Tag deafness [52 articles] Export

Recent papers classified by the tag deafness.

	Is Visual Selective Attention in Deaf Individuals Enhanced or Deficient? The Case of the Useful Field of View [My Copy] PLoS ONE, Vol. 4, No. 5. (20 May 2009), e5640. by Matthew W. Dye, Peter C. Hauser, Daphne Bavelier posted to deafness visual_attention by ybysk on 2009-06-23 09:48:46 as along with 1 person and 1 group sherdim EPLab
	Exploring the perceptual characteristics of voice-hallucinations in deaf people [My Copy] Cognitive Neuropsychiatry, Vol. 12, No. 4. (2007), pp. 339-361. by Joanna R. Atkinson, Kate Gleeson, Jim Cromwell, Sue O'Rourke posted to deafness language sign-language voices by yaxu on 2009-06-22 12:04:21 as
	Genetics: Deaf by design [My Copy] Nature, Vol. 431, No. 7011. (21 October 2004), pp. 894-896. by Carina Dennis posted to article deaf deafness genetics prenatal survey by pakoo on 2009-06-12 22:16:21 as along with 1 person and 1 group ladygoat CGREL
	Attitudes to Genetic Testing for Deafness: The Importance of Informed Choice [My Copy] Journal of Genetic Counseling, Vol. 15, No. 1. (February 2006), pp. 51-59. by Marilys Guillemin, Lynn Gillam posted to deaf deafness genetics prenatal survey testing by pakoo on 2009-06-12 22:13:25 as
	Genetic testing for hearing loss: different motivations for the same outcome. [My Copy] American journal of medical genetics, Vol. 113, No. 2. (22 November 2002), pp. 137-143. by O. Dagan, H. Hochner, H. Levi, A. Raas-Rothschild, M. Sagi posted to deaf deafness genetics prenatal survey testing by pakoo on 2009-06-12 22:07:53 as
	Genetic information but not termination: pregnant women's attitudes and willingness to pay for carrier screening for deafness genes [My Copy] Journal of Medical Genetics, Vol. 40, No. 6. (1 June 2003), e80. by M. Ryan, Z. Miedzybrodzka, L. Fraser, M. Hall posted to deaf deafness genetics prenatal survey testing by pakoo on 2009-06-12 22:04:14 as
	Prenatal diagnosis for inherited deafness--what is the potential demand? [My Copy] Journal of genetic counseling, Vol. 10, No. 2. (April 2001), pp. 121-131. by A. Middleton, J. Hewison, R. Mueller posted to deaf deafness genetics prenatal testing by pakoo on 2009-06-12 21:44:40 as
	Attitudes of deaf and hard of hearing subjects towards genetic testing and prenatal diagnosis of hearing loss. [My Copy] Journal of medical genetics, Vol. 39, No. 6. (June 2002), pp. 449-453. by S. J. Stern, K. S. Arnos, L. Murrelle, K. O. Welch, W. E. Nance, A. Pandya posted to deaf deafness genetics prenatal testing by pakoo on 2009-06-12 21:26:27 as
	Assessment of vestibular function of infants and children with congenital and acquired deafness using the ice-water caloric test, rotational chair test and vestibular-evoked myogenic potential recording. [My Copy] Acta oto-laryngologica, Vol. 127, No. 7. (July 2007), pp. 736-747. by Y. Shinjo, Y. Jin, K. Kaga posted to deafness neurology_physical_therapy physical_therapy rehabilitation vestibular_examination by DFellNeuroPT to the group Neurology Physical Therapy on 2009-02-12 22:20:43 as
	Prevalence of Deafness in Dogs Heterozygous or Homozygous for the Merle Allele. [My Copy] Journal of veterinary internal medicine / American College of Veterinary Internal Medicine (3 February 2009) by G M M. Strain, L A A. Clark, J M M. Wahl, A E E. Turner, K E E. Murphy posted to deafness merle by r_vdham on 2009-02-05 23:00:58 as
	Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness [My Copy] Nature Genetics, Vol. 41, No. 1. (30 November 2008), pp. 106-111. by Chantal Lagresle-Peyrou, Emmanuelle M. Six, Capucine Picard, et al.Frédéric Rieux-Laucat, Vincent Michel, Andrea Ditadi, Corinne D. Chappedelaine, Estelle Morillon, Françoise Valensi, Karen L. Simon-Stoos, James C. Mullikin, Lenora M. Noroski, Céline Besse, Nicolas M. Wulffraat, Alina Ferster, Manuel M. Abecasis, Fabien Calvo, Christine Petit, Fabio Candotti, Laurent Abel, Alain Fischer, Marina Cavazzana-Calvo posted to ak2 deafness by dchughes on 2009-01-07 14:45:11 as
	Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip [My Copy] European Journal of Human Genetics, Vol. aop, No. current. by Marianne Lévêque, Sandrine Marlin, Laurence Jonard, et al.Vincent Procaccio, Pascal Reynier, Patrizia Amati-Bonneau, Sylvain Baulande, Denis Pierron, Didier Lacombe, Françoise Duriez, Christine Francannet, Thierry Mom, Hubert Journel, Hélène Catros, Valérie Drouin-Garraud, Marie-Françoise Obstoy, Hélène Dollfus, Marie-Madeleine Eliot, Laurence Faivre, Christian Duvillard, Remy Couderc, Eréa-Noël Garabedian, Christine Petit, Delphine Feldmann, Françoise Denoyelle posted to a1555g a3243g a3397g a7445g c1494t c1537t chip deafness g12236a g15077a g7444a g8078a mitochip mtdna reqsequencing t669c t7510c t7511c by LHON on 2008-12-21 03:03:51 as along with 1 person giovanni
	The role of audition in infant babbling. [My Copy] Child development, Vol. 59, No. 2. (April 1988), pp. 441-449. by D. K. Oller, R. E. Eilers posted to articulation audition babbling canonical-babbling deafness vocal-development by awarlau on 2008-12-12 18:59:34 as
	Electrical stimulation of the auditory nerve. I. Correlation of physiological responses with cochlear status [My Copy] Hearing Research (June 1997), pp. 112-144. by R. K. Shepherd, E. Javel posted to auditory-nerve cochlear-histopathology cochlear-implant deafness electrical-stimulation by lumiste on 2008-11-18 14:32:19 as along with 1 person bdahl
	MtDNA mutations in maternally inherited diabetes: presence of the 3397 ND1 mutation previously associated with Alzheimer's and Parkinson's disease. [My Copy] Hereditas, Vol. 135, No. 1. (2001), pp. 65-70. by L. Cavelier, I. Erikson, M. Tammi, et al.P. Jalonen, E. Lindholm, E. Jazin, P. Smith, H. Luthman, U. Gyllensten posted to alzheimers deafness inherited_diabetes mtdna parkinsons by HEIRS to the group HEIRS Neurology on 2008-11-16 02:34:01 as along with 2 people and 3 groups Archaeogenetics tkandell HEIRS LIfespan and Ageing HEIRS - Environmental Illness Research HEIRS Diabetes, Insulin Resistance and Metabolic Syndrome Research
	Encoding, Rehearsal, and Recall in Signers and Speakers: Shared Network but Differential Engagement [My Copy] Cereb. Cortex, Vol. 18, No. 10. (1 October 2008), pp. 2263-2274. by D. Bavelier, A. J. Newman, M. Mukherjee, et al.P. Hauser, S. Kemeny, A. Braun, M. Boutla posted to american_sign_language deafness fmri short-term_memory sign_language by ybysk on 2008-10-28 01:02:03 as along with 1 person espressofiend
	Connexin 26 mutations in autosomal recessive deafness disorders: A review [My Copy] International Journal of Audiology, Vol. 46, No. 2. (2007), pp. 75-81. by Stacey A. Apps, Wayne A. Rankin, Andrew P. Kurmis posted to cx26 deafness gjb2 by shirleym on 2008-09-29 01:12:27 as
