizophrenia patients
Leslie G Nucifora, Koko Ishizuka, Nagat El Demerdash, et al.
Schizophrenia Bulletin
|
August 20, 2016
Abnormal Grey Matter Arteriolar Cerebral Blood Volume in Schizophrenia Measured With 3D Inflow-Based Vascular-Space-Occupancy MRI at 7T
Jun Hua, Allison S Brandt, SeungWook Lee, et al.
The American Journal of Psychiatry
|
May 7, 2019
Increased Protein Insolubility in Brains From a Subset of Patients With Schizophrenia
Leslie G Nucifora, Matthew L MacDonald, Brian J Lee, et al.
Human Mutation
|
August 21, 2010
Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias
Claudia Cagnoli, Giovanni Stevanin, Alessandro Brussino, et al.
Nature Reviews. Neurology
|
March 12, 2014
Huntington disease: natural history, biomarkers and prospects for therapeutics
Christopher A Ross, Elizabeth H Aylward, Edward J Wild, et al.
Annals of Neurology
|
July 12, 2002
Trinucleotide repeat expansions in the junctophilin-3 gene are not found in Caucasian patients with a Huntington's disease-like phenotype
Ingrid Bauer, Martin Gencik, Franco Laccone, et al.
Psychiatric Genetics
|
August 13, 2009
Long tandem repeats as a form of genomic copy number variation: structure and length polymorphism of a chromosome 5p repeat in control and schizophrenia populations
Heather A Bruce, Nancy Sachs, Dobrila D Rudnicki, et al.
Nature Communications
|
March 4, 2021
Pharmacological rescue in patient iPSC and mouse models with a rare DISC1 mutation
Nam-Shik Kim, Zhexing Wen, Jing Liu, et al.
Page
of 13