Street VA[au] - Search Results

Year	Number of Results
1992	2
1994	1
1995	1
1996	1
1997	2
1998	2
2001	1
2002	2
2003	2
2004	2
2005	1
2008	3
2011	1
2014	1
2024	0

1

Vestibular function in families with inherited autosomal dominant hearing loss.

Street VA, Kallman JC, Strombom PD, Bramhall NF, Phillips JO. Street VA, et al. J Vestib Res. 2008;18(1):51-8. J Vestib Res. 2008. PMID: 18776598 Free PMC article. Review.

2

New gene for CMT.

Street VA, Bennett CL, Bird TD, Chance PF. Street VA, et al. J Peripher Nerv Syst. 2003 Dec;8(4):206. doi: 10.1111/j.1085-9489.2003.03025.x. J Peripher Nerv Syst. 2003. PMID: 14641644 No abstract available.

3

SIMPLE mutation in demyelinating neuropathy and distribution in sciatic nerve.

Bennett CL, Shirk AJ, Huynh HM, Street VA, Nelis E, Van Maldergem L, De Jonghe P, Jordanova A, Guergueltcheva V, Tournev I, Van Den Bergh P, Seeman P, Mazanec R, Prochazka T, Kremensky I, Haberlova J, Weiss MD, Timmerman V, Bird TD, Chance PF. Bennett CL, et al. Among authors: street va. Ann Neurol. 2004 May;55(5):713-20. doi: 10.1002/ana.20094. Ann Neurol. 2004. PMID: 15122712

4

Mutations in a plasma membrane Ca2+-ATPase gene cause deafness in deafwaddler mice.

Street VA, McKee-Johnson JW, Fonseca RC, Tempel BL, Noben-Trauth K. Street VA, et al. Nat Genet. 1998 Aug;19(4):390-4. doi: 10.1038/1284. Nat Genet. 1998. PMID: 9697703

5

Physical and genetic maps of the deafwaddler region on distal mouse Chr 6.

McKee-Johnson JW, Street VA, Erford SK, Robinson LC, Tempel BL. McKee-Johnson JW, et al. Among authors: street va. Genomics. 1998 May 1;49(3):371-7. doi: 10.1006/geno.1998.5274. Genomics. 1998. PMID: 9615221

6

In search of the DFNA11 myosin VIIA low- and mid-frequency auditory genetic modifier.

Kallman JC, Phillips JO, Bramhall NF, Kelly JP, Street VA. Kallman JC, et al. Among authors: street va. Otol Neurotol. 2008 Sep;29(6):860-7. doi: 10.1097/MAO.0b013e3181825651. Otol Neurotol. 2008. PMID: 18667942 Free PMC article.

7

Resistance to noise-induced hearing loss in 129S6 and MOLF mice: identification of independent, overlapping, and interacting chromosomal regions.

Street VA, Kujawa SG, Manichaikul A, Broman KW, Kallman JC, Shilling DJ, Iwata AJ, Robinson LC, Robbins CA, Li J, Liberman MC, Tempel BL. Street VA, et al. J Assoc Res Otolaryngol. 2014 Oct;15(5):721-38. doi: 10.1007/s10162-014-0472-x. Epub 2014 Jun 21. J Assoc Res Otolaryngol. 2014. PMID: 24952082 Free PMC article.

8

The type 1 inositol 1,4,5-trisphosphate receptor gene is altered in the opisthotonos mouse.

Street VA, Bosma MM, Demas VP, Regan MR, Lin DD, Robinson LC, Agnew WS, Tempel BL. Street VA, et al. J Neurosci. 1997 Jan 15;17(2):635-45. doi: 10.1523/JNEUROSCI.17-02-00635.1997. J Neurosci. 1997. PMID: 8987786 Free PMC article.

9

Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1C.

Street VA, Bennett CL, Goldy JD, Shirk AJ, Kleopa KA, Tempel BL, Lipe HP, Scherer SS, Bird TD, Chance PF. Street VA, et al. Neurology. 2003 Jan 14;60(1):22-6. doi: 10.1212/wnl.60.1.22. Neurology. 2003. PMID: 12525712

10

Charcot-Marie-Tooth neuropathy: clinical phenotypes of four novel mutations in the MPZ and Cx 32 genes.

Street VA, Meekins G, Lipe HP, Seltzer WK, Carter GT, Kraft GH, Bird TD. Street VA, et al. Neuromuscul Disord. 2002 Oct;12(7-8):643-50. doi: 10.1016/s0960-8966(02)00021-4. Neuromuscul Disord. 2002. PMID: 12207932

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