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MS BRONWYN GRINTON



Contact Details

Organization: Medicine - Austin Health and Northern Health
Position: RESEARCH ASSISTANT
Email:
Work: 9496 2761
Room: 77
Building: No Building
Campus: Repatriation Hospital

Research Expertise and International Linkages

Research Expertise

Research Interest Key Words Country of Expertise
Epilepsy Genetics Epilepsy, genetics Australia

Qualifications, Honours, Fellowships and Other Awards

Qualifications

Title Institution Date Awarded Abbreviation
Bachelor of Science (honours) University of Melbourne 31-Dec-1998
Graduate Diploma of Information Management Royal Melbourne Institute of Technology 31-Dec-2004

Government Research Classifications

Research Fields, Courses and Discipline Classifications

Socio-Economic Objective Classifications

Publications

Publications produced at the University of Melbourne and reported in the Annual Publications Collection and 'Research Report' since 2001. The Themis Publications module, released in November 2006, allows additional publications from previous institutions and publications from past years to be entered.

Publications in 2007

Journal Articles

  • Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures

    Year: 2007
    Journal: Journal of Medical Genetics
    Volume: 44
    Issue: 12
    Page numbers: 791-796
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  • Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study
    Year: 2007
    Journal: The Lancet Neurology
    Volume: 6
    Issue: 11
    Page numbers: 970-980
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  • SCN2A mutations and benign familial neonatal-infantile seizures: the phenotypic spectrum
    Year: 2007
    Journal: Epilepsia
    Volume: 48
    Issue: 6
    Page numbers: 1138-1142
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  • Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations
    Year: 2007
    Journal: Brain
    Volume: 130
    Issue: 2007
    Page numbers: 100-109
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Publications in 2006

Journal Articles

  • Invited comments on the Shostak and Ottman review. Genetic research on the epilepsies.
    Year: 2006
    Journal: Epilepsia
    Volume: 47
    Issue: 2006
    Page numbers: 1751-1752
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  • The non-neurologists' view on epilepsy syndromes classification
    Year: 2006
    Journal: Epileptic Disorders
    Volume: 8
    Issue: 2
    Page numbers: 81-85
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Publications in 2005

Journal Articles

  • Familial clustering of seizure types within the idiopathic generalized epilepsies
    Year: 2005
    Journal: Neurology
    Volume: 65
    Page numbers: 523-528
    Publisher: Lippincott Williams & Wilkins(Pennsylvania)
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Publications in 2004

Journal Articles

  • Benign familial neonatal-infantile seizures: Characterization of a new sodium channelopathy
    Year: 2004
    Journal: Annals of Neurology
    Volume: 55
    Page numbers: 550-557
    Publisher: Wiley-Liss(New York)
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  • Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex families
    Year: 2004
    Journal: Epilepsia
    Volume: 45
    Issue: 5
    Page numbers: 467-478
    Publisher: Blackwell Science(Massachusetts)
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  • Novel mutations in the KCNQ2 gene link epilepsy to a dysfunction of the KCNQ2-calmodulin interaction
    Year: 2004
    Journal: Journal of Medical Genetics
    Volume: 41
    Issue: 3
    Page numbers: e35
    Publisher: BMJ Publishing Group(London)
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Publications in 2003

Journal Articles

  • Sodium channel α1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms
    Year: 2003
    Journal: Neurology
    Volume: 61
    Page numbers: 765-769
    Publisher: Lippincott Williams & Wilkins(Pennsylvania)
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  • The health-related quality of life of childhood epilepsy syndromes
    Year: 2003
    Journal: Journal of Paediatrics and Child Health
    Volume: 39
    Page numbers: 690-696
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