The World Federation of Neurology Research Group on Huntington's Disease,
The International Huntington Association, The Hereditary Disease Foundation,
The Huntington's Disease Association of America, The Huntington Society of Canada
and The Huntington Study Group present the

World Congress on Huntington's Disease

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Updated! Poster Abstract List

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Poster Abstract Detailed Listing

92 posters have been accepted for presentation at the World Congress on Huntington's Disease. All 92 posters will be displayed from Sunday morning until Monday evening. There are two poster sessions, and poster presenters are asked to stand by their poster at their designated session time (either Sunday, August 17 from 7:45 a.m. to 8:45 a.m., or, Monday, August 18 from 8:00 a.m. to 9:00 a.m.). These poster abstract lists are organized by poster session and poster topic.


POSTER ABSTRACT SESSION #1

Sunday, August 17th, 2003 - Staffed from 7:45 a.m. - 8:45 a.m.

Number
Genetics (6)
Presenting Author
008 European Molecular Genetics Quality Network: External Quality Assessment for the Molecular Diagnosis of Huntington Disease in Europe (1997-2002) Monique Losekoot, PhD
009

Monozygotic Twins Displaying Mosaicism of an Expanded and an Intermediate Allele of the CAG Repeat in the Huntington Disease Gene

Anne Norremolle, PhD
020 Study of Juvenile Huntington Disease Patients of Italian Origin Ferdinando Squitieri, MD, PhD
036

Molecular Analysis of Turkish Huntington's Disease Patients

Nazli Basak, PhD
057 Sequence and Haplotype Analysis of GRIK2 (GluR6) in Huntington Disease: Assessment of a Modifier Gene Wen-Qi Zeng, MD, PhD
071 Molecular Study of Huntington Disease in Iranian Families Fabiola Hormozian, Ms.c in Genetics
 
Genetic Counseling (7)
 
010 UK Study of Reduced Penetrance Alleles in Huntington's Disease Oliver Quarrell, MD, FRCP
012 Reproductive Decision Making Before and After Predictive Testing for Huntington Disease: An Australian Perspective Fiona Richards, Master of Social Work
019

Predictive Testing in Huntington Disease Families With Patients Homozygous for CAG Mutation

Ferdinando Squitieri, MD, PhD
021 Non-Consensual Predictive Testing: Testing at 25% risk-Some Legal and Counseling Issues Encountered in Australia Roslyn Tassicker, Master of Social Work
044 Preimplantation Diagnosis for Huntington Disease-The London Experience Alison Lashwood, MSc. Genetic Counseling
046 The Impact of Presymptomatic Predictive Testing for Huntington's Disease on Partners and Marital Relationships: Secrets, Lies and Truths Anita Bruce, BSc
060 Personality Traits in Probands Undergoing Predictive Testing for Huntington Disease Elisabeth Almqvist, PhD, RN
 
Psychosocial Issues (8)
 
005 Adverse Effects of Predictive Testing for Huntington Disease Underestimated: Long Term Effects 7-10 Years After the Test Reinier Timman, MA
006 Informing Relatives About Genetic Risk: A Qualitative Study of Patients At Risk For Huntington's Disease or Hereditary Breast/Ovarian Cancer Karen Forrest, MLitt
014 Innovative Approaches to Improving the Acceptance of Texture Karen Keast, BSc
023 Effects of Rehabilitation on Motor Performance, Mood State and Everyday Life of HD Patients Paola Zinzi, psychology
047 Improving Psychiatric Outcomes in an Outpatient HD Population Teresa Tempkin, RNC, MSN, ANP
062 Parenting Patterns in Patients with Huntington's Disease Ellizabeth McCusker, MBBS, FRACP
066 Who Killed That Lady? A HD Murder Case in Japan Kaori Muto, PhD
092 Self-Understanding and Identity: The Experience of Adolescents At Risk for Huntington's Disease Jessica Easton, M.A.
 
Pathogenetic Mechanisms (3)
 
004

Homozygosity For CAG Mutation in Huntington Disease is Associated With a More Severe Clinical Course

Ferdinando Squitieri, MD, PhD
017 Genetic Disruption of Tissue Transglutaminase Delays Disease Progression in a Mouse Model of Huntington's Disease Craig Bailey, PhD
051 Analysis of Huntingtin Protein-Protein Interactions Using the Yeast Two-Hybrid System Heike Goehler
 
Cell Dysfunction (5)
 
015 Specific Progressive cAMP Reduction Implicates Energy Deficits in Presymptomatic HD Knock-in Mice Silvia Gines-Padros, PhD Biochemistry
039 Abnormal Morphology of HD Fibroblasts Grown in Enriched Culture Medium Lis Hasholt, Dr. Med.Sci.
058 A Quantitative Gene Expression Analysis Of Laser-Dissected Striatal Neurons In The R6/2 Mouse Model Of Huntington's Disease Birgit Zucker, MD
074 Heat Shock Protein 27 Protects Monkey Cos Cells Against Oxidative Stress Generated by the Expression of Mutant Huntington Exon 1 Wance J.J. Firdaus, DEA, MSc
075 Huntington Expression Results in a Decrease of Proteasome Activity and Triggers Apoptosis in PC12 Cells George Lawless
 
