Baas F - 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: baas f. Neuromuscul Disord. 1998 Jun;8(5):317-20. doi: 10.1016/s0960-8966(98)00020-0. Neuromuscul Disord. 1998. PMID: 9673985

2

The gene for X-linked myotubular myopathy is located in an 8 Mb region at the border of Xq27.3 and Xq28.

Janssen EA, Hensels GW, van Oost BA, Hamel BC, Kemp S, Baas F, Weber JW, Barth PG, Bolhuis PA. Janssen EA, et al. Among authors: baas f. Neuromuscul Disord. 1994 Sep-Nov;4(5-6):455-61. doi: 10.1016/0960-8966(94)90084-1. Neuromuscul Disord. 1994. PMID: 7881289

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: baas f. Neurology. 1996 Mar;46(3):779-82. doi: 10.1212/wnl.46.3.779. Neurology. 1996. PMID: 8618682

4

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: baas f. Neuromuscul Disord. 1991;1(2):93-7. doi: 10.1016/0960-8966(91)90055-w. Neuromuscul Disord. 1991. PMID: 1822787

5

Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28.

Bolhuis PA, Hensels GW, Hulsebos TJ, Baas F, Barth PG. Bolhuis PA, et al. Among authors: baas f. Am J Hum Genet. 1991 Mar;48(3):481-5. Am J Hum Genet. 1991. PMID: 1998334 Free PMC article.

6

Alternatively sized duplication in Charcot-Marie-Tooth disease type 1A.

Valentijn LJ, Baas F, Zorn I, Hensels GW, de Visser M, Bolhuis PA. Valentijn LJ, et al. Among authors: baas f. Hum Mol Genet. 1993 Dec;2(12):2143-6. doi: 10.1093/hmg/2.12.2143. Hum Mol Genet. 1993. PMID: 8111385 No abstract available.

7

Evidence for genetic heterogeneity underlying hereditary neuropathy with liability to pressure palsies.

Mariman EC, Gabreëls-Festen AA, van Beersum SE, Jongen PJ, van de Looij E, Baas F, Bolhuis PA, Ropers HH, Gabreëls FJ. Mariman EC, et al. Among authors: baas f. Hum Genet. 1994 Feb;93(2):151-6. doi: 10.1007/BF00210601. Hum Genet. 1994. PMID: 8112739

8

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: baas f. Nat Genet. 1996 Sep;14(1):113-5. doi: 10.1038/ng0996-113. Nat Genet. 1996. PMID: 8782832

9

Autosomal dominant cerebellar ataxia with retinal degeneration (ADCA II): clinical and neuropathological findings in two pedigrees and genetic linkage to 3p12-p21.1.

Jöbsis GJ, Weber JW, Barth PG, Keizers H, Baas F, van Schooneveld MJ, van Hilten JJ, Troost D, Geesink HH, Bolhuis PA. Jöbsis GJ, et al. Among authors: baas f. J Neurol Neurosurg Psychiatry. 1997 Apr;62(4):367-71. doi: 10.1136/jnnp.62.4.367. J Neurol Neurosurg Psychiatry. 1997. PMID: 9120450 Free PMC article.

10

Upper motor neuron and extra-motor neuron involvement in amyotrophic lateral sclerosis: a clinical and brain imaging review.

van der Graaff MM, de Jong JM, Baas F, de Visser M. van der Graaff MM, et al. Among authors: baas f. Neuromuscul Disord. 2009 Jan;19(1):53-8. doi: 10.1016/j.nmd.2008.10.002. Epub 2008 Dec 12. Neuromuscul Disord. 2009. PMID: 19070491 Review.

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