[BIC-announce] FW: Next week's Killam Speaker - A genetic approach to Parkinson's diseases: neurodegeneration due to dardarin mutations

Jennifer Chew, Ms. jennifer.chew at mcgill.ca
Thu Oct 13 11:52:44 EDT 2005


PLEASE DISCARD IF THIS IS A DUPLICATE.  THANK YOU.  JENNIFER 
 

 
________________________________

From: MNISTAFF - Montreal Neurological Institute Staff
[mailto:MNISTAFF at LISTS.MCGILL.CA] On Behalf Of Enza Ferracane, Ms.
Sent: Thursday, October 13, 2005 9:56 AM
To: MNISTAFF at LISTS.MCGILL.CA
Subject: Next week's Killam Speaker



Killam Speaker: Dr. Jordi Perez Tur

Title: A genetic approach to Parkinson's diseases:  Neurodegeneration
due to dardarin mutations
  
October 18, 4 PM, De Grandpre Communications Centre


Dr. Jordi Perez Tur (http://ugm.ibv.csic.es/) will be visiting the MNI
to give a Killam seminar on Oct 18. Jordi is a prolific neurogeneticist
and cell biologist with wide-ranging interests. His lab has ongoing
projects related to genes involved in movement disorders, epilepsy and
MS - some of his recent publications are listed below. 

Jordi is an engaging speaker and I am sure all will enjoy his seminar on
Tuesday, October 18th. I hope to see you there.

Best regards,
Phil Barker


Zarranz et al. A novel mutation (K317M) in the MAPT gene causes FTDP and
motor neuron disease. Neurology. 2005 May 10;64(9):1578-85.

Morris et al. Genome-wide analysis of the parkinsonism-dementia complex
of Guam. Arch Neurol. 2004 Dec;61(12):1889-97.

Paisan-Ruiz et al. Cloning of the gene containing mutations that cause
PARK8-linked Parkinson's disease. Neuron. 2004 Nov 18;44(4):595-600.

Goertsches et al. A genomic screen of Spanish multiple sclerosis
patients reveals multiple loci associated with the disease. J
Neuroimmunol. 2003 Oct;143(1-2):124-8.

Morante-Redolat et al. Mutations in the LGI1/Epitempin gene on 10q24
cause autosomal dominant lateral temporal epilepsy. Hum Mol Genet. 2002
May 1;11(9):1119-28.

Otaegui et al. Mitochondrial polymporphisms in Parkinson's Disease.
Neurosci Lett. 2004 Nov 11;370(2-3):171-4.


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