Publications by authors named "Geraldine Bailey"

Claim this Profile
M
MEGF10 related myopathies: A new case with adult onset disease with prominent respiratory failure and review of reported phenotypes.
Elizabeth Harris, Chiara Marini-Bettolo, Ana Töpf, Rita Barresi, Tuomo Polvikoski, Geraldine Bailey

Neuromuscul Disord· January 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Respiratory involvement in ambulant and non-ambulant patients with facioscapulohumeral muscular dystrophy.
Sandra Moreira, Libby Wood, Debbie Smith, Chiara Marini-Bettolo, Michela Guglieri, Geraldine Bailey

J Neurol· June 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
ANO5 gene analysis in a large cohort of patients with anoctaminopathy: confirmation of male prevalence and high occurrence of the common exon 5 gene mutation.
Anna Sarkozy, Debbie Hicks, Judith Hudson, Steve H Laval, Rita Barresi, Geraldine Bailey

Hum Mutat· August 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Charcot-Marie-Tooth disease in Northern England.
Charlotte Foley, Ian Schofield, Gail Eglon, Geraldine Bailey, Patrick F Chinnery

J Neurol Neurosurg Psychiatry· May 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A founder mutation in Anoctamin 5 is a major cause of limb-girdle muscular dystrophy.
Debbie Hicks, Anna Sarkozy, Nuria Muelas, Katrin Köehler, Angela Huebner, Geraldine Bailey

Brain· January 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis