Browsing publications by Dr Rumaisa Bashir

Newcastle AuthorsTitleYear
Dr Anna Sarkozy
Dr Rumaisa Bashir
Dr Debbie Hicks
Dr Rita Barresi
Dr Steven Laval
et al.
The first UK family with Ano5-associated myopathy2010
Rebecca Harrison
Dr Steven Laval
Dr Rumaisa Bashir
Professor Katherine Bushby
Characterisation of the dysferlin muscle promoter2001
Dr Elizabeth Vafiadaki
Dr Alexandra Reis
Ruth Harrison
Dr Louise VB Anderson
Professor Katherine Bushby
et al.
Cloning of the mouse dysferlin gene and genomic characterization of the SJL-Dysf mutation2001
Dr Louise VB Anderson
Dr Rumaisa Bashir
Professor Volker Straub
Professor Katherine Bushby
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C2001
Dr Rumaisa Bashir
Professor Katherine Bushby
Muscular dystrophy due to dysferlin deficiency in Libyan Jews - Clinical and genetic features2000
Dr Rumaisa Bashir
Professor Katherine Bushby
Muscular dystrophy due to dysferlin deficiency in Libyan Jews: Clinical and genetic features.2000
Dr Janet Lindsey
Dr Meryl Lusher
Dr Kathleen White
Dr Rumaisa Bashir
Professor Pamela Shaw
et al.
Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis2000
Dr Louise VB Anderson
Dr Roger Harrison
Dr Robert Pogue
Dr Elizabeth Vafiadaki
Jennifer Moss
et al.
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)2000
Stephen Britton
Dr Elizabeth Vafiadaki
Sharon Foster
Rebecca Harrison
Professor Katherine Bushby
et al.
The third human FER-1-like protein is highly similar to dysferlin2000
Dr Louise VB Anderson
Dr Rumaisa Bashir
Dr Elizabeth Vafiadaki
Rebecca Harrison
Professor Katherine Bushby
et al.
Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B1999
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