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287 results

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Page 1
Presymptomatic genetic testing in CADASIL.
Reyes S, Kurtz A, Hervé D, Tournier-Lasserve E, Chabriat H. Reyes S, et al. Among authors: herve d. J Neurol. 2012 Oct;259(10):2131-6. doi: 10.1007/s00415-012-6468-8. Epub 2012 Mar 15. J Neurol. 2012. PMID: 22418996
Longitudinal diffusion changes in cerebral hemispheres after MCA infarcts.
Buffon F, Molko N, Hervé D, Porcher R, Denghien I, Pappata S, Le Bihan D, Bousser MG, Chabriat H. Buffon F, et al. Among authors: herve d. J Cereb Blood Flow Metab. 2005 May;25(5):641-50. doi: 10.1038/sj.jcbfm.9600054. J Cereb Blood Flow Metab. 2005. PMID: 15689956
White matter changes contribute to corpus callosum atrophy in the elderly: the LADIS study.
Ryberg C, Rostrup E, Sjöstrand K, Paulson OB, Barkhof F, Scheltens P, van Straaten EC, Fazekas F, Schmidt R, Erkinjuntti T, Wahlund LO, Basile AM, Pantoni L, Inzitari D, Waldemar G; LADIS study group. Ryberg C, et al. AJNR Am J Neuroradiol. 2008 Sep;29(8):1498-504. doi: 10.3174/ajnr.A1169. Epub 2008 Jun 12. AJNR Am J Neuroradiol. 2008. PMID: 18556357 Free PMC article.
Three-dimensional MRI analysis of individual volume of Lacunes in CADASIL.
Hervé D, Godin O, Dufouil C, Viswanathan A, Jouvent E, Pachaï C, Guichard JP, Bousser MG, Dichgans M, Chabriat H. Hervé D, et al. Stroke. 2009 Jan;40(1):124-8. doi: 10.1161/STROKEAHA.108.520825. Epub 2008 Oct 23. Stroke. 2009. PMID: 18948610 Free PMC article.
Location of lacunar infarcts correlates with cognition in a sample of non-disabled subjects with age-related white-matter changes: the LADIS study.
Benisty S, Gouw AA, Porcher R, Madureira S, Hernandez K, Poggesi A, van der Flier WM, Van Straaten EC, Verdelho A, Ferro J, Pantoni L, Inzitari D, Barkhof F, Fazekas F, Chabriat H; LADIS Study group. Benisty S, et al. J Neurol Neurosurg Psychiatry. 2009 May;80(5):478-83. doi: 10.1136/jnnp.2008.160440. Epub 2009 Feb 11. J Neurol Neurosurg Psychiatry. 2009. PMID: 19211595 Free article.
Changes in white matter as determinant of global functional decline in older independent outpatients: three year follow-up of LADIS (leukoaraiosis and disability) study cohort.
Inzitari D, Pracucci G, Poggesi A, Carlucci G, Barkhof F, Chabriat H, Erkinjuntti T, Fazekas F, Ferro JM, Hennerici M, Langhorne P, O'Brien J, Scheltens P, Visser MC, Wahlund LO, Waldemar G, Wallin A, Pantoni L; LADIS Study Group. Inzitari D, et al. BMJ. 2009 Jul 6;339:b2477. doi: 10.1136/bmj.b2477. BMJ. 2009. PMID: 19581317 Free PMC article.
A hereditary moyamoya syndrome with multisystemic manifestations.
Hervé D, Touraine P, Verloes A, Miskinyte S, Krivosic V, Logeart D, Alili N, Laredo JD, Gaudric A, Houdart E, Metzger JP, Tournier-Lasserve E, Woimant F. Hervé D, et al. Neurology. 2010 Jul 20;75(3):259-64. doi: 10.1212/WNL.0b013e3181e8ee3f. Neurology. 2010. PMID: 20644152
287 results