Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Bulantrisna Djelantik"'
Autor:
Kuswandewi Mutyara, Riskiana Djamin, Widya W. Hartanto, Cissy B. Kartasasmita, Tri Mulyani, Sutji Pratiwi Rahardjo, Bulantrisna Djelantik, Abla Ghanie, Anna Mailasari Kusuma Dewi, Ratna Anggraeni, Eric A. F. Simões, Suprihati Winarto, Erica Lukman, Denny Satria Utama, Eka Putra Setiawan, Phyllis Carosone-Link
Publikováno v:
International journal of pediatric otorhinolaryngology. 125
Objective There are scant recent studies from low middle-income countries that investigate the impact of otitis media (OM) on hearing loss (HL) in school children. Methods This was a prospective epidemiological survey conducted by otorhinolaryngologi
Publikováno v:
American journal of medical genetics : part A
Although hereditary hearing loss is a very heterogeneous disorder, variants in one gene, GJB2 (connexin 26), account for up to 50% of autosomal recessive nonsyndromal sensorineural hearing loss in most populations. This study investigates the contrib
Autor:
Sutji Pratiwi Rahardjo, Eka Putra Setiawan, Kuswandewi Mutyara, Suprihati Asmuni, Widya W. Hartanto, Chintriany Hardiningsih, Tri Mulyani, Cissy B. Kartasasmita, Abla Ghanie, Denny Satria Utama, Erica Lukman, Eric A. F. Simões, Bulantrisna Djelantik, Riskiana Djamin, Ratna Anggraeni, Rery Budiarti, Phyllis Carosone-Link
Publikováno v:
The Pediatric infectious disease journal. 33(10)
BACKGROUND Although the epidemiology of otitis media is well-known in industrialized countries, the extent of otitis media in developing Asian countries, especially in south East Asia is not well studied. METHODS To define the burden of otitis media
Autor:
P. van Hauwe, Frank Declau, Richard J.H. Smith, Henri A. M. Marres, M. van Ewijk, G. Van Camp, Cor W. R. J. Cremers, P. Van de Heyning, D. van Velzen, Isabelle Schatteman, Paul Coucke, P.H.G.M. Willems, J. B. Kenyon, J. Meyers, Bulantrisna Djelantik, Shelley D. Smith, Henricus P. M. Kunst
Publikováno v:
Genomics : International Journal of Gene Mapping and Nucleotide Sequencing Emphasizing Analyses of the Human and Other Complex Genomes, 70-74
STARTPAGE=70;ENDPAGE=74;ISSN=0888-7543;TITLE=Genomics : International Journal of Gene Mapping and Nucleotide Sequencing Emphasizing Analyses of the Human and Other Complex Genomes
Genomics : International Journal of Gene Mapping and Nucleotide Sequencing Emphasizing Analyses of the Human and Other Complex Genomes, 41, 1, pp. 70-83
Genomics : International Journal of Gene Mapping and Nucleotide Sequencing Emphasizing Analyses of the Human and Other Complex Genomes, 41, pp. 70-74
Genomics : International Journal of Gene Mapping and Nucleotide Sequencing Emphasizing Analyses of the Human and Other Complex Genomes, 41, 70-83
Genomics: international journal of gene mapping and nucleotide sequencing
STARTPAGE=70;ENDPAGE=74;ISSN=0888-7543;TITLE=Genomics : International Journal of Gene Mapping and Nucleotide Sequencing Emphasizing Analyses of the Human and Other Complex Genomes
Genomics : International Journal of Gene Mapping and Nucleotide Sequencing Emphasizing Analyses of the Human and Other Complex Genomes, 41, 1, pp. 70-83
Genomics : International Journal of Gene Mapping and Nucleotide Sequencing Emphasizing Analyses of the Human and Other Complex Genomes, 41, pp. 70-74
Genomics : International Journal of Gene Mapping and Nucleotide Sequencing Emphasizing Analyses of the Human and Other Complex Genomes, 41, 70-83
Genomics: international journal of gene mapping and nucleotide sequencing
Thus far, 13 genes for autosomal dominant hearing loss have been localized to specific chromosomal regions, but none of the genes has been cloned. Only a single family has been linked to each of these loci, with the exception of DFNA2. DFNA2 was orig
Publikováno v:
Hearing Impairment ISBN: 9784431223269
The far reaching implications of hearing loss, both in respect of development of communication skills, as well as in social, economic and quality of life, warrants an urgent need to highlight the magnitude and severity of the problem. Although it is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::efdb518dd2f7204e6f5e7c2767366ef0
https://doi.org/10.1007/978-4-431-68397-1_62
https://doi.org/10.1007/978-4-431-68397-1_62
Autor:
Frank Declau, Henricus Kunst, Bulantrisna Djelantik, R.J.H. Ensink, P.M. Kelley, Paul Coucke, Henri A. Marres, van Peter Hauwe, C.W.R.J. Cremers, van Guy Camp, Shelley D. Smith, van de Paul Heyning
Publikováno v:
Nature Genetics, 21, 3, pp. 263
Nature Genetics, 21, 263
ResearcherID
Nature genetics
Nature Genetics, 21, 263
ResearcherID
Nature genetics
Item does not contain fulltext
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e3063363d73722559cd36f14a5b302f
https://hdl.handle.net/2066/188704
https://hdl.handle.net/2066/188704
Publikováno v:
Asian Theatre Journal. 22:361-362
Publikováno v:
Community Ear and Hearing Health. 7:1
Autor:
Genoveva Noirury Nostalgia
Publikováno v:
Urban: Jurnal Seni Urban. 1:157-180
This paper is an analysis of the creative process done by Retno Maruti when making his dance work. I focus on Maruti’s work, titled Legong Calonarang. This work is a collaboration between Retno Maruti and Bulantrisna Djelantik; it combines bedhaya,
Autor:
Anggraeni, Ratna, Hartanto, Widya W., Djelantik, Bulantrisna, Ghanie, Abla, Utama, Denny S., Setiawan, Eka P., Lukman, Erica, Hardiningsih, Chintriany, Asmuni, Suprihati, Budiarti, Rery, Rahardjo, Sutji Pratiwi, Djamin, Riskiana, Mulyani, Tri, Mutyara, Kuswandewi, Carosone-Link, Phyllis, Kartasasmita, Cissy B., Simões, Eric A. F.
Publikováno v:
Pediatric Infectious Disease Journal; Oct2014, Vol. 33 Issue 10, p1010-1015, 6p