-
1
-
-
34447500724
-
Causative factors and epidemiology of bilateral vestibulopathy in 255 patients
-
Zingler V.C., Cnyrim C., Jahn K., Weintz E., Fernbacher J., Frenzel C., Brandt T., and Strupp M. Causative factors and epidemiology of bilateral vestibulopathy in 255 patients. Ann. Neurol. 61 (2007) 524-532
-
(2007)
Ann. Neurol.
, vol.61
, pp. 524-532
-
-
Zingler, V.C.1
Cnyrim, C.2
Jahn, K.3
Weintz, E.4
Fernbacher, J.5
Frenzel, C.6
Brandt, T.7
Strupp, M.8
-
2
-
-
27644450442
-
Vestibular loss causes hippocampal atrophy and impaired spatial memory in humans
-
Brandt T., Schautzer F., Hamilton D.A., Brüning R., Markowitsch H.J., Kalla R., Darlington C., Smith P., and Strupp M. Vestibular loss causes hippocampal atrophy and impaired spatial memory in humans. Brain 128 (2005) 2732-2741
-
(2005)
Brain
, vol.128
, pp. 2732-2741
-
-
Brandt, T.1
Schautzer, F.2
Hamilton, D.A.3
Brüning, R.4
Markowitsch, H.J.5
Kalla, R.6
Darlington, C.7
Smith, P.8
Strupp, M.9
-
4
-
-
37849038231
-
Recent advances in the genetics of recurrent vertigo and vestibulopathy
-
Jen J.C. Recent advances in the genetics of recurrent vertigo and vestibulopathy. Curr. Opin. Neurol. 21 (2008) 3-7
-
(2008)
Curr. Opin. Neurol.
, vol.21
, pp. 3-7
-
-
Jen, J.C.1
-
5
-
-
50249178612
-
Susceptibility genes for gentamicin-induced vestibular dysfunction
-
Roth S.M., Williams S.M., Jiang L., Menon K.S., and Jeka J.J. Susceptibility genes for gentamicin-induced vestibular dysfunction. J. Vestib. Res. 18 (2008) 59-68
-
(2008)
J. Vestib. Res.
, vol.18
, pp. 59-68
-
-
Roth, S.M.1
Williams, S.M.2
Jiang, L.3
Menon, K.S.4
Jeka, J.J.5
-
6
-
-
35548963935
-
Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip
-
Lévêque M., Marlin S., Jonard L., Procaccio V., Reynier P., Amati-Bonneau P., Baulande S., Pierron D., Lacombe D., Duriez F., Francannet C., Mom T., Journel H., Catros H., Drouin-Garraud V., Obstoy M.F., Dollfus H., Eliot M.M., Faivre L., Duvillard C., Couderc R., Garabedian E.N., Petit C., Feldmann D., and Denoyelle F. Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip. Eur. J. Hum. Genet. 15 (2007) 1145-1155
-
(2007)
Eur. J. Hum. Genet.
, vol.15
, pp. 1145-1155
-
-
Lévêque, M.1
Marlin, S.2
Jonard, L.3
Procaccio, V.4
Reynier, P.5
Amati-Bonneau, P.6
Baulande, S.7
Pierron, D.8
Lacombe, D.9
Duriez, F.10
Francannet, C.11
Mom, T.12
Journel, H.13
Catros, H.14
Drouin-Garraud, V.15
Obstoy, M.F.16
Dollfus, H.17
Eliot, M.M.18
Faivre, L.19
Duvillard, C.20
Couderc, R.21
Garabedian, E.N.22
Petit, C.23
Feldmann, D.24
Denoyelle, F.25
more..
-
7
-
-
33644547013
-
Molecular understanding of aminoglycoside action and resistance
-
Jana S., and Deb J.K. Molecular understanding of aminoglycoside action and resistance. Appl. Microbiol. Biotechnol. (2006) 1-11
-
(2006)
Appl. Microbiol. Biotechnol.
