Similar articles for PMID: 1334371

Year	Number of Results
1989	2
1990	2
1991	5
1992	10
1993	13
1994	5
1995	7
1996	8
1997	2
1998	5
1999	5
2000	5
2001	1
2003	1
2004	2
2005	6
2006	5
2007	1
2008	1
2014	4
2015	2
2018	1
2024	0

1

Genetic and radiation hybrid mapping of the hyperekplexia region on chromosome 5q.

Ryan SG, Dixon MJ, Nigro MA, Kelts KA, Markand ON, Terry JC, Shiang R, Wasmuth JJ, O'Connell P. Ryan SG, et al. Am J Hum Genet. 1992 Dec;51(6):1334-43. Am J Hum Genet. 1992. PMID: 1334371 Free PMC article.

2

Startle disease, or hyperekplexia: response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysis.

Ryan SG, Sherman SL, Terry JC, Sparkes RS, Torres MC, Mackey RW. Ryan SG, et al. Ann Neurol. 1992 Jun;31(6):663-8. doi: 10.1002/ana.410310615. Ann Neurol. 1992. PMID: 1355335

3

Mutations in the alpha 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia.

Shiang R, Ryan SG, Zhu YZ, Hahn AF, O'Connell P, Wasmuth JJ. Shiang R, et al. Nat Genet. 1993 Dec;5(4):351-8. doi: 10.1038/ng1293-351. Nat Genet. 1993. PMID: 8298642

4

Confirmation of the localization of the human GABAA receptor alpha 1-subunit gene (GABRA1) to distal 5q by linkage analysis.

Johnson KJ, Sander T, Hicks AA, van Marle A, Janz D, Mullan MJ, Riley BP, Darlison MG. Johnson KJ, et al. Genomics. 1992 Nov;14(3):745-8. doi: 10.1016/s0888-7543(05)80178-8. Genomics. 1992. PMID: 1330891

5

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. Arch Neurol. 1995 Jun;52(6):578-82. doi: 10.1001/archneur.1995.00540300052012. Arch Neurol. 1995. PMID: 7763205 Free article.

6

Genetic investigation of chromosome 5q GABAA receptor subunit genes in schizophrenia.

Petryshen TL, Middleton FA, Tahl AR, Rockwell GN, Purcell S, Aldinger KA, Kirby A, Morley CP, McGann L, Gentile KL, Waggoner SG, Medeiros HM, Carvalho C, Macedo A, Albus M, Maier W, Trixler M, Eichhammer P, Schwab SG, Wildenauer DB, Azevedo MH, Pato MT, Pato CN, Daly MJ, Sklar P. Petryshen TL, et al. Mol Psychiatry. 2005 Dec;10(12):1074-88, 1057. doi: 10.1038/sj.mp.4001739. Mol Psychiatry. 2005. PMID: 16172613 Clinical Trial.

7

Genetic and physical mapping of the Treacher Collins syndrome locus with respect to loci in the chromosome 5q3 region.

Jabs EW, Li X, Lovett M, Yamaoka LH, Taylor E, Speer MC, Coss C, Cadle R, Hall B, Brown K, et al. Jabs EW, et al. Genomics. 1993 Oct;18(1):7-13. doi: 10.1006/geno.1993.1420. Genomics. 1993. PMID: 8276417

8

A combined genetic and radiation hybrid map surrounding the Treacher Collins syndrome locus on chromosome 5q.

Loftus SK, Edwards SJ, Scherpbier-Heddema T, Buetow KH, Wasmuth JJ, Dixon MJ. Loftus SK, et al. Hum Mol Genet. 1993 Nov;2(11):1785-92. doi: 10.1093/hmg/2.11.1785. Hum Mol Genet. 1993. PMID: 8281138

9

Hyperekplexia in two siblings.

Kulkarni ML, Kannan B, Mathadh P. Kulkarni ML, et al. Indian J Pediatr. 2006 Dec;73(12):1109-11. doi: 10.1007/BF02763057. Indian J Pediatr. 2006. PMID: 17202641

10

[Hyperekplexia -- a treatable neuropediatric disease].

Freilinger M, Jalowetz S, Reiter E, Schubert MT, Seidl R. Freilinger M, et al. Klin Padiatr. 2005 Jul-Aug;217(4):220-1. doi: 10.1055/s-2004-820286. Klin Padiatr. 2005. PMID: 16032547 German.

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