	Predicting candidate genes for human deafness disorders: a bioinformatics approach [My Copy] BMC Genomics, Vol. 7 (19 July 2006), 180. by Rami Alsaber, Christopher J. Tabone, Raj P. Kandpal posted to bioinformatics deafness by shirleym on 2008-09-18 16:10:59 as along with 1 person and 2 groups dchughes G4ID Genetics-of-Gambling
	On the Robustness of Vocal Development: An Examination of Infants With Moderate-to-Severe Hearing Loss and Additional Risk Factors [My Copy] J Speech Lang Hear Res, Vol. 50, No. 6. (1 December 2007), pp. 1425-1444. by Suneeti Nathani, Kimbrough D. Oller, Rebecca A. Neal posted to babbling deafness early-identification hearing-impairment infancy infant-vocalization som-project by awarlau on 2008-08-25 23:13:53 as
	From 1-word to 2-words with cochlear implant and cued speech: A case study [My Copy] Clinical Linguistics & Phonetics, Vol. 22, No. 7. (2008), pp. 491-508. by Ignacio Moreno-Torres, Santiago Torres posted to acquisition cochlear deafness implant language by imoreno on 2008-07-23 20:07:41 as
	Tune Deafness: Processing Melodic Errors Outside of Conscious Awareness as Reflected by Components of the Auditory ERP [My Copy] PLoS ONE, Vol. 3, No. 6. (11 June 2008), e2349. by Allen Braun, Joe Mcardle, Jennifer Jones, et al.Vladimir Nechaev, Christopher Zalewski, Carmen Brewer, Dennis Drayna posted to deafness tune by skumagai on 2008-06-11 13:40:29 as along with 1 person and 1 group sherdim EPLab
	More on compulsory registration of clinical trials: Complete clinical trial register is already reality for paediatrics [My Copy] BMJ, Vol. 330, No. 7489. (26 February 2005), 480. by M. Bonati, C. Pandolfini, Dec-Net C. Group posted to childhood countries deafness developing in by vezdolphin on 2008-06-11 11:48:06 as
	The implications of genetic testing for deafness. [My Copy] Ear and hearing, Vol. 24, No. 4. (August 2003), pp. 324-331. by K. S. Arnos posted to deafness ethical-issues genetic-testing by PredictER on 2008-04-08 22:08:17 as
	Self-Esteem Scores Among Deaf College Students: An Examination of Gender and Parents' Hearing Status and Signing Ability [My Copy] J. Deaf Stud. Deaf Educ., Vol. 8, No. 2. (1 April 2003), pp. 199-206. by Teresa V. Crowe posted to deafness by adamou on 2008-03-02 14:51:08 as along with 1 person cmy
	DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24. [My Copy] Am J Hum Genet, Vol. 68, No. 1. (January 2001), pp. 254-260. by C. C. Greene, P. M. McMillan, S. E. Barker, et al.P. Kurnool, M. I. Lomax, M. Burmeister, M. M. Lesperance posted to deafness dfna25 ube3b by dchughes on 2008-01-09 10:51:29 as
	Molecular characterization of a 12q22-q24 deletion associated with congenital deafness: Confirmation and refinement of the DFNA25 locus [My Copy] American Journal of Medical Genetics, Vol. 117A, No. 2. (2003), pp. 122-126. by Erwin Petek, Christian Windpassinger, Monika Mach, et al.Ludwig Rauter, Stephen W. Scherer, Klaus Wagner, Peter M. Kroisel posted to deafness dfna25 ube3b by dchughes on 2008-01-09 10:50:03 as
	Genotype–phenotype correlations for SLC26A4- related deafness [My Copy] Human Genetics, Vol. 122, No. 5. (21 December 2007), pp. 451-457. by Hela Azaiez, Tao Yang, Sai Prasad, et al.Jessica Sorensen, Carla Nishimura, William Kimberling, Richard Smith posted to deafness slc26a4 by dchughes on 2007-11-26 10:10:44 as
