Suchergebnisse - "Poulter, Mark"

PubPharm (58)

1

Rare structural genetic variation in human prion diseases

enthalten in: Neurobiology of aging | 2015

von Lukic, A. | Uphill, J. | Brown, C. | +11

2

Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansion

enthalten in: Neurobiology of aging | 2015

von Fratta, P. | Polke, J. | Newcombe, J. | +27

3

Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansion

enthalten in: Neurobiology of aging | 2015

von Fratta, P. | Polke, J. | Newcombe, J. | +27

4

Rare structural genetic variation in human prion diseases

enthalten in: Neurobiology of aging | 2015

von Lukic, A. | Uphill, J. | Brown, C. | +11

5

In vitro screen of prion disease susceptibility genes using the scrapie cell assay

enthalten in: Human molecular genetics | 2014

von Brown, C. | Schmidt, C. | Poulter, M. | +6

6

Abstracts of the Rehabilitation and Therapy Research Society 9th Annual Conference

enthalten in: Physical therapy reviews | 2014

von French, H. | Foley, G. | Timonen, V. | +96

7

C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies

enthalten in: Neurology | 2014

von Hensman Moss, D. | Poulter, M. | Beck, J. | +12

ErratumIn: Neurology. 2014 May 13;82(19):1753. - PMID 24936621

8

Validation of next-generation sequencing technologies in genetic diagnosis of dementia

enthalten in: Neurobiology of aging | 2014

von Beck, J. | Pittman, A. | Adamson, G. | +16

9

Validation of next-generation sequencing technologies in genetic diagnosis of dementia

enthalten in: Neurobiology of aging | 2014

von Beck, J. | Pittman, A. | Adamson, G. | +16

10

Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic : large scale survey

enthalten in: BMJ (Clinical research ed.) | 2013

von Gill, O. | Spencer, Y. | Richard-Loendt, A. | +14

CommentIn: BMJ. 2013 Oct 15;347:f5994. - PMID 24129060

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