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Drug companies 'chasing wrong Alzheimer's target'
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Roger Highfield reports on new evidence to suggest scientists could have missed the basic cause of this devastating dementia
Gene Hunters Find Cause of Rare Movement Disorder | Science ...
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Natalio Fejerman, Steve Frucht, Christina A. Gurnett, Edouard Hirsch, Henry Houlden, Joseph Jankovic, Wei-Ling Lee, David R. Lynch, Shehla Mohammed, Ulrich Müller, Mark P. Nespeca, David Renner, Jacques Rochette, ...
The Cyprus Institute of Neurology and Genetics - CING Lectures:...
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Genetics of Locomotor Disorders
Prof Henry Houlden, PhD
Houlden, H; UCL Institute of Neuro
DNA_GWAS Belgium
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Henry Houlden. It gives me personally a warm feeling that even my husband, who passed away on December 27, 2009, his DNA will still be ...
Network Profiles
LinkedIn: Henry Houlden | Professional Profile - LinkedIn
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Interests
Genetic mutation causes ataxia in humans and dogs | EurekAlert!...
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Cerebellar ataxia is a condition of the cerebellum that causes an inability to coordinate muscle movements. A study publishing June 16 in Cell Reports now...
Stem cell study offers hope for Parkinson's patients -- ScienceDaily
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Scientists have for the first time generated stem cells from one of the most rapidly progressing forms of Parkinson's disease. The development will help...
Education
Investigation of next-generation sequencing technologies as a...
kclpure.kcl.ac.uk
Ammar Al-Chalabi and Andrea Malaspina and Henry Houlden and John Hardy ...
Heritage
Michael-Peter-Johnson - User Trees - Genealogy.com
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Family Tree Maker user home page for Michael-Peter-Johnson.
Books & Literature
authors:"Henry Houlden" - Search | Paperity
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Henry Houlden | XanEdu Customization Platform
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Author: Henry Houlden. Results. Call for participation in the neurogenetics consortium within the Human Variome Project Springer Science+Business ...
PLOS ONE: Coenzyme Q10 Levels Are Decreased in the Cerebellum of...
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About the Authors. Lucia V. Schottlaender, Conceição Bettencourt, Iain Hargreaves, Henry Houlden: Department of Molecular Neuroscience, ...
Challenging Concepts in Neurology: Cases with Expert Commentarybooks.google.nl › books
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Sara Ajina and Angela Gall Parkinsonism with little response to levodopa Karen M. Doherty and Henry Houlden Non-convulsive status epilepticus Jan Novy, ...
Related Documents
Marriage of Henry Houlden and Dorothy Parker | The National Archives
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Coexpression Networks Predict Ataxia Genes | Genetics and Genomics |...
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The genomics revolution has introduced novel platforms and bioinformatics approaches to the study of human diseases and model organisms. In this issue of JAMA N
Philip Henry HOULDEN - Personal Appointments (free information from...
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A 6.4 Mb Duplication of the α-Synuclein Locus Causing Frontotemporal...
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Kara and colleagues report a novel family carrying a heterozygous 6.4 Mb duplication of the alpha-synuclein locus with an atypical clinical presentation strongl
Scientific Publications
Hereditary Sensory And Autonomic Neuropathy Type 2 - PMC - NCBI
www.ncbi.nlm.nih.gov
... Rébecca Gaudet, Anne-Marie Mes-Masson, Jonathan Baets, Henry Houlden, Bernard Brais ... PMC Images search for Hereditary Sensory And Autonomic Neuropathy Type 2
Concomitant progressive supranuclear palsy and chronic traumatic...
actaneurocomms.biomedcentral.com
We report the case of a 75-year-old ex-professional boxer who developed diplopia and eye movement abnormalities in his 60’s followed by memory impairment, low...
dblp: BibTeX records: Henry Houlden
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List of computer science publications by BibTeX records: Henry Houlden
Neuropathological features of genetically confirmed DYT1 dystonia:...
actaneurocomms.biomedcentral.com
John Hardy, Hyder A Jinnah, Kailash Bhatia, Henry Houlden and ...
Publications
Publications Authored by Henry Houlden | PubFacts
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Publications Authored by Henry Houlden
JCM | Free Full-Text | Utility of Whole Blood Thiamine Pyrophosphate ...
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... Simon Heales 3, Rosaline Quinlivan 1,2,6, Henry Houlden 1,2, Johannes A. Mayr 4, Michael G. Hanna 1,2 and Robert D.S. Pitceathly 1,2,*. 1.
