Matthijs G - Search Results

1

Familial juvenile focal amyotrophy of the upper extremity (Hirayama disease). Superoxide dismutase 1 genotype and activity.

Robberecht W, Aguirre T, Van den Bosch L, Theys P, Nees H, Cassiman JJ, Matthijs G. Robberecht W, et al. Among authors: matthijs g. Arch Neurol. 1997 Jan;54(1):46-50. doi: 10.1001/archneur.1997.00550130032012. Arch Neurol. 1997. PMID: 9006413

2

D90A heterozygosity in the SOD1 gene is associated with familial and apparently sporadic amyotrophic lateral sclerosis.

Robberecht W, Aguirre T, Van den Bosch L, Tilkin P, Cassiman JJ, Matthijs G. Robberecht W, et al. Among authors: matthijs g. Neurology. 1996 Nov;47(5):1336-9. doi: 10.1212/wnl.47.5.1336. Neurology. 1996. PMID: 8909456

3

Mutational analysis of the Cu/Zn superoxide dismutase gene in 23 familial and 69 sporadic cases of amyotrophic lateral sclerosis in Belgium.

Aguirre T, Matthijs G, Robberecht W, Tilkin P, Cassiman JJ. Aguirre T, et al. Among authors: matthijs g. Eur J Hum Genet. 1999 Jul;7(5):599-602. doi: 10.1038/sj.ejhg.5200337. Eur J Hum Genet. 1999. PMID: 10439968

4

Clinical and molecular genetic features of congenital spinal muscular atrophy.

Devriendt K, Lammens M, Schollen E, Van Hole C, Dom R, Devlieger H, Cassiman JJ, Fryns JP, Matthijs G. Devriendt K, et al. Among authors: matthijs g. Ann Neurol. 1996 Nov;40(5):731-8. doi: 10.1002/ana.410400509. Ann Neurol. 1996. PMID: 8957014

5

Lack of homozygotes for the most frequent disease allele in carbohydrate-deficient glycoprotein syndrome type 1A.

Matthijs G, Schollen E, Van Schaftingen E, Cassiman JJ, Jaeken J. Matthijs G, et al. Am J Hum Genet. 1998 Mar;62(3):542-50. doi: 10.1086/301763. Am J Hum Genet. 1998. PMID: 9497260 Free PMC article.

6

Demographic characteristics and prognosis in a Flemish amyotrophic lateral sclerosis population.

Thijs V, Peeters E, Theys P, Matthijs G, Robberecht W. Thijs V, et al. Among authors: matthijs g. Acta Neurol Belg. 2000 Jun;100(2):84-90. Acta Neurol Belg. 2000. PMID: 10934559

7

The occurrence of mutations in FUS in a Belgian cohort of patients with familial ALS.

Damme PV, Goris A, Race V, Hersmus N, Dubois B, Bosch LV, Matthijs G, Robberecht W. Damme PV, et al. Among authors: matthijs g. Eur J Neurol. 2010 May;17(5):754-6. doi: 10.1111/j.1468-1331.2009.02859.x. Epub 2009 Nov 13. Eur J Neurol. 2010. PMID: 19922450

8

Expanded ATXN2 CAG repeat size in ALS identifies genetic overlap between ALS and SCA2.

Van Damme P, Veldink JH, van Blitterswijk M, Corveleyn A, van Vught PW, Thijs V, Dubois B, Matthijs G, van den Berg LH, Robberecht W. Van Damme P, et al. Among authors: matthijs g. Neurology. 2011 Jun 14;76(24):2066-72. doi: 10.1212/WNL.0b013e31821f445b. Epub 2011 May 11. Neurology. 2011. PMID: 21562247

9

Unusual molecular findings in autosomal recessive spinal muscular atrophy.

Matthijs G, Schollen E, Legius E, Devriendt K, Goemans N, Kayserili H, Apäk MY, Cassiman JJ. Matthijs G, et al. J Med Genet. 1996 Jun;33(6):469-74. doi: 10.1136/jmg.33.6.469. J Med Genet. 1996. PMID: 8782046 Free PMC article.

10

Non-syndromic deafness associated with a mutation and a polymorphism in the mitochondrial 12S ribosomal RNA gene in a large Zairean pedigree.

Matthijs G, Claes S, Longo-Mbenza B, Cassiman JJ. Matthijs G, et al. Eur J Hum Genet. 1996;4(1):46-51. doi: 10.1159/000472169. Eur J Hum Genet. 1996. PMID: 8800928

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