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

Year Number of Results
1967 1
1968 1
1969 2
1970 4
1973 3
1974 1
1975 2
1976 2
1977 2
1978 4
1979 1
1980 3
1981 4
1982 4
1983 2
1984 8
1985 4
1986 5
1987 4
1988 5
1989 2
1990 2
1991 3
1992 1
1993 5
1994 4
1995 5
1996 5
1997 6
1998 8
1999 5
2000 3
2001 2
2002 3
2003 9
2004 5
2005 2
2006 2
2008 2
2009 6
2010 5
2011 1
2012 1
2014 2
2015 1
2018 1
2025 0

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151 results

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Page 1
Myasthenia gravis: prolonged treatment with steroids.
Sghirlanzoni A, Peluchetti D, Mantegazza R, Fiacchino F, Cornelio F. Sghirlanzoni A, et al. Among authors: cornelio f. Neurology. 1984 Feb;34(2):170-4. doi: 10.1212/wnl.34.2.170. Neurology. 1984. PMID: 6538004
Hepatic ketogenesis and muscle carnitine deficiency.
DiDonato S, Cornelio F, Storchi G, Rimoldi M. DiDonato S, et al. Among authors: cornelio f. Neurology. 1979 Jun;29(6):780-5. doi: 10.1212/wnl.29.6.780. Neurology. 1979. PMID: 572000
Chloroquine myopathy and myasthenia-like syndrome.
Sghirlanzoni A, Mantegazza R, Mora M, Pareyson D, Cornelio F. Sghirlanzoni A, et al. Among authors: cornelio f. Muscle Nerve. 1988 Feb;11(2):114-9. doi: 10.1002/mus.880110205. Muscle Nerve. 1988. PMID: 3343986
Fetal myosin immunoreactivity in human dystrophic muscle.
Schiaffino S, Gorza L, Dones I, Cornelio F, Sartore S. Schiaffino S, et al. Among authors: cornelio f. Muscle Nerve. 1986 Jan;9(1):51-8. doi: 10.1002/mus.880090108. Muscle Nerve. 1986. PMID: 3513005
Narcolepsy is a common phenotype in HSAN IE and ADCA-DN.
Moghadam KK, Pizza F, La Morgia C, Franceschini C, Tonon C, Lodi R, Barboni P, Seri M, Ferrari S, Liguori R, Donadio V, Parchi P, Cornelio F, Inzitari D, Mignarri A, Capocchi G, Dotti MT, Winkelmann J, Lin L, Mignot E, Carelli V, Plazzi G. Moghadam KK, et al. Among authors: cornelio f. Brain. 2014 Jun;137(Pt 6):1643-55. doi: 10.1093/brain/awu069. Epub 2014 Apr 10. Brain. 2014. PMID: 24727570 Free article.
Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy.
Winkelmann J, Lin L, Schormair B, Kornum BR, Faraco J, Plazzi G, Melberg A, Cornelio F, Urban AE, Pizza F, Poli F, Grubert F, Wieland T, Graf E, Hallmayer J, Strom TM, Mignot E. Winkelmann J, et al. Among authors: cornelio f. Hum Mol Genet. 2012 May 15;21(10):2205-10. doi: 10.1093/hmg/dds035. Epub 2012 Feb 9. Hum Mol Genet. 2012. PMID: 22328086 Free PMC article.
Heterogeneity of carnitine-palmitoyltransferase deficiency.
Di Donato S, Castiglione A, Rimoldi M, Cornelio F, Vendemia F, Cardace G, Bertagnolio B. Di Donato S, et al. Among authors: cornelio f. J Neurol Sci. 1981 May;50(2):207-15. doi: 10.1016/0022-510x(81)90167-2. J Neurol Sci. 1981. PMID: 7229666
A unique case of dystrophinopathy.
Worzak FD, Mora M, Morandi L, Bernasconi P, Cornelio F, Ripamonti D. Worzak FD, et al. Among authors: cornelio f. J Neurol Neurosurg Psychiatry. 1994 Sep;57(9):1136-7. doi: 10.1136/jnnp.57.9.1136-a. J Neurol Neurosurg Psychiatry. 1994. PMID: 8089689 Free PMC article. No abstract available.
151 results