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Newcastle AuthorsTitleYearFull text
Dr Ana Topf
Professor Volker Straub
POGLUT1 biallelic mutations cause myopathy with reduced satellite cells, α-dystroglycan hypoglycosylation and a distinctive radiological pattern2020
Dr Ana Topf
Professor Volker Straub
First clinical and myopathological description of a myofibrillar myopathy with congenital onset and homozygous mutation in FLNC2020
Dr Ana Topf
Rachel Thompson
Professor Volker Straub
Improved Criteria for the Classification of Titin Variants in Inherited Skeletal Myopathies2020
Dr Ana Topf
Dr Alison Blain
Dr Jennifer Duff
Magdalena Mroczek
Dr Monica Ensini
et al.
Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness2020
Professor Volker Straub
The clinical-phenotype continuum in DYNC1H1-related disorders—genomic profiling and proposal for a novel classification2020
Dr Simon Cockell
Dr Rachel Queen
Dr Federico Ravaioli
Dr Jeremy Palmer
Dr Rebecca Darlay
et al.
Transcriptomic profiling across the nonalcoholic fatty liver disease spectrum reveals gene signatures for steatohepatitis and fibrosis2020
Dr Ana Topf
Professor Volker Straub
POPDC3 Gene Variants Associate with a New Form of Limb Girdle Muscular Dystrophy2019
Dr Ana Topf
Professor Volker Straub
ANO5 mutations in the Polish limb girdle muscular dystrophy patients: Effects on the protein structure2019
Dr Ana Topf
Professor Volker Straub
Characterization of three TRAPPC11 variants suggests a critical role for the extreme carboxy terminus of the protein2019
Dr Ana Topf
Dr Rita Barresi
Professor Volker Straub
Extending the clinical and mutational spectrum of TRIM32-related myopathies in a non-Hutterite population2019
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