S. Grew

发表

Nasal High Flow in Room Air for Hypoxemic Bronchiolitis Infants

J. Fraser, F. Babl, S. Moloney, 2019, Front. Pediatr..

Histopathological Findings in Hereditary Motor and Sensory Neuropathy of Axonal Type With Onset in Early Childhood Associated With Mitofusin 2 Mutations

J. Pollard, J. Vallat, M. Ryan, 2008, Journal of neuropathology and experimental neurology.

Severe early-onset axonal neuropathy with homozygous and compound heterozygous MFN2 mutations

J. Vallat, M. Ryan, F. Sturtz, 2008, Neurology.

Multicentre, randomised trial to investigate early nasal high—flow therapy in paediatric acute hypoxaemic respiratory failure: a protocol for a randomised controlled trial—a Paediatric Acute respiratory Intervention Study (PARIS 2)

J. Fraser, F. Babl, S. Moloney, 2019, BMJ Open.

Mechanisms of disease and clinical features of mutations of the gene for mitofusin 2: an important cause of hereditary peripheral neuropathy with striking clinical variability in children and adults

R. Ouvrier, S. Grew, 2010, Developmental medicine and child neurology.

Al 9 BSi 2 O 19 , a new mineral from granulite-facies metapelites , Mount Sta ff ord , central Australia : a natural analogue of a synthetic “ boron-mullite ”

Armbruster, G. Yates, S. Grew, 2008 .

Mechanisms of disease and clinical features of mutations of the gene for mitofusin 2: an important cause of hereditary peripheral neuropathy with striking clinical variability in children and adults

R. Ouvrier, S. Grew, 2010, Developmental medicine and child neurology.

Effect of Early High-Flow Nasal Oxygen vs Standard Oxygen Therapy on Length of Hospital Stay in Hospitalized Children With Acute Hypoxemic Respiratory Failure: The PARIS-2 Randomized Clinical Trial.

F. Babl, S. Moloney, J. Acworth, 2023, JAMA.

Severe early-onset axonal neuropathy with homozygous and compound heterozygous MFN2 mutations

R. Ouvrier, C. Magdelaine, S. Grew, 2008, Neurology.