Reema Paudel

Hammersmith Campus, Du Cane Road
London, ENG W120NN, United Kingdom

Last Updated: 09/26/2026

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Found 10 publications

Tumor and local lymphoid tissue interaction determines prognosis in high-grade serous ovarian cancer.

Tumor and local lymphoid tissue interaction determines prognosis in high-grade serous ovarian cancer.

Journal: Cell reports. Medicine

Published: July 20, 2022

Pure Cerebellar Ataxia with Homozygous Mutations in the PNPLA6 Gene.

Pure Cerebellar Ataxia with Homozygous Mutations in the PNPLA6 Gene.

Journal: Cerebellum (London, England)

Published: March 21, 2016

DYT6 Dystonia: A Neuropathological Study.

DYT6 Dystonia: A Neuropathological Study.

Journal: Neuro-degenerative diseases

Published: May 21, 2015

Forebrain deletion of the dystonia protein torsinA causes dystonic-like movements and loss of striatal cholinergic neurons.

Forebrain deletion of the dystonia protein torsinA causes dystonic-like movements and loss of striatal cholinergic neurons.

Journal: eLife

Published: April 26, 2015

Neuropathological features of genetically confirmed DYT1 dystonia: investigating disease-specific inclusions.

Neuropathological features of genetically confirmed DYT1 dystonia: investigating disease-specific inclusions.

Journal: Acta neuropathologica communications

Published: September 18, 2014

C19orf12 mutation leads to a pallido-pyramidal syndrome.

C19orf12 mutation leads to a pallido-pyramidal syndrome.

Journal: Gene

Published: April 22, 2013

Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia.

Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia.

Journal: Annals of neurology

Published: August 05, 2012

Analysis of ATP13A2 in large neurodegeneration with brain iron accumulation (NBIA) and dystonia-parkinsonism cohorts.

Analysis of ATP13A2 in large neurodegeneration with brain iron accumulation (NBIA) and dystonia-parkinsonism cohorts.

Journal: Neuroscience letters

Published: April 19, 2012

Analysis of spinocerebellar ataxias due to expanded triplet repeats in Greek patients with cerebellar ataxia.

Analysis of spinocerebellar ataxias due to expanded triplet repeats in Greek patients with cerebellar ataxia.

Journal: Journal of the neurological sciences

Published: February 10, 2012

THAP1 mutations and dystonia phenotypes: genotype phenotype correlations.

THAP1 mutations and dystonia phenotypes: genotype phenotype correlations.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: November 24, 2011

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Last Updated: 09/26/2026