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Items: 1 to 20 of 29

1.

Quality of life and functional outcome in early school-aged children after neonatal stroke: a prospective cohort study.

Darteyre S, Renaud C, Vuillerot C, Presles E, Kossorotoff M, Dinomais M, Lazaro L, Gautheron V, Chabrier S; AVCnn Group.

Eur J Paediatr Neurol. 2014 May;18(3):347-53. doi: 10.1016/j.ejpn.2014.01.006. Epub 2014 Jan 25.

PMID:
24503061
2.

Morbidity and mortality from ataxia-telangiectasia are associated with ATM genotype.

Micol R, Ben Slama L, Suarez F, Le Mignot L, Beauté J, Mahlaoui N, Dubois d'Enghien C, Laugé A, Hall J, Couturier J, Vallée L, Delobel B, Rivier F, Nguyen K, Billette de Villemeur T, Stephan JL, Bordigoni P, Bertrand Y, Aladjidi N, Pedespan JM, Thomas C, Pellier I, Koenig M, Hermine O, Picard C, Moshous D, Neven B, Lanternier F, Blanche S, Tardieu M, Debré M, Fischer A, Stoppa-Lyonnet D; CEREDIH Network Investigators.

J Allergy Clin Immunol. 2011 Aug;128(2):382-9.e1. doi: 10.1016/j.jaci.2011.03.052. Epub 2011 Jun 12.

PMID:
21665257
3.

Motor outcomes after neonatal arterial ischemic stroke related to early MRI data in a prospective study.

Husson B, Hertz-Pannier L, Renaud C, Allard D, Presles E, Landrieu P, Chabrier S; AVCnn Group.

Pediatrics. 2010 Oct;126(4):912-8. doi: 10.1542/peds.2009-3611. Epub 2010 Sep 20. Erratum in: Pediatrics. 2010 Nov;126(5):1053.

PMID:
20855393
4.

Low prevalence of coagulation F2 and F5 polymorphisms in mothers and children in a large cohort of patients with neonatal arterial ischemic stroke.

Renaud C, Tardy-Poncet B, Presles E, Chabrier S; AVCnn group.

Br J Haematol. 2010 Sep;150(6):709-12. doi: 10.1111/j.1365-2141.2010.08259.x. Review. No abstract available. Erratum in: Br J Haematol. 2010 Oct;151(1):110.

PMID:
20528875
5.

Lipoprotein (a), birth weight and neonatal stroke.

Renaud C, Bonneau C, Presles E, Laporte S, Depeyre A, Varlet MN, Chabrier S; AVCnn Group.

Neonatology. 2010;98(3):225-8. doi: 10.1159/000281015. Epub 2010 Apr 13.

PMID:
20428016
6.

Bilateral periventricular nodular heterotopia in France: frequency of mutations in FLNA, phenotypic heterogeneity and spectrum of mutations.

Solé G, Coupry I, Rooryck C, Guérineau E, Martins F, Devés S, Hubert C, Souakri N, Boute O, Marchal C, Faivre L, Landré E, Debruxelles S, Dieux-Coeslier A, Boulay C, Chassagnon S, Michel V, Routon MC, Toutain A, Philip N, Lacombe D, Villard L, Arveiler B, Goizet C.

J Neurol Neurosurg Psychiatry. 2009 Dec;80(12):1394-8. doi: 10.1136/jnnp.2008.162263.

PMID:
19917821
7.

Clinically observed chickenpox and the risk of childhood-onset multiple sclerosis.

Mikaeloff Y, Caridade G, Suissa S, Tardieu M; KIDSEP Study Group.

Am J Epidemiol. 2009 May 15;169(10):1260-6. doi: 10.1093/aje/kwp039. Epub 2009 Mar 27.

PMID:
19329530
8.

Effectiveness of early beta interferon on the first attack after confirmed multiple sclerosis: a comparative cohort study.

Mikaeloff Y, Caridade G, Tardieu M, Suissa S; KIDSEP study group of the French Neuropediatric Society.

Eur J Paediatr Neurol. 2008 May;12(3):205-9. Epub 2007 Sep 19.

