de Visser M - Search Results

1

Genetic heterogeneity in Miyoshi-type distal muscular dystrophy.

Linssen WH, de Visser M, Notermans NC, Vreyling JP, Van Doorn PA, Wokke JH, Baas F, Bolhuis PA. Linssen WH, et al. Among authors: de visser m. Neuromuscul Disord. 1998 Jun;8(5):317-20. doi: 10.1016/s0960-8966(98)00020-0. Neuromuscul Disord. 1998. PMID: 9673985

2

An unusual variant of Becker muscular dystrophy.

de Visser M, Bakker E, Defesche JC, Bolhuis PA, van Ommen GJ. de Visser M, et al. Ann Neurol. 1990 May;27(5):578-81. doi: 10.1002/ana.410270521. Ann Neurol. 1990. PMID: 2193611

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

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

5

Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21.

van der Kooi AJ, van Meegen M, Ledderhof TM, McNally EM, de Visser M, Bolhuis PA. van der Kooi AJ, et al. Among authors: de visser m. Am J Hum Genet. 1997 Apr;60(4):891-5. Am J Hum Genet. 1997. PMID: 9106535 Free PMC article.

6

Miyoshi-type distal muscular dystrophy. Clinical spectrum in 24 Dutch patients.

Linssen WH, Notermans NC, Van der Graaf Y, Wokke JH, Van Doorn PA, Höweler CJ, Busch HF, De Jager AE, De Visser M. Linssen WH, et al. Among authors: de jager ae, de visser m. Brain. 1997 Nov;120 ( Pt 11):1989-96. doi: 10.1093/brain/120.11.1989. Brain. 1997. PMID: 9397016 Free article.

7

A novel gamma-sarcoglycan mutation causing childhood onset, slowly progressive limb girdle muscular dystrophy.

van der Kooi AJ, de Visser M, van Meegen M, Ginjaar HB, van Essen AJ, Jennekens FG, Jongen PJ, Leschot NJ, Bolhuis PA. van der Kooi AJ, et al. Among authors: de visser m. Neuromuscul Disord. 1998 Jun;8(5):305-8. doi: 10.1016/s0960-8966(98)00040-6. Neuromuscul Disord. 1998. PMID: 9673983

8

Long-term follow-up study on patients with Miyoshi phenotype of distal muscular dystrophy.

Linssen WH, de Voogt WG, Krahn M, Bernard R, Levy N, Wokke JH, Ginjaar HB, de Visser M. Linssen WH, et al. Among authors: de voogt wg, de visser m. Eur J Neurol. 2013 Jun;20(6):968-74. doi: 10.1111/ene.12129. Epub 2013 Mar 26. Eur J Neurol. 2013. PMID: 23530687

9

Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a). The HMSN Collaborative Research Group.

Raeymaekers P, Timmerman V, Nelis E, De Jonghe P, Hoogendijk JE, Baas F, Barker DF, Martin JJ, De Visser M, Bolhuis PA, et al. Raeymaekers P, et al. Among authors: de jonghe p, de visser m. Neuromuscul Disord. 1991;1(2):93-7. doi: 10.1016/0960-8966(91)90055-w. Neuromuscul Disord. 1991. PMID: 1822787

10

Genetic linkage of hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease) to markers of chromosomes 1 and 17.

Defesche JC, Hoogendijk JE, de Visser M, de Visser O, Bolhuis PA. Defesche JC, et al. Among authors: de visser o, de visser m. Neurology. 1990 Sep;40(9):1450-3. doi: 10.1212/wnl.40.9.1450. Neurology. 1990. PMID: 2392234

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

508 results

Search Page

Filters