de Visser M - Search Results

1

Bethlem myopathy: a slowly progressive congenital muscular dystrophy with contractures.

Jöbsis GJ, Boers JM, Barth PG, de Visser M. Jöbsis GJ, et al. Among authors: de visser m. Brain. 1999 Apr;122 ( Pt 4):649-55. doi: 10.1093/brain/122.4.649. Brain. 1999. PMID: 10219778

2

Limb girdle muscular dystrophy: reappraisal of a rejected entity.

van der Kooi AJ, de Visser M, Barth PG. van der Kooi AJ, et al. Among authors: de visser m. Clin Neurol Neurosurg. 1994 Aug;96(3):209-18. doi: 10.1016/0303-8467(94)90070-1. Clin Neurol Neurosurg. 1994. PMID: 7988088 Review.

3

Genetic localization of Bethlem myopathy.

Jobsis GJ, Bolhuis PA, Boers JM, Baas F, Wolterman RA, Hensels GW, de Visser M. Jobsis GJ, et al. Among authors: de visser m. Neurology. 1996 Mar;46(3):779-82. doi: 10.1212/wnl.46.3.779. Neurology. 1996. PMID: 8618682

4

Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contractures.

Jöbsis GJ, Keizers H, Vreijling JP, de Visser M, Speer MC, Wolterman RA, Baas F, Bolhuis PA. Jöbsis GJ, et al. Among authors: de visser m. Nat Genet. 1996 Sep;14(1):113-5. doi: 10.1038/ng0996-113. Nat Genet. 1996. PMID: 8782832

5

The clinical spectrum of limb girdle muscular dystrophy. A survey in The Netherlands.

van der Kooi AJ, Barth PG, Busch HF, de Haan R, Ginjaar HB, van Essen AJ, van Hooff LJ, Höweler CJ, Jennekens FG, Jongen P, Oosterhuis HJ, Padberg GW, Spaans F, Wintzen AR, Wokke JH, Bakker E, van Ommen GJ, Bolhuis PA, de Visser M. van der Kooi AJ, et al. Among authors: de haan r, de visser m. Brain. 1996 Oct;119 ( Pt 5):1471-80. doi: 10.1093/brain/119.5.1471. Brain. 1996. PMID: 8931572

6

The heart in limb girdle muscular dystrophy.

van der Kooi AJ, de Voogt WG, Barth PG, Busch HF, Jennekens FG, Jongen PJ, de Visser M. van der Kooi AJ, et al. Among authors: de voogt wg, de visser m. Heart. 1998 Jan;79(1):73-7. doi: 10.1136/hrt.79.1.73. Heart. 1998. PMID: 9505924 Free PMC article.

7

Limb-girdle muscular dystrophy in the Netherlands: gene defect identified in half the families.

van der Kooi AJ, Frankhuizen WS, Barth PG, Howeler CJ, Padberg GW, Spaans F, Wintzen AR, Wokke JH, van Ommen GJ, de Visser M, Bakker E, Ginjaar HB. van der Kooi AJ, et al. Among authors: de visser m. Neurology. 2007 Jun 12;68(24):2125-8. doi: 10.1212/01.wnl.0000264853.40735.3b. Neurology. 2007. PMID: 17562833

8

Differential diagnosis in spinal and bulbar muscular atrophy clinical and molecular aspects.

Jöbsis GJ, Louwerse ES, de Visser M, Wolterman RA, Bolhuis PA, Busch HF, Brüggenwirth HT, Baas F, Wiersinga WM, Koelman JH, et al. Jöbsis GJ, et al. Among authors: de visser m. J Neurol Sci. 1995 May;129 Suppl:56-7. doi: 10.1016/0022-510x(95)00064-9. J Neurol Sci. 1995. PMID: 7595622 Free article. Clinical Trial.

9

Machado-Joseph disease presenting as severe asymmetric proximal neuropathy.

van Schaik IN, Jöbsis GJ, Vermeulen M, Keizers H, Bolhuis PA, de Visser M. van Schaik IN, et al. Among authors: de visser m. J Neurol Neurosurg Psychiatry. 1997 Oct;63(4):534-6. doi: 10.1136/jnnp.63.4.534. J Neurol Neurosurg Psychiatry. 1997. PMID: 9343141 Free PMC article.

10

Limb girdle muscular dystrophy: a pathological and immunohistochemical reevaluation.

van der Kooi AJ, Ginjaar HB, Busch HF, Wokke JH, Barth PG, de Visser M. van der Kooi AJ, et al. Among authors: de visser m. Muscle Nerve. 1998 May;21(5):584-90. doi: 10.1002/(sici)1097-4598(199805)21:5<584::aid-mus4>3.0.co;2-4. Muscle Nerve. 1998. PMID: 9572237

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