, pp. 1-11
-
-
Jana, S.1
Deb, J.K.2
-
8
-
-
0030827973
-
Specific binding of aminoglycosides to a human rRNA construct based on a DNA polymorphism which causes aminoglycoside-induced deafness
-
Hamasaki K., and Rando R.R. Specific binding of aminoglycosides to a human rRNA construct based on a DNA polymorphism which causes aminoglycoside-induced deafness. Biochemistry 36 (1997) 12323-12380
-
(1997)
Biochemistry
, vol.36
, pp. 12323-12380
-
-
Hamasaki, K.1
Rando, R.R.2
-
9
-
-
46249111398
-
Mitochondrial non-syndromic sensorineural hearing loss: a clinical, audiological and pathological study from Italy, and revision of the literature
-
Berrettini S., Forli F., Passetti S., Rocchi A., Pollina L., Cecchetti D., Mancuso M., and Siciliano G. Mitochondrial non-syndromic sensorineural hearing loss: a clinical, audiological and pathological study from Italy, and revision of the literature. Biosci. Rep. 28 (2008) 49-59
-
(2008)
Biosci. Rep.
, vol.28
, pp. 49-59
-
-
Berrettini, S.1
Forli, F.2
Passetti, S.3
Rocchi, A.4
Pollina, L.5
Cecchetti, D.6
Mancuso, M.7
Siciliano, G.8
-
10
-
-
17344365276
-
Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides
-
Estivill X., Govea N., Barceló E., Badenas C., Romero E., Moral L., Scozzri R., D'Urbano L., Zeviani M., and Torroni A. Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides. Am. J. Hum. Genet. 62 (1998) 27-35
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 27-35
-
-
Estivill, X.1
Govea, N.2
Barceló, E.3
Badenas, C.4
Romero, E.5
Moral, L.6
Scozzri, R.7
D'Urbano, L.8
Zeviani, M.9
Torroni, A.10
-
11
-
-
33847000885
-
Histopathology of the vestibular end organs after intratympanic gentamicin failure for Meniere's disease
-
Ishiyama G., Lopez I., Baloh R.W., and Ishiyama A. Histopathology of the vestibular end organs after intratympanic gentamicin failure for Meniere's disease. Acta Otolaryngol. 127 (2007) 34-40
-
(2007)
Acta Otolaryngol.
, vol.127
, pp. 34-40
-
-
Ishiyama, G.1
Lopez, I.2
Baloh, R.W.3
Ishiyama, A.4
-
12
-
-
35248821352
-
Vestibular system in infants after systemic aminoglycoside therapy
-
Zagólski O. Vestibular system in infants after systemic aminoglycoside therapy. Int. J. Pediatr. Otorhinolaryngol. 71 (2007) 1797-1802
-
(2007)
Int. J. Pediatr. Otorhinolaryngol.
, vol.71
, pp. 1797-1802
-
-
Zagólski, O.1
-
13
-
-
0030716844
-
Clinical-pathologic correlation in a patient with selective loss of hair cells in the vestibular endorgans
-
Baloh R.W., Lopez I., Beykirch K., Ishiyama A., and Honrubia V. Clinical-pathologic correlation in a patient with selective loss of hair cells in the vestibular endorgans. Neurology 49 (1997) 1377-1820
-
(1997)
Neurology
, vol.49
, pp. 1377-1820
-
-
Baloh, R.W.1
Lopez, I.2
Beykirch, K.3
Ishiyama, A.4
Honrubia, V.5
-
14
-
-
0027226069
-
Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness
-
Prezant T.R., Agapian J.V., Bohlman M.C., Bu X., Oztas S., Qiu W.Q., Arnos K.S., Cortopassi G.A., Jaber L., Rotter J.I., et al. Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness. Nat. Genet. 4 (1993) 289-294
-
(1993)
Nat. Genet.