	Differential display and gene arrays to examine auditory plasticity. [My Copy] Hear Res, Vol. 147, No. 1-2. (September 2000), pp. 293-302. by M. I. Lomax, L. Huang, Y. Cho, T. L. Gong, R. A. Altschuler posted to deafness mir ube3b by dchughes on 2007-11-13 14:44:43 as along with 1 person Schmidtc
	Differential Gene Expression Following Noise Trauma in Birds and Mammals. [My Copy] Noise Health, Vol. 3, No. 11. (2001), pp. 19-35. by Margaret I. Lomax, Tzy-Wen W. Gong, Younsook Cho, et al.Li Huang, Seung-Ha H. Oh, Henry J. Adler, Yehoash Raphael, Richard A. Altschuler posted to deafness ear mir ube3b ubiquitin by dchughes on 2007-11-13 13:24:25 as along with 1 person suizan
	Congenital sensorineural deafness in dogs: a molecular genetic approach toward unravelling the responsible genes. [My Copy] Vet J, Vol. 169, No. 2. (March 2005), pp. 188-196. by S. G. Rak, O. Distl posted to deafness dog by dchughes on 2007-10-31 13:08:58 as along with 1 person melissa21
	Analysis of the 5' region of the canine PAX3 gene and exclusion as a candidate for Dalmatian deafness1 [My Copy] Animal Genetics, Vol. 34, No. 1. (2003), pp. 47-50. by B. Brenig, I. Pfeiffer, A. Jaggy, et al.I. Kathmann, M. Balzari, C. Gaillard, G. Dolf posted to deafness dog by dchughes on 2007-10-31 13:05:25 as
	Tectorial membrane stiffness gradients. [My Copy] Biophys J, Vol. 93, No. 6. (15 September 2007), pp. 2265-2276. by C. P. Richter, G. Emadi, G. Getnick, A. Quesnel, P. Dallos posted to deafness tectorin by dchughes on 2007-10-24 11:42:33 as
	Evaluation of ESPN, MYO3A, SLC26A5 and USH1C as candidates for hereditary non-syndromic deafness (congenital sensorineural deafness) in Dalmatian dogs [My Copy] Animal Genetics, Vol. 38, No. 5. (October 2007), pp. 533-534. by Mieskes, K., Distl, O. posted to deafness dog by dchughes on 2007-10-12 14:24:24 as
	<I>MYO15A</I> (<I>DFNB3</I>) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation [My Copy] American Journal of Medical Genetics Part A, Vol. 143A, No. 20. (2007), pp. 2382-2389. by Ersan Kalay, Abdullah Uzumcu, Elmar Krieger, et al.Refik Çaylan, Oya Uyguner, Melike Ulubil-Emiroglu, Hidayet Erdol, Hülya Kayserili, Gunter Hafiz, Nermin Ba&scedil;erer, Angelien J. G. M. Heister, Hans C. Hennies, Peter Nürnberg, Seher Ba&scedil;aran, Han G. Brunner, Cor W. R. J. Cremers, Ahmet Karaguzel, Bernd Wollnik, Hannie Kremer posted to deafness mir myo15a myosin by dchughes on 2007-09-27 11:10:17 as along with 1 person shirleym
	Mutant beta-spectrin 4 causes auditory and motor neuropathies in quivering mice. [My Copy] Nat Genet, Vol. 29, No. 1. (September 2001), pp. 61-65. by N. J. Parkinson, C. L. Olsson, J. L. Hallows, et al.J. McKee-Johnson, B. P. Keogh, K. Noben-Trauth, S. G. Kujawa, B. L. Tempel posted to deafness sptbn4 by N0131826 on 2007-09-24 12:09:13 as
	Novel syndrome of cataracts, retinitis pigmentosa, late onset deafness and sperm abnormalities: A new Usher syndrome subtype with X-linked inheritance? [My Copy] American Journal of Medical Genetics Part A, Vol. 143A, No. 14. (2007), pp. 1646-1652. by Mahdi Malekpour, Arash Shahidi, Mohammad, Masoud M. Zarandy posted to deafness male-fertility sperm sperm-morphology sperm-motility by dchughes on 2007-08-17 12:53:38 as along with 2 groups G4ID Genetics-of-Gambling
