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

Year Number of Results
1974 1
1981 1
1982 3
1983 2
1985 1
1986 1
1987 2
1988 3
1990 2
1991 3
1992 4
1993 6
1994 4
1995 6
1996 5
1997 2
1998 3
1999 1
2000 3
2001 2
2002 6
2005 3
2006 2
2007 1
2012 1
2024 0

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67 results

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Page 1
Polyglucosan bodies in sural nerve biopsies.
Busard HL, Gabreëls-Festen AA, van 't Hof MA, Renier WO, Gabreëls FJ. Busard HL, et al. Among authors: gabreels festen aa. Acta Neuropathol. 1990;80(5):554-7. doi: 10.1007/BF00294618. Acta Neuropathol. 1990. PMID: 2251913
Phenotype of Charcot-Marie-Tooth disease Type 2.
Bienfait HM, Baas F, Koelman JH, de Haan RJ, van Engelen BG, Gabreëls-Festen AA, Ongerboer de Visser BW, Meggouh F, Weterman MA, De Jonghe P, Timmerman V, de Visser M. Bienfait HM, et al. Among authors: gabreels festen aa. Neurology. 2007 May 15;68(20):1658-67. doi: 10.1212/01.wnl.0000263479.97552.94. Neurology. 2007. PMID: 17502546
Histology of hereditary neuralgic amyotrophy.
van Alfen N, Gabreëls-Festen AA, Ter Laak HJ, Arts WF, Gabreëls FJ, van Engelen BG. van Alfen N, et al. Among authors: gabreels festen aa. J Neurol Neurosurg Psychiatry. 2005 Mar;76(3):445-7. doi: 10.1136/jnnp.2004.044370. J Neurol Neurosurg Psychiatry. 2005. PMID: 15716548 Free PMC article.
The status of HMSN type III.
Gabreëls-Festen AA, Gabreëls FJ, Jennekens FG, Janssen-van Kempen TW. Gabreëls-Festen AA, et al. Neuromuscul Disord. 1994 Jan;4(1):63-9. doi: 10.1016/0960-8966(94)90049-3. Neuromuscul Disord. 1994. PMID: 8173353
Recurrent neuropathy associated with Ehlers-Danlos syndrome.
Voermans NC, Drost G, van Kampen A, Gabreëls-Festen AA, Lammens M, Hamel BC, Schalkwijk J, van Engelen BG. Voermans NC, et al. Among authors: gabreels festen aa. J Neurol. 2006 May;253(5):670-1. doi: 10.1007/s00415-005-0056-0. Epub 2005 Nov 29. J Neurol. 2006. PMID: 16311893 No abstract available.
Regulation and expression of the murine PMP22 gene.
van de Wetering RA, Gabreëls-Festen AA, Kremer H, Kalscheuer VM, Gabreëls FJ, Mariman EC. van de Wetering RA, et al. Among authors: gabreels festen aa. Mamm Genome. 1999 Apr;10(4):419-22. doi: 10.1007/s003359901015. Mamm Genome. 1999. PMID: 10087306 No abstract available.
De-novo mutation in hereditary motor and sensory neuropathy type I.
Hoogendijk JE, Hensels GW, Gabreëls-Festen AA, Gabreëls FJ, Janssen EA, de Jonghe P, Martin JJ, van Broeckhoven C, Valentijn LJ, Baas F, et al. Hoogendijk JE, et al. Among authors: gabreels festen aa. Lancet. 1992 May 2;339(8801):1081-2. doi: 10.1016/0140-6736(92)90668-s. Lancet. 1992. PMID: 1349106
67 results