Gabreëls FJ - 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. Among authors: gabreels festen a, gabreels fj. 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 fj. 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

Two new mutations in the sterol 27-hydroxylase gene in two families lead to cerebrotendinous xanthomatosis.

Verrips A, Steenbergen-Spanjers GC, Luyten JA, van den Heuvel LP, Keyser A, Gabreëls FJ, Wevers RA. Verrips A, et al. Among authors: gabreels fj. Hum Genet. 1996 Dec;98(6):735-7. doi: 10.1007/s004390050294. Hum Genet. 1996. PMID: 8931710

4

Exon skipping in the sterol 27-hydroxylase gene leads to cerebrotendinous xanthomatosis.

Verrips A, Steenbergen-Spanjers GC, Luyten JA, Wevers RA, Wokke JH, Gabreëls FJ, Wolthers BG, van den Heuvel LP. Verrips A, et al. Among authors: gabreels fj. Hum Genet. 1997 Aug;100(2):284-6. doi: 10.1007/s004390050506. Hum Genet. 1997. PMID: 9254865

5

Spinal xanthomatosis: a variant of cerebrotendinous xanthomatosis.

Verrips A, Nijeholt GJ, Barkhof F, Van Engelen BG, Wesseling P, Luyten JA, Wevers RA, Stam J, Wokke JH, van den Heuvel LP, Keyser A, Gabreëls FJ. Verrips A, et al. Among authors: gabreels fj. Brain. 1999 Aug;122 ( Pt 8):1589-95. doi: 10.1093/brain/122.8.1589. Brain. 1999. PMID: 10430841

6

Presence of diarrhea and absence of tendon xanthomas in patients with cerebrotendinous xanthomatosis.

Verrips A, van Engelen BG, Wevers RA, van Geel BM, Cruysberg JR, van den Heuvel LP, Keyser A, Gabreëls FJ. Verrips A, et al. Among authors: gabreels fj. Arch Neurol. 2000 Apr;57(4):520-4. doi: 10.1001/archneur.57.4.520. Arch Neurol. 2000. PMID: 10768627 Review.

7

Clinical and molecular genetic characteristics of patients with cerebrotendinous xanthomatosis.

Verrips A, Hoefsloot LH, Steenbergen GC, Theelen JP, Wevers RA, Gabreëls FJ, van Engelen BG, van den Heuvel LP. Verrips A, et al. Among authors: gabreels fj. Brain. 2000 May;123 ( Pt 5):908-19. doi: 10.1093/brain/123.5.908. Brain. 2000. PMID: 10775536

8

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. Among authors: gabreels fj, gabreels festen aa. Neuromuscul Disord. 2002 Oct;12(7-8):651-5. doi: 10.1016/s0960-8966(02)00025-1. Neuromuscul Disord. 2002. PMID: 12207933

9

Hereditary demyelinating motor and sensory neuropathy.

Gabreëls-Festen A, Gabreëls F. Gabreëls-Festen A, et al. Brain Pathol. 1993 Apr;3(2):135-46. doi: 10.1111/j.1750-3639.1993.tb00738.x. Brain Pathol. 1993. PMID: 8293175 Review.

10

Complex regional pain syndrome type I (RSD): pathology of skeletal muscle and peripheral nerve.

van der Laan L, ter Laak HJ, Gabreëls-Festen A, Gabreëls F, Goris RJ. van der Laan L, et al. Neurology. 1998 Jul;51(1):20-5. doi: 10.1212/wnl.51.1.20. Neurology. 1998. PMID: 9674773

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