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Results by year

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

Year Number of Results
1956 1
1958 2
1959 1
1960 1
1961 2
1963 4
1964 3
1965 8
1966 3
1967 5
1968 4
1969 5
1970 4
1971 3
1972 7
1973 1
1974 4
1975 5
1977 2
1978 3
1979 4
1981 1
1982 1
1983 1
1984 1
1985 4
1986 2
1987 3
1989 2
1990 1
1991 2
1992 3
1993 3
1994 3
1995 2
1996 2
1997 3
1998 2
1999 3
2000 2
2001 2
2002 3
2003 3
2004 5
2005 1
2006 3
2007 2
2008 2
2009 1
2011 2
2012 1
2014 1
2020 1
2024 0

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Search Results

140 results

Results by year

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Page 1
Respiratory problems in spinal muscular atrophies.
Barois A, Estournet-Mathiaud B. Barois A, et al. Pediatr Pulmonol Suppl. 1997;16:140-1. doi: 10.1002/ppul.1950230875. Pediatr Pulmonol Suppl. 1997. PMID: 9443243 Review. No abstract available.
Congenital muscular dystrophy with merosin deficiency.
Tomé FM, Evangelista T, Leclerc A, Sunada Y, Manole E, Estournet B, Barois A, Campbell KP, Fardeau M. Tomé FM, et al. Among authors: barois a. C R Acad Sci III. 1994 Apr;317(4):351-7. C R Acad Sci III. 1994. PMID: 8000914
Riluzole pharmacokinetics in young patients with spinal muscular atrophy.
Abbara C, Estournet B, Lacomblez L, Lelièvre B, Ouslimani A, Lehmann B, Viollet L, Barois A, Diquet B. Abbara C, et al. Among authors: barois a. Br J Clin Pharmacol. 2011 Mar;71(3):403-10. doi: 10.1111/j.1365-2125.2010.03843.x. Br J Clin Pharmacol. 2011. PMID: 21284699 Free PMC article. Clinical Trial.
[Congenital myasthenic syndromes due to mutations in the rapsyn gene].
Eymard B, Ioos C, Barois A, Estournet B, Mayer M, Fournier E, Yasaki E, Prioleau C, Bauché S, Gaudon K, Leroy JP, Koenig J, Richard P, Hantaï D. Eymard B, et al. Among authors: barois a. Rev Neurol (Paris). 2004 May;160(5 Pt 2):S78-84. doi: 10.1016/s0035-3787(04)71009-7. Rev Neurol (Paris). 2004. PMID: 15269664 Review. French.
De novo LMNA mutations cause a new form of congenital muscular dystrophy.
Quijano-Roy S, Mbieleu B, Bönnemann CG, Jeannet PY, Colomer J, Clarke NF, Cuisset JM, Roper H, De Meirleir L, D'Amico A, Ben Yaou R, Nascimento A, Barois A, Demay L, Bertini E, Ferreiro A, Sewry CA, Romero NB, Ryan M, Muntoni F, Guicheney P, Richard P, Bonne G, Estournet B. Quijano-Roy S, et al. Among authors: barois a. Ann Neurol. 2008 Aug;64(2):177-86. doi: 10.1002/ana.21417. Ann Neurol. 2008. PMID: 18551513
Evoked potentials in spinal muscular atrophy.
Cheliout-Heraut F, Barois A, Urtizberea A, Viollet L, Estournet-Mathiaud B. Cheliout-Heraut F, et al. Among authors: barois a. J Child Neurol. 2003 Jun;18(6):383-90. doi: 10.1177/08830738030180061101. J Child Neurol. 2003. PMID: 12886971
Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutation.
Ben Yaou R, Navarro C, Quijano-Roy S, Bertrand AT, Massart C, De Sandre-Giovannoli A, Cadiñanos J, Mamchaoui K, Butler-Browne G, Estournet B, Richard P, Barois A, Lévy N, Bonne G. Ben Yaou R, et al. Among authors: barois a. Eur J Hum Genet. 2011 Jun;19(6):647-54. doi: 10.1038/ejhg.2010.256. Epub 2011 Jan 26. Eur J Hum Genet. 2011. PMID: 21267004 Free PMC article.
140 results