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Items: 22

1.

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
2.

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
3.

[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
4.

[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
5.

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
6.

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
7.

[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
8.

[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
9.

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.

10.

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
11.

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
12.

[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
13.

[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
14.

[Intravenous immunoglobulins and aseptic meningitis].

Mselati JC, Carlier JC, Routon MC, Noui Mehidi F, de Gennes C.

Arch Fr Pediatr. 1992 Mar;49(3):216. French. No abstract available.

PMID:
1610283
15.

[Congenital hereditary motor and sensory neuropathy].

Routon MC, Robain O, Mayer M, Jardin L, Ponsot G.

Rev Neurol (Paris). 1991;147(8-9):577-85. Review. French.

PMID:
1962067
16.

["Blueberry muffin baby": neonatal extramedullary hematopoiesis? Involutive congenital monoblastic leukemia? Or involutive congenital histiocytosis?].

Enjolras O, Leibowitch M, Guillemette J, Mathieu AM, Routon MC, Escande JP.

Ann Dermatol Venereol. 1990;117(11):810-2. French. No abstract available.

PMID:
2099688
17.

[Giant axonal neuropathy: intermediate filament disease with involvement of the peripheral and central nervous system].

Buissonnière RF, Routon MC, Robain O, Ponsot G, Arthuis M.

Rev Neurol (Paris). 1989;145(5):355-61. Review. French.

PMID:
2662338
18.

Menkes disease: a Golgi and electron microscopic study of the cerebellar cortex.

Robain O, Aubourg P, Routon MC, Dulac O, Ponsot G.

Clin Neuropathol. 1988 Mar-Apr;7(2):47-52.

PMID:
3390973
19.

Peripheral neuropathy associated with erythrophagocytic lymphohistiocytosis.

Boutin B, Routon MC, Rocchiccioli F, Mayer M, Leverger G, Robain O, Ponsot G, Arthuis M.

J Neurol Neurosurg Psychiatry. 1988 Feb;51(2):291-4.

20.

[Heatstroke in children].

Routon MC, Mselati JC.

Rev Prat. 1982 Apr 11;32(21):1441-5. French. No abstract available.

PMID:
7089457
21.

[Neonatal cardiac tumour: diagnostic and therapeutic problems. One case (author's transl)].

Routon MC, Lavaud J, Lejeune C, Batisse A, Bex J, Cloup M.

Nouv Presse Med. 1979 Jun 16;8(27):2265-8. French.

PMID:
492999
22.

[Hemineurine: an always present hazard in children].

Lavaud J, Himon F, Laudignon N, Routon MC, Cloup M.

Arch Fr Pediatr. 1979 Jan;36(1):56-8. French.

PMID:
444000

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