	Identification of three novel <I>TECTA</I> mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus [My Copy] American Journal of Medical Genetics Part A, Vol. 143A, No. 14. (2007), pp. 1623-1629. by Nicole C. Meyer, Fatemeh Alasti, Carla J. Nishimura, et al.Parisa Imanirad, Kimia Kahrizi, Yasser Riazalhosseini, Mahdi Malekpour, Nafiseh Kochakian, Payman Jamali, Guy Van Camp, Richard J. H. Smith, Hossein Najmabadi posted to deafness tecta tectorin by dchughes on 2007-08-17 12:52:37 as along with 1 person and 2 groups shirleym G4ID Genetics-of-Gambling
	Towards a Systems Biology of Mouse Inner Ear Organogenesis: Gene Expression Pathways, Patterns and Network Analysis [My Copy] Genetics (29 July 2007), genetics.107.078584. by Samin A. Sajan, Mark E. Warchol, Michael Lovett posted to inner-ear deafness by dchughes to the group G4ID on 2007-07-30 07:53:28 as along with 1 group Genetics-of-Gambling
	Audioprofiling identifies TECTA and GJB2-related deafness segregating in a single extended pedigree [My Copy] Clinical Genetics, Vol. 72, No. 2. (2007), pp. 130-137. by Nc Meyer, Cj Nishimura, S. Mcmordie, Rjh Smith posted to tectorin tecta deafness by dchughes to the group G4ID on 2007-07-28 09:46:42 as along with 1 group Genetics-of-Gambling
	A novel DFNA5 mutation does not cause hearing loss in an Iranian family [My Copy] Journal of Human Genetics, Vol. 52, No. 6. (26 June 2007), pp. 549-552. by Lut Van Laer, Nicole Meyer, Mahdi Malekpour, et al.Yasser Riazalhosseini, Mahdi Moghannibashi, Kimia Kahrizi, Ann Vandevelde, Fatemeh Alasti, Hossein Najmabadi, Guy Van Camp, Richard Smith posted to deafness by dchughes on 2007-06-01 10:10:41 as along with 2 groups G4ID Genetics-of-Gambling
	Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in Japanese [My Copy] Journal of Human Genetics, Vol. 52, No. 6. (26 June 2007), pp. 510-515. by Hisakuni Fukuoka, Yukihiko Kanda, Shuji Ohta, Shin-Ichi Usami posted to deafness by dchughes to the group Genetics-of-Gambling on 2007-06-01 10:09:20 as along with 1 group G4ID
	Molecular analysis of hearing loss associated with enlarged vestibular aqueduct in the mainland Chinese: a unique SLC26A4 mutation spectrum [My Copy] Journal of Human Genetics, Vol. 52, No. 6. (26 June 2007), pp. 492-497. by Hao Hu, Lingqian Wu, Yong Feng, et al.Qian Pan, Zhigao Long, Juan Li, Heping Dai, Kun Xia, Desheng Liang, Norio Niikawa, Jiahui Xia posted to deafness by dchughes to the group G4ID on 2007-06-01 10:08:21 as along with 1 group Genetics-of-Gambling
	Snaring Otoferlin's Role in Deafness [My Copy] Cell, Vol. 127, No. 2. (20 October 2006), pp. 258-260. by William M. Roberts posted to deafness by dchughes to the group Genetics-of-Gambling on 2007-03-01 10:21:48 as along with 1 group G4ID
	Sharpened cochlear tuning in a mouse with a genetically modified tectorial membrane [My Copy] Nature Neuroscience, Vol. 10, No. 2. (14 January 2007), pp. 215-223. by Ian J. Russell, Kevin P. Legan, Victoria A. Lukashkina, Andrei N. Lukashkin, Richard J. Goodyear, Guy P. Richardson posted to zp-domain tectorin deafness by dchughes on 2007-01-30 15:51:21 as along with 2 people and 2 groups shirleym thenose G4ID Genetics-of-Gambling
	Mitochondrial diabetes and its lessons for common Type 2 diabetes. [My Copy] Biochem Soc Trans, Vol. 34, No. Pt 5. (October 2006), pp. 819-823. by J. A. Maassen, L. M. 't Hart, G. M. Janssen, E. Reiling, J. A. Romijn, H. H. Lemkes posted to a3243g deafness melas midd mt non-obese trna type_2_diabetes by Archaeogenetics on 2006-11-14 18:06:25 as