PMID:
17881262
9.

A gene for an autosomal recessive lower motor neuron disease with childhood onset maps to 1p36.

Maystadt I, Zarhrate M, Leclair-Richard D, Estournet B, Barois A, Renault F, Routon MC, Durand MC, Lefebvre S, Munnich A, Verellen-Dumoulin C, Viollet L.

Neurology. 2006 Jul 11;67(1):120-4. Epub 2006 May 25.

PMID:
16728649
10.

[Maxillary and sphenoid sinusitis complicated by acute inflammatory optic neuritis in a 12-year-old patient].

Chanzy S, Routon MC, Bursztyn J, Maitrepierre E, Cheminée M, Msélati JC.

Arch Pediatr. 2005 Jan;12(1):46-8. French.

PMID:
15653054
11.

[The presentation of childhood systemic lupus erythematosus with neurological symptoms: three-case reports].

Chanzy S, Routon MC, Prieur AM, Larroche C, Mselati JC.

Rev Neurol (Paris). 2004 Sep;160(8-9):817-20. French.

PMID:
15454868
12.

Clinical findings and cytogenetic analysis of small supernumerary ring chromosomes 7: report of two new cases.

Chantot-Bastaraud S, Muti C, Pipiras E, Routon MC, Roubergue A, Burglen L, Siffroi JP, Simon-Bouy B.

Ann Genet. 2004 Jul-Sep;47(3):241-9. Review.

PMID:
15337469
13.

Demyelinating peripheral neuropathy associated with hemophagocytic lymphohistiocytosis. An immuno-electron microscopic study.

De Armas R, Sindou P, Gelot A, Routon MC, Ponsot G, Vallat JM.

Acta Neuropathol. 2004 Oct;108(4):341-4. Epub 2004 Jul 9.

PMID:
15243760
14.

[Loss of consciousness in a child due to loperamide].

Chanzy S, Moretti S, Mayet H, Routon MC, De Gennes C, Msélati JC.

Arch Pediatr. 2004 Jul;11(7):826-7. French.

PMID:
15234380
15.

[Unusual good prognosis for X-linked myotubular myopathy].

Chanzy S, Routon MC, Moretti S, de Gennes C, Mselati JC.

Arch Pediatr. 2003 Aug;10(8):707-9. French.

PMID:
12922003
16.

Possible founder effect of rapsyn N88K mutation and identification of novel rapsyn mutations in congenital myasthenic syndromes.

Richard P, Gaudon K, Andreux F, Yasaki E, Prioleau C, Bauché S, Barois A, Ioos C, Mayer M, Routon MC, Mokhtari M, Leroy JP, Fournier E, Hainque B, Koenig J, Fardeau M, Eymard B, Hantaï D.

J Med Genet. 2003 Jun;40(6):e81. No abstract available.

17.

Congenital insensitivity to pain with anhydrosis. Report of two unrelated cases.

Vital A, Fontan D, Julien J, Talon P, Héron B, Routon MC, Ponsot G, Vital C.

J Peripher Nerv Syst. 1998;3(2):125-32.

PMID:
10959246
18.

X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: clinical and electrophysiologic study.

Birouk N, LeGuern E, Maisonobe T, Rouger H, Gouider R, Tardieu S, Gugenheim M, Routon MC, Léger JM, Agid Y, Brice A, Bouche P.

Neurology. 1998 Apr;50(4):1074-82.

PMID:
9566397
19.

[Biopercular polymicrogyria associated with congenital ophthalmoplegia caused by nuclear lesion of the common oculomotor nerve].

Routon MC, Expert-Bezançon MC, Bursztyn J, Mselati JC, Robain O.

Rev Neurol (Paris). 1994;150(5):363-9. French.

PMID:
7878323
20.

[Herpes encephalitis in newborn infants. Retrospective study of 12 cases].

Bigotte J, Mselati JC, Routon MC, Noui Mehidi F, Lebon P, Ponsot G.

Arch Fr Pediatr. 1993 Mar;50(3):209-14. French.

PMID:
8338413

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