Publications by Dr Sally Spendiff - ePrints

Browsing publications by Dr Sally Spendiff.

Newcastle Authors	Title	Year
Cecilia Jimenez Moreno Dr Nikoletta Nikolenko Professor Grainne Gorman Gabriella-Denisa Hathazi Dr Sally Spendiff et al.	Periostin as a blood biomarker of muscle cell fibrosis, cardiomyopathy and disease severity in myotonic dystrophy type 1	2023
Dr Sally Spendiff Rachel Howarth Dr Grace McMacken Tracey Davey Dr Andreas Roos et al.	Modulation of the Acetylcholine Receptor Clustering Pathway Improves Neuromuscular Junction Structure and Muscle Strength in a Mouse Model of Congenital Myasthenic Syndrome	2020
Dr Grace McMacken Dr Sally Spendiff Professor Roger Whittaker Emily O'Connor Rachel Howarth et al.	Salbutamol modifies the neuromuscular junction in a mouse model of ColQ myasthenic syndrome	2019
Daniel Cox Silvia Cipriani Dr Sally Spendiff Emily O'Connor Professor Rita Horvath et al.	SIL1 deficiency causes degenerative changes of peripheral nerves and neuromuscular junctions in fish, mice and human	2019
Emily O'Connor Dr Ana Topf Dr Sally Spendiff Daniel Cox Dr Andreas Roos et al.	Clinical and research strategies for limb-girdle congenital myasthenic syndromes	2018
Dr Sally Spendiff Emeritus Professor Clarke Slater Dr Andreas Roos Professor Hanns Lochmuller	GFPT1 deficiency in muscle leads to myasthenia and myopathy in mice	2018
Dr Emma Brunton Dr Sally Spendiff Professor Kianoush Nazarpour	Influence of nerve cuff channel count and implantation site on the separability of afferent ENG	2018
Silvia Cipriani Professor Rita Horvath Professor Hanns Lochmuller Dr Andreas Roos Dr Sally Spendiff et al.	Neuromuscular junction changes in a mouse model of charcot-marie-tooth disease type 4C	2018
Dr Emma Brunton Dr Sally Spendiff Professor Kianoush Nazarpour	Positioning the nerve cuff distally on the sciatic nerve improves the classification of ankle-movement proprioceptive ENG signals	2018
Dr Grace McMacken Dr Teresinha Evangelista Dr Sally Spendiff Professor Hanns Lochmuller	The Increasing Genetic and Phenotypical Diversity of Congenital Myasthenic Syndromes	2017