Publications by Dr Nuria Muelas Gomez - ePrints

Browsing publications by Dr Nuria Muelas Gomez.

Newcastle Authors	Title	Year
Roberto Fernandez-Torron Dr ursula Moore Dr German Moris Dr Nuria Muelas Gomez	Muscle MRI characteristic pattern for late-onset TK2 deficiency diagnosis	2022
Dr Ana Topf Professor Jordi Diaz Manera Dr Nuria Muelas Gomez Dr Teresinha Evangelista Dr Yoshiteru Azuma et al.	Molecular characterization of congenital myasthenic syndromes in Spain	2017
Professor Jordi Diaz Manera Aida Alejaldre Dr Nuria Muelas Gomez Roberto Fernandez-Torron	Muscle imaging in muscle dystrophies produced by mutations in the EMD and LMNA genes	2016
Dr Amina Chaouch Dr Nuria Muelas Gomez Professor Hanns Lochmuller	A retrospective clinical study of the treatment of slow-channel congenital myasthenic syndrome	2012
Dr Amina Chaouch Ana Nascimento Dr Nuria Muelas Gomez Professor Hanns Lochmuller	A retrospective clinical study of the treatment of slow-channel congenital myasthenic syndrome	2012
Dr Nuria Muelas Gomez Professor Michael Hanna Dr Amina Chaouch Professor Volker Straub Emerita Professor Katherine Bushby et al.	Congenital myasthenic syndrome with tubular aggregates caused by GFPT1 mutations	2012
Dr Debbie Hicks Dr Anna Sarkozy Dr Nuria Muelas Gomez Professor Gavin Hudson Professor Patrick Chinnery et al.	A founder mutation in Anoctamin 5 is a major cause of limb girdle muscular dystrophy	2011
Dr Debbie Hicks Dr Anna Sarkozy Dr Nuria Muelas Gomez Professor Gavin Hudson Professor Patrick Chinnery et al.	A founder mutation in Anoctamin 5 is a major cause of limb-girdle muscular dystrophy	2011
Dr Debbie Hicks Dr Anna Sarkozy Dr Nuria Muelas Gomez Professor Gavin Hudson Dr Rita Barresi et al.	Mutations in ANO5 represent a common cause of non-dysferlin LGMD2B and Miyoshi myopathy	2010