Publications by authors named "Neil Stoodley"

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Rate and severity of radiological features of physical abuse in children during the first UK-wide COVID-19 enforced national lockdown.
Stavros Stivaros, Michael Paddock, Azita Rajai, Helen Cliffe, Daniel Ja Connolly, Neil Stoodley

Arch Dis Child· June 2022

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Clinical and Functional Characterization of the Recurrent TUBA1A p.(Arg2His) Mutation.
Jennifer F Gardner, Thomas D Cushion, Georgios Niotakis, Heather E Olson, P Ellen Grant, Neil Stoodley

Brain Sci· August 2018

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De novo mutations in GRIN1 cause extensive bilateral polymicrogyria.
Andrew E Fry, Katherine A Fawcett, Nathanel Zelnik, Hongjie Yuan, Belinda A N Thompson, Neil Stoodley

Brain· March 2018

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Initial response of the European Society of Paediatric Radiology and Society for Pediatric Radiology to the Swedish Agency for Health Technology Assessment and Assessment of Social Services' document on the triad of shaken baby syndrome.
Amaka C Offiah, Sabah Servaes, Catherine S Adamsbaum, Maria I Argyropoulou, Katharine E Halliday, Neil Stoodley

Pediatr Radiol· April 2017

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Neuropsychiatric disease in patients with periventricular heterotopia.
Andrew E Fry, Michael P Kerr, Frances Gibbon, Peter D Turnpenny, Khalid Hamandi, Neil Stoodley

J Neuropsychiatry Clin Neurosci· September 2013

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Every picture does not (always) tell a story.
Neil Stoodley

Dev Med Child Neurol· July 2013

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Overlapping cortical malformations and mutations in TUBB2B and TUBA1A.
Thomas D Cushion, William B Dobyns, Jonathan G L Mullins, Neil Stoodley, Seo-Kyung Chung

Brain· February 2013

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Childhood presentation of COL4A1 mutations.
Siddharth Shah, Sian Ellard, Rachel Kneen, Ming Lim, Nigel Osborne, Neil Stoodley

Dev Med Child Neurol· June 2012

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Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patients.
Richard J Leventer, Anna Jansen, Daniela T Pilz, Neil Stoodley, Carla Marini

Brain· May 2010

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A dominantly inherited mutation in collagen IV A1 (COL4A1) causing childhood onset stroke without porencephaly.
Siddharth Shah, Yadlapalli Kumar, Brendan McLean, Amanda Churchill, Neil Stoodley

Eur J Paediatr Neurol· March 2010

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Mutation of the variant alpha-tubulin TUBA8 results in polymicrogyria with optic nerve hypoplasia.
Mohammad R Abdollahi, Ewan Morrison, Tamara Sirey, Zoltan Molnar, Bruce E Hayward, Neil Stoodley

Am J Hum Genet· November 2009

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Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation.
Nathaniel H Robin, Clare J Taylor, Donna M McDonald-McGinn, Elaine H Zackai, Peter Bingham, Neil Stoodley

Am J Med Genet A· November 2006

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Mutation in Rab3 GTPase-activating protein (RAB3GAP) noncatalytic subunit in a kindred with Martsolf syndrome.
Irene A Aligianis, Neil V Morgan, Marina Mione, Colin A Johnson, Elisabeth Rosser, Neil Stoodley

Am J Hum Genet· April 2006

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Non-accidental head injury in children: gathering the evidence.
Neil Stoodley

Lancet· July 2002

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Neuronal migration, cerebral cortical development, and cerebral cortical anomalies.
Daniela Pilz, Neil Stoodley, Jeffrey A Golden

J Neuropathol Exp Neurol· January 2002

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