Search filters

List of works by Thomas T. Warner

A 24-Hour Study of the Hypothalamo-Pituitary Axes in Huntington's Disease.

scientific article published on 2 October 2015

A Histologic Study of the Circadian System in Parkinson Disease, Multiple System Atrophy, and Progressive Supranuclear Palsy.

scientific article

A Retrospective Evaluation of the Frequency of Impulsive Compulsive Behaviors in Parkinson's Disease Patients Treated with Continuous Waking Day Apomorphine Pumps

scientific article published on 11 August 2016

A clinical and molecular genetic study of dentatorubropallidoluysian atrophy in four European families

scientific article published on 01 April 1995

A clinical, genetic and candidate gene study of Silver syndrome, a complicated form of hereditary spastic paraplegia

scientific article published on 01 September 2004

A critical evaluation of inflammatory markers in Huntington's Disease plasma.

scientific article published in January 2013

A large Indian family with rearrangement of chromosome 4p16 and 3p26.3 and divergent clinical presentations

scientific article published on 10 November 2015

A large family with hereditary spastic paraparesis due to a frame shift mutation of the spastin (SPG4) gene: association with multiple sclerosis in two affected siblings and epilepsy in other affected family members.

scientific article

A new locus for autosomal recessive complicated hereditary spastic paraplegia (SPG26) maps to chromosome 12p11.1-12q14.

scientific article published in January 2005

A partially inactivating mutation in the sodium-dependent lysophosphatidylcholine transporter MFSD2A causes a non-lethal microcephaly syndrome

scientific article published on 25 May 2015

A systematic evaluation of integration free reprogramming methods for deriving clinically relevant patient specific induced pluripotent stem (iPS) cells

scientific article

Abrogation of LRRK2 dependent Rab10 phosphorylation with TLR4 activation and alterations in evoked cytokine release in immune cells

scientific article published on 15 May 2021

Analysis of White Adipose Tissue Gene Expression Reveals CREB1 Pathway Altered in Huntington's Disease.

scientific article published in December 2015

Analysis of macroautophagy related proteins in G2019S LRRK2 Parkinson's disease brains with Lewy body pathology

scientific article published on 25 July 2018

Analysis of the epsilon-sarcoglycan gene in familial and sporadic myoclonus-dystonia: evidence for genetic heterogeneity.

scientific article

Association between diabetes and subsequent Parkinson disease: A record-linkage cohort study

scientific article published on 13 June 2018

Association of Autonomic Dysfunction With Disease Progression and Survival in Parkinson Disease.

scientific article

Association of autonomic symptoms with disease progression and survival in progressive supranuclear palsy

scientific article published on 31 December 2018

Astrogliopathy predominates the earliest stage of corticobasal degeneration pathology

scientific article

Autonomic Dysfunction in Parkinson's Disease: The Hidden Game Changer?

scientific article published on 14 May 2018

Basic genetics for the clinical neurologist

scientific article

CDIP-58 can measure the impact of botulinum toxin treatment in cervical dystonia.

scientific article published in December 2006

Central alveolar hypoventilation associated with paraneoplastic brain-stem encephalitis and anti-Hu antibodies.

scientific article published in August 1994

Cervical dystonia is associated with a polymorphism in the dopamine (D5) receptor gene

scientific article

Chromosomes from the epithelium of plucked human telogen hairs.

scientific article

Churg-Strauss syndrome presenting with visual loss

scientific article published on 01 December 2000

Clinical diagnosis of cervical dystonia

scientific article published on 01 June 2004

Clinical presentations of Wilson disease.

scientific article published in April 2019

Colonic transit, high-resolution anorectal manometry and MRI defecography study of constipation in Parkinson's disease

scientific article published on 28 August 2019

Complex I function in familial and sporadic dystonia

scientific article published on 01 April 1997

Copy number variation of in familial dystonic tremor

scientific article published on 04 February 2019

Creatine therapy for Huntington's disease: clinical and MRS findings in a 1-year pilot study.

