Bruyn RP - Search Results

1

Pure hereditary spastic paraparesis: an exclusion map covering more than 40% of the autosomal genome.

van Deutekom JC, Bruyn RP, van den Boorn N, Sandkuijl LA, Padberg GW, Frants RR. van Deutekom JC, et al. Among authors: bruyn rp. Hum Genet. 1994 Apr;93(4):408-14. doi: 10.1007/BF00201665. Hum Genet. 1994. PMID: 8168811

2

Hereditary spastic paraparesis. Clinical and genetic data from a large Dutch family.

Bruyn RP, van Deutekom J, Frants RR, Padberg GW. Bruyn RP, et al. Clin Neurol Neurosurg. 1993 Jun;95(2):125-9. doi: 10.1016/0303-8467(93)90006-3. Clin Neurol Neurosurg. 1993. PMID: 8344010

3

Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p.

Hazan J, Fontaine B, Bruyn RP, Lamy C, van Deutekom JC, Rime CS, Dürr A, Melki J, Lyon-Caen O, Agid Y, et al. Hazan J, et al. Among authors: bruyn rp. Hum Mol Genet. 1994 Sep;3(9):1569-73. doi: 10.1093/hmg/3.9.1569. Hum Mol Genet. 1994. PMID: 7833913

4

Familial spastic paraplegia: evidence for a fourth locus.

Bruyn RP, van Veen MM, Kremer H, Scheltens PH, Padberg GW. Bruyn RP, et al. Clin Neurol Neurosurg. 1997 May;99(2):87-90. doi: 10.1016/s0303-8467(97)00602-1. Clin Neurol Neurosurg. 1997. PMID: 9213050

5

[From gene to disease; spastin and hereditary spastic paraparesis].

Bruyn RP, Frants RR. Bruyn RP, et al. Ned Tijdschr Geneeskd. 2004 Jan 24;148(4):179-81. Ned Tijdschr Geneeskd. 2004. PMID: 14974310 Review. Dutch.

6

A Dutch family with autosomal dominant pure spastic paraparesis (Strümpell's disease).

Scheltens P, Bruyn RP, Hazenberg GJ. Scheltens P, et al. Among authors: bruyn rp. Acta Neurol Scand. 1990 Sep;82(3):169-73. doi: 10.1111/j.1600-0404.1990.tb04484.x. Acta Neurol Scand. 1990. PMID: 2270744 Review.

7

The neuropathology of hereditary spastic paraparesis.

Bruyn RP. Bruyn RP. Clin Neurol Neurosurg. 1992;94 Suppl:S16-8. doi: 10.1016/0303-8467(92)90010-z. Clin Neurol Neurosurg. 1992. PMID: 1320499 Review.

8

Clinically silent dysfunction of dorsal columns and dorsal spinocerebellar tracts in hereditary spastic paraparesis.

Bruyn RP, van Dijk JG, Scheltens P, Boezeman EH, Ongerboer de Visser BW. Bruyn RP, et al. J Neurol Sci. 1994 Sep;125(2):206-11. doi: 10.1016/0022-510x(94)90037-x. J Neurol Sci. 1994. PMID: 7807169

9

Differentiation of hereditary spastic paraparesis from primary lateral sclerosis in sporadic adult-onset upper motor neuron syndromes.

Brugman F, Veldink JH, Franssen H, de Visser M, de Jong JM, Faber CG, Kremer BH, Schelhaas HJ, van Doorn PA, Verschuuren JJ, Bruyn RP, Kuks JB, Robberecht W, Wokke JH, van den Berg LH. Brugman F, et al. Among authors: bruyn rp. Arch Neurol. 2009 Apr;66(4):509-14. doi: 10.1001/archneurol.2009.19. Arch Neurol. 2009. PMID: 19364936

10

Autosomal recessive paraparesis with amyotrophy of the hands and feet.

Bruyn RP, Scheltens P, Lycklama à Nijeholt J, de Jong JM. Bruyn RP, et al. Acta Neurol Scand. 1993 Jun;87(6):443-5. doi: 10.1111/j.1600-0404.1993.tb04133.x. Acta Neurol Scand. 1993. PMID: 8395130

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