, vol.4
, pp. 289-294
-
-
Prezant, T.R.1
Agapian, J.V.2
Bohlman, M.C.3
Bu, X.4
Oztas, S.5
Qiu, W.Q.6
Arnos, K.S.7
Cortopassi, G.A.8
Jaber, L.9
Rotter, J.I.10
-
15
-
-
0029832209
-
Audiovestibular findings in patients with deafness caused by a mitochondrial susceptibility mutation and precipitated by an inherited nuclear mutation or aminoglycosides
-
Braverman I., Jaber L., Levi H., Adelman C., Arons K.S., Fischel-Ghodsian N., Shohat M., and Elidan J. Audiovestibular findings in patients with deafness caused by a mitochondrial susceptibility mutation and precipitated by an inherited nuclear mutation or aminoglycosides. Arch. Otolaryngol. Head Neck Surg. 122 (1996) 1001-1004
-
(1996)
Arch. Otolaryngol. Head Neck Surg.
, vol.122
, pp. 1001-1004
-
-
Braverman, I.1
Jaber, L.2
Levi, H.3
Adelman, C.4
Arons, K.S.5
Fischel-Ghodsian, N.6
Shohat, M.7
Elidan, J.8
-
16
-
-
0035134021
-
Different clinical characteristics of aminoglycoside-induced profound deafness with and without the 1555 A>G mitochondrial mutation
-
Tono T., Kiyomizu K., Matsuda K., Komune S., Usami S., Abe S., and Shinkawa H. Different clinical characteristics of aminoglycoside-induced profound deafness with and without the 1555 A>G mitochondrial mutation. ORL J. Otorhinolaryngol. Relat. Spec. 63 (2001) 25-30
-
(2001)
ORL J. Otorhinolaryngol. Relat. Spec.
, vol.63
, pp. 25-30
-
-
Tono, T.1
Kiyomizu, K.2
Matsuda, K.3
Komune, S.4
Usami, S.5
Abe, S.6
Shinkawa, H.7
-
17
-
-
0842277862
-
Audiovestibular findings in patients with mitochondrial A1555G mutation
-
Noguchi Y., Yashima T., Ito T., Sumi T., Tsuzuku T., and Kitamura K. Audiovestibular findings in patients with mitochondrial A1555G mutation. Laryngoscope 114 (2004) 344-348
-
(2004)
Laryngoscope
, vol.114
, pp. 344-348
-
-
Noguchi, Y.1
Yashima, T.2
Ito, T.3
Sumi, T.4
Tsuzuku, T.5
Kitamura, K.6
-
18
-
-
33644875533
-
MtDB: Human Mitochondrial Genome Database, a resource for population genetics and medical sciences
-
Ingman M., and Gyllensten U. MtDB: Human Mitochondrial Genome Database, a resource for population genetics and medical sciences. Nucleic Acids Res. 34 (2006) D749-D751
-
(2006)
Nucleic Acids Res.
, vol.34
-
-
Ingman, M.1
Gyllensten, U.2
-
19
-
-
36448991500
-
Clustal W and Clustal X version 2.0
-
Larkin M.A., Blackshields G., Brown N.P., Chenna R., McGettigan P.A., McWilliam H., Valentin F., Wallace I.M., Wilm A., Lopez R., Thompson J.D., Gibson T.J., and Higgins D.G. Clustal W and Clustal X version 2.0. Bioinformatics 23 (2007) 2947-2948
-
(2007)
Bioinformatics
, vol.23
, pp. 2947-2948
-
-
Larkin, M.A.1
Blackshields, G.2
Brown, N.P.3
Chenna, R.4
McGettigan, P.A.5
McWilliam, H.6
Valentin, F.7
Wallace, I.M.8
Wilm, A.9
Lopez, R.10
Thompson, J.D.11
Gibson, T.J.12
Higgins, D.G.13
-
21
-
-
7444244924
-
Assigning pathogenicity to mitochondrial tRNA mutations: when "definitely maybe" is not good enough
-
McFarland R., Elson J.L., Taylor R.W., Howell N., and Turnbull D.M. Assigning pathogenicity to mitochondrial tRNA mutations: when "definitely maybe" is not good enough. Trends Genet. 20 (2004) 591-596
-
(2004)
Trends Genet.
