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American Academy of Pediatrics Committee on Children with Handicaps. The physician and the deaf child.

Pediatrics

[No authors listed]
PMID: 4710448
Pediatrics. 1973 Jun;51(6):1100-1.

No abstract available.

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American Academy of Pediatrics Committee on Children with Handicaps. The physician and the deaf child. Pediatrics. 1973;51(6):1100-1
(1973). American Academy of Pediatrics Committee on Children with Handicaps. The physician and the deaf child. Pediatrics, 51(6), 1100-1.
"American Academy of Pediatrics Committee on Children with Handicaps. The physician and the deaf child." Pediatrics vol. 51,6 (1973): 1100-1.
American Academy of Pediatrics Committee on Children with Handicaps. The physician and the deaf child. Pediatrics. 1973 Jun;51(6):1100-1. PMID: 4710448.
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[Deafness in children].

Revue medicale de Bruxelles

Mansbach AL.
PMID: 17091887
Rev Med Brux. 2006 Sep;27(4):S250-7.

Considerable progress has been achieved these last years in the field of hearing screening, diagnosis of hearing loss in children and rehabilitation methods. It is now generally accepted that every child with hearing impairment must receive intervention before six...

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Mansbach AL. La surdité de l'enfant. [Deafness in children]. Rev Med Brux. 2006;27(4):S250-7
Mansbach, A. L. (2006). La surdité de l'enfant. [Deafness in children]. Revue medicale de Bruxelles, 27(4), S250-7.
Mansbach, A L. "La surdité de l'enfant." [Deafness in children]. Revue medicale de Bruxelles vol. 27,4 (2006): S250-7.
Mansbach AL. La surdité de l'enfant. [Deafness in children]. Rev Med Brux. 2006 Sep;27(4):S250-7. French. PMID: 17091887.
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[Improving the diagnosis and treatment skills by establishing new platform of gene diagnosis].

Zhonghua yi xue za zhi

Ou QS, Cheng ZJ.
PMID: 20137611
Zhonghua Yi Xue Za Zhi. 2009 Sep 29;89(36):2523-5.

No abstract available.

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Ou QS, Cheng ZJ. [Improving the diagnosis and treatment skills by establishing new platform of gene diagnosis]. Zhonghua Yi Xue Za Zhi. 2009;89(36):2523-5
Ou, Q. S., & Cheng, Z. J. (2009). [Improving the diagnosis and treatment skills by establishing new platform of gene diagnosis]. Zhonghua yi xue za zhi, 89(36), 2523-5.
Ou, Qi-shui, and Cheng, Zu-jian. "[Improving the diagnosis and treatment skills by establishing new platform of gene diagnosis]." Zhonghua yi xue za zhi vol. 89,36 (2009): 2523-5.
Ou QS, Cheng ZJ. [Improving the diagnosis and treatment skills by establishing new platform of gene diagnosis]. Zhonghua Yi Xue Za Zhi. 2009 Sep 29;89(36):2523-5. Chinese. PMID: 20137611.
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Deafness in young children.

Nursing mirror and midwives journal

Reading PV.
PMID: 5175634
Nurs Mirror Midwives J. 1966 Feb 04;6-8.

No abstract available.

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Reading PV. Deafness in young children. Nurs Mirror Midwives J. 1966;6-8
Reading, P. V. (1966). Deafness in young children. Nursing mirror and midwives journal, 6-8.
Reading, P V. "Deafness in young children." Nursing mirror and midwives journal vol. (1966): 6-8.
Reading PV. Deafness in young children. Nurs Mirror Midwives J. 1966 Feb 04;6-8. PMID: 5175634.
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The hard of hearing child.

The Medical journal of Australia

Bulteau V.
PMID: 5576830
Med J Aust. 1971 May 08;1(19):1034.

No abstract available.

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Bulteau V. The hard of hearing child. Med J Aust. 1971;1(19):1034
Bulteau, V. (1971). The hard of hearing child. The Medical journal of Australia, 1(19), 1034.
Bulteau, V. "The hard of hearing child." The Medical journal of Australia vol. 1,19 (1971): 1034.
Bulteau V. The hard of hearing child. Med J Aust. 1971 May 08;1(19):1034. PMID: 5576830.
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[The doctor and the deaf child: early detection, diagnosis and rehabilitation].

