Publications by authors named "Malcolm Howard"

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Correction: Seven years on from the Canadian Airway Focus Group Difficult Airway Guidelines: an observational survey.
Malcolm Howard, Ruediger Noppens, Nelson Gonzalez, Philip M Jones, Sonja M Payne

Can J Anaesth· July 2024

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Inhaled milrinone for the management of severe pulmonary hypertension in non-cardiac surgery.
Philip Stamov, Malcolm Howard, Craig Railton, Wilfredo Puentes

Anaesthesiol Intensive Ther· January 2024

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Seven years on from the Canadian Airway Focus Group Difficult Airway Guidelines: an observational survey.
Malcolm Howard, Ruediger Noppens, Nelson Gonzalez, Philip M Jones, Sonja M Payne

Can J Anaesth· September 2021

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Analysis of exome data for 4293 trios suggests GPI-anchor biogenesis defects are a rare cause of developmental disorders.
Alistair T Pagnamenta, Yoshiko Murakami, John M Taylor, Consuelo Anzilotti, Malcolm F Howard

Eur J Hum Genet· June 2017

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Activation of an exonic splice-donor site in exon 30 of in a patient with severe microcephaly and pigmentary abnormalities.
Alistair T Pagnamenta, Malcolm F Howard, Samantha J L Knight, David A Keays, Gerardine Quaghebeur

Clin Case Rep· October 2016

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Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin-Siris syndrome.
Annmarie Hempel, Alistair T Pagnamenta, Moira Blyth, Sahar Mansour, Vivienne McConnell, Malcolm F Howard

J Med Genet· March 2016

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Mutations in PIGY: expanding the phenotype of inherited glycosylphosphatidylinositol deficiencies.
Biljana Ilkovski, Alistair T Pagnamenta, Gina L O'Grady, Taroh Kinoshita, Malcolm F Howard

Hum Mol Genet· November 2015

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Germline recessive mutations in PI4KA are associated with perisylvian polymicrogyria, cerebellar hypoplasia and arthrogryposis.
Alistair T Pagnamenta, Malcolm F Howard, Eva Wisniewski, Niko Popitsch, Samantha J L Knight

Hum Mol Genet· July 2015

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Factors influencing success of clinical genome sequencing across a broad spectrum of disorders.
Jenny C Taylor, Hilary C Martin, Stefano Lise, John Broxholme, Jean-Baptiste Cazier, Malcolm Howard

Nat Genet· July 2015

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Mutations in PGAP3 impair GPI-anchor maturation, causing a subtype of hyperphosphatasia with mental retardation.
Malcolm F Howard, Yoshiko Murakami, Alistair T Pagnamenta, Cornelia Daumer-Haas, Björn Fischer

Am J Hum Genet· February 2014

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Social buffering by God: prayer and measures of stress.
Jennifer N Belding, Malcolm G Howard, Anne M McGuire, Amanda C Schwartz, Janie H Wilson

J Relig Health· June 2010

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