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MRS JACINTA MCMAHON



Contact Details

Organization: Medicine - Austin Health and Northern Health
Position: RESEARCH ASSISTANT, EPILEPSY
Email:
Work: 9496 2096
Building: No Building
Campus: Repatriation Hospital

Qualifications, Honours, Fellowships and Other Awards

Qualifications

Title Institution Date Awarded Abbreviation
Bachelor of Science (honours) University of Melbourne 31-Dec-2001

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 2009

Journal Articles

  • Periventricular heterotopia, mental retardation and epilepsy associated with 5q14.3-q15 deletion
    Year: 2009
    Journal: Neurology
    Volume: 72
    Page numbers: 784-792
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Publications in 2008

Journal Articles

  • Severe autosomal dominant nocturnal frontal lobe epilepsy associated with psychiatric disorders and intellectual disability
    Year: 2008
    Journal: Epilepsia
    Volume: 49
    Issue: 5
    Page numbers: 2125-2129
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Publications in 2007

Journal Articles

  • Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsy


    Year: 2007
    Journal: Epilepsy Research
    Volume: 76
    Issue: 1
    Page numbers: 41-48
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  • The spectrum of SCN1A-related infantile epileptic encephalopathies


    Year: 2007
    Journal: Brain
    Volume: 130
    Issue: pt 3
    Page numbers: 843-852
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  • Increased nicotinamide nucleotide transhydrogenase levels predispose to insulin hypersecretion in a mouse strain susceptible to diabetes
    Year: 2007
    Journal: Diabetologia
    Volume: 50
    Issue: 2007
    Page numbers: 2476-2485
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Publications in 2006

Journal Articles

  • A new molecular mechanism for severe myoclonic epilepsy of infancy: Exonic deletions in SCN1A
    Year: 2006
    Journal: Neurology
    Volume: 67
    Issue: 2006
    Page numbers: 1094-1095
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  • De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective study
    Year: 2006
    Journal: The Lancet Neurology
    Volume: 5
    Issue: 2006
    Page numbers: 488-492
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  • Severe myoclonic epilepsy of infancy (Dravet syndrome): Recognition and diagnosis in adults
    Year: 2006
    Journal: Neurology
    Volume: 67
    Issue: 2006
    Page numbers: 2224-2226
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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 2004

Journal Articles

  • Failure to confrim association of a polymorphism in ABCB1 with multidrug-resistant epilepsy
    Year: 2004
    Journal: Neurology
    Volume: 63
    Issue: 6
    Page numbers: 1090-1092
    Publisher: Lippincott Williams & Wilkins(Pennsylvania)
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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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  • LGI1 mutations in temporal lobe epilepsies
    Year: 2004
    Journal: Neurology
    Volume: 62
    Page numbers: 1115-1119
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