L'union medicale du Canada

Desjardins R.
PMID: 549237
Union Med Can. 1979 Nov;108(11):1326-7.

No abstract available.

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Desjardins R. Le médecin et l'enfant sourd: dépistage précoce, diagnostic et réadaptation. [The doctor and the deaf child: early detection, diagnosis and rehabilitation]. Union Med Can. 1979;108(11):1326-7
Desjardins, R. (1979). Le médecin et l'enfant sourd: dépistage précoce, diagnostic et réadaptation. [The doctor and the deaf child: early detection, diagnosis and rehabilitation]. L'union medicale du Canada, 108(11), 1326-7.
Desjardins, R. "Le médecin et l'enfant sourd: dépistage précoce, diagnostic et réadaptation." [The doctor and the deaf child: early detection, diagnosis and rehabilitation]. L'union medicale du Canada vol. 108,11 (1979): 1326-7.
Desjardins R. Le médecin et l'enfant sourd: dépistage précoce, diagnostic et réadaptation. [The doctor and the deaf child: early detection, diagnosis and rehabilitation]. Union Med Can. 1979 Nov;108(11):1326-7. French. PMID: 549237.
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Towards integrated practices in early detection of and intervention for deaf and hard of hearing children.

American annals of the deaf

Storbeck C, Calvert-Evers J.
PMID: 18807406
Am Ann Deaf. 2008;153(3):314-21. doi: 10.1353/aad.0.0047.

It is well documented that undetected hearing loss can have a profound effect on a child's holistic development, including communicative, language and cognitive development. It is crucial therefore that deaf and hard of hearing infants are detected as early...

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Storbeck C, Calvert-Evers J. Towards integrated practices in early detection of and intervention for deaf and hard of hearing children. Am Ann Deaf. 2008;153(3):314-21doi: 10.1353/aad.0.0047.
Storbeck, C., & Calvert-Evers, J. (2008). Towards integrated practices in early detection of and intervention for deaf and hard of hearing children. American annals of the deaf, 153(3), 314-21. https://doi.org/10.1353/aad.0.0047
Storbeck, Claudine, and Calvert-Evers, Jennifer. "Towards integrated practices in early detection of and intervention for deaf and hard of hearing children." American annals of the deaf vol. 153,3 (2008): 314-21. doi: https://doi.org/10.1353/aad.0.0047
Storbeck C, Calvert-Evers J. Towards integrated practices in early detection of and intervention for deaf and hard of hearing children. Am Ann Deaf. 2008;153(3):314-21. doi: 10.1353/aad.0.0047. PMID: 18807406.
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Pure word deafness and frontotemporal dementia.

European journal of neurology

Boban M.
PMID: 17880554
Eur J Neurol. 2007 Oct;14(10):e3; author reply e4. doi: 10.1111/j.1468-1331.2007.01899.x.

No abstract available.

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Boban M. Pure word deafness and frontotemporal dementia. Eur J Neurol. 2007;14(10):e3; author reply e4doi: 10.1111/j.1468-1331.2007.01899.x.
Boban, M. (2007). Pure word deafness and frontotemporal dementia. European journal of neurology, 14(10), e3; author reply e4. https://doi.org/10.1111/j.1468-1331.2007.01899.x
Boban, M. "Pure word deafness and frontotemporal dementia." European journal of neurology vol. 14,10 (2007): e3; author reply e4. doi: https://doi.org/10.1111/j.1468-1331.2007.01899.x
Boban M. Pure word deafness and frontotemporal dementia. Eur J Neurol. 2007 Oct;14(10):e3; author reply e4. doi: 10.1111/j.1468-1331.2007.01899.x. PMID: 17880554.
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[Etiological diagnosis of deafmutism].

Revue medicale de la Suisse romande

DE REYNIER JP, DUPONT-HUBER M.
PMID: 13668268
Rev Med Suisse Romande. 1959 May;79(5):283-9.

