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List of works by Dominic B Rowe

A Temporal Association between Accumulated Petrol (Gasoline) Lead Emissions and Motor Neuron Disease in Australia

scientific article published on 19 December 2015

A functional polymorphism in the parkin gene promoter affects the age of onset of Parkinson's disease

scientific article published on 7 January 2007

A possible role for humoral immunity in the pathogenesis of Parkinson's disease

scientific article

Adult onset leucodystrophy with neuroaxonal spheroids and pigmented glia (ALSP): report of a new kindred

scientific article published on 01 February 2012

Adult-onset Alexander's disease mimicking degenerative disease

scientific article

An inflammatory review of Parkinson's disease.

scientific article

Antibodies from patients with Parkinson's disease react with protein modified by dopamine oxidation.

scientific article

Anticipation of onset age in familial Parkinson's disease without SCA gene mutations

article

Breakdown and quantitation of the forked termination of replication intermediate of Bacillus subtilis

scientific article published on 01 August 1987

CMS-01 Genetic testing for familial amyotrophic lateral sclerosis (ALS): insights and challenges

scientific article published on 01 November 2019

Common and rare variant association analyses in Amyotrophic Lateral Sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

preprint

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

scholarly article

Corticomotoneuronal function in asymptomatic SOD-1 mutation carriers.

scientific article published in April 2010

Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.

scientific article published on 20 September 2017

Differential effects of human neuromelanin and synthetic dopamine melanin on neuronal and glial cells.

scientific article published on 31 August 2005

Diffusion kurtosis and quantitative susceptibility mapping MRI are sensitive to structural abnormalities in amyotrophic lateral sclerosis

scientific article published on 22 July 2019

Do polymorphisms in the familial Parkinsonism genes contribute to risk for sporadic Parkinson's disease?

scientific article published in April 2009

Effects of cerebrospinal fluid from patients with Parkinson disease on dopaminergic cells.

scientific article published on February 1999

Evidence for polygenic and oligogenic basis of Australian sporadic amyotrophic lateral sclerosis

scientific article published on 14 May 2020

Focal vertebral artery dissection causing Brown-Sequard's syndrome

scientific article published on March 1, 1998

Genetic Analysis of Tryptophan Metabolism Genes in Sporadic Amyotrophic Lateral Sclerosis

scientific article published on 14 June 2021

Genetic and Pathological Assessment of hnRNPA1, hnRNPA2/B1, and hnRNPA3 in Familial and Sporadic Amyotrophic Lateral Sclerosis

scientific article published on 11 November 2017

Genetic and immunopathological analysis of CHCHD10 in Australian amyotrophic lateral sclerosis and frontotemporal dementia and transgenic TDP-43 mice

scientific article published on 05 November 2019

Genetic contributions to Parkinson's disease

scientific article published on 01 August 2004

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

scientific article published on 25 July 2016

Haplotype analysis of the IGF2-INS-TH gene cluster in Parkinson's disease

scientific article

Identification and outcomes of clinical phenotypes in amyotrophic lateral sclerosis/motor neuron disease: Australian National Motor Neuron Disease observational cohort.

scientific article published on 30 September 2016

Identifying the pattern of olfactory deficits in Parkinson disease using the brief smell identification test

scientific article

Identity by descent analysis identifies founder events and links SOD1 familial and sporadic ALS cases

scientific article published on 07 August 2020

Increased peripheral inflammation in asymptomatic leucine-rich repeat kinase 2 mutation carriers

scientific article published on 25 February 2016

Inflammasome inhibition prevents α-synuclein pathology and dopaminergic neurodegeneration in mice

scientific article published on 01 October 2018

Inhibitor treatment of peripheral mononuclear cells from Parkinson's disease patients further validates LRRK2 dephosphorylation as a pharmacodynamic biomarker

scientific article published on 9 August 2016

Interaction between α-Synuclein and Tau Genotypes and the Progression of Parkinson's Disease

scientific article published on January 1, 2011

Interleukin-12 and interferon-gamma are not detectable in the cerebrospinal fluid of patients with amyotrophic lateral sclerosis

scientific article published in June 2004

Involvement of quinolinic acid in the neuropathogenesis of amyotrophic lateral sclerosis.

scientific article published on 2 June 2016

Isolated fascicular oculomotor nerve palsy as the initial presentation of the antiphospholipid syndrome

scientific article published in November 2002

Isolated trochlear nerve palsy as a presenting feature of primary polycythemia rubra vera

scientific article published on 01 June 2004

Limitations of Electromyography in the Assessment of Abdominal Wall Muscle Contractility Following Botulinum Toxin A Injection

scientific article published on 09 April 2019

Measurement of LRRK2 and Ser910/935 phosphorylated LRRK2 in peripheral blood mononuclear cells from idiopathic Parkinson's disease patients.

scientific article

Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disorders

scientific article published on 26 March 2021

Mitochondrial DNA haplogroups J and K are not protective for Parkinson's disease in the Australian community

article

Monozygotic twins and triplets discordant for amyotrophic lateral sclerosis display differential methylation and gene expression.

scientific article published on 4 June 2019

Motor neuron disease mortality and lifetime petrol lead exposure: Evidence from national age-specific and state-level age-standardized death rates in Australia.

scientific article

Neuronal intranuclear inclusion disease is genetically heterogeneous

scientific article published on 10 August 2020

Nocturnal hypoxia in motor neuron disease is not predicted by standard respiratory function tests.

scientific article published in July 2006

Novel TBK1 truncating mutation in a familial amyotrophic lateral sclerosis patient of Chinese origin.

scientific article published on 18 August 2015

Novel prion protein gene mutation presenting with subacute PSP-like syndrome.

scientific article published in March 2007

Predicting a positive response to intravenous immunoglobulin in isolated lower motor neuron syndromes

scientific article

Predictive genetic testing for amyotrophic lateral sclerosis and frontotemporal dementia: genetic counselling considerations.

scientific article published on 6 June 2017

Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's disease

scientific article published in May 2007

Reduced T helper and B lymphocytes in Parkinson's disease

scientific article published on 19 August 2012

SNCA Gene, but Not MAPT, Influences Onset Age of Parkinson's Disease in Chinese and Australians

scientific article published on 15 April 2015

Safety and tolerability of Triumeq in amyotrophic lateral sclerosis: the Lighthouse trial

scientific article published on 08 July 2019

Significant out-of-sample classification from methylation profile scoring for amyotrophic lateral sclerosis

scientific article published on 27 February 2020

The C9orf72 hexanucleotide repeat expansion presents a challenge for testing laboratories and genetic counseling

scientific article published on 23 March 2019

The genotype-phenotype landscape of familial amyotrophic lateral sclerosis in Australia.

scientific article published on 20 January 2017

The mRNA-based reprogramming of fibroblasts from a SOD1E101G familial amyotrophic lateral sclerosis patient to induced pluripotent stem cell line UOWi007

scientific article published on 16 January 2020

VISA--a pass to innate immunity

scientific article published on 14 September 2006

Whole genome sequencing for the genetic diagnosis of heterogenous dystonia phenotypes

scientific article published on 07 November 2019