Pure Cerebellar Ataxia with Homozygous Mutations in the PNPLA6 Gene |...
link.springer.com
Authors; Authors and affiliations. Sarah WiethoffEmail author; Conceição
Bettencourt; Reema Paudel; Prochi Madon; Yo-Tsen Liu; Joshua Hersheson;
Noshir Wadia; Joy Desai; Henry Houlden. Sarah Wiethoff. 1; 2; 3. Email author ...
Henry Houlden - Wikidatawww.wikidata.org › wiki
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Language, Label, Description, Also known as. English. Henry Houlden. researcher. Statements. instance of · human. 0 references.
Reports & Statements
eBOOk--- GeneReviews :: 네이버 블로그
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; Spinocerebellar Ataxia Type 10 SCA10 Tohru Matsuura and Tetsuo Ashizawa Initial Posting: April 23, 2002Last Update: March 9, 2010; Spinocerebellar Ataxia Type 11SCA11 Henry Houlden Initial Posting: July 22, ...
Henry Houlden | SPATAX Network : Clinical and Genetic Analysis of...
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Posts about Henry Houlden written by spatax
Exome sequencing in neurodegeneration post-doc - UCL London -...
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Exome sequencing in neurodegeneration post-doc - UCL London Academic/Non-Profit Jobs
Miscellaneous
Henry Houlden | LinkedIn
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View Henry Houlden's professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Henry Houlden discover inside ...
Henry Houlden - Google Scholar Citations
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Henry Houlden. Prof Neurology and Neurogenetics. Neurology and genetics. Verified email at ucl.ac.uk - Homepage. Scholar. Get my own profile. Google Scholar. Citation ...
Henry Houlden - Google Scholar Citationsscholar.google.co.uk › citations
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J Simon-Sanchez, C Schulte, JM Bras, M Sharma, JR Gibbs, D Berg, ... Nature genetics 41 (12), 1308Early-onset Alzheimer's disease ...
Henry Houlden - Google Scholar
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Prof Neurology and Neurogenetics - 引用: 44,999 件 - Neurology and genetics
Overcoming Movement Disorder: Impending NIH Visit
www.overcomingmovementdisorder.com
Below is a paraphrase of a paper entitled "Clinical and genetic characterization of families with triple A (Allgrove) syndrome" by Henry Houlden et al. published in BRAIN. Triple A (Allgrove) syndrome is characterized by ...
Two Michael J Fox awards for UCL Parkinson's research
www.ucl.ac.uk
Drs Henry Houlden and Coro Paisan-Ruiz applied for funds for a study on 'The Glucosylceramide Pathway in Parkinson's Disease and Other Synucleinopathies: Genetic Defects, Neuropathological Characterization and Cell ...
Five Questions with CMT Researcher Henry Houlden - Muscular Dystrophy...
strongly.mda.org
Henry Houlden is working to identify genes that, when flawed, can cause CMT. His work could help optimize treatment strategies and accelerate new therapy...
Professor Henry Houlden - Rare Mitochondrial Disorders ...mitochondrialdisease.nhs.uk › nhs-mitochondrial-services › london
mitochondrialdisease.nhs.uk
Professor Henry Houlden is a Professor in Clinical Neurology & Clinical lead of the Neurogenetics Laboratory and Clinical Service. He co-leads for the Genomics England Clinical Interpretation Partnership (GeCIP) and sits on the Genomics England committee representing rare diseases.
Professor Henry Houlden – Multiple System Atrophy Trust
www.msatrust.org.uk
Professor Henry Houlden at the University College London (UCL) and grant-holder of the Trust-funded UK MSA Network: The Trust grant round funded a research team ...
Lincolnshire County Board Premier League
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Player Henry Houlden ( SKEG ). Rules Type: Pairs, Standard. Batting; Bowling; Fielding; Game Results. Bowling Summary; Dismissals; Top 5 Bowling ...
Henry Houlden | UCL Queen Square Institute of Neurology - UCL –...
www.ucl.ac.uk
Henry Houlden. My laboratory works on the genetics of neurodegeneration, peripheral nerve disease, ataxias, and paroxysmal movement disorders. I also have an interest ...
Henry Houlden, PhD | Parkinson's Disease
www.michaeljfox.org
Dr. Houldin works in a small but expanding laboratory at the Institute of Neurology in London. The inistutute specializes in Parkinson’s disease and...
Houlden, Henry
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Life story: John Henry Houlden | Lives of the First World War
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Play-Cricket
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Rate, Strike Rate, Average, % Team Wickets. All25, 808, 54, 4/11, 0, 3.6929.0, 5, 118, 5, 2/15, 0, 4.0750.0, 4, 183, 10, 3/14, 0, 3.6651.0, 5, 175, 11, 2/5,
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