No abstract available.

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DE REYNIER JP, DUPONT-HUBER M. A propos du diagnostic étiologique de la surdi-mutité. [Etiological diagnosis of deafmutism]. Rev Med Suisse Romande. 1959;79(5):283-9
DE REYNIER, J. P., & DUPONT-HUBER, M. (1959). A propos du diagnostic étiologique de la surdi-mutité. [Etiological diagnosis of deafmutism]. Revue medicale de la Suisse romande, 79(5), 283-9.
DE REYNIER, J P, and DUPONT-HUBER, M. "A propos du diagnostic étiologique de la surdi-mutité." [Etiological diagnosis of deafmutism]. Revue medicale de la Suisse romande vol. 79,5 (1959): 283-9.
DE REYNIER JP, DUPONT-HUBER M. A propos du diagnostic étiologique de la surdi-mutité. [Etiological diagnosis of deafmutism]. Rev Med Suisse Romande. 1959 May;79(5):283-9. French. PMID: 13668268.
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Investigation of the child with permanent hearing impairment.

Archives of disease in childhood. Education and practice edition

Ardle BM, Bitner-Glindzicz M.
PMID: 20145014
Arch Dis Child Educ Pract Ed. 2010 Feb;95(1):14-23. doi: 10.1136/adc.2008.150987.

No abstract available.

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Ardle BM, Bitner-Glindzicz M. Investigation of the child with permanent hearing impairment. Arch Dis Child Educ Pract Ed. 2010;95(1):14-23doi: 10.1136/adc.2008.150987.
Ardle, B. M., & Bitner-Glindzicz, M. (2010). Investigation of the child with permanent hearing impairment. Archives of disease in childhood. Education and practice edition, 95(1), 14-23. https://doi.org/10.1136/adc.2008.150987
Ardle, Breege Mac, and Bitner-Glindzicz, Maria. "Investigation of the child with permanent hearing impairment." Archives of disease in childhood. Education and practice edition vol. 95,1 (2010): 14-23. doi: https://doi.org/10.1136/adc.2008.150987
Ardle BM, Bitner-Glindzicz M. Investigation of the child with permanent hearing impairment. Arch Dis Child Educ Pract Ed. 2010 Feb;95(1):14-23. doi: 10.1136/adc.2008.150987. PMID: 20145014.
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[Genetic hearing loss].

Presse medicale (Paris, France : 1983)

Tanaka-Ouyang L, Marlin S, Nevoux J.
PMID: 29089220
Presse Med. 2017 Nov;46(11):1089-1096. doi: 10.1016/j.lpm.2017.09.005. Epub 2017 Oct 28.

Deafness is the most common sensory disability in developed countries affecting more than 2 births in 1000. Eighty percent of congenital deafness is genetic. Universal newborn hearing screening has been in place since 2012 in France. All genetic hearing...

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Tanaka-Ouyang L, Marlin S, Nevoux J. Les surdités d’origine génétique. [Genetic hearing loss]. Presse Med. 2017;46(11):1089-1096doi: 10.1016/j.lpm.2017.09.005.
Tanaka-Ouyang, L., Marlin, S., & Nevoux, J. (2017). Les surdités d’origine génétique. [Genetic hearing loss]. Presse medicale (Paris, France : 1983), 46(11), 1089-1096. https://doi.org/10.1016/j.lpm.2017.09.005
Tanaka-Ouyang, Lei, et al. "Les surdités d’origine génétique." [Genetic hearing loss]. Presse medicale (Paris, France : 1983) vol. 46,11 (2017): 1089-1096. doi: https://doi.org/10.1016/j.lpm.2017.09.005
Tanaka-Ouyang L, Marlin S, Nevoux J. Les surdités d’origine génétique. [Genetic hearing loss]. Presse Med. 2017 Nov;46(11):1089-1096. doi: 10.1016/j.lpm.2017.09.005. Epub 2017 Oct 28. French. PMID: 29089220.
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Showing 1 to 11 of 11 entries