ter Laak HJ - Search Results

1

Galanin-like immunoreactivity within Ch2 neurons in the vertical limb of the diagonal band of Broca in aging and Alzheimer's disease.

Vogels OJ, Renkawek K, Broere CA, ter Laak HJ, van Workum F. Vogels OJ, et al. Among authors: ter laak hj. Acta Neuropathol. 1989;78(1):90-5. doi: 10.1007/BF00687407. Acta Neuropathol. 1989. PMID: 2472041

2

The olfactory bulb in Alzheimer disease: a morphologic study of neuron loss, tangles, and senile plaques in relation to olfaction.

ter Laak HJ, Renkawek K, van Workum FP. ter Laak HJ, et al. Alzheimer Dis Assoc Disord. 1994 Spring;8(1):38-48. Alzheimer Dis Assoc Disord. 1994. PMID: 8185881

3

Cell loss and shrinkage in the nucleus basalis Meynert complex in Alzheimer's disease.

Vogels OJ, Broere CA, ter Laak HJ, ten Donkelaar HJ, Nieuwenhuys R, Schulte BP. Vogels OJ, et al. Among authors: ter laak hj. Neurobiol Aging. 1990 Jan-Feb;11(1):3-13. doi: 10.1016/0197-4580(90)90056-6. Neurobiol Aging. 1990. PMID: 2183081 Review.

4

Neuropathological findings in muscle-eye-brain disease (MEB-D). Neuropathological delineation of MEB-D from congenital muscular dystrophy of the Fukuyama type.

Leyten QH, Renkawek K, Renier WO, Gabreëls FJ, Mooy CM, ter Laak HJ, Mullaart RA. Leyten QH, et al. Among authors: ter laak hj. Acta Neuropathol. 1991;83(1):55-60. doi: 10.1007/BF00294430. Acta Neuropathol. 1991. PMID: 1792864

5

Congenital muscular dystrophy. A study on the variability of morphological changes and dystrophin distribution in muscle biopsies.

Leyten QH, ter Laak HJ, Gabreëls FJ, Renier WO, Renkawek K, Sengers RC. Leyten QH, et al. Among authors: ter laak hj. Acta Neuropathol. 1993;86(4):386-92. doi: 10.1007/BF00369452. Acta Neuropathol. 1993. PMID: 8256590

6

Congenital muscular dystrophy and severe central nervous system atrophy in two siblings.

Leyten QH, Barth PG, Gabreëls FJ, Renkawek K, Renier WO, Gabreëls-Festen AA, ter Laak HJ, Smits MG. Leyten QH, et al. Among authors: ter laak hj. Acta Neuropathol. 1995;90(6):650-6. doi: 10.1007/BF00318580. Acta Neuropathol. 1995. PMID: 8615088

7

Myositis during long-term interferon-alpha treatment.

Hengstman GJ, Vogels OJ, ter Laak HJ, de Witte T, van Engelen BG. Hengstman GJ, et al. Among authors: ter laak hj. Neurology. 2000 Jun 13;54(11):2186. doi: 10.1212/wnl.54.11.2186. Neurology. 2000. PMID: 10851394 No abstract available.

8

Congenital muscular dystrophy with eye and brain malformations in six Dutch patients.

Leyten QH, Gabreëls FJ, Renier WO, Renkawek K, ter Laak HJ, Mullaart RA. Leyten QH, et al. Among authors: ter laak hj. Neuropediatrics. 1992 Dec;23(6):316-20. doi: 10.1055/s-2008-1071365. Neuropediatrics. 1992. PMID: 1491751

9

A new phenotype of autosomal dominant nemaline myopathy.

Gommans IM, van Engelen BG, ter Laak HJ, Brunner HG, Kremer H, Lammens M, Vogels OJ. Gommans IM, et al. Among authors: ter laak hj. Neuromuscul Disord. 2002 Jan;12(1):13-8. doi: 10.1016/s0960-8966(01)00231-0. Neuromuscul Disord. 2002. PMID: 11731279

10

A locus on chromosome 15q for a dominantly inherited nemaline myopathy with core-like lesions.

Gommans IM, Davis M, Saar K, Lammens M, Mastaglia F, Lamont P, van Duijnhoven G, ter Laak HJ, Reis A, Vogels OJ, Laing N, van Engelen BG, Kremer H. Gommans IM, et al. Among authors: ter laak hj. Brain. 2003 Jul;126(Pt 7):1545-51. doi: 10.1093/brain/awg162. Epub 2003 Jun 4. Brain. 2003. PMID: 12805120

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