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Human Molecular Genetics
|
July 8, 2005
The H1c haplotype at the MAPT locus is associated with Alzheimer's disease
A J Myers, M Kaleem, L Marlowe, et al.
Neuropathology and Applied Neurobiology
|
April 8, 2006
Quantification of Alzheimer pathology in ageing and dementia: age-related accumulation of amyloid-beta(42) peptide in vascular dementia
H Lewis, D Beher, N Cookson, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
August 21, 2004
Phase II study of ISIS 3521, an antisense oligodeoxynucleotide to protein kinase C alpha, in patients with previously treated low-grade non-Hodgkin's lymphoma
S Rao, D Watkins, D Cunningham, et al.
Bone Marrow Transplantation
|
June 29, 2022
Association of genetic variants with patient reported quality of life and pain experience in patients in the UK NCRI Myeloma X Relapse [Intensive]) trial; an exploratory study
John A Snowden, Sam H Ahmedzai, Angela Cox, et al.
Annals of the New York Academy of Sciences
|
May 20, 2000
Hereditary vascular dementia linked to notch 3 mutations. CADASIL in British families
N J Thomas, C M Morris, F Scaravilli, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 19, 2005
Rate of progression of cognitive decline in Alzheimer's disease: effect of butyrylcholinesterase K gene variation
C Holmes, C Ballard, D Lehmann, et al.
Brain : a Journal of Neurology
|
December 2, 2000
Pathology of early-onset Alzheimer's disease cases bearing the Thr113-114ins presenilin-1 mutation
A B Singleton, R Hall, C G Ballard, et al.
Journal of Neural Transmission. Supplementum
|
January 1, 1996
Molecular biology of APO E alleles in Alzheimer's and non-Alzheimer's dementias
C M Morris, H M Massey, R Benjamin, et al.
Brain : a Journal of Neurology
|
January 20, 2007
Hereditary multi-infarct dementia of the Swedish type is a novel disorder different from NOTCH3 causing CADASIL
W C Low, M Junna, A Börjesson-Hanson, et al.
Neuropathology and Applied Neurobiology
|
May 29, 2020
Neuropathological and biochemical investigation of Hereditary Ferritinopathy cases with ferritin light chain mutation: Prominent protein aggregation in the absence of major mitochondrial or oxidative stress
M Kurzawa-Akanbi, M Keogh, E Tsefou, et al.
Page
of 21
Search research articles
Search
Showing results (181-190 of 201) with videos related to
Sort By:
Page
of 21
Human Molecular Genetics
|
July 8, 2005
The H1c haplotype at the MAPT locus is associated with Alzheimer's disease
A J Myers, M Kaleem, L Marlowe, et al.
Neuropathology and Applied Neurobiology
|
April 8, 2006
Quantification of Alzheimer pathology in ageing and dementia: age-related accumulation of amyloid-beta(42) peptide in vascular dementia
H Lewis, D Beher, N Cookson, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
August 21, 2004
Phase II study of ISIS 3521, an antisense oligodeoxynucleotide to protein kinase C alpha, in patients with previously treated low-grade non-Hodgkin's lymphoma
S Rao, D Watkins, D Cunningham, et al.
Bone Marrow Transplantation
|
June 29, 2022
Association of genetic variants with patient reported quality of life and pain experience in patients in the UK NCRI Myeloma X Relapse [Intensive]) trial; an exploratory study
John A Snowden, Sam H Ahmedzai, Angela Cox, et al.
Annals of the New York Academy of Sciences
|
May 20, 2000
Hereditary vascular dementia linked to notch 3 mutations. CADASIL in British families
N J Thomas, C M Morris, F Scaravilli, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 19, 2005
Rate of progression of cognitive decline in Alzheimer's disease: effect of butyrylcholinesterase K gene variation
C Holmes, C Ballard, D Lehmann, et al.
Brain : a Journal of Neurology
|
December 2, 2000
Pathology of early-onset Alzheimer's disease cases bearing the Thr113-114ins presenilin-1 mutation
A B Singleton, R Hall, C G Ballard, et al.
Journal of Neural Transmission. Supplementum
|
January 1, 1996
Molecular biology of APO E alleles in Alzheimer's and non-Alzheimer's dementias
C M Morris, H M Massey, R Benjamin, et al.
Brain : a Journal of Neurology
|
January 20, 2007
Hereditary multi-infarct dementia of the Swedish type is a novel disorder different from NOTCH3 causing CADASIL
W C Low, M Junna, A Börjesson-Hanson, et al.
Neuropathology and Applied Neurobiology
|
May 29, 2020
Neuropathological and biochemical investigation of Hereditary Ferritinopathy cases with ferritin light chain mutation: Prominent protein aggregation in the absence of major mitochondrial or oxidative stress
M Kurzawa-Akanbi, M Keogh, E Tsefou, et al.
Page
of 21