Julie Hall

发表

Outcome after surgical or conservative management of cerebral cavernous malformations

C. Warlow, G. Murray, C. Counsell, 2014, Neurology.

LRPPRC mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population

Robert W. Taylor, H. Prokisch, M. Simpson, 2015, Brain : a journal of neurology.

Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits

Robert W. Taylor, H. Prokisch, M. Simpson, 2017, neurogenetics.

WE-146. Whole-body fasciculation detection in Amyotrophic Lateral Sclerosis (ALS) using motor unit MRI (MUMRI)

I. Schofield, R. Whittaker, L. Heskamp, 2022, Clinical Neurophysiology.

Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder

Matthew H. Brush, Sarah E. Gould, Jean M. Davidson, 2018, American journal of human genetics.

Nature, frequency and natural history of intracranial cavernous malformations in adults

Julie M Hall, Julie Hall, 2014 .

Forecasting stroke-like episodes and outcomes in mitochondrial disease

Robert W. Taylor, D. Erskine, N. Lax, 2021, Brain : a journal of neurology.

Ultrasound‐guided motor unit scanning electromyography

I. Schofield, R. Whittaker, B. Stenberg, 2022, Muscle & nerve.

Diagnosis and management of multiple sclerosis: MRI in clinical practice

V. Tomassini, O. Pearson, V. Sawlani, 2020, Journal of Neurology.