Gabreëls-Festen A - Search Results

1

Cerebrotendinous xanthomatosis. Controversies about nerve and muscle: observations in ten patients.

Verrips A, van Engelen BG, ter Laak H, Gabreëls-Festen A, Janssen A, Zwarts M, Wevers RA, Gabreëls FJ. Verrips A, et al. Neuromuscul Disord. 2000 Aug;10(6):407-14. doi: 10.1016/s0960-8966(00)00112-7. Neuromuscul Disord. 2000. PMID: 10899446 Clinical Trial.

2

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.

3

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

4

Hereditary neuropathy with liability to pressure palsies with a small deletion interrupting the PMP22 gene.

van de Wetering RA, Gabreëls-Festen AA, Timmerman V, Padberg GM, Gabreëls FJ, Mariman EC. van de Wetering RA, et al. Neuromuscul Disord. 2002 Oct;12(7-8):651-5. doi: 10.1016/s0960-8966(02)00025-1. Neuromuscul Disord. 2002. PMID: 12207933

5

Hereditary neuropathy with liability to pressure palsies in childhood.

Gabreëls-Festen AA, Gabreëls FJ, Joosten EM, Vingerhoets HM, Renier WO. Gabreëls-Festen AA, et al. Neuropediatrics. 1992 Jun;23(3):138-43. doi: 10.1055/s-2008-1071329. Neuropediatrics. 1992. PMID: 1322507

6

Autosomal recessive form of hereditary motor and sensory neuropathy type I.

Gabreëls-Festen AA, Gabreëls FJ, Jennekens FG, Joosten EM, Janssen-van Kempen TW. Gabreëls-Festen AA, et al. Neurology. 1992 Sep;42(9):1755-61. doi: 10.1212/wnl.42.9.1755. Neurology. 1992. PMID: 1513466

7

Early morphological features in dominantly inherited demyelinating motor and sensory neuropathy (HMSN type I).

Gabreëls-Festen AA, Joosten EM, Gabreëls FJ, Jennekens FG, Janssen-van Kempen TW. Gabreëls-Festen AA, et al. J Neurol Sci. 1992 Feb;107(2):145-54. doi: 10.1016/0022-510x(92)90282-p. J Neurol Sci. 1992. PMID: 1564512

8

Sensory axonopathy in hereditary distal spinal muscular atrophy.

Frequin ST, Gabreëls FJ, Gabreëls-Festen AA, Joosten EM. Frequin ST, et al. Clin Neurol Neurosurg. 1991;93(4):323-6. doi: 10.1016/0303-8467(91)90099-b. Clin Neurol Neurosurg. 1991. PMID: 1665767

9

Hereditary motor and sensory neuropathy of neuronal type with onset in early childhood.

Gabreëls-Festen AA, Joosten EM, Gabreëls FJ, Jennekens FG, Gooskens RH, Stegeman DF. Gabreëls-Festen AA, et al. Brain. 1991 Aug;114 ( Pt 4):1855-70. doi: 10.1093/brain/114.4.1855. Brain. 1991. PMID: 1884182

10

Polyglucosan bodies in sural nerve biopsies.

Busard HL, Gabreëls-Festen AA, van 't Hof MA, Renier WO, Gabreëls FJ. Busard HL, et al. Acta Neuropathol. 1990;80(5):554-7. doi: 10.1007/BF00294618. Acta Neuropathol. 1990. PMID: 2251913

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