Julie M Hall

发表

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.

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.

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.

Forecasting stroke-like episodes and outcomes in mitochondrial disease

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

Untreated clinical course of cerebral cavernous malformations: a prospective, population-based cohort study

C. Warlow, G. Murray, R. Salman, 2012, The Lancet Neurology.

Outcome after surgical or conservative management of cerebral cavernous malformations

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

Ventriculitis from a pituitary prolactinoma: bacterial or chemical?

S. Pearce, A. Jenkins, B. P. Jayasekera, 2017, British journal of neurosurgery.

Comparison of the Retinomax autorefractor with hand‐held retinoscopy in 1‐year‐old infants

G. Gole, D. Colville, P. Schluter, 2003, Clinical & experimental ophthalmology.

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

Julie M Hall, Julie Hall, 2014 .

Diagnosis and management of multiple sclerosis: MRI in clinical practice

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

Ultrasound‐guided motor unit scanning electromyography

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