Results 261 to 270 of about 365,870 (389)

Critical Management Studies: From One‐Dimensional Critique to Three‐Dimensional Scepticism

Journal of Management Studies, EarlyView.
Abstract Critical Management Studies (CMS) has largely relied on one‐dimensional critique which focus on the negation of a dominant social order. This strong focus has made the field increasingly stale and preoccupied with standard objects for critique.
Mats Alvesson, André Spicer
wiley   +1 more source

Genetic and Environmental Factors Shaping Hearing Loss: Xenobiotics, Mechanisms and Translational Perspectives. [PDF]

J Xenobiot
Esteves F, Caria H.
europepmc   +1 more source

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.

American Journal of Human Genetics, 2001
Julie M. Bork, Linda M Peters, S. Riazuddin, S. Riazuddin, S. Bernstein, Zubair M. Ahmed, Zubair M. Ahmed, S. Ness, R. Polomeno, Arabandi Ramesh, Arabandi Ramesh, M. Schloss, C. R. S. Srisailpathy, C. R. S. Srisailpathy, S. Wayne, S. Bellman, Dilip Desmukh, Zahoor Ahmed, Shaheen N. Khan, V. Kaloustian, X. C. Li, A. Lalwani, Sheikh Riazuddin, M. Bitner-Glindzicz, W. Nance, Xue Liu, G. Wistow, Richard J. H. Smith, A. J. Griffith, E. Wilcox, T. Friedman, R. Morell   +31 more
semanticscholar   +1 more source

The writing of deaf students: a study about the teaching and learning of the Portuguese language

, 2023
Samara Machado Pereira
openalex   +1 more source

Distal Renal Tubular Acidosis With Sensorineural Deafness in a Saudi Female: A Case Report of an ATP6V1B1 Mutation in a Consanguineous Family. [PDF]

Cureus
Alrasheed A, Alyabis N, Alrasheed SA, Alrasheed R.   +3 more
europepmc   +1 more source

Retinitis pigmentosa and sensorineural deafness associated with a <i>de novo DHX16</i> mutation: case report. [PDF]

Front Genet
Wang L, Gao J, Sun M, Fan L, Wang S, Li X, Gu S, Han B.   +7 more
europepmc   +1 more source

With Their Own Hands: A Community Lawyering Approach to Improving Law Enforcement Practices in the Deaf Community [PDF]

, 2011
McAnnany, Kelly, Shah, Aditi Kothekar
core   +2 more sources

Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosity. [PDF]

Proc Natl Acad Sci U S A
Riahi Z, Boucher S, Abdi S, Wong Jun Tai F, Singh-Estivalet A, Aghaie A, Niasme-Grare M, Hardelin JP, Behlouli A, Dahmani M, Talbi S, Bouyacoub Y, Mkaouar R, Charfeddine C, Amalou G, Bakhchane A, Bousfiha A, Salime S, Elrharchi S, Salame M, Hadrami M, Boussaty E, Charoute H, Detsouli M, Snoussi K, Rouba H, Hachmi HE, Veten F, Meiloud G, Marrakchi J, Zainine R, Chahed H, Besbes G, Trabelsi M, Mrad R, Kraoua I, Ouhab S, Djennaoui D, Boudjenah F, Chouery E, Mustapha M, Houmeida A, Barakat A, Khodja FA, Makrelouf M, Zenati A, Beltaief N, Abdelhak S, Petit C, Bonnet C.   +49 more
europepmc   +1 more source

Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness.

New England Journal of Medicine, 1998
R. Morell, H. J. Kim, L. Hood, L. Goforth, K. Friderici, R. Fisher, G. Van Camp, C. Berlin, C. Oddoux, H. Ostrer, B. Keats, T. Friedman, T. S. Agustin, J. Dumon   +13 more
semanticscholar   +1 more source

Shared Decision‐Making for Genetic Tests With Children and Young People With Intellectual Disability: Considerations for Inclusive, Person‐Centred, and Respectful Approaches

Journal of Paediatrics and Child Health, EarlyView.
ABSTRACT With over 1000 genetic causes for neurodevelopmental conditions, genetic testing (including exome sequencing) is recommended for people with intellectual disability to guide clinical care, as well as improve empowerment, connection to peer supports, and access to funded therapies.
Manjekah Dunn, Iva Strnadová, Michelle Tso, Claudia Pantoja Mardones, Jackie Boyle, Erica Longhurst, Julie Loblinzk Refalo, Skie Sarfaraz, Bronwyn Terrill, Elizabeth Emma Palmer   +9 more
wiley   +1 more source