ter Laak HJ - Search Results

1

Dystrophic myopathy of the diaphragm in a neonate with severe respiratory failure during infectious episodes.

Leyten QH, Renier WO, Gabreëls FJ, ter Laak HJ, Hinkofer LH. Leyten QH, et al. Among authors: ter laak hj. Neuromuscul Disord. 1993 Jan;3(1):51-5. doi: 10.1016/0960-8966(93)90041-h. Neuromuscul Disord. 1993. PMID: 8329889

2

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.

3

Familial adult-onset muscular dystrophy with leukoencephalopathy.

van Engelen BG, Leyten QH, Bernsen PL, Gabreëls FJ, Barkhof F, Joosten EM, Hamel BC, ter Laak HJ, Ruijs MB, Cruysberg JR, et al. van Engelen BG, et al. Among authors: ter laak hj. Ann Neurol. 1992 Oct;32(4):577-80. doi: 10.1002/ana.410320415. Ann Neurol. 1992. PMID: 1456743

4

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

5

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

6

Congenital muscular dystrophy.

Leyten QH, Gabreëls FJ, Renier WO, Ter Laak HJ, Sengers RC, Mullaart RA. Leyten QH, et al. Among authors: ter laak hj. J Pediatr. 1989 Aug;115(2):214-21. doi: 10.1016/s0022-3476(89)80068-x. J Pediatr. 1989. PMID: 2754551

7

White matter abnormalities in congenital muscular dystrophy.

Leyten QH, Gabreëls FJ, Renier WO, van Engelen BG, ter Laak HJ, Sengers RC, Thijssen HO. Leyten QH, et al. Among authors: ter laak hj. J Neurol Sci. 1995 Apr;129(2):162-9. doi: 10.1016/0022-510x(94)00264-o. J Neurol Sci. 1995. PMID: 7608731 Free article.

8

Coxsackie B1 virus-induced murine myositis: relationship of disease severity to virus dose and antiviral antibody response.

Jongen PJ, Heessen FW, ter Laak HJ, Galama JM, Gabreëls FJ. Jongen PJ, et al. Among authors: ter laak hj. Neuromuscul Disord. 1994 Jan;4(1):17-23. doi: 10.1016/0960-8966(94)90044-2. Neuromuscul Disord. 1994. PMID: 8173348

9

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

10

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

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