de Haan A - Search Results

1

Parental origin of the fra(X) gene is a major determinant of the cytogenetic expression and the CGG repeat length in female carriers.

Smits A, Smeets D, Dreesen J, Hamel B, de Haan A, van Oost B. Smits A, et al. Among authors: de haan a. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):261-7. doi: 10.1002/ajmg.1320430141. Am J Med Genet. 1992. PMID: 1605199

2

Prediction of mental status in carriers of the fragile X mutation using CGG repeat length.

Smits A, Smeets D, Hamel B, Dreesen J, de Haan A, van Oost B. Smits A, et al. Among authors: de haan a. Am J Med Genet. 1994 Jul 15;51(4):497-500. doi: 10.1002/ajmg.1320510440. Am J Med Genet. 1994. PMID: 7943027

3

Rapid antibody test for diagnosing fragile X syndrome: a validation of the technique.

Willemsen R, Smits A, Mohkamsing S, van Beerendonk H, de Haan A, de Vries B, van den Ouweland A, Sistermans E, Galjaard H, Oostra BA. Willemsen R, et al. Among authors: de haan a, de vries b. Hum Genet. 1997 Mar;99(3):308-11. doi: 10.1007/s004390050363. Hum Genet. 1997. PMID: 9050914 Free article.

4

Reduced quantitative muscle function in tenascin-X deficient Ehlers-Danlos patients.

Voermans NC, Altenburg TM, Hamel BC, de Haan A, van Engelen BG. Voermans NC, et al. Among authors: de haan a. Neuromuscul Disord. 2007 Aug;17(8):597-602. doi: 10.1016/j.nmd.2007.04.004. Epub 2007 Jun 27. Neuromuscul Disord. 2007. PMID: 17588758

5

Clinical and molecular overlap between myopathies and inherited connective tissue diseases.

Voermans NC, Bönnemann CG, Huijing PA, Hamel BC, van Kuppevelt TH, de Haan A, Schalkwijk J, van Engelen BG, Jenniskens GJ. Voermans NC, et al. Among authors: de haan a. Neuromuscul Disord. 2008 Nov;18(11):843-56. doi: 10.1016/j.nmd.2008.05.017. Epub 2008 Sep 24. Neuromuscul Disord. 2008. PMID: 18818079 Review.

6

Cytoarchitectural and metabolic adaptations in muscles with mitochondrial and cytosolic creatine kinase deficiencies.

Steeghs K, Oerlemans F, de Haan A, Heerschap A, Verdoodt L, de Bie M, Ruitenbeek W, Benders A, Jost C, van Deursen J, Tullson P, Terjung R, Jap P, Jacob W, Pette D, Wieringa B. Steeghs K, et al. Among authors: de haan a, de bie m. Mol Cell Biochem. 1998 Jul;184(1-2):183-94. Mol Cell Biochem. 1998. PMID: 9746321 Free article.

7

Muscle characteristics and altered myofascial force transmission in tenascin-X-deficient mice, a mouse model of Ehlers-Danlos syndrome.

Huijing PA, Voermans NC, Baan GC, Busé TE, van Engelen BG, de Haan A. Huijing PA, et al. Among authors: de haan a. J Appl Physiol (1985). 2010 Oct;109(4):986-95. doi: 10.1152/japplphysiol.00723.2009. Epub 2010 Jun 24. J Appl Physiol (1985). 2010. PMID: 20576846 Free article.

8

Neuromuscular properties of the thigh muscles in patients with Ehlers-Danlos syndrome.

Gerrits KH, Voermans NC, de Haan A, van Engelen BG. Gerrits KH, et al. Among authors: de haan a. Muscle Nerve. 2013 Jan;47(1):96-104. doi: 10.1002/mus.23482. Epub 2012 Nov 21. Muscle Nerve. 2013. PMID: 23169204

9

Compound heterozygous mutations of the TNXB gene cause primary myopathy.

Voermans NC, Gerrits K, van Engelen BG, de Haan A. Voermans NC, et al. Among authors: de haan a. Neuromuscul Disord. 2014 Jan;24(1):88-9. doi: 10.1016/j.nmd.2013.10.007. Epub 2013 Nov 5. Neuromuscul Disord. 2014. PMID: 24300784 No abstract available.

10

Muscle slowness in a family with nemaline myopathy.

Pauw-Gommans IM, Gerrits KH, de Haan A, van Engelen BG. Pauw-Gommans IM, et al. Among authors: de haan a. Neuromuscul Disord. 2006 Aug;16(8):477-80. doi: 10.1016/j.nmd.2006.05.003. Epub 2006 Jun 21. Neuromuscul Disord. 2006. PMID: 16793268

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