scientific article published in July 2003

DRD1 rare variants associated with tardive-like dystonia: A pilot pathway sequencing study in dystonia

scientific article published on 13 April 2014

Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutations

scientific article published on 01 January 1999

Diagnosis Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal Syndrome

scientific article published on 20 December 2019

Dopamine reuptake transporter-single-photon emission computed tomography and transcranial sonography as imaging markers of prediagnostic Parkinson's disease

scientific article published on 30 January 2018

Dystonia

scientific article published on 01 January 2018

Dystonia.

scientific article published in September 2017

Dystonia: an update on genetics and treatment.

scientific article

Early presentation of urinary retention in multiple system atrophy: can the disease begin in the sacral spinal cord?

scientific article published on 12 November 2019

Elevated salivary protein in Parkinson's disease and salivary DJ-1 as a potential marker of disease severity

scientific article published on 23 July 2015

Emerging common molecular pathways for primary dystonia.

scientific article published on June 2013

Encephalomyelitis in primary hypogammaglobulinaemia.

scientific article published in February 1996

Erratum to: Strategies for treatment of dystonia.

scientific article published on 6 November 2015

Evidence-based guidelines for using the Short Form 36 in cervical dystonia.

scientific article published in January 2007

Exclusion of the DYT1 locus in familial torticollis

scientific article published on 01 October 1996

Focal dystonia is associated with a polymorphism of the dopamine D5 receptor gene.

scientific article published in January 2004

Friedreich's ataxia presenting as an isolated spastic paraparesis ⬇️

scientific article published on November 1, 2001

Fulminant corticobasal degeneration: a distinct variant with predominant neuronal tau aggregates

scientific article published on 16 January 2020

Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: Evidence for a third EKD gene

article

Genetic and phenotypic characterization of complex hereditary spastic paraplegia

scientific article published on 23 May 2016

Genetic counselling in mitochondrial diseases ⬇️

scientific article published on October 1, 1997

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

scientific article published on 15 February 2021

Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approaches

scientific article published on 31 July 2019

High-dose creatine therapy for Huntington disease: a 2-year clinical and MRS study.

scientific article published in May 2005

Hypokalaemia mimicking Guillain-Barré syndrome.

scientific article

Hypothalamic α-synuclein and its relation to weight loss and autonomic symptoms in Parkinson's disease.

scientific article published on 28 November 2016

Iatrogenic B12-deficient peripheral neuropathy following nitrous oxide administration for functional tonic leg spasm: A case report

scientific article published on 06 July 2017

Impact of cervical dystonia on quality of life.

scientific article published in July 2002

Increased rate of whole-brain atrophy over 6 months in early Huntington disease.

scientific article published in August 2006

Investigation of somatic CNVs in brains of synucleinopathy cases using targeted SNCA analysis and single cell sequencing

scientific article published on 23 December 2019

Lamotrigine-induced carbamazepine toxicity: an interaction with carbamazepine-10,11 -epoxide

article

Linkage analysis with chromosome 9 markers in hereditary essential tremor

scientific article published on 01 July 1993

Loss of phosphatidylinositol 4-kinase 2alpha activity causes late onset degeneration of spinal cord axons

scientific article

Lower nucleus accumbens α-synuclein load and D3 receptor levels in Parkinson's disease with impulsive compulsive behaviours

scientific article published on 01 November 2019

MIR-NATs repress MAPT translation and aid proteostasis in neurodegeneration

scientific article published on 19 May 2021

MSA-C or SCA 17? A clinicopathological case update

scientific article published in August 2016

Mutant torsinA, which causes early-onset primary torsion dystonia, is redistributed to membranous structures enriched in vesicular monoamine transporter in cultured human SH-SY5Y cells.

scientific article

Myoclonus-dystonia syndrome with severe depression is caused by an exon-skipping mutation in the epsilon-sarcoglycan gene

scientific article published on 01 June 2007

Neuroendocrine abnormalities in Parkinson's disease

scientific article published on 31 October 2016

Neuropathology of Circadian Alterations in Parkinson Disease-Reply

scientific article published on 01 January 2019

No association with common Caucasian genotypes in exons 8, 13 and 14 of the human cytoplasmic dynein heavy chain gene (DNCHC1) and familial motor neuron disorders

article

No evidence of iatrogenic human transmission in autopsy confirmed multiple system atrophy

scientific article published on 23 March 2018

Overactive prefrontal and underactive motor cortical areas in idiopathic dystonia

scientific article published on 01 March 1995

Paroxysmal exercise-induced dyskinesia of the hands

scientific article published on 04 October 2012

Plasma melatonin is reduced in Huntington's disease.