, vol.20
, pp. 591-596
-
-
McFarland, R.1
Elson, J.L.2
Taylor, R.W.3
Howell, N.4
Turnbull, D.M.5
-
22
-
-
18444373246
-
Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation
-
Giordano C., Pallotti F., Walker W.F., Checcarelli N., Musumeci O., Santorelli F., d'Amati G., Schon E.A., DiMauro S., Hirano M., and Davidson M.M. Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation. Biochem. Biophys. Res. Commun. 293 (2002) 521-529
-
(2002)
Biochem. Biophys. Res. Commun.
, vol.293
, pp. 521-529
-
-
Giordano, C.1
Pallotti, F.2
Walker, W.F.3
Checcarelli, N.4
Musumeci, O.5
Santorelli, F.6
d'Amati, G.7
Schon, E.A.8
DiMauro, S.9
Hirano, M.10
Davidson, M.M.11
-
23
-
-
0030601096
-
Mutant mtDNA at 1555 A to G in 12S rRNA gene and hypersusceptibility of mitochondrial translation to streptomycin can be co-transferred to rho 0 HeLa cells
-
Inoue K., Takai D., Soejima A., Isobe K., Yamasoba T., Oka Y., Goto Y., and Hayashi J. Mutant mtDNA at 1555 A to G in 12S rRNA gene and hypersusceptibility of mitochondrial translation to streptomycin can be co-transferred to rho 0 HeLa cells. Biochem. Biophys. Res. Commun. 223 (1996) 496-501
-
(1996)
Biochem. Biophys. Res. Commun.
, vol.223
, pp. 496-501
-
-
Inoue, K.1
Takai, D.2
Soejima, A.3
Isobe, K.4
Yamasoba, T.5
Oka, Y.6
Goto, Y.7
Hayashi, J.8
-
24
-
-
0347003512
-
Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family
-
Zhao H., Li R., Wang Q., Yan Q., Deng J.H., Han D., Bai Y., Young W.Y., and Guan M.X. Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family. Am. J. Hum. Genet. 74 (2004) 139-152
-
(2004)
Am. J. Hum. Genet.
, vol.74
, pp. 139-152
-
-
Zhao, H.1
Li, R.2
Wang, Q.3
Yan, Q.4
Deng, J.H.5
Han, D.6
Bai, Y.7
Young, W.Y.8
Guan, M.X.9
-
25
-
-
19944430235
-
Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation
-
Wang Q., Li R., Zhao H., Peters J.L., Liu Q., Yang L., Han D., Greinwald J.H.J., Young W.Y., and Guan M.X. Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation. Am. J. Med. Genet. A 133A (2005) 27-30
-
(2005)
Am. J. Med. Genet. A
, vol.133 A
, pp. 27-30
-
-
Wang, Q.1
Li, R.2
Zhao, H.3
Peters, J.L.4
Liu, Q.5
Yang, L.6
Han, D.7
Greinwald, J.H.J.8
Young, W.Y.9
Guan, M.X.10
-
26
-
-
33646185290
-
A reappraisal of complete mtDNA variation in East Asian families with hearing impairment
-
Yao Y.G., Salas A., Bravi C.M., and Bandelt H.J. A reappraisal of complete mtDNA variation in East Asian families with hearing impairment. Hum. Genet. 119 (2006) 505-515
-
(2006)
Hum. Genet.
