Gabreëls-Festen A - Search Results

1

Neurophysiologic studies in early-onset cerebellar ataxia.

Schelhaas HJ, van de Warrenburg BP, Bos MM, Houtman CJ, Scheffer H, Gabreëls-Festen A, Kremer B, Zwarts MJ. Schelhaas HJ, et al. Among authors: gabreels festen a. J Clin Neurophysiol. 2006 Aug;23(4):381-7. doi: 10.1097/01.wnp.0000216262.54227.7a. J Clin Neurophysiol. 2006. PMID: 16885713 Clinical Trial.

2

Dejerine-Sottas syndrome grown to maturity: overview of genetic and morphological heterogeneity and follow-up of 25 patients.

Gabreëls-Festen A. Gabreëls-Festen A. J Anat. 2002 Apr;200(4):341-56. doi: 10.1046/j.1469-7580.2002.00043.x. J Anat. 2002. PMID: 12090401 Free PMC article. Review.

3

Human Nerve Pathology Caused by Different Mutational Mechanisms of the PMP22 Gene.

Gabreëls-Festen A, VAN DE Wetering R. Gabreëls-Festen A, et al. Ann N Y Acad Sci. 1999 Oct;883(1):336-343. doi: 10.1111/j.1749-6632.1999.tb08595.x. Ann N Y Acad Sci. 1999. PMID: 29086940

4

Human nerve pathology caused by different mutational mechanisms of the PMP22 gene.

Gabreëls-Festen A, Wetering RV. Gabreëls-Festen A, et al. Ann N Y Acad Sci. 1999 Sep 14;883:336-43. Ann N Y Acad Sci. 1999. PMID: 10586258 Review.

5

Identical point mutations of PMP-22 in Trembler-J mouse and Charcot-Marie-Tooth disease type 1A.

Valentijn LJ, Baas F, Wolterman RA, Hoogendijk JE, van den Bosch NH, Zorn I, Gabreëls-Festen AW, de Visser M, Bolhuis PA. Valentijn LJ, et al. Nat Genet. 1992 Dec;2(4):288-91. doi: 10.1038/ng1292-288. Nat Genet. 1992. PMID: 1303281

6

Severe Dejerine-Sottas disease with respiratory failure and dysmorphic features in association with a PMP22 point mutation and a 3q23 microdeletion.

Voermans NC, Kleefstra T, Gabreëls-Festen AA, Faas BH, Kamsteeg EJ, Houlden H, Laurá M, Polke JM, Pandraud A, van Ruissen F, van Engelen BG, Reilly MM. Voermans NC, et al. Among authors: gabreels festen aa. J Peripher Nerv Syst. 2012 Jun;17(2):223-5. doi: 10.1111/j.1529-8027.2012.00402.x. J Peripher Nerv Syst. 2012. PMID: 22734911 No abstract available.

7

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

8

Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations.

Azzedine H, Ravisé N, Verny C, Gabrëels-Festen A, Lammens M, Grid D, Vallat JM, Durosier G, Senderek J, Nouioua S, Hamadouche T, Bouhouche A, Guilbot A, Stendel C, Ruberg M, Brice A, Birouk N, Dubourg O, Tazir M, LeGuern E. Azzedine H, et al. Among authors: gabreels festen a. Neurology. 2006 Aug 22;67(4):602-6. doi: 10.1212/01.wnl.0000230225.19797.93. Neurology. 2006. PMID: 16924012

9

Late onset axonal Charcot-Marie-Tooth phenotype caused by a novel myelin protein zero mutation.

Bienfait HM, Faber CG, Baas F, Gabreëls-Festen AA, Koelman JH, Hoogendijk JE, Verschuuren JJ, Wokke JH, de Visser M. Bienfait HM, et al. Among authors: gabreels festen aa. J Neurol Neurosurg Psychiatry. 2006 Apr;77(4):534-7. doi: 10.1136/jnnp.2005.073437. J Neurol Neurosurg Psychiatry. 2006. PMID: 16543539 Free PMC article.

10

Macrophage clustering as a diagnostic marker in sural nerve biopsies of patients with CIDP.

Sommer C, Koch S, Lammens M, Gabreels-Festen A, Stoll G, Toyka KV. Sommer C, et al. Among authors: gabreels festen a. Neurology. 2005 Dec 27;65(12):1924-9. doi: 10.1212/01.wnl.0000188879.19900.b7. Neurology. 2005. PMID: 16380614

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