Dr Lou Wiblin
@dr_wiblin
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Joined January 2016
Find about quality of life in people with PSP and MSA by @neurobear at poster 258 #MDSCongress2017 #psp #msa
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https://t.co/Lo6RuoXmbn at last, some progress for MND
FDA approves first new drug for ALS treatment in 22 years #ALS #MND #neurodegeneration #edavarone
https://t.co/jRss4YaL5s
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'Exciting' blood test spots cancer a year early
bbc.co.uk
The discovery allows doctors to detect returning tumours earlier and increases chances of a cure.
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Rare subtypes of rare diseases; PSP, MSA or other AP. Second try! #RareDiseaseDay
pubmed.ncbi.nlm.nih.gov
PubMed® comprises more than 39 million citations for biomedical literature from MEDLINE, life science journals, and online books. Citations may include links to full text content from PubMed Central...
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Rare forms of a rare disease...the importance of research in facilitating diagnosis in PSP and MSA https://t.co/SXRqCd152P…
#RareDiseaseDay
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Vital in conditions like PSP, MSA and DLB as well as Parkinson's. So much we don't know!
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A review on Palliative Care and how it applies to MSA and PSP. With thanks to Mark Lee and David Burn.
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A decade of deadlock over Alzheimer's treatment may be drawing to a close
theguardian.com
The next phase of trials for a new Alzheimer’s drug will answer the real question: are brain plaques the root cause of the disease, or just a symptom?
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We're delighted Palliative Care Consultant Dr Venkata Chaitanya is sharing his expertise with our delegates in #Newcastle #TeamPSPA
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'Stay hopeful' says researcher @dr_wiblin closing our study day in #Newcastle, thanks to our delegates and speakers, it's been a great day
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This exciting (but early) result has indications for other tauopathies like PSP.
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Great day spent with @PSPASSOCIATION discussing updates from the PROSPECT study. Exciting research in the pipeline!
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PSP Association meeting looking at research from around the UK in the PROSPECT project. @PSPASSOCIATION
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Because Parkinson's and related conditions affect us all. The R4 presenter Richard Coles lost his father recently
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A small but significant presence of MSA & PSP research at the Palliative Care Congress #PCC2016 from the North-East!
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It's #RareDiseaseDay - at least 4,000 people are living with Progressive Supranuclear Palsy (PSP) in the UK
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