, vol.119
, pp. 505-515
-
-
Yao, Y.G.1
Salas, A.2
Bravi, C.M.3
Bandelt, H.J.4
-
27
-
-
0029003553
-
Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafness
-
Bacino C., Prezant T.R., Bu X., Fournier P., and Fischel-Ghodsian N. Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafness. Pharmacogenetics 5 (1995) 165-172
-
(1995)
Pharmacogenetics
, vol.5
, pp. 165-172
-
-
Bacino, C.1
Prezant, T.R.2
Bu, X.3
Fournier, P.4
Fischel-Ghodsian, N.5
-
28
-
-
13044279515
-
Inherited susceptibility to aminoglycoside ototoxicity: genetic heterogeneity and clinical implications
-
Casano R.A., Johnson D.F., Bykhovskaya Y., Torricelli F., Bigozzi M., and Fischel-Ghodsian N. Inherited susceptibility to aminoglycoside ototoxicity: genetic heterogeneity and clinical implications. Am. J. Otolaryngol. 20 (1999) 151-156
-
(1999)
Am. J. Otolaryngol.
, vol.20
, pp. 151-156
-
-
Casano, R.A.1
Johnson, D.F.2
Bykhovskaya, Y.3
Torricelli, F.4
Bigozzi, M.5
Fischel-Ghodsian, N.6
-
29
-
-
0344167734
-
Cosegregation of C-insertion at position 961 with the A1555G mutation of the mitochondrial 12S rRNA gene in a large Chinese family with maternally inherited hearing loss
-
Li R., Xing G., Yan M., Cao X., Liu X.Z., Bu X., and Guan M.X. Cosegregation of C-insertion at position 961 with the A1555G mutation of the mitochondrial 12S rRNA gene in a large Chinese family with maternally inherited hearing loss. Am. J. Med. Genet. A 124 (2004) 113-117
-
(2004)
Am. J. Med. Genet. A
, vol.124
, pp. 113-117
-
-
Li, R.1
Xing, G.2
Yan, M.3
Cao, X.4
Liu, X.Z.5
Bu, X.6
Guan, M.X.7
-
30
-
-
4043089861
-
Molecular analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in paediatric subjects with non-syndromic hearing loss
-
Li R., Greinwald J.H.J., Yang L., Choo D.I., Wenstrup R.J., and Guan M.X. Molecular analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in paediatric subjects with non-syndromic hearing loss. J. Med. Genet. 41 (2004) 615-620
-
(2004)
J. Med. Genet.
, vol.41
, pp. 615-620
-
-
Li, R.1
Greinwald, J.H.J.2
Yang, L.3
Choo, D.I.4
Wenstrup, R.J.5
Guan, M.X.6
-
31
-
-
20344407298
-
Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss
-
Li Z., Li R., Chen J., Liao Z., Zhu Y., Qian Y., Xiong S., Heman-Ackah S., Wu J., Choo D.I., and Guan M.X. Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss. Hum. Genet. 117 (2005) 9-15
-
(2005)
Hum. Genet.
, vol.117
, pp. 9-15
-
-
Li, Z.1
Li, R.2
Chen, J.3
Liao, Z.4
Zhu, Y.5
Qian, Y.6
Xiong, S.7
Heman-Ackah, S.8
Wu, J.9
Choo, D.I.10
Guan, M.X.11
-
32
-
-
8844236333
-
Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation
-
Zhao L., Young W.Y., Li R., Wang Q., Qian Y., and Guan M.X. Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation. Biochem. Biophys. Res. Commun. 325 (2004) 1503-1508
-
(2004)
Biochem. Biophys. Res. Commun.
, vol.325
, pp. 1503-1508
-
-
Zhao, L.1
Young, W.Y.2
Li, R.3
Wang, Q.4
Qian, Y.5
Guan, M.X.6
-
33
-
-
0036726578
-
Genetic susceptibility to aminoglycoside ototoxicity: how many are at risk?
-
Tang H.Y., Hutcheson E., Neill S., Drummond-Borg M., Speer M., and Alford R.L. Genetic susceptibility to aminoglycoside ototoxicity: how many are at risk?. Genet. Med. 4 (2002) 336-345
-
(2002)
Genet. Med.
, vol.4
, pp. 336-345
-
-
Tang, H.Y.1
Hutcheson, E.2
Neill, S.3
Drummond-Borg, M.4
Speer, M.5
Alford, R.L.6
|