يعرض 1 - 10 نتائج من 353 نتيجة بحث عن '"Tropitzsch A"', وقت الاستعلام: 1.16s تنقيح النتائج
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    دورية أكاديمية
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    دورية أكاديمية
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    دورية أكاديمية
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    مؤتمر

    المصدر: Abstract- und Posterband - 93. Jahresversammlung der Deutschen Gesellschaft für HNO-Heilkunde, Kopf- und Hals-Chirurgie e.V., Bonn Interface - Fokus Mensch im Zeitalter der technisierten Medizin ; Laryngo-Rhino-Otologie ; ISSN 1438-8685

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    مؤتمر

    المصدر: Abstract- und Posterband - 93. Jahresversammlung der Deutschen Gesellschaft für HNO-Heilkunde, Kopf- und Hals-Chirurgie e.V., Bonn Interface - Fokus Mensch im Zeitalter der technisierten Medizin ; Laryngo-Rhino-Otologie ; ISSN 1438-8685

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    دورية أكاديمية
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    دورية أكاديمية
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    دورية أكاديمية
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    مؤتمر

    المصدر: 37. Wissenschaftliche Jahrestagung der Deutschen Gesellschaft für Phoniatrie und Pädaudiologie (DGPP); 20210917-20210918; sine loco [digital]; DOCV6 /20211028/

    مصطلحات موضوعية: ddc: 610

    العلاقة: Cunningham LL, Tucci DL. Hearing Loss in Adults. N Engl J Med. 2017;377(25):2465-73. DOI:10.1056/NEJMra1616601; Fuller C, Mallinckrodt L, Maat B, Baskent D, Free R. Music and quality of life in early-deafened late-implanted adult cochlear implant users. Otol Neurotol. 2013;34(6):1041-7. DOI:10.1097/MAO.0b013e31828f47dd; GBD 2019 Hearing Loss Collaborators. Hearing loss prevalence and years lived with disability, 1990-2019: findings from the Global Burden of Disease Study 2019. Lancet. 2021;397(10278):996-1009. DOI:10.1016/S0140-6736(21)00516-X; Korver AM, Smith RJ, Van Camp G, Schleiss MR, Bitner-Glindzicz MA, Lustig LR, Usami SI, Boudewyns AN. Congenital hearing loss. Nat Rev Dis Primers. 2017;3:16094. DOI:10.1038/nrdp.2016.94; Oza AM, DiStefano MT, Hemphill SE, Cushman BJ, Grant AR, Siegert RK, Shen J, Chapin A, Boczek NJ, Schimmenti LA, Murry JB, Hasadsri L, Nara K, Kenna M, Booth KT, Azaiez H, Griffith A, Avraham KB, Kremer H, Rehm HL, Amr SS, Abou Tayoun AN; ClinGen Hearing Loss Clinical Domain Working Group. Expert specification of the ACMG/AMP variant interpretation guidelines for genetic hearing loss. Hum Mutat. 2018;39(11):1593-613. DOI:10.1002/humu.23630; Parker M, Bitner-Glindzicz M. Genetic investigations in childhood deafness. Arch Dis Child. 2015;100(3):271-8. DOI:10.1136/archdischild-2014-306099; Sharma A, Dorman MF, Spahr AJ. A sensitive period for the development of the central auditory system in children with cochlear implants: implications for age of implantation. Ear Hear. 2002;23(6):532-9. DOI:10.1097/00003446-200212000-00004; Shearer AE, Hildebrand MS, Smith RJH. Hereditary hearing loss and deafness overview. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, Amemiya A, editors. GeneReviews((R)). Seattle, WA: University of Washington; 2017. p. 1993-2021.; Shearer AE, Shen J, Amr S, Morton CC, Smith RJ; Newborn Hearing Screening Working Group of the National Coordinating Center for the Regional Genetics Networks. A proposal for comprehensive newborn hearing screening to improve identification of deaf and hard-of-hearing children. Genet Med. 2019;21(11):2614-30. DOI:10.1038/s41436-019-0563-5; Sloan-Heggen CM, Bierer AO, Shearer AE, Kolbe DL, Nishimura CJ, Frees KL, Ephraim SS, Shibata SB, Booth KT, Campbell CA, Ranum PT, Weaver AE, Black-Ziegelbein EA, Wang D, Azaiez H, Smith RJH. Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss. Hum Genet. 2016;135(4):441-50. DOI:10.1007/s00439-016-1648-8; Van Camp G, Smith RJH. Hereditary Hearing Loss Homepage; 2021. Available from: https://hereditaryhearingloss.orgTest; Vona B, Müller T, Nanda I, Neuner C, Hofrichter MA, Schröder J, Bartsch O, Läßig A, Keilmann A, Schraven S, Kraus F, Shehata-Dieler W, Haaf T. Targeted next-generation sequencing of deafness genes in hearing-impaired individuals uncovers informative mutations. Genet Med. 2014;16(12):945-53. DOI:10.1038/gim.2014.65; http://dx.doi.org/10.3205/21dgpp23Test; http://nbn-resolving.de/urn:nbn:de:0183-21dgpp233Test; http://www.egms.de/en/meetings/dgpp2021/21dgpp23.shtmlTest

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    مؤتمر

    المصدر: 37. Wissenschaftliche Jahrestagung der Deutschen Gesellschaft für Phoniatrie und Pädaudiologie (DGPP); 20210917-20210918; sine loco [digital]; DOCP16 /20211028/

    مصطلحات موضوعية: ddc: 610

    العلاقة: Apaydin F, Bereketoglu M, Turan O, Hribar K, Maassen MM, Günhan O, Zenner HP, Pfister M. Waardenburg-Syndrom. Eine heterogene Erkrankung mit variabler Penetranz [Waardenburg syndrome. A heterogenic disorder with variable penetrance]. HNO. 2004;52(6):533-7. DOI:10.1007/s00106-003-0938-3; Azaiez H, Booth KT, Ephraim SS, Crone B, Black-Ziegelbein EA, Marini RJ, Shearer AE, Sloan-Heggen CM, Kolbe D, Casavant T, Schnieders MJ, Nishimura C, Braun T, Smith RJH. Genomic Landscape and Mutational Signatures of Deafness-Associated Genes. Am J Hum Genet. 2018;103(4):484-97. DOI:10.1016/j.ajhg.2018.08.006; Parker M, Bitner-Glindzicz M. Genetic investigations in childhood deafness. Arch Dis Child. 2015;100(3):271-8. DOI:10.1136/archdischild-2014-306099; Read AP, Newton VE. Waardenburg syndrome. J Med Genet. 1997;34(8):656-65. DOI:10.1136/jmg.34.8.656; Song J, Feng Y, Acke FR, Coucke P, Vleminckx K, Dhooge IJ. Hearing loss in Waardenburg syndrome: a systematic review. Clin Genet. 2016;89(4):416-25. DOI:10.1111/cge.12631; http://dx.doi.org/10.3205/21dgpp31Test; http://nbn-resolving.de/urn:nbn:de:0183-21dgpp316Test; http://www.egms.de/en/meetings/dgpp2021/21dgpp31.shtmlTest