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

Year Number of Results
1974 1
1975 1
1976 4
1977 4
1978 1
1979 4
1980 5
1981 1
1982 3
1983 1
1984 5
1985 1
1986 5
1987 1
1988 3
1990 2
1991 1
1992 5
1993 5
1994 4
1995 1
1996 3
1997 3
1998 2
1999 6
2000 2
2001 3
2002 7
2003 7
2005 3
2006 2
2024 0

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96 results

Results by year

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Page 1
Adrenomyeloneuropathy. A report on two families.
Martin JJ, Lowenthal A, Ceuterick C, Gacoms H. Martin JJ, et al. Among authors: ceuterick c. J Neurol. 1982;226(4):221-32. doi: 10.1007/BF00313395. J Neurol. 1982. PMID: 6174703
Marshall-Smith syndrome: new aspects.
Roodhooft AM, Van Acker KJ, Van Thienen MN, Martin JJ, Ceuterick C. Roodhooft AM, et al. Among authors: ceuterick c. Neuropediatrics. 1988 Nov;19(4):179-82. doi: 10.1055/s-2008-1052441. Neuropediatrics. 1988. PMID: 3205374
Early-onset Alzheimer's disease in 2 large Belgian families.
Martin JJ, Gheuens J, Bruyland M, Cras P, Vandenberghe A, Masters CL, Beyreuther K, Dom R, Ceuterick C, Lübke U, et al. Martin JJ, et al. Among authors: ceuterick c. Neurology. 1991 Jan;41(1):62-8. doi: 10.1212/wnl.41.1.62. Neurology. 1991. PMID: 1985297
MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2.
Verhoeven K, Claeys KG, Züchner S, Schröder JM, Weis J, Ceuterick C, Jordanova A, Nelis E, De Vriendt E, Van Hul M, Seeman P, Mazanec R, Saifi GM, Szigeti K, Mancias P, Butler IJ, Kochanski A, Ryniewicz B, De Bleecker J, Van den Bergh P, Verellen C, Van Coster R, Goemans N, Auer-Grumbach M, Robberecht W, Milic Rasic V, Nevo Y, Tournev I, Guergueltcheva V, Roelens F, Vieregge P, Vinci P, Moreno MT, Christen HJ, Shy ME, Lupski JR, Vance JM, De Jonghe P, Timmerman V. Verhoeven K, et al. Among authors: ceuterick c. Brain. 2006 Aug;129(Pt 8):2093-102. doi: 10.1093/brain/awl126. Epub 2006 May 19. Brain. 2006. PMID: 16714318
Periaxin mutations cause a broad spectrum of demyelinating neuropathies.
Takashima H, Boerkoel CF, De Jonghe P, Ceuterick C, Martin JJ, Voit T, Schröder JM, Williams A, Brophy PJ, Timmerman V, Lupski JR. Takashima H, et al. Among authors: ceuterick c. Ann Neurol. 2002 Jun;51(6):709-15. doi: 10.1002/ana.10213. Ann Neurol. 2002. PMID: 12112076
Mutations in GDAP1: autosomal recessive CMT with demyelination and axonopathy.
Nelis E, Erdem S, Van Den Bergh PY, Belpaire-Dethiou MC, Ceuterick C, Van Gerwen V, Cuesta A, Pedrola L, Palau F, Gabreëls-Festen AA, Verellen C, Tan E, Demirci M, Van Broeckhoven C, De Jonghe P, Topaloglu H, Timmerman V. Nelis E, et al. Among authors: ceuterick c. Neurology. 2002 Dec 24;59(12):1865-72. doi: 10.1212/01.wnl.0000036272.36047.54. Neurology. 2002. PMID: 12499475
96 results