Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1979 2
1982 1
1988 2
1989 1
1990 1
1991 1
1992 1
1993 1
1994 1
1998 2
2003 2
2004 4
2005 1
2006 1
2009 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

22 results

Results by year

Filters applied: . Clear all
Page 1
Peripheral neuropathy associated with erythrophagocytic lymphohistiocytosis.
Boutin B, Routon MC, Rocchiccioli F, Mayer M, Leverger G, Robain O, Ponsot G, Arthuis M. Boutin B, et al. Among authors: routon mc. J Neurol Neurosurg Psychiatry. 1988 Feb;51(2):291-4. doi: 10.1136/jnnp.51.2.291. J Neurol Neurosurg Psychiatry. 1988. PMID: 3346698 Free PMC article.
[Heatstroke in children].
Routon MC, Mselati JC. Routon MC, et al. Rev Prat. 1982 Apr 11;32(21):1441-5. Rev Prat. 1982. PMID: 7089457 French. No abstract available.
[Intravenous immunoglobulins and aseptic meningitis].
Mselati JC, Carlier JC, Routon MC, Noui Mehidi F, de Gennes C. Mselati JC, et al. Among authors: routon mc. Arch Fr Pediatr. 1992 Mar;49(3):216. Arch Fr Pediatr. 1992. PMID: 1610283 French. No abstract available.
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. Solé G, et al. Among authors: routon mc. J Neurol Neurosurg Psychiatry. 2009 Dec;80(12):1394-8. doi: 10.1136/jnnp.2008.162263. J Neurol Neurosurg Psychiatry. 2009. PMID: 19917821
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. Richard P, et al. Among authors: routon mc. J Med Genet. 2003 Jun;40(6):e81. doi: 10.1136/jmg.40.6.e81. J Med Genet. 2003. PMID: 12807980 Free PMC article. No abstract available.
22 results