scientific article published on 27 August 2014

Primary dystonia and dystonia-plus syndromes: clinical characteristics, diagnosis, and pathogenesis.

scientific article published on 24 October 2011

Prognosis and Neuropathologic Correlation of Clinical Subtypes of Parkinson Disease

scientific article published on 01 April 2019

Recent advances in the molecular pathogenesis of dystonia-plus syndromes and heredodegenerative dystonias.

scientific article published on January 2013

Reply to: Young- onset multiple system atrophy

scientific article published on 01 December 2018

Review: Clinical, neuropathological and genetic features of Lewy body dementias

scientific article published on 20 May 2019

Review: Induced pluripotent stem cell models of frontotemporal dementia

scientific article

SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotype.

scientific article published on 11 September 2014

SGCE mutations cause psychiatric disorders: clinical and genetic characterization

scientific article

SPG3A mutation screening in English families with early onset autosomal dominant hereditary spastic paraplegia

scientific article (publication date: 15 December 2003)

Saccadic Direction Errors are Associated with Impulsive Compulsive Behaviours in Parkinson's Disease Patients

scientific article published on 01 January 2019

Screening of patients with hereditary spastic paraplegia reveals seven novel mutations in the SPG4 (Spastin) gene.

scientific article published in February 2003

Sensitivity and Specificity of the ECAS in Parkinson's Disease and Progressive Supranuclear Palsy.

scientific article

Silver syndrome is not linked to any of the previously established autosomal dominant hereditary spastic paraplegia loci

scientific article published on 01 July 2001

Spastin and microtubules: Functions in health and disease.

scientific article published on September 2007

Strategies for treatment of dystonia.

scientific article published on 14 September 2015

Structures of α-synuclein filaments from human brains with Lewy pathology

scientific article published in 2022

Systematic review and meta-analysis of salivary protein concentration in Parkinson's disease

scientific article published on 19 November 2015

The BRadykinesia Akinesia INcoordination (BRAIN) Tap Test: Capturing the Sequence Effect

scientific article published on 25 June 2019

The Outcome of Dopamine Dysregulation Syndrome in Parkinson's Disease: A Retrospective Postmortem Study

scientific article published on 01 September 2018

The dystonia-associated protein torsinA modulates synaptic vesicle recycling

scientific article

The dystonias

scientific article published on 01 April 1998

The genetic and clinico-pathological profile of early-onset progressive supranuclear palsy

scientific article published on 12 July 2019

The genetics of Parkinson's disease and parkinsonian syndromes

scientific article published on 01 October 1998

The long-term outcome of impulsive compulsive behaviours in Parkinson's disease

scientific article published on 01 February 2019

The molecular genetics of the dystonias ⬇️

scientific article published on April 1, 1998

The neuropsychological profile of Othello syndrome in Parkinson's disease

scientific article published on 16 August 2017

The role of the alpha -synuclein gene mutation in patients with sporadic Parkinson's disease in the United Kingdom ⬇️

scientific article published on September 1, 1998

The role of torsinA in dystonia.

scientific article published on July 2010

Three novel spastin (SPG4) mutations in families with autosomal dominant hereditary spastic paraplegia

scientific article (publication date: 15 September 2002)

TorsinA and dystonia: from nuclear envelope to synapse.

scientific article published on 08 April 2009

Training in neurology: lessons learnt

scientific article published on 13 May 2019

Verbal adynamia in parkinsonian syndromes: behavioral correlates and neuroanatomical substrate

scientific article published in August 2018

White matter DNA methylation profiling reveals deregulation of HIP1, LMAN2, MOBP, and other loci in multiple system atrophy

scientific article published on 18 September 2019

Xeroderma pigmentosum is a definite cause of Huntington's disease-like syndrome.

scientific article published on 4 December 2017

Young-onset multiple system atrophy: Clinical and pathological features

scientific article published on 01 July 2018

Paulina is supported by:

About Paulina

Help