Thanks to all the listeners for joining us and supporting this campaign to fight PD together.
On behalf of MDSI, we are grateful to be a partner in your journey with PD.
MDSI is always there to provide the best possible care and support for you.
#WorldParkinsonsDay

Share with your PD patients and caregivers
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#WorldParkinsonsDay
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Beautiful talk by Dr Suvasini Sharma on Hypermanganesemia at Indian Rare Movement Disorders Consortium
Thanks for sharing a nice video on '🐔 walk'
youtu.be/z3FvkwGcWtU?si…

'May we continue to learn from each other's Zebbras and Unicorns'

Fantastic talk by Dr Ai-Huey Tan on approach to ataxia at Indian Rare Movement disorders Consortium

Nice talk on diagnostic approach to Mitochondrial disorders from Professor Carolyn Sue at Indian Rare Movement disorders Consortium
doi.org/10.1016/j.bbag…
dx.doi.org/10.20517/jtgg.…

#WorldParkinsonsDay

📢 Registration is now open
#MDSCongress

A comprehensive summary of monogenic PD from Dr Kishore Kumar #NeuroTwitter
Monogenic Parkinson’s Disease: Genotype, Phenotype, Pathophysiology, and Genetic Testing mdpi.com/1532012 #mdpigenes via Genes MDPI

Palmaris brevis spasm syndrome: The treatable hypothenar dimpling, published in AOMD
- Occupational overuse of a computer keyboard, mouse, pipette, vibratory tools
- Can be spontaneous
- Excellent response to botulinum toxin
journals.lww.com/aomd/fulltext/…

Khat consumption as a modifiable risk factor for chewing dystonia - a study from Mehta et al. published in AOMD
- Chewing khat leaves (Catha edulis) is common in East Africa and Yemen
- Khat contains cathinone, analogue of d-amphetamine and cathine
journals.lww.com/aomd/fulltext/…

Quadrupedal locomotion in Uner Tan syndrome: A neurological viewpoint - Things to ponder, from Prof GM Wali, just published in AOMD
- Devolution
- Adaptive behavior
- Clinical vignette
- Genetics
- Role of Cerebellum
- Role of Spinal pattern generators

journals.lww.com/aomd/fulltext/…

Our preprints with The Lancet unveil biallelic NOTCH3 variants: truncating ones cause neurodevelopmental disorder, while cysteine missense resemble CADASIL. Missense carriers exhibit CADASIL; truncating carriers are mostly asymptomatic unless affecting last exon, leading to LMS.

MDSGene Systematic review on ATX-ANO10 Movement Disorders Journal
▶️ Conjunctival vessel tortuosity and early facial muscle denervation are some interesting clues #NeuroTwitter
doi.org/10.1002/mds.29…

Machado-Joseph disease (SCA3) was originally described in descendants from São Miguel Island, Azores, Portugal in the 1970s. In the 1990s, the pathogenic variant was found in chromosome 14 and originally named MJD1 and was later changed to ATXN3. loom.ly/BKwJkbg

🧬🧬How Do I Report Genes in a Paper?🧬🧬
A nice article from Prof. Christine Klein Movement Disorders Clinical Practice #neurotwitter
…mentdisorders.onlinelibrary.wiley.com/doi/full/10.10…

MDS Video Challenge 2024 MDS
#MDSCongress

A comprehensive MDS review on the management of ICD, Punding, DDS in PD Movement Disorders Journal #neurotwitter
doi.org/10.1002/mds.29…

A nice depiction of 'Synucleinopathy' Vs 'Synucleinopenia' hypothesis in PD Alberto J Espay Andrew Lees #NeuroTwitter #Lewybodies