	Maternally Inherited Diabetes and Deafness in a North American Kindred: Tips for Making the Diagnosis and Review of Unique Management Issues. [My Copy] J Clin Endocrinol Metab (3 October 2006) by Lois E E. Donovan, Naomi E E. Severin posted to a3423g co-q10 deafness melas midd mt non-obese trna type_ii_diabetes by Archaeogenetics on 2006-11-14 05:07:02 as
	Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy [My Copy] Nature Genetics, Vol. 38, No. 7. (25 June 2006), pp. 770-778. by Sedigheh Delmaghani, Francisco, Vincent Michel, et al.Michel Leibovici, Asadollah Aghaie, Uri Ron, Lut Van Laer, Nir Ben-Tal, Guy Van Camp, Dominique Weil, Francina Langa, Mark Lathrop, Paul Avan, Christine Petit posted to deafness by dchughes to the group G4ID on 2006-07-05 10:46:21 as along with 1 person and 1 group daforerog Genetics-of-Gambling
	Molecular cloning and domain structure of human myosin-VIIa, the gene product defective in Usher syndrome 1B. [My Copy] Genomics, Vol. 36, No. 3. (15 September 1996), pp. 440-448. by Z. Y. Chen, T. Hasson, P. M. Kelley, et al.B. J. Schwender, M. F. Schwartz, M. Ramakrishnan, W. J. Kimberling, M. S. Mooseker, D. P. Corey posted to deafness mir myosin-viia by dchughes to the group G4ID on 2006-07-04 17:21:35 as along with 1 group Genetics-of-Gambling
	Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure. [My Copy] Nat Genet, Vol. 29, No. 3. (November 2001), pp. 310-314. by R. Birkenhäger, E. Otto, M. J. Schürmann, et al.M. Vollmer, E. M. Ruf, I. Maier-Lutz, F. Beekmann, A. Fekete, H. Omran, D. Feldmann, D. V. Milford, N. Jeck, M. Konrad, D. Landau, N. V. Knoers, C. Antignac, R. Sudbrak, A. Kispert, F. Hildebrandt posted to bartter bsnd deafness failure kidney syndrome by Odi on 2006-06-01 13:56:11 as
	A Novel TECTA Mutation in a Dutch DFNA8/12 Family Confirms Genotype-Phenotype Correlation. [My Copy] J Assoc Res Otolaryngol (25 April 2006) by Rutger F. Plantinga, Arjan P. de Brouwer, Patrick L. Huygen, Henricus P. Kunst, Hannie Kremer, Cor W. Cremers posted to deafness tecta by dchughes to the group G4ID on 2006-04-26 14:40:35 as along with 1 group Genetics-of-Gambling

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tectorin	10
tecta	9
deaf	6
genetics	6
mir	6
mtdna	6
prenatal	6
alzheimers	5
inherited_diabetes	5
parkinsons	5
testing	5
bioinformatics	4
hair_cell	4
otoferlin	4
survey	4
ube3b	4
dog	3
inner-ear	3
male-fertility	3
myosin-viia	3
sperm	3
sperm-morphology	3
sperm-motility	3
vglut	3
zp-domain	3
a3243g	2
auditory-nerve	2
babbling	2
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cochlear-implant	2
dfna25	2
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mt	2
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physical_therapy	2
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transmitter_release	2
trna	2
vestibular_examination	2
a1555g	1
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ak2	1
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rab_proteins	1
sign-language	1
som-project	1
syndrome	1
t669c	1
t7510c	1
t7511c	1
tune	1
type_2_diabetes	1
type_ii_diabetes	1
usher_syndrome	1
vglut3	1
vocal-development	1
voices	1

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