Frants RR - Search Results

1

Molecular genetic reevaluation of the Dutch hyperekplexia family.

Tijssen MA, Shiang R, van Deutekom J, Boerman RH, Wasmuth JJ, Sandkuijl LA, Frants RR, Padberg GW. Tijssen MA, et al. Among authors: frants rr. Arch Neurol. 1995 Jun;52(6):578-82. doi: 10.1001/archneur.1995.00540300052012. Arch Neurol. 1995. PMID: 7763205 Free article.

2

Facioscapulohumeral muscular dystrophy in the Dutch population.

Padberg GW, Frants RR, Brouwer OF, Wijmenga C, Bakker E, Sandkuijl LA. Padberg GW, et al. Among authors: frants rr. Muscle Nerve Suppl. 1995;2:S81-4. Muscle Nerve Suppl. 1995. PMID: 7739631 Free article.

3

Facioscapulohumeral muscular dystrophy in early childhood.

Brouwer OF, Padberg GW, Wijmenga C, Frants RR. Brouwer OF, et al. Among authors: frants rr. Arch Neurol. 1994 Apr;51(4):387-94. doi: 10.1001/archneur.1994.00540160085011. Arch Neurol. 1994. PMID: 8155016 Review.

4

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. Among authors: frants rr. Clin Neurol Neurosurg. 1993 Jun;95(2):125-9. doi: 10.1016/0303-8467(93)90006-3. Clin Neurol Neurosurg. 1993. PMID: 8344010

5

Hyperekplexia-like syndromes without mutations in the GLRA1 gene.

Vergouwe MN, Tijssen MA, Shiang R, van Dijk JG, al Shahwan S, Ophoff RA, Frants RR. Vergouwe MN, et al. Among authors: frants rr. Clin Neurol Neurosurg. 1997 Aug;99(3):172-8. doi: 10.1016/s0303-8467(97)00022-x. Clin Neurol Neurosurg. 1997. PMID: 9350397

6

Hyperekplexia phenotype due to compound heterozygosity for GLRA1 gene mutations.

Vergouwe MN, Tijssen MA, Peters AC, Wielaard R, Frants RR. Vergouwe MN, et al. Among authors: frants rr. Ann Neurol. 1999 Oct;46(4):634-8. doi: 10.1002/1531-8249(199910)46:4<634::aid-ana12>3.0.co;2-9. Ann Neurol. 1999. PMID: 10514101

7

Pulsed-field gel electrophoresis of the D4F104S1 locus reveals the size and the parental origin of the facioscapulohumeral muscular dystrophy (FSHD)-associated deletions.

Wijmenga C, van Deutekom JC, Hewitt JE, Padberg GW, van Ommen GJ, Hofker MH, Frants RR. Wijmenga C, et al. Among authors: frants rr. Genomics. 1994 Jan 1;19(1):21-6. doi: 10.1006/geno.1994.1006. Genomics. 1994. PMID: 7910579

8

Genetic heterogeneity of familial hemiplegic migraine.

Ophoff RA, van Eijk R, Sandkuijl LA, Terwindt GM, Grubben CP, Haan J, Lindhout D, Ferrari MD, Frants RR. Ophoff RA, et al. Among authors: frants rr. Genomics. 1994 Jul 1;22(1):21-6. doi: 10.1006/geno.1994.1340. Genomics. 1994. PMID: 7959770

9

Genetics of seven Dutch familial atypical multiple mole-melanoma syndrome families: a review of linkage results including chromosomes 1 and 9.

Bergman W, Gruis NA, Sandkuijl LA, Frants RR. Bergman W, et al. Among authors: frants rr. J Invest Dermatol. 1994 Nov;103(5 Suppl):122S-125S. doi: 10.1111/1523-1747.ep12399430. J Invest Dermatol. 1994. PMID: 7963673 Free article.

10

Facioscapulohumeral muscular dystrophy: the impact of genetic research.

Brouwer OF, Wijmenga C, Frants RR, Padberg GW. Brouwer OF, et al. Among authors: frants rr. Clin Neurol Neurosurg. 1993 Mar;95(1):9-21. doi: 10.1016/0303-8467(93)90086-v. Clin Neurol Neurosurg. 1993. PMID: 8095870 Review.

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