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Alan King

Showing results (41-50 of 45) with videos related to

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Acta Neuropathologica Communications|April 27, 2019
Hippocampal CA2 Lewy pathology is associated with cholinergic degeneration in Parkinson's disease with cognitive declineAlan King Lun Liu, Tsz Wing Chau, Ernest Junwei Lim, et al.
Nature Communications|July 11, 2018
Author Correction: Next generation histology methods for three-dimensional imaging of fresh and archival human brain tissuesHei Ming Lai, Alan King Lun Liu, Harry Ho Man Ng, et al.
Nature Communications|March 16, 2018
Next generation histology methods for three-dimensional imaging of fresh and archival human brain tissuesHei Ming Lai, Alan King Lun Liu, Harry Ho Man Ng, et al.
Plos One|July 1, 2016
Rationalisation and Validation of an Acrylamide-Free Procedure in Three-Dimensional Histological ImagingHei Ming Lai, Alan King Lun Liu, Wai-Lung Ng, et al.
Human Molecular Genetics|August 22, 2002
A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotypeTim Cundy, Madhuri Hegde, Dorit Naot, et al.
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Showing results (41-50 of 45) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 45 results.
Acta Neuropathologica Communications|April 27, 2019
Hippocampal CA2 Lewy pathology is associated with cholinergic degeneration in Parkinson's disease with cognitive declineAlan King Lun Liu, Tsz Wing Chau, Ernest Junwei Lim, et al.
Nature Communications|July 11, 2018
Author Correction: Next generation histology methods for three-dimensional imaging of fresh and archival human brain tissuesHei Ming Lai, Alan King Lun Liu, Harry Ho Man Ng, et al.
Nature Communications|March 16, 2018
Next generation histology methods for three-dimensional imaging of fresh and archival human brain tissuesHei Ming Lai, Alan King Lun Liu, Harry Ho Man Ng, et al.
Plos One|July 1, 2016
Rationalisation and Validation of an Acrylamide-Free Procedure in Three-Dimensional Histological ImagingHei Ming Lai, Alan King Lun Liu, Wai-Lung Ng, et al.
Human Molecular Genetics|August 22, 2002
A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotypeTim Cundy, Madhuri Hegde, Dorit Naot, et al.
Pageof 5