Starr A - Search Results

1

OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele.

Varga R, Avenarius MR, Kelley PM, Keats BJ, Berlin CI, Hood LJ, Morlet TG, Brashears SM, Starr A, Cohn ES, Smith RJ, Kimberling WJ. Varga R, et al. Among authors: starr a. J Med Genet. 2006 Jul;43(7):576-81. doi: 10.1136/jmg.2005.038612. Epub 2005 Dec 21. J Med Genet. 2006. PMID: 16371502 Free PMC article.

2

Non-syndromic recessive auditory neuropathy is the result of mutations in the otoferlin (OTOF) gene.

Varga R, Kelley PM, Keats BJ, Starr A, Leal SM, Cohn E, Kimberling WJ. Varga R, et al. Among authors: starr a. J Med Genet. 2003 Jan;40(1):45-50. doi: 10.1136/jmg.40.1.45. J Med Genet. 2003. PMID: 12525542 Free PMC article. No abstract available.

3

A gene responsible for autosomal dominant auditory neuropathy (AUNA1) maps to 13q14-21.

Kim TB, Isaacson B, Sivakumaran TA, Starr A, Keats BJ, Lesperance MM. Kim TB, et al. Among authors: starr a. J Med Genet. 2004 Nov;41(11):872-6. doi: 10.1136/jmg.2004.020628. J Med Genet. 2004. PMID: 15520414 Free PMC article. No abstract available.

4

Auditory neuropathy.

Starr A, Picton TW, Sininger Y, Hood LJ, Berlin CI. Starr A, et al. Brain. 1996 Jun;119 ( Pt 3):741-53. doi: 10.1093/brain/119.3.741. Brain. 1996. PMID: 8673487

5

Hereditary auditory, vestibular, motor, and sensory neuropathy in a Slovenian Roma (Gypsy) kindred.

Butinar D, Zidar J, Leonardis L, Popovic M, Kalaydjieva L, Angelicheva D, Sininger Y, Keats B, Starr A. Butinar D, et al. Among authors: starr a. Ann Neurol. 1999 Jul;46(1):36-44. doi: 10.1002/1531-8249(199907)46:1<36::aid-ana7>3.0.co;2-j. Ann Neurol. 1999. PMID: 10401778

6

Pathology and physiology of auditory neuropathy with a novel mutation in the MPZ gene (Tyr145->Ser).

Starr A, Michalewski HJ, Zeng FG, Fujikawa-Brooks S, Linthicum F, Kim CS, Winnier D, Keats B. Starr A, et al. Brain. 2003 Jul;126(Pt 7):1604-19. doi: 10.1093/brain/awg156. Epub 2003 May 6. Brain. 2003. PMID: 12805115

7

A dominantly inherited progressive deafness affecting distal auditory nerve and hair cells.

Starr A, Isaacson B, Michalewski HJ, Zeng FG, Kong YY, Beale P, Paulson GW, Keats BJ, Lesperance MM. Starr A, et al. J Assoc Res Otolaryngol. 2004 Dec;5(4):411-26. doi: 10.1007/s10162-004-5014-5. J Assoc Res Otolaryngol. 2004. PMID: 15675004 Free PMC article.

8

Hereditary motor and sensory neuropathy--Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries.

Chandler D, Angelicheva D, Heather L, Gooding R, Gresham D, Yanakiev P, de Jonge R, Baas F, Dye D, Karagyozov L, Savov A, Blechschmidt K, Keats B, Thomas PK, King RH, Starr A, Nikolova A, Colomer J, Ishpekova B, Tournev I, Urtizberea JA, Merlini L, Butinar D, Chabrol B, Voit T, Baethmann M, Nedkova V, Corches A, Kalaydjieva L. Chandler D, et al. Among authors: starr a. Neuromuscul Disord. 2000 Dec;10(8):584-91. doi: 10.1016/s0960-8966(00)00148-6. Neuromuscul Disord. 2000. PMID: 11053686

9

Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome.

Simon M, Richard EM, Wang X, Shahzad M, Huang VH, Qaiser TA, Potluri P, Mahl SE, Davila A, Nazli S, Hancock S, Yu M, Gargus J, Chang R, Al-Sheqaih N, Newman WG, Abdenur J, Starr A, Hegde R, Dorn T, Busch A, Park E, Wu J, Schwenzer H, Flierl A, Florentz C, Sissler M, Khan SN, Li R, Guan MX, Friedman TB, Wu DK, Procaccio V, Riazuddin S, Wallace DC, Ahmed ZM, Huang T, Riazuddin S. Simon M, et al. Among authors: starr a. PLoS Genet. 2015 Mar 25;11(3):e1005097. doi: 10.1371/journal.pgen.1005097. eCollection 2015 Mar. PLoS Genet. 2015. PMID: 25807530 Free PMC article.

10

Audibility, speech perception and processing of temporal cues in ribbon synaptic disorders due to OTOF mutations.

Santarelli R, del Castillo I, Cama E, Scimemi P, Starr A. Santarelli R, et al. Among authors: starr a. Hear Res. 2015 Dec;330(Pt B):200-12. doi: 10.1016/j.heares.2015.07.007. Epub 2015 Jul 15. Hear Res. 2015. PMID: 26188103 Review.

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