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196 results

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Page 1
Infantile bilateral striatal necrosis following measles.
Cambonie G, Houdon L, Rivier F, Bongrand AF, Echenne B. Cambonie G, et al. Among authors: rivier f. Brain Dev. 2000 Jun;22(4):221-3. doi: 10.1016/s0387-7604(00)00105-4. Brain Dev. 2000. PMID: 10838107
[Acute motor deficit in childhood: diagnosis management].
Roubertie A, Soëte S, Meyer P, Echenne B, Rivier F, Langlois C. Roubertie A, et al. Among authors: rivier f. Arch Pediatr. 2010 Mar;17(3):325-32. doi: 10.1016/j.arcped.2009.11.017. Epub 2009 Dec 31. Arch Pediatr. 2010. PMID: 20045298 Review. French.
[Convulsions of infants and children].
Carneiro M, Meyer P, Rivier F. Carneiro M, et al. Among authors: rivier f. Rev Prat. 2010 Apr 20;60(4):543-50. Rev Prat. 2010. PMID: 20465134 French. No abstract available.
[Childhood parvovirus B19 encephalitis].
Meyer P, Jeziorski E, Bott-Gilton L, Foulongne V, Rivier F, Rondoin G, Rodière M. Meyer P, et al. Among authors: rivier f. Arch Pediatr. 2011 Dec;18(12):1315-9. doi: 10.1016/j.arcped.2011.08.013. Epub 2011 Oct 1. Arch Pediatr. 2011. PMID: 21963073 French.
Partial acute transverse myelitis is a predictor of multiple sclerosis in children.
Meyer P, Leboucq N, Molinari N, Roubertie A, Carneiro M, Walther-Louvier U, Cuntz-Shadfar D, Leydet J, Cheminal R, Cambonie G, Echenne B, Rondouin G, Deiva K, Mikaeloff Y, Rivier F. Meyer P, et al. Among authors: rivier f. Mult Scler. 2014 Oct;20(11):1485-93. doi: 10.1177/1352458514526943. Epub 2014 Mar 11. Mult Scler. 2014. PMID: 24619933
[Mitochondrial neurogastrointestinal encephalopathy disease].
Benureau A, Meyer P, Maillet O, Leboucq N, Legras S, Jeziorski E, Fournier-Favre S, Jeandel C, Gaignard P, Slama A, Rivier F, Roubertie A, Carneiro M. Benureau A, et al. Among authors: rivier f. Arch Pediatr. 2014 Dec;21(12):1370-4. doi: 10.1016/j.arcped.2014.08.006. Epub 2014 Oct 2. Arch Pediatr. 2014. PMID: 25282463 French.
Mutation in NDUFA13/GRIM19 leads to early onset hypotonia, dyskinesia and sensorial deficiencies, and mitochondrial complex I instability.
Angebault C, Charif M, Guegen N, Piro-Megy C, Mousson de Camaret B, Procaccio V, Guichet PO, Hebrard M, Manes G, Leboucq N, Rivier F, Hamel CP, Lenaers G, Roubertie A. Angebault C, et al. Among authors: rivier f. Hum Mol Genet. 2015 Jul 15;24(14):3948-55. doi: 10.1093/hmg/ddv133. Epub 2015 Apr 21. Hum Mol Genet. 2015. PMID: 25901006
Mosaic parental germline mutations causing recurrent forms of malformations of cortical development.
Zillhardt JL, Poirier K, Broix L, Lebrun N, Elmorjani A, Martinovic J, Saillour Y, Muraca G, Nectoux J, Bessieres B, Fallet-Bianco C, Lyonnet S, Dulac O, Odent S, Rejeb I, Ben Jemaa L, Rivier F, Pinson L, Geneviève D, Musizzano Y, Bigi N, Leboucq N, Giuliano F, Philip N, Vilain C, Van Bogaert P, Maurey H, Beldjord C, Artiguenave F, Boland A, Olaso R, Masson C, Nitschké P, Deleuze JF, Bahi-Buisson N, Chelly J. Zillhardt JL, et al. Among authors: rivier f. Eur J Hum Genet. 2016 Apr;24(4):611-4. doi: 10.1038/ejhg.2015.192. Epub 2015 Sep 23. Eur J Hum Genet. 2016. PMID: 26395554 Free PMC article.
196 results