Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 2
2006 2
2009 2
2010 2
2012 1
2013 3
2017 1
2018 2
2022 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

15 results

Results by year

Filters applied: . Clear all
Page 1
Childhood presentation of COL4A1 mutations.
Shah S, Ellard S, Kneen R, Lim M, Osborne N, Rankin J, Stoodley N, van der Knaap M, Whitney A, Jardine P. Shah S, et al. Among authors: stoodley n. Dev Med Child Neurol. 2012 Jun;54(6):569-74. doi: 10.1111/j.1469-8749.2011.04198.x. Epub 2012 Jan 16. Dev Med Child Neurol. 2012. PMID: 22574627 Free article. Review.
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.
Offiah AC, Servaes S, Adamsbaum CS, Argyropoulou MI, Halliday KE, Jaspan T, Owens CM, Raissaki M, Rosendahl K, Stoodley N, Van Rijn RR, Callahan MJ, Chung T, Donaldson JS, Jaramillo D, Slovis TL, Strouse PJ. Offiah AC, et al. Among authors: stoodley n. Pediatr Radiol. 2017 Apr;47(4):369-371. doi: 10.1007/s00247-017-3808-y. Epub 2017 Feb 23. Pediatr Radiol. 2017. PMID: 28233046 Free article. No abstract available.
De novo mutations in GRIN1 cause extensive bilateral polymicrogyria.
Fry AE, Fawcett KA, Zelnik N, Yuan H, Thompson BAN, Shemer-Meiri L, Cushion TD, Mugalaasi H, Sims D, Stoodley N, Chung SK, Rees MI, Patel CV, Brueton LA, Layet V, Giuliano F, Kerr MP, Banne E, Meiner V, Lerman-Sagie T, Helbig KL, Kofman LH, Knight KM, Chen W, Kannan V, Hu C, Kusumoto H, Zhang J, Swanger SA, Shaulsky GH, Mirzaa GM, Muir AM, Mefford HC, Dobyns WB, Mackenzie AB, Mullins JGL, Lemke JR, Bahi-Buisson N, Traynelis SF, Iago HF, Pilz DT. Fry AE, et al. Among authors: stoodley n. Brain. 2018 Mar 1;141(3):698-712. doi: 10.1093/brain/awx358. Brain. 2018. PMID: 29365063 Free PMC article.
Clinical and Functional Characterization of the Recurrent TUBA1A p.(Arg2His) Mutation.
Gardner JF, Cushion TD, Niotakis G, Olson HE, Grant PE, Scott RH, Stoodley N, Cohen JS, Naidu S, Attie-Bitach T, Bonnières M, Boutaud L, Encha-Razavi F, Palmer-Smith SM, Mugalaasi H, Mullins JGL, Pilz DT, Fry AE. Gardner JF, et al. Among authors: stoodley n. Brain Sci. 2018 Aug 7;8(8):145. doi: 10.3390/brainsci8080145. Brain Sci. 2018. PMID: 30087272 Free PMC article.
Rate and severity of radiological features of physical abuse in children during the first UK-wide COVID-19 enforced national lockdown.
Stivaros S, Paddock M, Rajai A, Cliffe H, Connolly DJ, Dineen RA, Dixon R, Edwards H, Evans E, Halliday K, Jackson K, Landes C, Oates AJ, Stoodley N, Offiah AC. Stivaros S, et al. Among authors: stoodley n. Arch Dis Child. 2022 Jun;107(6):575-581. doi: 10.1136/archdischild-2021-323444. Epub 2022 Feb 17. Arch Dis Child. 2022. PMID: 35177407 Free article.
Every picture does not (always) tell a story.
Stoodley N. Stoodley N. Dev Med Child Neurol. 2013 Jul;55(7):589-90. doi: 10.1111/dmcn.12134. Epub 2013 Apr 1. Dev Med Child Neurol. 2013. PMID: 23550843 Free article. No abstract available.
Overlapping cortical malformations and mutations in TUBB2B and TUBA1A.
Cushion TD, Dobyns WB, Mullins JG, Stoodley N, Chung SK, Fry AE, Hehr U, Gunny R, Aylsworth AS, Prabhakar P, Uyanik G, Rankin J, Rees MI, Pilz DT. Cushion TD, et al. Among authors: stoodley n. Brain. 2013 Feb;136(Pt 2):536-48. doi: 10.1093/brain/aws338. Epub 2013 Jan 29. Brain. 2013. PMID: 23361065
Neuropsychiatric disease in patients with periventricular heterotopia.
Fry AE, Kerr MP, Gibbon F, Turnpenny PD, Hamandi K, Stoodley N, Robertson SP, Pilz DT. Fry AE, et al. Among authors: stoodley n. J Neuropsychiatry Clin Neurosci. 2013 Winter;25(1):26-31. doi: 10.1176/appi.neuropsych.11110336. J Neuropsychiatry Clin Neurosci. 2013. PMID: 23487190
15 results