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Oncogene
|
May 4, 2004
E2F3 amplification and overexpression is associated with invasive tumor growth and rapid tumor cell proliferation in urinary bladder cancer
Martin Oeggerli, Sanja Tomovska, Peter Schraml, et al.
Parkinsonism & Related Disorders
|
December 12, 2025
Assessment of SLC25A46 variants in idiopathic Parkinson's disease
Zachary Schneider, Hui Liu, Mohammad Dehestani, et al.
Dementia and Geriatric Cognitive Disorders
|
November 30, 2011
Association of clusterin gene polymorphisms with late-onset Alzheimer's disease
Huiying Gu, Xing Wei, Shirley Chen, et al.
Neurosurgical Review
|
August 11, 2010
Spontaneous cerebellar hemorrhage--experience with 57 surgically treated patients and review of the literature
Philipp Dammann, Siamak Asgari, Hischam Bassiouni, et al.
Frontiers in Molecular Neuroscience
|
October 30, 2016
Rare Variants in Neurodegeneration Associated Genes Revealed by Targeted Panel Sequencing in a German ALS Cohort
Stefanie Krüger, Florian Battke, Andrea Sprecher, et al.
Annals of Neurology
|
October 22, 2005
Myoclonus-dystonia due to genomic deletions in the epsilon-sarcoglycan gene
Friedrich Asmus, Farid Salih, Lena Elisabeth Hjermind, et al.
Journal of Alzheimer'S Disease : JAD
|
February 17, 2010
The CST3 BB genotype and low cystatin C cerebrospinal fluid levels are associated with dementia in Lewy body disease
Walter Maetzler, Benjamin Schmid, Matthis Synofzik, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
December 29, 2007
Genetic variability in the SNCA gene influences alpha-synuclein levels in the blood and brain
Julia Fuchs, Ales Tichopad, Yulia Golub, et al.
Neurobiology of Disease
|
June 2, 2009
No differences of butyrylcholinesterase protein activity and allele frequency in Lewy body diseases
Walter Maetzler, Stefanie Keller, Joan Michelis, et al.
Journal of Medical Genetics
|
March 8, 2024
Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insights
Burcu Atasu, Javier Simón-Sánchez, Hasmet Hanagasi, et al.
Page
of 48
Search research articles
Search
Showing results (181-190 of 476) with videos related to
Sort By:
Page
of 48
Oncogene
|
May 4, 2004
E2F3 amplification and overexpression is associated with invasive tumor growth and rapid tumor cell proliferation in urinary bladder cancer
Martin Oeggerli, Sanja Tomovska, Peter Schraml, et al.
Parkinsonism & Related Disorders
|
December 12, 2025
Assessment of SLC25A46 variants in idiopathic Parkinson's disease
Zachary Schneider, Hui Liu, Mohammad Dehestani, et al.
Dementia and Geriatric Cognitive Disorders
|
November 30, 2011
Association of clusterin gene polymorphisms with late-onset Alzheimer's disease
Huiying Gu, Xing Wei, Shirley Chen, et al.
Neurosurgical Review
|
August 11, 2010
Spontaneous cerebellar hemorrhage--experience with 57 surgically treated patients and review of the literature
Philipp Dammann, Siamak Asgari, Hischam Bassiouni, et al.
Frontiers in Molecular Neuroscience
|
October 30, 2016
Rare Variants in Neurodegeneration Associated Genes Revealed by Targeted Panel Sequencing in a German ALS Cohort
Stefanie Krüger, Florian Battke, Andrea Sprecher, et al.
Annals of Neurology
|
October 22, 2005
Myoclonus-dystonia due to genomic deletions in the epsilon-sarcoglycan gene
Friedrich Asmus, Farid Salih, Lena Elisabeth Hjermind, et al.
Journal of Alzheimer'S Disease : JAD
|
February 17, 2010
The CST3 BB genotype and low cystatin C cerebrospinal fluid levels are associated with dementia in Lewy body disease
Walter Maetzler, Benjamin Schmid, Matthis Synofzik, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
December 29, 2007
Genetic variability in the SNCA gene influences alpha-synuclein levels in the blood and brain
Julia Fuchs, Ales Tichopad, Yulia Golub, et al.
Neurobiology of Disease
|
June 2, 2009
No differences of butyrylcholinesterase protein activity and allele frequency in Lewy body diseases
Walter Maetzler, Stefanie Keller, Joan Michelis, et al.
Journal of Medical Genetics
|
March 8, 2024
Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insights
Burcu Atasu, Javier Simón-Sánchez, Hasmet Hanagasi, et al.
Page
of 48