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Brain dopamine-serotonin vesicular transport disease presenting as a severe infantile hypotonic parkinsonian disorder

Journal of inherited metabolic disease, 2016-03, Vol.39 (2), p.305-308

2016

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A Comparison of Cognitive Function in Former Rugby Union Players Compared with Former Non-Contact-Sport Players and the Impact of Concussion History

Sports medicine (Auckland), 2017-06, Vol.47 (6), p.1209-1220

2017

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Exome and genome sequencing results refine diagnoses and provide treatment options in a cohort of New Zealanders with neurodevelopmental disorders (P1.304)

Neurology, 2018-04, Vol.90 (15_supplement)

2018

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Whole Exome Sequencing Reveals Compound Heterozygosity for Ethnically Distinct PEX7 Mutations Responsible for Rhizomelic Chondrodysplasia Punctata, Type 1

Case reports in genetics, 2015-01, Vol.2015 (2015), p.1-4

2015

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Hemodynamic and Metabolic Aspects of Photosensitive Epilepsy Revealed by Functional Magnetic Resonance Imaging and Magnetic Resonance Spectroscopy

Epilepsia (Copenhagen), 1999-07, Vol.40 (7), p.912-920

1999

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Genetic diagnostic outcomes from a 10-year research programme in autism in Aotearoa New Zealand

Journal of the Royal Society of New Zealand, 2024-09, p.1-17

2024

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COGNITION IN FORMER RUGBY UNION PLAYERS AND IMPACT OF CONCUSSION HISTORY

British journal of sports medicine, 2017-02, Vol.51 (4), p.333-333

2017

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The New Zealand minds for minds autism spectrum disorder self-reported cohort

Research in autism spectrum disorders, 2017-04, Vol.36, p.1-7

2017

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Compound heterozygous SLC19A3 mutations further refine the critical promoter region for biotin-thiamine-responsive basal ganglia disease

Cold Spring Harbor molecular case studies, 2017-11, Vol.3 (6), p.a001909

2017

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Compound Heterozygous Inheritance of Mutations in Coenzyme Q8A Results in Autosomal Recessive Cerebellar Ataxia and Coenzyme Q10 Deficiency in a Female Sib-Pair

JIMD Reports, Volume 42, 2018, Vol.42, p.31-36

2018

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Compound Heterozygous Inheritance of Mutations in Coenzyme Q8A Results in Autosomal Recessive Cerebellar Ataxia and Coenzyme Q 10 Deficiency in a Female Sib-Pair

JIMD reports, 2018, Vol.42, p.31

2018

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Photosensitive Epilepsy Studied by Functional Magnetic Resonance Imaging and Magnetic Resonance Spectroscopy

Epilepsia (Copenhagen), 1999-01, Vol.40 (s4), p.3-7

1999

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Electrophysiologic monitoring in the intensive care unit

Canadian journal of neurological sciences, 1994-05, Vol.21 (2), p.S12-S16

1994

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EEG during MR imaging: differentiation of movement artifact from paroxysmal cortical activity

Neurology, 1995-10, Vol.45 (10), p.1942-1943

1995

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Epilepsy and Mental Decline

Neurologic clinics, 1994-02, Vol.12 (1), p.101-114

1994

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Evaluation and prognostication in coma

Electroencephalography and clinical neurophysiology, 1998-02, Vol.106 (2), p.149-155

1998

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The revised global yellow fever risk map and recommendations for vaccination, 2010: consensus of the Informal WHO Working Group on Geographic Risk for Yellow Fever

The Lancet infectious diseases, 2011-08, Vol.11 (8), p.622-632

2011

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Epidemiology of Human Mpox - Worldwide, 2018-2021

MMWR. Morbidity and mortality weekly report, 2023-01, Vol.72 (3), p.68-72

2023

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Epidemiology of human monkeypox --worldwide, 2018-2021/Epidemiologie de la variole simienne chez l'humain--dans le monde, 2018-2021

Weekly epidemiological record, 2023-01, Vol.98 (3), p.29

2023

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Epidemiology of human monkeypox (mpox) – worldwide, 2018–2021

Weekly Epidemiological Record, 2023-01, Vol.98 (3), p.29-36

2023

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Central child abuse registers: The British experience

Child abuse & neglect, 1979, Vol.3 (1), p.157-166

1979

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Brain dopamine-serotonin vesicular transport disease presenting as a severe infantile hypotonic parkinsonian disorder

A Comparison of Cognitive Function in Former Rugby Union Players Compared with Former Non-Contact-Sport Players and the Impact of Concussion History

Exome and genome sequencing results refine diagnoses and provide treatment options in a cohort of New Zealanders with neurodevelopmental disorders (P1.304)

Whole Exome Sequencing Reveals Compound Heterozygosity for Ethnically Distinct PEX7 Mutations Responsible for Rhizomelic Chondrodysplasia Punctata, Type 1

Hemodynamic and Metabolic Aspects of Photosensitive Epilepsy Revealed by Functional Magnetic Resonance Imaging and Magnetic Resonance Spectroscopy

Genetic diagnostic outcomes from a 10-year research programme in autism in Aotearoa New Zealand

COGNITION IN FORMER RUGBY UNION PLAYERS AND IMPACT OF CONCUSSION HISTORY

The New Zealand minds for minds autism spectrum disorder self-reported cohort

Compound heterozygous SLC19A3 mutations further refine the critical promoter region for biotin-thiamine-responsive basal ganglia disease

Compound Heterozygous Inheritance of Mutations in Coenzyme Q8A Results in Autosomal Recessive Cerebellar Ataxia and Coenzyme Q10 Deficiency in a Female Sib-Pair

Compound Heterozygous Inheritance of Mutations in Coenzyme Q8A Results in Autosomal Recessive Cerebellar Ataxia and Coenzyme Q 10 Deficiency in a Female Sib-Pair

Photosensitive Epilepsy Studied by Functional Magnetic Resonance Imaging and Magnetic Resonance Spectroscopy

Electrophysiologic monitoring in the intensive care unit

EEG during MR imaging: differentiation of movement artifact from paroxysmal cortical activity

Epilepsy and Mental Decline

Evaluation and prognostication in coma

The revised global yellow fever risk map and recommendations for vaccination, 2010: consensus of the Informal WHO Working Group on Geographic Risk for Yellow Fever

Epidemiology of Human Mpox - Worldwide, 2018-2021

Epidemiology of human monkeypox --worldwide, 2018-2021/Epidemiologie de la variole simienne chez l'humain--dans le monde, 2018-2021

Epidemiology of human monkeypox (mpox) – worldwide, 2018–2021

Central child abuse registers: The British experience

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