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Year Number of Results
1978 1
1979 1
1980 3
1981 1
1982 2
1984 1
1991 2
1992 4
1993 2
1994 2
1995 6
1996 4
1997 9
1998 6
1999 1
2000 2
2001 2
2003 3
2004 6
2005 3
2006 4
2007 5
2008 10
2010 5
2011 2
2012 4
2013 3
2014 3
2015 4
2016 1
2017 1
2019 1
2020 1
2021 1
2022 1
2024 0

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99 results

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Page 1
Diagnostic accuracy and usability of the EMBalance decision support system for vestibular disorders in primary care: proof of concept randomised controlled study results.
Bamiou DE, Kikidis D, Bibas T, Koohi N, Macdonald N, Maurer C, Wuyts FL, Ihtijarevic B, Celis L, Mucci V, Maes L, Van Rompaey V, Van de Heyning P, Nazareth I, Exarchos TP, Fotiadis D, Koutsouris D, Luxon LM. Bamiou DE, et al. Among authors: luxon lm. J Neurol. 2022 May;269(5):2584-2598. doi: 10.1007/s00415-021-10829-7. Epub 2021 Oct 20. J Neurol. 2022. PMID: 34669009 Free PMC article. Clinical Trial.
The Pediatric Vestibular Symptom Questionnaire: A Validation Study.
Pavlou M, Whitney S, Alkathiry AA, Huett M, Luxon LM, Raglan E, Godfrey EL, Eva-Bamiou D. Pavlou M, et al. Among authors: luxon lm. J Pediatr. 2016 Jan;168:171-177.e1. doi: 10.1016/j.jpeds.2015.09.075. Epub 2015 Oct 30. J Pediatr. 2016. PMID: 26522978 Free article.
A detailed clinical and molecular survey of subjects with nonsyndromic USH2A retinopathy reveals an allelic hierarchy of disease-causing variants.
Lenassi E, Vincent A, Li Z, Saihan Z, Coffey AJ, Steele-Stallard HB, Moore AT, Steel KP, Luxon LM, Héon E, Bitner-Glindzicz M, Webster AR. Lenassi E, et al. Among authors: luxon lm. Eur J Hum Genet. 2015 Oct;23(10):1318-27. doi: 10.1038/ejhg.2014.283. Epub 2015 Feb 4. Eur J Hum Genet. 2015. PMID: 25649381 Free PMC article.
Clinical heterogeneity in a family with mutations in USH2A.
Lenassi E, Robson AG, Luxon LM, Bitner-Glindzicz M, Webster AR. Lenassi E, et al. Among authors: luxon lm. JAMA Ophthalmol. 2015 Mar;133(3):352-5. doi: 10.1001/jamaophthalmol.2014.5163. JAMA Ophthalmol. 2015. PMID: 25521520 No abstract available.
Mobile telephone use effects on perception of verticality.
Bamiou DE, Ceranic B, Vickers D, Zamyslowska-Szmytke E, Cox R, Chadwick P, Luxon LM. Bamiou DE, et al. Among authors: luxon lm. Bioelectromagnetics. 2015 Jan;36(1):27-34. doi: 10.1002/bem.21877. Epub 2014 Sep 26. Bioelectromagnetics. 2015. PMID: 25263937
Screening for duplications, deletions and a common intronic mutation detects 35% of second mutations in patients with USH2A monoallelic mutations on Sanger sequencing.
Steele-Stallard HB, Le Quesne Stabej P, Lenassi E, Luxon LM, Claustres M, Roux AF, Webster AR, Bitner-Glindzicz M. Steele-Stallard HB, et al. Among authors: luxon lm. Orphanet J Rare Dis. 2013 Aug 8;8:122. doi: 10.1186/1750-1172-8-122. Orphanet J Rare Dis. 2013. PMID: 23924366 Free PMC article.
99 results