Other (11)
 
002 Huntington Disease in Cuba Tatiana Zaldivar Vaillant, MD
007 The Effect of Huntington's Disease on the Ability to Respond to Conflicting Spatial Stimuli Nellie Georgiou-Karistianis, PhD
011 Small Compounds That Inhibit Mutant Huntingtin Aggregation: Potential Therapeutics of HD Patients Wang Jin, PhD
013 An Abnormal Sleep Pattern and Excessive Movements Can Characterize Patients With Huntington's Disease Marieta Anca, MD
025 Comparisons of CAG Repeat Distributions for Familial and Sporadic HD Cases & Intermediate Allele Frequencies For Different Populations Support a Stepwise Model for CAG Expansion Lilias Barron, BSc
027 Multidisciplinary Care in the Information Age a System for Coordination of Care Amongst Geographically Dispersed Providers Ronald Risley, MD
029 The Huntingtin-Interacting Protein Endophilin A3 Forms Filamentous Structures Which Associate With Microtubules But Not With Actin Filaments Alis Hughes, Ms
040 High Throughput Screen To Identify Compounds That Downregulate Intracellular Mutant Huntingtin Expression Deborah Russel, BA
045 PEG Feeding In End Stage Huntington's Disease: An Examination of the Clinical and Ethical Issues, Including the Views of the Doctor, Patient and the Patient's Family Sheila Simpson, MBChB, BSc, MD
052 Motor Deficits and Striosome Volume in the YAC72 Mouse Model of Huntington's Disease Collene Lawhorn, BS, MS Ed
076 Bilateral GP Stimulation for Huntington's Disease Elena Moro, MD, PhD

POSTER ABSTRACT SESSION #2

Monday, August 18th, 2003 - Staffed from 8:00 a.m. - 9:00 a.m.

 
Neuronal Vulnerability and Survival (1)
 
061 mRNA Profiling of Two Striatal Neuron Populations with Differential Vulnerability in HD: A Study Utilizing LCM, Real-Time PCR, and cDNA Microarrays Sarah Augood, PhD
 
Cellular-Based and Genetic Animal Models (5)
 
037 Interaction Between Huntingtin and the Nuclear Receptor Corepressor Nagehan Ersoy, MSc
042 Identification in Cell Culture of Small, Recruitment Positive Polyglutamine Aggregates: Aggregation Foci Erica Johnson, BS
054 Toxicity of a Carboxyl-Terminal Huntingtin Fragment in Drosophila Hui Zhu, PhD
064 Suppression of a Polyglutamine Toxicity by a Drosophila Ortholog of MRJ Parsa Kazemi-Esfarjani, B.Sc., PhD
077 The Role of Calpain in Huntington's Disease Lisa Ellerby, PhD
 
Animal Model Experimental Therapeutics (5)
 
003 A Strategy for Drug Discovery in Huntington's Disease Laure Jamot, PhD
026 A Dual Role of Adenosine A2A Receptors in 3-Nitropropionic Acid-Induced Striatal Lesions: Implications for the Neuroprotective Potential of A2A Antagonists David Blum, PhD
038 PEI Mediated In Vivo Gene Transfer in Transgenic Huntington's Disease Mice. Evaluation of Transfection Method, Effect and Biomarkers Bjarke Naver, MSc
043 Histone Deacetylase Inhibitors Prevent Oxidative Neuronal Death Independent of Expanded Polyglutamine Repeats via a Sp1-Dependent Pathway Hoon Ryu, PhD
053 Use of Adult Bone Marrow Stem Cell Transplants to Counteract Cognitive Deficits in a Rat Model of Huntington's Disease Gary Dunbar, PhD
 
Clinical Characteristics (20)
 
