NEW!

Presenters Stand by Posters 5:30 p.m.–7:00 p.m.
P5.390 Co-Existence of Novel KIF1A
Mutation (SPG30) and Intronic Expansion
of BEAN (SCA31) in a Family: Clinical
and Genetic Characterization —Arika
Hasegawa, Ryoko Koike, Akio Kawakami,
Kishin Koh, Yoshihisa Takiyama, Takeshi
Ikeuchi
P5.391 Novel CACNB4 Variant
Associated with a Case of Progressive
Ataxia —Alexandra Lloyd-Smith, Shyamal
Mehta, Sian Spacey
P5.392 X-linked Spinocerebellar
Ataxia (SCA) Type 1A: a Novel Late Onset
Phenotype of the ATP2B3 Mutation —
Christopher Stephen, Kathleen Sweadner,
John Penniston, Jeremy Schmahmann
P5.393 Neuropathology of
Parkinsonism in Spinocerebellar Ataxia
Type 6: a Case Report —Diviya Kaul, Keith
Morley, Marius Pakalniskis, William Hickey,
Stephen Lee
Movement Disorders: Ataxia and
Dystonia
P5.394 A Mutation Causing Reduced
BK Channel Activity Leads to Cognitive
Inpairment and Progressive Cerebellar
Ataxia —Julia Staisch, Xiaofei Du, Joao
Carvalho-de-Souza, Tomoya Kubota,
Francisco Bezanilla, Christopher Gomez
P5.395 49 Year Old Male with Rapidly
Progressive Cerebellar Ataxia Secondary
to Non-Paraneoplastic Voltage-Gated
Calcium Channel Antibodies (VGCC): Case
Report —Shnehal Patel, Ilia Itin
P5.396 Prolonged Cerebellar
Syndrome After Legionnaire’s Disease —
Brandon Barton
P5.397 The Broadening Clinical
Spectrum Associated with ATP1A3
Mutations —Inge Meijer, Naomi Lubarr, Paul
Greene, Steven Frucht, Deborah Raymond,
William Severt, Vicki Shanker, Rivka Sachdev,
Susan Bressman, Laurie Ozelius, Rachel
Saunders-Pullman
P5.398 Likely Underrecognized
Mosaicism in Genetic Disease: High
Frequency of Mosaic Mutations in
ADCY5-Related Dyskinesia —Dong-Hui
Chen, Jennifer Friedman, Aurélie Méneret,
Emily Bonkowski, Fuki Hisama, Marie Davis,
Phillip Swanson, Saunder Bernes, Marie
Vidailhet, Emmanuel Roze, Thomas Bird,
Wendy Raskind
P5.399 Clinical Characteristics and
Natural History of Oromandibular and
Lingual Dystonia —Laura Scorr, Stewart
Factor, H. Jinnah
P5.400 Functional Dystonia: 10-year
Experience in a Specialized Dystonia
Clinic —Christopher Stephen, David Perez,
Nutan Sharma
P5.401 The Role of Acetyl-L-Carnitine
Levels and 95A>G Mutations in the
SLC22A5 Gene on Parkinson’s Disease in
Faroe Islands —Maria Skaalum Petersen,
Jónrit Halling, Debes Christiansen, Sára Bech
P5.402 Preclinical Model of
Parkinson’s Disease Using Circuit Specific
Optogenetics —Neel Patel, Vishakh
Iyer, Kala Venkiteswaran, Erin Handly,
Caitlin White, Naila Iqbal, Pooja Sridhar,
Kedar Thiagarajan, Zhiwen Liu, Charu
Ramakrishnan, Karl Deisseroth, Thyagarajan
Subramanian
Frequently Asked Questions
Wed· April 20
Do I need to register for the Annual Meeting
courses that I want to take?
No. A big change this year is that most courses no longer
require pre-registration. You are free to attend any course you
like. Courses that require pre-registration are clearly marked.
How do I plan my Annual Meeting schedule?
The Annual Meeting Mobile App and Itinerary Planner
(available within the registration site) are optional tools
available to assist you in customizing your itinerary. You can
edit your itinerary at any time; adding course(s) or event(s) to
your schedule does not require you to attend.
During the meeting, you are free to move between sessions,
as you wish. We only ask that you are mindful of the speakers
and other attendees and enter and exit with as little disruption
as possible.
How can I guarantee that I have a seat in a
particular session?
The sessions that do not require pre-registration are first-come,
first-serve seating. Please arrive early to any session(s) that
you must attend. Full session(s) may be overflowed to a second
room.
How can I access my course syllabi?
New for 2016, all attendees will receive complimentary online
access to all Annual Meeting Syllabi for one year. Notifications
will be sent out prior to the meeting with instructions for
access. Attendees may choose to upgrade to a USB drive for
permanent access.
Fast and easy registration · AAN.com/view/AM16 121