-
2
-
-
66049150303
-
Permanent bilateral sensory and neural hearing loss of children after neonatal intensive care because of extreme prematurity: A thirty-year study
-
Robertson CM, Howarth TM, Bork DL, et al. Permanent bilateral sensory and neural hearing loss of children after neonatal intensive care because of extreme prematurity: A thirty-year study. Pediatrics 2009;123:e797-807.
-
(2009)
Pediatrics
, vol.123
-
-
Robertson, C.M.1
Howarth, T.M.2
Bork, D.L.3
-
3
-
-
0025980075
-
Genetic aspects of antibiotic induced deafness: Mitochondrial inheritance
-
Hu DN, Qui WQ, Wu BT, et al. Genetic aspects of antibiotic induced deafness: mitochondrial inheritance. J Med Genet 1991;28:79-83.
-
(1991)
J Med Genet
, vol.28
, pp. 79-83
-
-
Hu, D.N.1
Qui, W.Q.2
Wu, B.T.3
-
4
-
-
0024360825
-
Unique inheritance of streptomycin-induced deafness
-
Higashi K. Unique inheritance of streptomycin-induced deafness. Clin Genet 1989;35:433-6. (Pubitemid 19149832)
-
(1989)
Clinical Genetics
, vol.35
, Issue.6
, pp. 433-436
-
-
Higashi, K.1
-
5
-
-
0021365039
-
Risk factors for the development of auditory toxicity in patients receiving aminoglycosides
-
Moore RD, Smith CR, Lietman PS. Risk factors for the development of auditory toxicity in patients with aminoglycosides. J Infect Dis 1984;149:23-30. (Pubitemid 14179885)
-
(1984)
Journal of Infectious Diseases
, vol.149
, Issue.1
, pp. 23-30
-
-
Moore, R.D.1
Smith, C.R.2
Lietman, P.S.3
-
6
-
-
0033858002
-
A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity
-
Guan MX, Fischel-Ghodsian N, Attardi G. A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity. Hum Mol Genet 2000;9:1787-93. (Pubitemid 30608612)
-
(2000)
Human Molecular Genetics
, vol.9
, Issue.12
, pp. 1787-1793
-
-
Guan, M.-X.1
Fischel-Ghodsian, N.2
Attardi, G.3
-
7
-
-
4043089861
-
Ser(UCN) genes in paediatric subjects with non-syndromic hearing loss
-
Li R, Greinwald JH, Yang L, et al. Molecular analysis of the mito-chondrial 12S rRNA and tRNASer (UCN) genes in paediatric subjects with non-syndromic hearing loss. J Med Genet 2004;41:615-20. (Pubitemid 39061268)
-
(2004)
Journal of Medical Genetics
, vol.41
, Issue.8
, pp. 615-620
-
-
Li, R.1
Greinwald Jr., J.H.2
Yang, L.3
Choo, D.I.4
Wenstrup, R.J.5
Guan, M.-X.6
-
8
-
-
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
-
DOI 10.1086/381133
-
Zhao H, Li R, Wang Q, et al. Maternally inherited aminoglycoside-induced and nonsyndromic deafness associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family. Am J Hum Genet 2004;74:139-52. (Pubitemid 38085245)
-
(2004)
American Journal of Human Genetics
, vol.74
, Issue.1
, 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
-
9
-
-
0033058511
-
Mitochondrial deafness mutations reviewed
-
DOI 10.1002/(SICI)1098-1004(1999)13:4 <261::AID-HUMU1> 3.0.CO;2-W
-
Fischel-Ghodsian N. Mitochondrial deafness mutations reviewed. Hum Mutat 1999;13:261-70. (Pubitemid 29307069)
-
(1999)
Human Mutation
, vol.13
, Issue.4
, pp. 261-270
-
-
Fischel-Ghodsian, N.1
-
11
-
-
0036726578
-
Genetic susceptibility to aminoglycoside ototoxicity: How many are at risk?
-
DOI 10.1097/00125817-200209000-00004
-
Tang HY, Hutcheson E, Neill S, et al. Genetic susceptibility to ami-noglycoside ototoxicity: How many are at risk? Genet Med 2002;4: 336-45. (Pubitemid 44698547)
-
(2002)
Genetics in Medicine
, vol.4
, Issue.5
, pp. 336-345
-
-
Tang, H.-Y.1
Hutcheson, E.2
Neill, S.3
Drummond-Borg, M.4
Speer, M.5
Alford, R.L.6
-
12
-
-
49949108551
-
Risk factors associated with sensorineural hearing loss in infants at the neonatal intensive care unit: 15-year experience at the National Institute of Perinatology (Mexico City)
-
Martinez-Cruz CF, Poblano A, Fernandez-Carrocera LA. Risk factors associated with sensorineural hearing loss in infants at the neonatal intensive care unit: 15-year experience at the National Institute of Perinatology (Mexico City). Arch Med Res 2008;39:686-94.
-
(2008)
Arch Med Res
, vol.39
, pp. 686-694
-
-
Martinez-Cruz, C.F.1
Poblano, A.2
Fernandez-Carrocera, L.A.3
-
13
-
-
18344396798
-
Comprehensive human genome amplification using multiple displacement amplification
-
DOI 10.1073/pnas.082089499
-
Dean FB, Hosono S, Fang L, et al. Comprehensive human genome amplification using multiple displacement amplification. Proc Natl Acad Sci U S A 2002;99:5261-6. (Pubitemid 34411536)
-
(2002)
Proceedings of the National Academy of Sciences of the United States of America
, vol.99
, Issue.8
, pp. 5261-5266
-
-
Dean, F.B.1
Hosono, S.2
Fang, L.3
Wu, X.4
Faruqi, A.F.5
Bray-Ward, P.6
Sun, Z.7
Zong, Q.8
Du, Y.9
Du, J.10
Driscoll, M.11
Song, W.12
Kingsmore, S.F.13
Egholm, M.14
Lasken, R.S.15
-
14
-
-
0038781878
-
Unbiased whole-genome amplification directly from clinical samples
-
DOI 10.1101/gr.816903
-
Hosono S, Faruqi AF, Dean FB, et al. Unbiased whole-genome amplification directly from clinical samples. Genome Res 2003;13:954-64. (Pubitemid 36621755)
-
(2003)
Genome Research
, vol.13
, Issue.5
, pp. 954-964
-
-
Hosono, S.1
Faruqi, A.F.2
Dean, F.B.3
Du, Y.4
Sun, Z.5
Wu, X.6
Du, J.7
Kingsmore, S.F.8
Egholm, M.9
Lasken, R.S.10
-
15
-
-
33749253041
-
A multisite study to examine the efficacy of the otoacoustic emission/automatic auditory brainstem response newborn hearing screening protocol: Recommendations for policy, practice, and research
-
Gravel JS, White KR, Johnson JL, et al. A multisite study to examine the efficacy of the otoacoustic emission/automatic auditory brainstem response newborn hearing screening protocol: recommendations for policy, practice, and research. Am J Audiol 2005;14:S217-28.
-
(2005)
Am J Audiol
, vol.14
-
-
Gravel, J.S.1
White, K.R.2
Johnson, J.L.3
-
16
-
-
1842678661
-
Molecular pathogenetic mechanisms of maternally inherited deafness
-
Guan MX. Molecular pathogenetic mechanisms of maternally inherited deafness. Ann N Y Acad Sci 2004;1011:259-71.
-
(2004)
Ann N y Acad Sci
, vol.1011
, pp. 259-271
-
-
Guan, M.X.1
|