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Results by year

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

Year Number of Results
1951 1
1952 1
1956 3
1957 1
1958 2
1960 1
1962 2
1965 1
1966 1
1967 1
1968 3
1969 2
1970 2
1972 3
1974 3
1976 2
1977 1
1978 4
1979 2
1980 2
1981 1
1982 3
1983 3
1984 3
1985 3
1986 1
1987 3
1988 3
1989 2
1991 5
1992 3
1993 10
1994 1
1995 2
1996 7
1997 2
1998 4
1999 10
2000 5
2001 5
2002 5
2003 3
2004 5
2005 4
2006 3
2007 2
2008 4
2009 2
2010 1
2011 3
2012 1
2024 0

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Article attribute

Article type

Publication date

PubMed (OMIM) for id: 4359

144 results

Results by year

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Page 1
Genetic spectrum of hereditary neuropathies with onset in the first year of life.
Baets J, Deconinck T, De Vriendt E, Zimoń M, Yperzeele L, Van Hoorenbeeck K, Peeters K, Spiegel R, Parman Y, Ceulemans B, Van Bogaert P, Pou-Serradell A, Bernert G, Dinopoulos A, Auer-Grumbach M, Sallinen SL, Fabrizi GM, Pauly F, Van den Bergh P, Bilir B, Battaloglu E, Madrid RE, Kabzińska D, Kochanski A, Topaloglu H, Miller G, Jordanova A, Timmerman V, De Jonghe P. Baets J, et al. Brain. 2011 Sep;134(Pt 9):2664-76. doi: 10.1093/brain/awr184. Epub 2011 Aug 11. Brain. 2011. PMID: 21840889 Free PMC article.
U1 snRNA mis-binding: a new cause of CMT1B.
Crehalet H, Latour P, Bonnet V, Attarian S, Labauge P, Bonello N, Bernard R, Millat G, Rousson R, Bozon D. Crehalet H, et al. Neurogenetics. 2010 Feb;11(1):13-9. doi: 10.1007/s10048-009-0199-8. Epub 2009 May 28. Neurogenetics. 2010. PMID: 19475438
144 results