016 Subcortical Mild Cognitive Impairment: A Novel Concept of Mental Dysfunction Raphael Bonelli, MD
018 Nature and Development of HD in a Nursing Home Population: The Further Development of the BOSH Rating Scale Hans Claus, MSC
024 Objective Assessment of Akinesia and Bradykinesia in Huntington's Disease Jeroen van Vugt, MD, PhD
028 Somatoform Disorders as the Initial Presentation of Huntington Disease Vicki Wheelock, MD
031 Does the Clinical Spectrum of Huntington's Disease Include Tremor Neil Mahant, MBBS
033 Stereotypic Leg Movements in a Family Member of Huntington's Disease Din-E Shan, MD, PhD
034 Psychomotor Slowing and Memory Disturbances Over a Three-Year Period in Presymptomatic' carriers for Huntington's Disease Marie-Noelle Witjes-Ane, MSc
035 Assessment of Change in Cognitive Function in Huntington's Disease Julie Snowden, PhD
041 Does the Cause of Functional Disability Change With Disease Progression in Patients with Huntington's Disease? Yvette Grimbergen, MD
048 Changes in Sexual Behaviour Associated with Huntington's Disease David Craufurd, FRCPsych
050 Walk and Drink Time; Objective Measures of Motor Progression in Huntington's Disease Elizabeth Howard, BSc, MB ChB, MRCGP
055 Social Cognition in Huntington's Disease and Frontotemporal Dementia Jennifer Thompson, B.Sc
069 Defining Progression in Huntington Disease Donald Higgins, MD
070 Safety and Feasibility of the Prospective Huntington At Risk Observational Study (PHAROS): A Progress Report Elise Kayson, MS, RNC
072 Clinical Predictors of Neuropathological Severity: A Prospective Autopsy Study of 100 Individuals with Huntington's Disease Adam Rosenblatt, MD
073 Risk factors for Osteoporosis in Women with Huntington's Disease in a Long-term Care Setting Ayana Duckett, BA
079 Peg Insertion Reflects Dysfunction in Huntington's Disease Carsten Saft, MD
082 Implicit Processes in People with Huntington's Disease Kristy Bolter, PhD
085 Episodic Memory Impairment in Huntington's Disease: a Meta-Analysis Alonso Montoya, MD
091 Pupillary Measure of Brainstem Activation is Reduced in Huntington's Disease Francois Richer, PhD
 
Neuroimaging (5)
 
030 Progression of Structural Neuropathology in Huntington's Disease Using Voxel and Tensor Based Morphometry Christopher Kipps, MBBS
056 Quantification of Caudate and Putamen Atrophy by Volumetric MRI in Patients with Huntington Disease. Association Between Length of the CAG Repeat and Age at Onset Heloisa Ruocco, PhD
059 Brain Energy Metabolism in Huntington's Disease Marguerite Wieler, BScPT
065 MRI and PET Assessment of Brain Involvement in Subjects With Presymptomatic, Initial and Advanced Huntington Disease Ferdinando Squitieri, MD, PhD
090 Frontal Hypoactivation and Reduced Voluntary Control in Early Huntington's Disease Francois Richer, PhD
 
Human Experimental Therapeutics (8)
 
001 Targeted Nucleotide Exchange in the CAG Repeat Region of the Human HD Gene Eric Kmiec, PhD
022 Increased Cell Proliferation and Neurogenesis in Huntington's Disease Maurice Curtis, BhSc, MSc
032 Treatment of Huntington's Disease Using Essential Fatty Acids (Long Term Follow Up Case Presentation) Krisna Vaddadi, FRC Psych
049 Measurement of Irritability in Huntington's Disease David Craufurd, FRC Psych
063 Ethyl-Eicosapentaenoate (Ethyl-Epa) in Huntington's Disease: A Randomised, Placebo-Controlled Trial Blair Leavitt, MD, CM
067 Management of Huntington's Disease: An Evidence-Based Review Raphael Bonelli, MD
088 Mechanism of Action of the Anti-Chorea Drug tetrabenazine: A Review Kathleen Clarence-Smith, MD, PhD

LATE-BREAKING RESEARCH (8 POSTERS)

 

Pathogenetic Mechanisms (1)
Poster will be staffed on Sunday, August 17th, 2003
7:45 a.m. - 8:45 a.m.

 
087-LBR- Msh2 Protein in Base-excision Mediated CAD Expansion Irina Kovtun
 
Cellular-Based and Genetic Animal Models (2)
Poster will be staffed on Monday, August 18th, 2003
8:00 a.m. - 9:00 a.m.
 
078-LBR Behavioral Manifestations of High Extracellular Dopamine in HdhQ92 Knock-in Mice Michel Cyr, PhD
083-LBR Cell Culture Screen Identifies Caspase Inhibitors as Potential Drugs for the Treatment of Huntington's Disease Charity Aiken
 
Animal Model Experimental Therapeutics (1)
Poster will be staffed on Monday, August 18th, 2003
8:00 a.m. - 9:00 a.m.
 
086-LBR Cop-1 Vaccination Reduces Motor Function Deficits and Increases Life Expectancy in a Transgenic Mouse Model of Huntington's Disease Yona Gefen, PhD
 
Clinical Characteristics (3)
Poster will be staffed on Monday, August 18th, 2003
8:00 a.m. - 9:00 a.m.
 
080-LBR Is 41 Better Than 45? Influence of Low CAG Ranges on Huntington's Disease Carsten Saft, MD
081-LBR Emerging Cohort Characteristics in the Prospective Huntington At Risk Observational Study (PHAROS) Kevin Biglan, MD
089-LBR Initial Baseline Characteristics in the PREDICT-HD (Neurobiological Predictors of HD) Study Jane Paulsen, PhD
 
Neuroimaging (1)
Poster will be staffed on Monday, August 18th, 2003
8:00 a.m. - 9:00 a.m.
 
084-LBR Onset and Rate of Change in Basal Ganglia Volume in Presymptomatic Subjects Elizabeth Aylward, PhD

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